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Much Ado About Nothing - 2013
Come to see 2 nights of one acts directed by the students of the Winter 2014 Directing II Class!
Where? At the Louis Armstrong Theatre - on stage!
When? April 23 and 24 at 7.30 pm
How Much are the Tickets? IT'S FREE!!
How can you miss it? YOU CAN'T !!!
April 23 - 7.30 pm:
Two Truths And A Lie by Mary Michael Wagner (directed by Amanda Furstenberg)
Land of the Dead by Neil LaBute (directed by Cody Robison)
Creep by James Christy (directed by Sammie Chaness)
Crazy Eights by David Lindsay-Abaire (directed by Kerissa Bradley)
April 24, 7,30 pm:
Guys by Robb Badlam (directed by Megan Prangley)
Great to See You by Theresa Rebeck (directed by Courtney Jenkins)
Baby Food by David Lindsay-Abaire (directed by Jessica Utter)
Counting to Three by Joe Anson (directed by Matt Fowler)
We are pleased to announce our 2014 - 2015 season! More details to come.
Grand Valley Shakespeare Festival presents
The Comedy of Errors
Sept. 26 to Oct. 5, 2014
Theatre at Grand Valley presents
The Women of Lockerbie
November 2014
Grand Valley Opera Theatre presents
February 2015
Theatre at Grand Valley presents
Restoration Comedy
March 2015
Plus our traveling Shakespeare troupe,
Bard To Go - visiting area high schools
ReACT! - our peer educational performing group
PS Series Shows - all student production
Dates and times yet to come!
The School of Communications and its major programs, in agreement with the university's mission, educates students to shape their lives, their professions, and their societies. The School of Communications curricula strive to accomplish this within a framework that integrates liberal and professional education.
The Theatre major provides quality undergraduate education and training in theatre within a traditional humanistic liberal arts environment.
2014 Will Power Summer Camp
Session 1:
July 14-18 - Hamlet: Ghosts and Graveyards
1st-3rd graders from 9:00am to noon
4th - 6th graders from 1:00pm to 4:00pm
Session 2:
July 21-25 - Twelfth Night: Tricks and Disguises
K-3rd graders from 9:00am to noon
4th - 6th graders from 1:00pm to 4:00pm
Click here for a printable registration form and to pay by check.
Click here to register on-line and pay with check or credit/debit cards.
Let your child expand their imagination, discover Shakespeare and get some Will Power this summer!
Grand Valley Shakespeare Festival is introducing its second summer education program Will Power!
Featuring teaching artists from Pigeon Creek Shakespeare Company, this week long day camp will focus on the process of drama. Using Shakespeares works, your camper will learn about theatre concepts and storytelling while having fun!
Please click here for pictures from last year's camp!
Please click here to read about the camp!
Click on the following links to find more information about other GVSU opportunities:
Grand Valley Shakespeare Festival
Grand Valley Shakespeare Conference - Pedagogy and Performance
Bard To Go, the Shakespeare Touring Troupe
ReACT! GVSU's Peer Theatre Education
Theatre at Grand Valley Faculty and Staff
Upcoming Auditions, Workshops, and Call for Actors
GVSU Department of Music and Dance
To read about Bard to Go's March 2014 trip to Genova, Italy and Prague, Czech Republic, please click here!
March 14 - 16, Alaine Alldaffer, Casting Director for Playwright Horizon, held two free workshops and a performance to culminate the workshops.
Alaine Alldaffer & GVSU Theatre students, March 2014
Last year Erin went to L.A. for two months and took a couple workshops: The first was at the Atlantic Theater School. She was among 9 people learning their technique from founding members.
Mary Tejeda (Theatre, 08) has been really busy promoting a season of new plays as the Educational/Outreach intern at Premiere Stages outside of New York City. Her work there also included marketing/PR and being the house manager for productions. She ran p
Katrina is currently starting her second season with The Arvada Center for Arts and Humanities, a LORT B equity theatre. She works in the costume shop as a costume crafts artisan and in wardrobe running shows. (Soon, hopefully she'll be able to announce t
In 2010-11, she served as the Stage Management Intern at Lexington Childrens Theatre (LCT) in Lexington, Kentucky. She fell in love with the theatre and the staff and so after taking the summer off, she returned this season (2011-12).
February 20, 2014
Five students affiliate with Theatre have been nominated for the 2013 - 2014 I Am Grand Valley Leadership Award.
February 12, 2014
Five students from GVSUs Theatre program were selected as nominees for The Kennedy Centers annual Irene Ryan Scholarships.
August 12, 2013
For two sessions in July, GVSU will host its third annual WILL POWER SUMMER CAMP and host dozens of local children. Link to our Facebook page and see more photos and comments! https://www.facebook.com/GVSUShakespeareFestivalWillPow
Let your children expand their imaginations, discover Shakespeare, and get some Will Power this summer! Grand Valley Shakespeare Festival is pleased to offer its summer education program Will Power....
Let your children expand their imaginations, discover Shakespeare, and get some Will Power this summer! Grand Valley Shakespeare Festival is pleased to offer its summer education program Will Power....


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"My son has gained self-control and self-esteem. I feel he is better for the rest of his life for being at Children's Care."
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subset: commoncrawl


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I recently bought a new (old and used) mountain bike frame at the Midwest bike show. ĀToday was its first real test on the trail. ĀI've ridden it by myself a couple of times on gravel and ran into a major problem; Āits hard to keep a chain on a 1×9 setup. ĀWith no front derailluer to keep it in place every large bump wanted to bounce it off the ring. ĀI built my own little chain catcher from spare parts and it helped, but wasn't exactly right.
I decided to skip the front chainring, derailuer and shifter because I've found that I wasn't using the granny gear very much on my mountain bike anymore, plus I'd be lying if I didn't mention the fact I wanted to save some weight. ĀYesterday I mounted my new Shimano HG-61 36-12 cassette, a heavy pie plate block of metal for sure, but the two extra teeth on the biggest cog over the 34-11 cassette should give me the lower gear I needed on a 1×9.


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Duncan's Cade Baldwin takes a swing during Friday night's district game against Chickasha at Sportsman's Park in Duncan. DHS will battle the Fighting Chicks today at 5 p.m. from Elliot Field in Chickasha.
- Poll
Who do you favor for the U.S. Senate seat that Tom Coburn is giving up?
- AP Video
- Captain of Sunken SKorean Ferry Arrested Raw: Fire Destroys 3 N.J. Beachfront Homes Raw: Pope Presides Over Good Friday Mass Raw: Space X Launches to Space Station Superheroes Descend on Capitol Mall Man Charged in Kansas City Highway Shootings Obama Awards Navy Football Trophy Anti-semitic Leaflets Posted in Eastern Ukraine Raw: Magnitude-7.2 Earthquake Shakes Mexico City Ceremony at MIT Remembers One of Boston's Finest Raw: Students Hurt in Colo. School Bus Crash Raw: Church Tries for Record With Chalk Jesus Raw: Faithful Celebrate Good Friday Worldwide Deadly Avalanche Sweeps Slopes of Mount Everest Police Arrest Suspect in Highway Shootings Drought Concerns May Hurt Lake Tourism Vermont Goat Meat Gives Refugees Taste of Home Calif. Investigators Re-construct Fatal Bus Cras Mayor Rob Ford Launches Re-election Campaign Appellate Court Hears Okla. Gay Marriage Case


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Federal Register Notices and other relevant regulatory documents related to the national OCS Renewable Energy Program, including the Cape Wind Project, are provided at the links below.
Additional Federal Register Notices related to BOEM Offshore initiatives are available on the BOEM Offshore Federal Register Notice web site.
BOEM has developed the following guidelines for renewable energy activities on the OCS. These informal documents are intended to provide lessees, operators and developers with additional information, clarification, description, or interpretation of a regulation, OCS standard or regional requirement; a better understanding of the scope and meaning of a regulation by explaining BOEM interpretation of a requirement; guidelines on the implementation of a special lease stipulation or regional requirement; or updated administrative information such as current telephone listings and a change in BOEM personnel or office address.
The United States Department of the Interior, Bureau of Ocean Energy Management (BOEM), formerly Minerals Management Service (MMS), prepared a final PEIS in support of the establishment of its program for authorizing alternative energy and alternate use (AEAU) activities on the Outer Continental Shelf (OCS), as authorized by Section 388 of the Energy Policy Act of 2005 (EPAct), and codified in subsection 8(p) of the Outer Continental Shelf Lands Act (OCSLA). The final PEIS examines the potential environmental effects of the program on the OCS and identifies policies and best management practices that may be adopted for the program. Under the program, BOEM has jurisdiction over AEAU projects on the OCS including, but not limited to: offshore wind energy, wave energy, ocean current energy, offshore solar energy, and hydrogen generation. BOEM will also have jurisdiction over other projects that make alternate use of existing oil and natural gas platforms in Federal waters on the OCS.


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Desktop Products Support
Elmer, OK 73539
Welcome to the WeatherBug Frequently Asked Questions (FAQ) and product support page for the WeatherBug family of desktop weather products. If you have a product question or issue that is not addressed here, you may want to visit the WeatherBug Forum to search related topics for posted feedback and discussion threads from users and WeatherBug representatives. Otherwise, please fill out a Support Request Form.
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You can also read manga online try the Ashita no Yoichi! manga!
You're reading Ashita no Yoichi! 22 online. You can try some of the related manga below or try some other manga from our manga list.
Users who read Ashita no Yoichi! also read Ranma, Zero no Tsukaima, Mahou Sensei Negima!, Rosario to Vampire Season II, Maken-Ki! and Spas-Pa.


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Clothing >J Jill
209 Newport Center Dr, Newport Beach, CA | Directions 9266033.612671 -117.875405
Mon. - Fri. 10am - 8pm;Sat. 10am - 7pm;Sun. 12am - 6pm
Casual, versatile women's fashions with earthy appeal. – In Short
Known for its popular mail-order catalogues, this women's apparel line is part sophisticated, part bohemian, with pretty, feminine accents and detailing. Breezy fashions in natural fibers include knit tops, skirts, sweaters, comfortable pants, denim and loungewear. Textures are soft; hues are primarily earth tones accented with romantic embroidery, buttons and rich patterns. Shoes are available at some locations, and through the catalogue and website.
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Do you have a review of J Jill on your blog? If you include the Citysearch image link (shown below) in your post, we'll automatically link to your review from the business profile page. Here's how our Linkback system works:
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To link to our business profile page, copy the html below to your web page.


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I have three of these. They dont always clear the braces as comfortably as I think they should. Seems the throat of the clamp should be deeper particularly when used with the associated clamping caul.
There is nothing wrong with this clamp, but after I bought it found the exact clamp much cheaper at a couple of different places.
This tool worked well for me. Just what I needed.
Without getting into specific detail of how we re-engineered this clamp to work in 99% of the bridge glue ups, especially when combined with the #4600 clamping caul; I'll just say;
[1]You will most likely find that you'll need to fit this clamp with cauls of your own to get it to butt up to the bridge plate. [2] You might need to relieve some material on the lower arm to get it to clear some of the taller X-Braces out there, and [3] you'll probably find that the nylon bushing is too large to clear over the average bridge when using a Bridge Clamp Caul..
Bottom line: Make sure your machinist and carpentry skills are up to snuff, before thinking that this clamp is true to it's name of Bridge Clamp.
As is, it's just a decent general soundhole clamp.
I SAY TO STEW MAC: Re-engineer this product with wider arm spacing and add lower arm adjustment screw, or aluminum "clip-on" cauls for butting up to the bridge plate, and you'd really have something!
The first time I pulled this out to use it was with the sister bridge clamp (with 2 screws for the wings)and it was to small for the job. I couldn't get it on so I pulled my out my old clamp and used that instead. I probably could have made a new caul for the underside, but I reckon this is too tight, it should open at least 10mm wider.
... but a too small opening throat for uses with a bit higher underside block.
for repair and new project but buy the complete kit for bridge
This is an outstanding item for using with the Bridge Clamping Caul. But the price is just ridiculous. I discovered after purchasing, I could get the same product elsewhere for less than half the price StewMac charges.
I'll have to disagree with the rest of my guitar making friends. Yep it's durable and can be used
applications. The depth of the throat is not enough especially if your using it's 'Sister' clamping caul!
This item is well made but sure has it's short comings! I'd like the throat opened at least 3/4" so you can attach any underside block for adhering a classical bridge. Stewmac are the 'best' and I know they will, at some point address this products applications.
This clamp does the job well and is gentle on the guitar. Definitely a worthy purchase.
To add items to your order, select the check box next to the item you want. You can edit the quantity you wish to purchase here, or in Your Order.
To add items to your saved list, select the check boxes next to the items you want. You can edit the quantity you wish to save here, or in your Saved List.


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Your shopping bag is empty - time to start shopping!
Printed Shirtdress
Final Sale
Special Offer
30% off Women's Markdowns Details
Offer valid through 4/30/2014 at 11:59 PM PST at JuicyCouture.com and participating Juicy Couture specialty retail stores. Offer not valid in department stores or outlet stores. Offer applies to all women's marked down apparel, excluding all girls' and baby styles and full-priced styles and colors. Other restrictions may apply. Consumer must pay applicable sales tax. Offer limited to stock on hand; no rain checks. Offer not applicable to prior or pending orders, and no adjustments can be made on previous purchases. Void where prohibited, taxed or otherwise restricted. Offer not valid in combination with any other merchandise sale, promotion, discount, code, coupon and/or offer. No cash value. Discount reflected in Checkout.
Style JG009175
Currently Sold Out
Please call 1-888-908-1160 for availability in our Specialty Stores
We explored the ins and outs of the shirtdress and came up with this printed design equipped with all the necessary shirtdress deets. Point collar. Long sleeves with button cuffs. Gemstone top button. Belt loops. Self belt with flat logo cord ends. 35" HPS.
- Machine wash
- Imported
- Polyester


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Because every family deserves the blessing of a child with Down Syndrome...
Girl, born Dec 2008
Mental delays, Cerebral Palsy, development delay. Atrophy of eye nerve. Cardiopathy.
From someone who met her in June 2013:
She was one of my absolute favorite kids I met! She is just the sweetest thing. She is diagnosed with MR not sure she really is. She was giggling and introduced herself by saying her name. She has a huge smile! She has a special nanny that does PT with her. She was bed bound when I met her but she came from a very good orphanage before she was transferred here. She needs out now!!
Boy, born November 2001
mental delay
His diagnosis is mental delay but I don't think they director was buying it- she brought him right down and said he should not be here- he needs a family!
He was found in a trash bag at the age of 5 along the road (break my heart!). He was able to easily talk – He told her he loves legos and does not mind going to school-sweet boy! He is said to have made great progress and they think he has great potential!
Girl, born October 2008
Mental delays, anomaly innate of development of central nervous system and spinal hernia with lower paraplegia, cross- eye. Chronic kidney infections (obstructive pyelonephritis, and congenital megaureter)
Available in Oct 2013, when she turns 5
From someone who met her, summer 2013:
This girl has my heart. I can not get her off my mind! I wish I was in a place to adopt or I would go get her. I really, really hope a family falls in love with her like I have! I got to kiss her and love on her for a little bit. No idea what she was saying to me but she gave the biggest smile- very photogenic. I can't bear to think about her just sitting in the wheelchair and watching the other kids play!
Boy, born July 2009
spina bifida (myelocele), hydrocephalus (subcompensation), moderate mental delays, functional systolic murmur, astigmatism, crossed eyes, delay of physical development, spastic talipes paralyticus, spastic dislocation of the hips.
Boy, born May 2002
is a wonderful boy; they kept him at his orphanage as long as they could and he was recently transferred to an internat.
A family met him recently as said he is very mild-mannered and very, very sweet.
Girl, born March 2003
Moderate mental delays; Microcephaly; Acquired deformity of chest and rib; Scoliosis
Girl, born July 2003
Moderate mental delays; Acquired deformity of chest and rib; Epilepsy
Girl, born Jan. 2004
Down syndrome, Severe mental delays, Congenital malformation of heart, unspecified; Kyphosis and lordosis (curved spine); malnutrition
Aislinn is in urgent need of an adoptive family. She is already 8 and in an institution. Please share her need!
Married couples only. Large families and older parents welcome. Travel required.
Mark (Latin America)
Boy, Born August 2006
Down syndrome
UPDATE Nov 2013: Mark is doing well, and his overall health is good!!
We did not receive any information on the treatment he received for leukemia — but GOOD HEALTH is GREAT news!!
UPDATE December 2012: It has been determined that sweet Mark is also battling leukemia. We are waiting for additional medical testing and details, but PLEASE pray for him and help us find his forever family! THANK GOD for a new photo, he has grown so much! Trying to get his new photo in a larger size, but SO glad to finally have one! Mark is up and walking and doing SO well! Updated info coming soon!
609-02 This gentle boy has smooth, baby soft skin. He has dark skin and dark hair, potentially from an African/black parent. He is just darling, with a round chubby face. He was born on 8/2006. He enjoys playing with toys and with other children. His legs are rather weak so he scoots around quickly to reach his destination. He smiles brightly when he is spoken to. He waits for his loving family because he has Down syndrome. His family will be so lucky to be able to help this angel reach his fullest potential!
Boy, born December 2009
Tetraparesis (which sounds like a degree of Cerebral palsy, or muscular weakness due to time in a crib)
Ulysses is blind; he won't have much of a life in an institution, but he can THRIVE in a family! Give this dear boy a chance at the world, help find his family.
He was born at 24 weeks. He can't speak but can understand everything. Ulysses is unable to walk but is trying to stand up. Will pull up to his knees.
Large families and older parents welcome.
Boy, born Feb 2006
Birth defect of central nervous system, hydrocephalus, mental delays, manifest deviation, cardipathy and protein-calorie deficiency
Elijah needs a family asap, because he needs constant care, and at the orphanage he doesn't receive it. They fed him with wheat cream only and how he is feeling sick all the time, it's hard to feed him, so that at orphanages he just remains hungry sometimes.
He can walk and likes music and playing with mobile phones. He likes watching TV and doesn't speak much.
Elijah really responds well to a male caregiver — he needs a Papa of his very own!
From someone who met him summer 2013:
Elijah is a beautiful, sweet child. He is nonverbal but he occasionally makes some noises. Unfortunately, when I saw him he had to be restrained most of the time because he would hit himself and bang his head … hard. He now has a one-on-one caregiver, and I hear he is doing very well. Elijah likes to watch tv, and he loves musical toys. When you play music for him, he just lights up in a huge smile. He has an infectious laugh. While I was visiting, Elijah had surgery to fix a malfunctioning shunt. I was able to visit him in the hospital. The dedication of the man who is now his personal caregiver was amazing. Elijah can walk with support, and he loves to be held and cuddled. This little blond-haired child looks like an angel, and he would bring nothing but joy to a family's life.
Boy, born September 2002
Severe mental delays
It wasn't clear if Julian was just sitting in the chair, or if he's not walking.
Boy, September 2003
Down syndrome, severe mental delays
Brooks is also believed to have FAS, as well.
Boy, born December 2003
Down syndrome
Paul is almost 10 years old. He is living in an institution and needs a family so badly.
Mixed hemangioma of face and neck, Chronic viral hepatitis C, Other specified deforming dorsopathies (carriage defect), Astigmatism, Iron deficiency anemia
Susana is a friendly and sociable girl!
BOY, born January 2008
From his medical records: internal hydrocephalus, multi cystic encephalomalacia, convulsive disorder, hernia, secondary cardiomyopathy, patent foramen ovale, anomalous chord of the left heart ventricle, secondary optic atrophy
Wesley is now available for international adoption, as he is 5 years old.
Girl, born December 1998
HIV, crossed eye
AnnaMarie loves school and was in 6th grade when I met her. Her favorite subject is math and likes working on the computer and with cameras. AnnaMarie is very quiet, sweet, and soft-spoken. She is very positive. She wants to have brothers and sisters of her own, and has many friends. She likes going out with her friends and dancing. She wants to go to college. I hope someone can help her make her dream come true!
AnnaMarie is in the same orphanage with several other available children. Interested and approved families could adopt multiple children together.
Trisha and Tyler
Girl, born November 2000
Such a beautiful girl!
Trisha has an older brother (born 1999), who is healthy. They will be available to be adopted together, in early 2014.
Trisha is in the same orphanage with several other available children. Interested and approved families could adopt multiple children together.
Girl, born July 2008
Goltz syndrome, severe mental delays, multiple malformations of upper and lower limbs, umbilical hernia, nasal septum deflection, congenital ptosis of the right eye, coloboma, hypermetropia of both eyes, dacryocystitis of the right eye, macula papilloma
Little Ariel is severely delayed and has a host of medical issues; she will need a family with access to good medical care.
From a family who met her in 2012:
She is so affectionate! She cruised over and wrapped her little arms around my legs as the nanny was giving me the run down of what my son would eat. I scooped her up and she is so light. I think we would have stayed and gone through the process all over again, had we been approved for 2 children!!
Darren #430
Boy, born March 2010
Darren is very calm and smiling, but doesn't sit or walk – he only lays because his head is too heavy.
He is happy when he sees the members of the staff, recognizes familiar people from strangers. He feels good when being around other children and adults. Grabs a toy when given to him and holds it for a while. Turns his head towards the direction of a sound. Makes active and passive movements with the limbs. Has a calm daily and night sleep.
He does not have a shunt, so his hydrocephalus remains untreated. His head circumference was 62cm in Feb 2013.
Because we only have this child's file for a short time, he will not be able to receive donations until a family is found for him.
Jacques #401 OD
Boy, born 2006
neuropsychological, motor and speech development delays
Jacques has severely delayed neuropsychological, motor and speech development. His behavior corresponds to that of an infant. He makes several steps independently and walks when held by one hand. He doesn't speak, but produces monotonous sound combinations. He sometimes seeks adults' physical closeness.
Girl, born 2003
Sarai should be in a family with no children or much older children; her behaviors are that of a younger child. She has FAS, HIV, and tests positive for TB on the skin test.
She is so cute!
Lucy and Linus #399 #400 OD
Lucy is a 5-year-old girl (born 2007) who has congenital microcephaly, infantile cerebral palsy, severe mental delay,delayed psychomotor development, multiple malformation syndrome. She rolls from back to belly and vice versa independently. She remains in a seated position for a short time when provided with some support. She shows interest in toys – she grabs and holds a toy in her hand, waves it around and examines it closely. She responds emotionally to seeing a familiar adult.
Linus is a 4-year-old boy(born 2009) who has microcephaly, congenital anomaly of the central nervous system, delayed psychomotor development, severe mental delay, multiple malformation syndrome. When put in a baby walker he steps on the floor with his whole feet and starts to slowly go around the room in the walker. The boy remains in a seated position for a short time with an adult's assistance. He follows each and every movement of a person or an object with his eyes and head. He loves to watch the other children playing and moving around.
These siblings have very similar diagnoses. Biotinidase deficiency is suspected. There is an emotional bond between the children and they often hold hands, smile, laugh, look for each other with their eyes and jest with each other when they are placed side by side.
Because we only have these files for a short time, they will not be able to receive donations until a family is found for them.
Carl #394 OD
Boy, born 2001
History of seizures, speech delays
Carl is an 11-year-old boy, who takes epilepsy medication, hasn't had a seizure ever since he was placed in the institution where he is at present (June 2009); has a speech difficulty; interacts freely with both familiar and unfamiliar people; loves playing with all children; shows a great interest in being involved in different activities; likes logic games; has normal physical development.
Because we only have this child's file for a short time, he will not be able to receive donations until a family is found for him.
Boy, born November 1999
HIV, astigmatism
Pics from 2013 – he wants to be adopted!
Ethan is in the same orphanage with several other available children. Interested and approved families could adopt multiple children together.
From a family who met him in Nov. & Dec. 2013:
Ethan is older than our daughter and so wasn't in her group. However, he clearly enjoys interacting with the younger kids, and he came into her group room at least two or three evenings each week to play-wrestle and to play games/video games with the younger kids. We met him our first weekend with our daughter, when Ethan came outside for about 2 hours on Saturday to play with the younger kids. He impressed me immensely in that short amount of time. He was gentle and kind with them, laughing and joking. Not once did he display any mean or bullying behavior, which some of the other older boys did. He was very respectful and polite to my husband and me, as well as toward the teachers. That behavior continued every time we saw him for the next six weeks. He especially likes play wrestling with the younger boys, although he is always very gentle with them. Many times he would be play wrestling with one of the younger, much smaller boys, and I'd see him get to a position where he could have easily taken the play too far and hurt the younger boy, but not once did he do so. He always gently set down the younger boy with a big smile. As a result, he is a favorite with the younger boys. He's also a bit goofy, in an understated way. For example, he likes to wear silly clothing combinations just to get a reaction from the other children. Once he was walking around with his skinny jeans rolled up his legs to look like shorts, but with huge gigantic cuffs. The other kids thought it was hilarious! Ethan told our daughter how much he wants a family. He will be a huge blessing and a wonderful addition to the family that chooses him.
Boy, born October 2001
Crossed-eyes, development delays
From someone who met him:
Marv is a very sweet, happy boy. He loves to play soccer, even though his vision problems make that very difficult for him. He has been living in a boarding school for typical kids, and receiving his own private lessons, but recently was transferred to a facility in another region specifically for children with special needs. His favorite class is math, and he gets great grades in math. His least favorite class is Ukrainian. He is said to learn more slowly than other children, which is why he has required private lessons.
He is cheerful, friendly, and sociable. He said several times he would like to be adopted by an American family.
Laynie #65-5
Girl, born 2006
Diagnosis: Delayed development
Laynie is described as having a positive attitude toward herself and others. Her motor skills are well developed. Her speech is delayed, but she speaks using single words and simple sentences. She's attending kindergarten and has the assistance of a resource teacher. She mimics the actions of adults and plays games with other children. She enjoys looking at books. She follows verbal directions, asks questions and is beginning to memorize short poems and songs.
Because we only have this child's file for a short time, she will not be able to receive donations until a family is found for her.
Girl, born December 1999
Cerebral palsy, deep mental handicap
Bedridden and quiet, so heartbreakingly alone.
10 day wait often waived here. Married couples only, larger families welcome.
Girl, born August 2000
Down syndrome and cerebral palsy
From someone who met her: She was in an almost empty room, just with another child next to her. She was rocking and gnawing at the bars of the cot and such a sad sight to behold. My heart just collapsed for her!
Every minute Velia spends here is a lost opportunity for life. There is a family out there who will want her, love her, cherish her, help her reach her true potential. Grant donations make all the difference!
10 day wait often waived here. Married couples only, larger families welcome.
Boy, born August 2000
Down syndrome
Lord, please, PLEASE let them see me here…please let my Mama and papa find me…please…..
Davian is 13 years old and stuffed in a stroller. Experienced adoptive families preferred. Large families and older parents welcome. Married couples only.
Boy, born Dec. 2004
Moderate mental delays
He is a very good boy, communicable, calm and friendly.
From a family who met him in Fall 2013:
Pearson is doing so good!! He is precious and sweet! I saw him from a distance every day. The first time, he was with a group of boys having their picture taken in the fall leaves. He always did what the nanny told him to. He walks very well, and he likes holding the nannies hands. My favorite day was when I walked past their group and he was right in front of me on the sidewalk, and before the nanny could move him, I bent down and in Russian told him how sweet he was. He took my face in both of his hands, and pulled me down so our foreheads were touching, and just stared in my eyes. I kissed his cheek, and his whole face lit up!! And he has the most adorable splatter of freckles! He is smaller than I would have thought too.
Boy, born January 1999
Cerebral palsy; Moderate mental delays
Boy, born May 2002
Cerebral palsy, spastic tetraparesis, epilepsy, hydrocephaly, deep mental handicap
From someone who met him:
Bedridden but still able to smile. They seemed particularly keen for me to photograph this child and kept turning his head for a better shot! I sensed that they too spot the potential within this child who smiled from inside his limited life. Somebody please go get this boy out of this cot!
10 day wait often waived here. Married couples only, larger families welcome.
Boy, born June 2003
Severe mental delays; cerebral palsy with low paraparesis
Boy, born Sept 2000
Сerebral palsy with mild tetraparesis; Severe mental delays
Boy, born March 2001
Significant mental delays, sequela after viral encephalitis, cerebral palsy, tetraparesis, epilepsy
He was a truly desperate sight. He sat rocking back and forth and moaning and staring into space. I wonder how a real life in a family could break the shell he is now locked in. My heart breaks for him even now!
10 day wait often waived here. Married couples only, larger families welcome.
Boy, born 2001
Significant mental delays, hydrocephaly, spastic paresis and inborn partial optic atrophy
From someone who met him:
He is a quiet child who smiled every time I looked his way.
10 day wait often waived here. Married couples only, larger families welcome.
Boy, born January, 2004
Down syndrome, mental delays, inborn partial optic atrophy of both eyes
From an adoptive family who visited with him in June 2013: I met Delmar today. He is really tiny … maybe the size of a 3 year old, very petite in build. He was quite shy and didn't want to come near me. He moved away when I tried to touch his hand. He was more open with the therapist who was there (a guy). Mostly he just sat on a mat, rocking and looking into space. Occasionally he waved his hands around. He's a beautiful little boy, and was adorable in a tiny pair of overalls.
10 day wait often waived here. Married couples only, larger families welcome.
Girl, born January 2006
cerebral palsy, bigeminal epilepsy, deep mental handicap, inner hydrocephaly, convergent squint
Kendall is a true orphans, as her mother has passed away.
From someone who met her:
She was gorgeous, when I spent time with her she had been taken into the playroom by a caretaker and she was lapping up every single second, she couldn't stop laughing and grinning; it was a joy to watch! when I compare to pictures I received of her later in her cot it does not look like the same child! She needs a life and love, she could bloom, I know it!
10 day wait often waived here. Married couples only, larger families welcome.
Boy, born January 2000
Cerebral palsy, difficult mental handicap
From someone who met him: When I met him I was heartbroken! More than any child in the institution the sight of this thin boy with his hands tied and blood on his sleeves made me weep! My own child self-harms and I think I connected with this sight…it could have been my angel!! The staff told me he was tied for his protection, as he hurts himself; the holes on his sleeves obviously points to this… my own child has a self-harming syndrome and lives a wondrously happy and fabulous family life! Yes it needs managing but this child in front of me was desperate and my heart literally broke! He needs help and the life I know he can lead!
From an adoptive family who visited with him in June 2013: I met Nehemiah today. He is in a groupa with 7 other boys. In the playroom he sat on a mat with a stuffed lion. He didn't really interact with me at all. Occasionally he would begin to cry loudly. Luckily, the caregivers responded to him quickly. He has sores all over his hands and wounds on his face. He's a very attractive little guy, though.
10 day wait often waived here. Married couples only, larger families welcome.
Boy, born March 2003
Sequels of encephalitis, convulsive disorder, sensorimotor alalia, deep mental handicap
A terribly sad rocking child whose face showed so much sorrow behind the eyes it was heart wrenching! He moaned and rocked and seemed untouchable! His eyes haunt me even now! How I wish I could have spent more time with him. He so needs a family to wipe away that sorrow.
10 day wait often waived here. Married couples only, larger families welcome.
Boy, born November 2002
Cerebral palsy, spastic tetraparesis, microcephaly, deep mental handicap, carditis, biliary dyskinesia
He was in the same room as Bobby and seemed quite quiet. I would love to see him outside of those stifling rooms.
10 day wait often waived here. Married couples only, larger families welcome.
Boy, born May 2001
Mental delays, inborn hydrocephaly, cerebral palsy, anemia
When I met him he was in the institution, but he has since moved to the first happy home (after another boy was adopted) so he is in a much better situation. I know emotionally he suffers, as he cries an awful lot.
10 day wait often waived here. Married couples only, larger families welcome.
Boy, born Sept 1999
Cerebral palsy, deep mental handicap, hydrocephaly, complete vascular leukoma, corneal staphyloma, inborn optic atrophy
This child is rather calm, but always smiles when somebody touches him, and always tries to walk with somebody's support.
From a family who met him in June 2013: I met Blaine today. When I arrived at the orphanage he was being stretched by the therapist. He seemed to really like the therapist and would crawl to him and hold up his hands so that he could stand up. He can walk if you hold both his hands, and I saw him in a gait trainer, too. It's very difficult for him to walk as he doesn't seem to be able to fully straighten his legs. Blaine smiles a lot and seemed to be a pretty happy kid. He did get mad about something and have a tantrum, but it passed quickly. He rocks a lot and makes repetitive noises. He came over to sit by me and took my hand from another child's so he could hold it. He was very interested in my iPhone.
From someone who met him: He was a bundle of smiles, just desperate to interact with us. [One of the men] picked him up and swung him, they obviously have built up a relationship and he shrieked with laughter…it was joyous! He was made to sit next to Tania for a picture, she hated it but he was just fine! He would blossom in a family and with a life!
10 day wait often waived here. Married couples only, larger families welcome.
Girl, born August 2007
Congenital malformations, deformations and chromosomal abnormalities, myopia
Miriam also has significant signs of FAS, although that is not diagnosed
From someone who met her:
I loved this child but she seemed so lost…she had only just arrived at the institution when I visited and she was bewildered! She is TINY. She is the child we all talk about, the child plucked from the baby house at 5 and left in a cot! She is the child forgotten and alone!
I was told she could walk, in fact she is the only child in the bedridden building who can walk, and then without warning she was swooped from her cot and paraded in front of me. A recent update says she is still moving and can still walk and she cries if she doesn't get her walk! And she is still laughing and playing; but for how much longer?
She needs OUT! She needs a Mama, NOW!
10 day wait often waived here. Married couples only, larger families welcome.
Boy, born Sept 2004
Coffin Lowry Syndrome, Hydrocephalus, moderate mental delays
Garrett does not speak, but understands speech addressed to him. Garrett can be adopted with Troy and Sammy.
From an adoptive family:
I met Garrett in May 2012 and I will always remember how sweet he was. He was usually the first one to greet me with a hug when I visited. He was always so excited to show off for me. When the care-taker announced that they were all going outside he promptly put his shoes on and helped some of the other kids with their shoes as well. He and the other boys in his group (Troy and Sammy) are very well loved by one of their care-takers and it shows. It is obvious that they have been taught manners and cooperation and they are very kind to one another. They are taught at least several days a week so do not let the diagnosis deceive you, they are fairly smart boys. They all have obvious delays but never had any problems following instructions and they understood everything they were told and all seemed to love to be helpful. When I show our son (who was adopted from this group) their pictures he remembers their names and tells me they were his friends. He told me he wants them to be adopted and to come to the U.S. How I pray that happens for Garrett and the other boys! Garrett is so sweet and innocent, I hate to see what will happen to him if he ages out of the orphanage.
Boy, born Feb 2005
Asthma and Moderate mental delays; Subcompensated hydrocephalus; possible FAS
What a great grin! Sammy can be adopted together with Troy or Garrett.
From an adoptive family:
I met Sammy in May 2012 and he was one of the sweetest kids I had ever met. Always ready with a smile and a hug! I brought things for all the kids in his group and he waited so patiently for his turn and gave me a big hug after. He was very kind and gentle with all the other kids, especially the one girl in the group. He and the other boys in his group (Troy and Garrett) are very well loved by one of their care-takers and it shows. It is obvious that they have been taught manners and cooperation and they are very kind to one another. They are taught at least several days a week so do not let the diagnosis deceive you, they are fairly smart boys.
They all have obvious delays but never had any problems following instructions and they understood everything they were told and all seemed to love to be helpful. When I show our son (who was adopted from this group) their pictures he remembers their names and tells me they were his friends. He told me he wants them to be adopted and to come to the U.S. How I pray that happens for Sammy and the other boys! Sammy is so sweet and innocent, I hate to see what will happen to him if he ages out of the orphanage.
Rebekah #69-3
Diagnosis: Cerebral Palsy
Rebekah was born premature at 27 weeks and has quadriplegic CP. She is delayed in all aspects of her development.
Additional information about her abilities and development are coming soon.
Because we only have this child's file for a short time, she will not be able to receive donations until a family is found for her.
Girl, Dec 2009
Congenital brain malformation (corpus collosum agenesia), spastic tetraparesis, epileptic syndrome, optic nerves atrophy, equinovarus, condition after exudative pericarditis, hypotrophy, deficiency anemia, mental retardation, convalescent bronchial pneumonia.
Bryannah #8-3
Diagnosis: Down syndrome
Bryannah has been in a mental institution since 2011. She has been in orphanages her entire life, but was just recently registered for adoption in 2013. She has waited 12 years for a chance to find a family! She walks, plays with toys, responds to her name and attends a special needs school each day. She is not talking and still requires help with daily self-help skills.
The agency also has a video available.
Doug #33-4
Doug has already been transfered to a mental institution!!!
This precious little boy has already been through several major transitions in his short life. He was raised by his birth family until he was 16 months old. He was then placed in an orphanage for young children for 7 months. A month before his 3rd birthday, he was transfered to a mental institution, where he currently lives.
Doug has moderate mental delays with no known cause. He walks and runs and climbs on objects. His visual-motor skills are developed but he still has difficulty with fine motor tasks. His speech is delayed and he is not talking at this time. He has recently begun showing an interest in toys and playing with them. He spends time each day in the sensory room. He does not like for the staff to try to direct his activities and prefers to do his own thing. He does play appropriately with toys and manipulates them in the correct ways. His favorite toys are balls, blocks, cars and trucks. He recognizes staff members and smiles at them. He seeks out interactions with them and will cuddle with them too. He tries to get them to follow him and to engage them in whatever activity he is doing. He doesn't yet seek out any interaction with the other children. He eats from a spoon and drinks from a cup with some assistance from the staff.
At 27 months of age, his skill level was tested at:
motor skills- 2 years
speech development- 5-6 months
cognitive development: 10-12 months
$18.00 is available towards the cost of my adoption!
Because we only have this child's file for a short time, he will not be able to receive further donations until a family is found for him.
Girl, born January 2009
Brain malformation (corpus callosum agenesia, optic septal dysplasia, ventriculomegalia, cerebral hemisphere hypotrophy), spastic tetraparesis with severe movement disorders Q 04.8, symptomatic focal partial epilepsy with complex partial and rare secondary generalized seizures G 40.2, optic nerves atrophy, convergent squint.
Sweet girl has a laundry list of diagnoses; she needs a family, or she'll spend so much of the rest of her life in a crib. She's got sparkle — a family could help her truly shine!
Boy, born December 2008
Delay of psychological and speech development, hip dysplasia, atrial septal defect (condition after surgery).
From a family who met him in late 2013:
He was in our son's groupa and we saw him several times in our 7 weeks of visits. He is sweet. He's a gentle boy. He's obedient/cooperative. He never stood out as mischievous or overly active (not hyper). Just a sweet, kind, joyous little guy. In the hustle and activity of the 11 kids in his groupa, I had to stop and look for him because he's not overly aggressive or assertive. Maybe a little on the shy side. But still friendly when approached (as far as we could tell.) His eyes are beautiful. Just a handsome little sweetie!! He needs a family!! He's in a good orphanage that provides good medical care. Such a sweet little boy. He needs a family!!
Boy, born July 2011
After-effects of meningocephalitis, tetraparesis, internal hydrocephalus, Hirschsprung disease, thymomegalia
Boy, Feb 2009
After-effects of neuroinfection, spastic tetraparesis with severe movement disorders G 09, symptomatic focal epilepsy with secondary generalized seizures, medicamental remission G 40.2, mental delays, partial atrophy of optic nerves.
Girl, born Nov 2008
Cerebral palsy, double hemiplegia with severe movement disorders, symptomatic epilepsy (frontal lobe, focal) with partial seizures with secondary generalization, significant mental delays, optic nerves atrophy.
This sweet girl needs a family to help her bloom!
Congenital hydrocephalus, paraplegia and tetraplegia (spastic tetraparesis), partial atrophy of optic discs of both eyes, additional chord of the left heart ventricle, hernia.
Look at the curls on this doll! Cameron is in urgent need of medical care!! Married couples only. Large families and older parents welcome. Travel required.
Boy, born 2001
Down syndrome
Vance is a cute, outgoing boy, with a winning smile! He loves to play outside – particularly swinging and playing soccer. He enjoys drawing and playing with puzzles and bricks.
Vance has a significant speech delay, but interacts with others using gestures and expresses himself well.
Girl, born October 2007
Hydrocephalus, spastic tetraparesis, epilepsy, adenoid vegetation, congenital partial atrophy of optic discs, recrudescent bronchitis in remission
Congenital heart disease (ASD), secondary cardiopathy.
Piper dear, where is your mama? Sweet girl has a lot of needs; a family could drastically change her life — otherwise, she is one who could be destined to spend her life in a laying down room.
Girl, born September 2007
Cerebral palsy
This little love is riding in a stroller — we don't know much about her mobility. Her wispy hair is beautiful, isn't it?
Update from a family who met her in late 2013:
Lydia is the sweetest little girl! Our kids were in the same groupa, so we got to see Lydia everyday we were in country. She is a joy! Lydia spends her days sitting in a stroller with hardly any interaction. Now that our kids are home, she is the only non-walker left in her groupa, so she is the only one who sits in a stroller all day long. She looks to be about the size of a four year old, but looks like she is a healthy weight. She's got a little chub on her legs. Her legs are not scissored, but when I lifted her legs up, they were definitely tight. She needs a Mama to stretch her legs! Her legs are always bent at the knee draped over the bar of the stroller (she's too big for her stroller). I couldn't tell how much head control she had because her head was always supported by her stroller, but her head was always upright, not bobbing. I never saw her move her body (except to arch her back when tickled), but one day I held both of her hands, and she was able to grasp my hands tightly in hers. Neither hand seemed weak. Lydia's vision looks pretty good. She could follow me with her eyes, but there's a good possibility she'll need glasses. Her poor teeth are rotten. We watched her eat lunch once and she seemed to eat well. She eats pureed food from a bottle. Did I mention she is SO sweet? Lydia seems to be very easy going. Once a child was hanging on her and pushing on her and she didn't respond except to make a face showing that she didn't like it. Lydia was my favorite child to interact with in the groupa. All I had to do was say hi to her and smile and she would light up EVERY single time and reward me with a big smile. We tickled her lots and she giggled away. One time she was left in a room all by herself and was crying. I peeked my head in the doorway and said hi to her and she immediately stopped crying and started smiling and giggling. She is very responsive when talked to. Even though she is non-verbal, she communicates with lots of smiles and giggles. This little lady is FULL of joy! She will truly BLESS any family! Please, please consider this sweet little one. She is still in the babyhouse, but is one of the oldest in her groupa, so she will be one of the next children to be transferred.
She does have an older brother who is eight years old and looks to be typically developing. I'm not sure if they will need to be adopted together or separately.
Boy, born June 2010
Microcephaly, spastic tetraparesis, epileptic syndrome with frequent seizures, chronic subdural hematoma
This sweet little tyke needs a family to love an care for him — he's said to have frequent seizures, so a neurologist should be overseeing his care and medications.
Girl, born February 2004
Chronic Hepatitis B
Tadee is a lovely young girl, hoping for a family of her own! Her hair is adorable, with the multiple braids.
Jaysen #378 OD
Boy, born June 2004
This 8 years old boy has been diagnosed with Fraccaro syndrome. He demonstrated a delayed neuropsychological development and hypogonadism, symptomatic epilepsy and mental delay. He needs a lot of positive emotions, individual work and positive reinforcement in order to master new skills and habits, and further acquire knowledge. His physical development is not correspondent to his biological age. He can sit independently but it is hard for him to walk on uneven surface and he is not always able to go down the stairs. This is main reason he cannot take part in sports games. He knows his name and responds with eyes when called by his name, especially when call by a familiar adult. He cannot speak yet and can pronounce a few words only.
Because we only have this child's file for a short time, he will not be able to receive donations until a family is found for him.
Amaris #377 OD
Girl, born September 2005
Her neuropsychological development is delayed. She has a surgically corrected heart malformation a weeks after she was born.
History of seizures, and increased muscle tone.
This 7-year-old girl is in a satisfactory general condition. She walks independently and takes part in music and dynamic games. She initiates contact with a caregiver in game play activity. She cannot speak and makes inarticulate sounds. She likes to play along with musical and singing toys.
Because we only have this child's file for a short time, she will not be able to receive donations until a family is found for her.
Ivy #379 OD
Girl, born May 2003
This girl is almost 10 years old and her neuropsychological development is delayed as a result of her congenital condition – hydrocephalus. She is small for her age. She seeks other people's closeness and responds with a smile when meeting unfamiliar adult. Her speech is underdeveloped and she doesn't use language as a means of communications. She tries to imitate sounds and says the word "mama"…. She studies a special educational program at school. She sleep good and wakes up calm and joyful. She likes to play alone or observe the other children playing.
Because we only have this child's file for a short time, she will not be able to receive donations until a family is found for her.
Autumn #380 OD
Girl, born October 2005
Blind (fourth degree of Retinopathy), Delayed physical and neuropsychological development
This 7 years old girl can walk independently. She attends special school and follows simple instructions. She likes the adults and wishes to spend most of her time in the group with children. The girl doesn't always like physical interactions. When she wants to be left alone she would wave her hands, spin around and cover her ears with hands. The child likes going out for walks. She is calm while traveling or when visiting a place she hasn't been to before. She likes musical toys. She knows her name and react to it but doesn't always like it when someone addresses her directly. She makes sounds which might be interpreted as joyful or expressing displeasure. She doesn't speak, she repeats syllables in imitation – "pa-pa", "ma-ma-ma", "da-da-da", "o-pa".
She shows preference to food – she likes sweets, pudding, and chicken and already tries to eat independently but needs adult's assistance. She is fed by a spoon. She hasn't yet mastered her skills to get dresses and undressed. She takes her shoes off.
Because we only have this child's file for a short time, she will not be able to receive donations until a family is found for her.
Bert and Ernie
What a handsome pair of boys! And so young!
Boy, born February 2008
Bert has cerebral palsy; we don't have any specific information
Boy, born March 2009
Younger brother, Ernie, is healthy. He is only available to be adopted WITH his brother.
Large families welcome; married couples only.
Sinclair #375 OD
Girl, born April 2005
Cerebral palsy and moderate mental delay
Listening to quiet music relaxes her. She seeks contact with another children from her group. She attends Daycare center for Children with disabilities but she is dependable on the care of adult. She repeats others's movements – giving a hand, clapping and raising both hands. She recognize her caregivers and rejoices in their presence. She will feel and do much better in a family setting where she will get a personal attention.
Because we only have this child's file for a short time, she will not be able to receive donations until a family is found for her.
Girl, born February 2002
Mental delay, HIV
Creative, eager
Devora is a real sweetie pie! She loves to have her head rubbed, and enjoys being tickled. Her smiles and giggles are absolutely heart melting! She does not talk, stand, or walk as far as I could tell. Her idea of mischief is to kick off a shoe or hide her arm inside of her sweatshirt, and she'd giggle as these things were corrected.
She seemed to find it very amusing when I would ask her where her hand was, then say "There it is" as I removed it from inside of her shirt. This became a game, and she would giggle as she hid her arm again as soon as I removed it from inside of her shirt. She is a very content little girl, and something as simple as a spiky ball could put a big grin on her face. I never saw her upset as long as she was allowed to play in either her bed or her chair, but she would become upset if I tried to move her to a more unfamiliar area to play.
Mason and Madison
Boy, Jan 2001
Cardiac abnormalities: mitral valve prolapse of 1 stage, supplemental oblique chord of the left ventricle. Scoliosis.
Girl, born Sept 1997
Abnormal development of cardiac system: mitral valve prolapse of 1 stage, humpback.
They are currently in the same orphanage, and need to be adopted together.
Girl, born 1998
Trudy is the older sister of Tristan and Tatiana.
All three children can be adopted together or separately; they are currently in the same region, but in different orphanages. We hope to find a family where they can stay together!
Boy, born 2003
Mental delays, but otherwise healthy
Tristan is the brother of Tatiana and Trudy. All three children can be adopted together or separately; they are currently in the same region, but in different orphanages. We hope to find a family where they can stay together!
George #19-2
Diagnosis: Down syndrome
George can walk with support. He will play with toys. He is described as friendly and as having a positive attitude. He is exposed to games and activities, but he does not always participate. He is not aggressive toward himself or others.
Boy, born February 2012
Congenital hydrocephalus, spastic tetraplegia, epileptic syndrome, open oval window
Boy, born 2003
Cerebral Palsy (spastic tetraparesis with moderate movement disorders), mixed astigmatism, amblyopia of both eyes, scoliosis of thoracic spine, dyslalia (speech disorder)
Girl, born 2001
CP spastic paraplegia with malfunction of lower limbs, convergent squint, myopic astigmatism of both eyes, S-type scoliosis of thoracic spine, flexion-adduction contracture of both hip joints, equinovarus feet, dysarthria.
Such a lovely young lady, such poise.
Girl, born 2006
Diagnoses: depression, impulsive, attention deficit disorder
It is suspected she has FAS; she suffered meningitis in past.
Look at sweet Edith, all dolled up for the New Year's party at her orphanage!
She has had a broken nose because when she lived in the family her mother's boyfriend pushed her and she fell and broke the nose. Two foreign families have visited her but did not end up adopting her.
One of our adoptive families has met her, and has video of her for inquiring families. They said she was begging for attention, desperately needing love.
Boy, born February 2001
cerebral palsy, cognitive delays, spastic diplegia, inborn hydrocephalus, secondary cardiopathy
Leroy is one of the cleverest kids there, and he speaks a lot – he is rather impudent
He gets sad, when other children get presents and he doesn't. He understands much and likes ice-cream.
From someone who met him in 2012:
I thought he was wonderful…again one of the lucky 9 boys to be in the small group home, picked because he is so very able. He is clever and could achieve much. He was full of smiles and laughter when I met him. He was very polite and enjoyed the excitement of a visit. He really would thrive in a home environment.
Boy, born 2004
HIV, hydrocephalus
Adam is a sweet, easy to please little cuddle bug. He is very much like a cuddly, curious little toddler. When I first met him he did not seem interested in me at all, but as time went by he began to want affection, and would grab my hands if I stopped rubbing his head and put them back on his head.
One day I picked him up and from that moment on he wanted to spend most of my time there in my arms. When I arrived he'd jump up from his little wooden chair, and hurry over to me with his arms raised. If I didn't pick him up fast enough he'd try to climb up into my arms using nearby chairs or beds, and he would not hesitate to grab items from my hands and set them down to free up my hands so I could hold him. He also began to cry whenever I left. He loves wind up toys and toys that vibrate, and would giggle happily and flap his hands to show how excited he was about them. His other favorite toys were a pony he enjoyed chewing on, any sort of car, and some legos that made a train. He is not verbal but was beginning to make noises to communicate. I tried to teach him to sign more one day, by signing hand over hand with him. When I asked him to sign it he took my hands and helped me sign it. He seems to me to have a need for love and affection that can only come from a loving family. I would love to see him thriving and meeting his full potential, as well as bringing joy to as many people as possible!
Girl, born June 2008
Cerebral palsy, focal symptomatic epileptic syndrome, complex local convulsions; rough delay of psychological and speech development
Lovely Harlowe!
She needs physical therapy and a loving home.
Boy, born September 2010
spina bifida (congenital malformation of the central nervous system, spina bifida of lower thoracic spine and upper lumbar spine)
lower paraplegia, pelvic organs dysfunction, hydrocephalus
So hard to see sweet Penn in this one little picture. He desperately needs a family to help him reach his full potential!
Girl, born March 2009
hydrocephalus (with shunt), spastic tetraparesis, convulsive disorder, Hep.B, valgus feet, optic discs atrophy
January 2010
microcephaly, Epilepsy, dystonic tetraparesis, brain degeneration
Kayson needs a family, to save him from a life in a crib.
July 2011
hydrocephalus (internal hydrocephalus as a result of suffered meningitis); spastic tetraparesis; prematurity; retinopathy of prematurity; collapse of lungs; prenatal infection;
heart disease: open arterial duct (condition after surgery on August 10, 2011), open oval window, anomalous chord of the left heart ventricle
Look at that white-blond hair! So pretty! Donna desperately needs a mama.
Boy, born June 2009
hydrocephalus (condition after ventriculoperitoneal shunt); cerebrospinal hernia of lumbar spine, post-surgery; congenital partial atrophy of optic discs; pelvic organs dysfunction; cytomegalovirus infection; anemia; rickets
Girl, born 2003
Diagnoses: Mild mental delays, Hydrocephalus, cleft palate, Anomaly (congenital) (unspecified type) of pupil function
She was so sweet! She was playing nice with all the kids. Very lovable. She came up to ask if I was her mama? It broke my heart. She loved to be held.
She followed the care givers directions & was very well behaved!! With love & patience she would fit right into a family.
Married couples only, large families welcome.
Girl, born 1999
Cerebral palsy
Additional information coming soon
Isolde is described as creative and eager.
From someone who met her: Isolde is lovely. First I thought she couldn't speak when I was there in the summer, 'cause it took her about 3 weeks before she would even say 'thank you.' But then she started to talk more and more. I started to do walking exercises with her. She could hardly stand on her legs by then. I practiced with her everyday and what I noticed is that she is a fighter. She worked so hard. She worked until she was bathing in sweat and totally tired. She wouldn't stop before her legs couldn't hold her anymore. Everyday we could walk further. First just one side of the building and in the end we could easily walk 2 rounds around the building. Though she needs quite some support. After the summer they gave her PT and she was walking way better when I was there in November again. She could walk with one hand then, which was totally impossible for her in the summer. And again she was fighting to learn more, but being inside the building all day would limit her. She is pretty smart too, I played games with her. One of the games was creating a 'picture' with little pins, just copying the example. The physical part of the game was the hardest. So we trained to pick up the pins, put them in and get them out. She is so wonderful! She smiles so sweet. She just stole my hard. In the beginning of the summer she had hardly any muscles in her leg and she was extremely skinny, but during the summer she got more muscles from exercising and in November she was doing even better. I'm so proud of this girl. If she will get the chance, she will reach so much, because she will fight for it. She would do so well in a family, because a family can give her the chance that she deserves and I know she will make the most of it.
Isolde's best friend is Duane; who is also listed for adoption.
MORE PHOTOS AVAILABLE. Married couples only, no parent age or family size restrictions, travel required.
Boy, born 2005
Justin does not always go to school because of blood transfusions. He is behind in each aspect compared to other children. Now he can go up and down stairs, can jump off the ground, can draw lines with holding pen, can draw circle, likes painting; knows "big and small", "inside and outside", "more and less" and "left and right"; recognize color of "red, yellow, blue, green, white and black". He can count from 1 to 10, but does not know number because of not receiving regular education.
His general language ability – he is talkative and can communicate simply, like telling you where he goes but not clearly. At the aspect of self-management, he can eat alone, can go to the toilet, can put on and off the clothes and socks. He also is a good helper, likes helping the caretaker do things like fetching things, helping the younger children.
FAS, cognitive delays, anemia, ADD, congenital malformation of ribs NOS: pectus excavatum congenital heart defect: Atrial septal defect
What a little doll! She may be a strawberry blonde? Cara is a sweet little girl with many of the challenges of fetal alcohol syndrome. Facial features, cognitive/academic delays, inattention, and heart condition are all common symptoms of FAS. She previously had a diagnosis of Hep C, but we believe that was preliminary at birth. Families should be aware of this and prepared, but not expect it to be the case. Cara will need to be followed by a cardiologist.
From one of our adoptive families who met her in 2013: Cara seems to be a very bright girl all around. She wanted to sneak out into the room where we were playing with our daughter. They all try When she was told to come in she would quickly sit by our side and say, "but I'm going to sit here nicely and play, I promise." I felt so bad when they would make her come in. She DID play very nicely. She didn't throw any tantrums. We gave her a mini slinkie to keep and she was so excited and said thank you and ran back into the room. Her hair is cut much shorter and she is petite. She got her shoes on and off by herself…and fast when told she could play after her shoes were on. She would really thrive in a family. This region waives the 10 day wait usually too which is extra nice.
Update March 2014:
Cara is a sweetie, but more shy. She's very pretty and has striking blue eyes and blond hair. She would watch me and sneak over to wave hello before the nannies would send her back to her chair. She's in a groupa that does a lot of preschool type work, and and is set up like a classroom so the kids come home with more age- appropriate skills. Our just-turned-3 year old daughter knows how to work puzzles, hold a crayon/pencil properly to write (and is showing pre-writing skills already), understands the concept of counting, etc- not the "norm" for orphanage life! So, kids from this groupa will likely come home knowing how to play appropriately with toys but also prepared to learn in a school-type setting as well. Cara does have obvious facial features of FAS, but the only behavioral/developmental issues that were apparent from casual glance was the sensory needs- she does rock back and forth on her chair when she has to sit for more than about 30 minutes. Otherwise, she seems to do very well. She follows instructions and sat quietly while waiting for her turn.
Gene is described as eager and easygoing.
From someone who met him: To really 'get access' to Gene, you need to try hard. Some days he's living in his own world and it's hard to 'reach' him. But it's worth the effort. I met Gene in the summer, and the other children in the group were all trying to get my attention, Gene wouldn't I tried to give some attention to every child in the group, so also to Gene. It took a while before I could get him out of his own world. I grabbed his hand and just stroke his fingers one at a time. He would look at his fingers, and after doing that for minutes, he would finally look at me. He looked who was stroking his hand.
Still he didn't allow me to touch him more than just stroking his hand. Next day I was wondering if he would still remember me and if I could touch his hand again. I didn't need to ask myself that question, because as soon as I walked in, he came up to me, reaching me his hand. I knew I broke through his wall that kept him safe in his own world. It still took me a while to really 'open him up'. In November I visited his group again, and again it took me a while to 'reach' him. But as I was tickling one of the other boys in his group, he came closer. So I grabbed his hand, to pull him on my lap, next to the other boy, and I tickled him. What happened was amazing! He started to laugh! He laughed out loud, the first time I heard him do that. And he couldn't stop anymore. His laugh was so contagious and so wonderful to hear it. It brought tears to my eyes. He was so open and he wanted me to tickle him more. Next day I could hardly touch him again, which was hard for me, because I wanted to get him out of his own world again. But I found out that I should not lose hope, because it depends on his mood if he will let you touch him. Another day I could tickle him again and he laughed again. This boy just needs more stimulation to stay out of his own world. Because of the lack of stimulation he normally just sits on the ground and rock back and forth. But he is able to walk, to run around and play games. He can have fun and interact with other children. It just takes a little more. This boy is already in the institute for a long time, and this is the price he paid for it.
He desperately needs a family — He needs a family committed to him before his 16th birthday, otherwise he'll be condemned to institution life forever.
Married couples only, large families welcome.
FAS (fetal alcohol syndrome), probable secondary CP
Julia has such happy, giant brown eyes and a smile that lights up a room!
From a family who met her in December 2013: "I have to shout for this precious girl for a moment…we are here now and we see her everyday at the orphanage. The pictures don't do this dear one justice at all; she is gorgeous and so very sweet!!! She can't walk on her own (she can if she is assisted!) but she is still quick! She comes over to me everyday and wants in my lap, to shake my hand, or give me a hug. She has SO much potential and I can just see the hunger for love and a Mothers touch in her eyes. She has been overlooked long enough!!! She is darling….truly!! "
From someone who met her: Julia is a girl that I know as the girl with the big smile. Somehow she just seem to smile almost always. She's a little monkey. Whenever somebody enters her group she would crawl up to that person and just start to climb on him/her. She doesn't even need you to give her a hand, she'll just climb up without any help and then she hangs on your neck, looking around, proud, as if she wants to say 'Did you see that? Do you see where I am?'
Her favorite toy is a doll. She plays with it as if it is a baby. Keeping the doll up straight, putting her down carefully. She feeds and clothes the doll. One of the nurses showed her how she should put a cotton diaper on the doll, she totally loved it. She even sings lullabies for the doll and she'll ask visitors to do the same. She also loves to play with long hair. She really tries to make ponytails or braids.
Julia is able to walk, but her legs are really crooked, and she needs help to keep standing or to walk. Julia is described as curious and enthusiastic.
Boy, born Oct 2011 congenital
internal hydrocephalus operated; anemia; protein-energy deficiency
Ezra has had a shunt placed, and is doing better. His adoption may necessitate consultations with medical personnel, to safely transport him home.
From someone who met Ezra in 2013: Ezra is absolutely precious! He is sweet and adorable and oh so lovable! He laughs when his toes are tickled, or when someone around him laughs or talks or sings to him. He often smiles or laughs so hard his chubby cheekers make his eyes close. He ha s learned to blow spit bubbles and coo. It is hard for me to tell if he is able to use his limbs normally, but he is able to move from his back to his side with little or no assistance. He has not yet learned to play with toys, but he has a very strong grip and enjoys holding my finger. I was told he can see, but not very well. I observed his eyes moving rapidly from side to side, and sometimes appearing to be looking in two different directions. In spite of this there were other times in which he appeared to be quite focused and looking right at us. He has absolutely stolen my heart, and I hope that he will find a family that can help him meet his full potential!
These pictures are from May, 2013.
Caius and Anne are in the same orphanage with Ezra.
Large families welcome; married couples only.
Boy, born April 2006
After-effects of traumatic brain injury, brain contusion, right hemiparesis, ptosis, OS
JEFFERSON HAS BEEN TRANSFERRED. He is at the older children's internat.
In May 2011 the boy fell off the third floor and his condition is the result of the injury. He has some vision and speech impairment but he is a very smart and nice boy.
He is still in the orphanage but will be transferred to the institution soon if we don't find him a family fast.
Ezra, Caius and Anne are in the same region with Jefferson.
Girl, born 2004
Unrepaired cleft palate
Kathleen is described as broadminded and cheerful.
From someone who met Kathleen in 2010: Kathleen is a very loving and social little girl who loves getting attention from adults. Whenever I was in her group, she was always right beside me, participating in whatever I was doing and engaging me in her own favorite activities. Kathleen has kept that silly, playfulness that most institutionalized children seem to lose. She was definitely a little mischievous getting into everything, but was also very quick to follow direction and obviously eager to please. I truly believe she would thrive in a family where she was showered with all the attention she deserves and allowed to simply be the fun-loving, silly little girl God created her to be.
From someone who met Kathleen in 2012: Kathleen is a happy little girl who would love to be able to communicate, but cannot because of an unrepaired cleft palate. She makes noises to communicate to the best of her ability. She is a very sweet little girl, and loves to play outside. Many missionaries who have met her loved her and spoke highly of her!
Sullivan is a sweet, loving little boy. He is described as cheerful and curious. The smile on his face when he is being held is absolutely precious! He is not talking, but appears to be very capable of learning sign language to communicate! He loves to play "If you're happy and you know it" and made up a sign for this, clapping his hands together.
Sullivan then quickly learned the ASL sign for more. In addition he has a sign for potty, and drink. He does not go right away to strangers, but wants those he is comfortable around to hold him and play with him. He is not able to stand or walk, but crawls to get around. When hurt by another child he will not attempt to defend himself, but will cry in hopes of someone comforting him. Sullivan is a very sweet boy who would do wonderfully in a family!
BOY, Born August 10, 2005
Don't mind this pink shirt, Porter is a BOY. He is HIV+, stage 3. He is cognitively delayed as well, and has some paralysis on half of his body.
From his medical records: HIV stage 3, without immunosuppression, delay of psychomotor and speech development, bacillosis
Update 2013: Severe mental retardation, HIV, congenital heart disease
Boy, born April 2008
Hepatitis C, rough mental delay, fish skin (ichthyosis)
What lovely blue eyes this little guy has … and cute mussed up hair!
Large families welcome, travel required. Married couples only.
Brett is a handsome young man who was born with CP. He is very smart, he gets around on his own by crawling, but he is not able to walk. Therapy will do wonders for him! He deserves to have a family!
From a volunteer who knows him: He plays with other children. He speaks with separate words. He understands the addressed speech. The boy is curious, likes classes. He loves when his nurse reads for him, he likes making pyramids.
Update December 2012:
Brett is very smart and curious. He has some learning and language delays associated with institutional life, but he does speak in complete phrases around people he trusts. He enjoys cars, coloring, and games. He got very excited when we showed him pictures of dogs and other animals, so he might do well with pets.
A family considering adopting him should be prepared to deal with some institutional behaviors and traumas. This is the area where Brett might need the most assistance in understanding rules, family, and nurturing relationships.His physical disability limits his lower body, specifically his legs and feet, but he is very strong in the upper body and crawls very quickly. He is a very active kid who needs some physical therapy, appropriate equipment, and perhaps braces to get where he needs to for walking. He is able to pull himself to standing. The orphanage has worked with him on potty training and he seems to be doing well with it.
More photos available, married couples only.
Boy, born December 1999
Rough mental delay, hydrocephalic syndrome
From someone who met him in 2012: Amos is a wonderful sweet boy! He will do anything you'll ask. In the summer the children will play outside and the more disabled children are sitting in a big box. Everyday he carries out the carpet to put in the box and he will carry out the benches and chairs to sit on as well. When the 'outside-time' is over, he would carry it all back in again. He doesn't really talk, but I'm pretty sure he would be able to. He does make sounds and he loves to 'sing'. While singing he makes sounds that could almost be words, but as long as he's lacking of stimulation, I think he will not talk. He likes to dance around to.
He is a big help for the nurses. When a child has to go to the shower or potty he brings them, when a child falls down, he picks the child up, even without somebody telling him to do that. He is a really social butterfly. He cares about the children around him and I'm sure that he would be an awesome big brother, because that's what he is for the children in his group.
The only self stimulating behavior that I saw in Amos was sticking things in his ears. You can easily distract him from that by offering him a toy. Once he has a toy, he will not be bored, he can play forever with just one toy.
Large families welcome, multiple children may be adopted together from the same orphanage. Married couples only; travel required.
Boy, born January 2002
DS, atrial septal defect, polydactyly of the left hand
Artemur is a handsome boy who has already been waiting far too long for a family of his own!
Large families welcome, multiple children may be adopted together from the same orphanage. Married couples only; travel required.
From someone who met Artemur in 2012: Artemur is aladies man He loves to greet visitors with a formal "Hello", a chair for the visitor to sit on, and for the ladies he'll kiss their hands and sometimes request a kiss by pointing to his cheek. He has ten toes and ten fingers, and appears healthy. He is one of the two highest functioning boys in his group and is a big helper. He is quite verbal, and he has good self-care skills, he is able to feed himself and ask to use the restroom. He likes to play with etch a sketches, toy phones, and bubbles. Artemur would probably do better in a family environment where he can be the youngest in the family.
Girl, born July 2003
Diagnosis: hydrocephaly, mental delays
She likes to play, tries to walk alone, but needs assistance. She doesn't speak, but understands much.
From someone who met her in 2012:
When I walked into the room packed with children, her smile and wave and joy stood out more than all the chaos and heartbreak and noise. She was a darling and I just know she would be amazing to have as a daughter.
Born December 1999
Diagnosis: cerebral palsy and down syndrome
From someone who met him in 2012:
Emil was the gentlest child ever! Unable to talk but the pleading in his eyes killed me! He grabbed my finger and wouldn't let go…what a grip! He also got really hit a few times by others wanting my attention, he didn't retaliate but fell in a heap and moved away, only to return when the coast was clear. I would love to see this child in a nurturing environment!
Emil is able to walk.
Boy, born May 2009
Cerebral palsy
Eldridge also has significant features of FAS (fetal alcohol syndrome), but this is not diagnosed.
Large families welcome, married couples only. Travel required.
Girl, born August 2009
After-effects of viral encephalitis in the form of microcephaly, movement disorders syndrome (cerebral palsy syndrome), epileptic syndrome of residual genesis, secondary hypothalamic syndrome, loop of thermal control
Brinli has pretty eyes, and such lovely long fingers. She desperately needs a family to save her from a life spent lying in a crib.
Large families welcome, married couples only. Travel required.
Boy, born October 2010
Cerebral palsy, spastic tetraparesis, optic atrophy, secondary internal hydrocephaly, seizure disorder
Polly #35-0 OD
Girl, born August 2000
Polly is a 12-year-old girl with a mild mental delay who has a developmental disorder of speech and language. She is in need of dental care due to some issues with her teeth.
Polly is relatively well-developed physically when compared to the age norms. The lack of parental care, a mother's caress and physical and emotional contact in early infancy has affected the child's psychological development negatively by lowering the quality of her behavioral activity.
There are no significant irregularities as regards Polly's psychomotor development. She demonstrates satisfactory verbal, non-verbal and eye contact. Her strength is correspondent to her bodily development. The child has normal mobility and well-coordinated movements. She would benefit from active physical activities and sports. The girl has adapted well to her classmates at school. Her attention is unsteady during the classes; she has limited attention span and low stability of concentration and can easily be distracted.
Additional medical information available.
Because we only have this child's file for a short time, she will not be able to receive donations until a family is found for her.
Robert #34-9 OD
Boy, born December 2002
Down syndrome
Robert is a handsome young man. His general development is delayed. He has good gross motor skills, and his fine motor skills need a bit of assistance; he likes to color. He enjoys listening to music, and dancing. He vocalizes, but his expressive speech is not developed yet.
Robert currently is a student in the fourth grade of a Special School. He has a good orientation in the academic environment and points at objects in the classroom. He understands instructions, but does not always follow them. He knows his name and reacts with a smile when called by name. He takes part in the educational activities with interest but he would soon lose his concentration. He shows positive attitude toward children and adults. He often takes part in organized events. The boy performs simple chores – when assisted and stimulated he cleans his work place and the classroom.
Additional information available from the agency.
Girl, born December 2009
Cerebral palsy, hemiplegia, movement disorders in combination with vision and hearing impairments
They really want a family for her in the orphanage before she has to be transferred.
Dani has beautiful blue eyes, and a darling little button nose!
Large families welcome, travel required.
Boy, born August 2008
Minimal hydrocephalus
Griffith is a very nice boy! He has a little bit of an impish look to him in this picture, doesn't he?
Married couples only, travel required. Large families welcome!
Girl, born April 2005
Mild to moderate delays, needs dental work
Sweet girl! She needs a mama to paint her nails and braid her hair. She's trying so hard to force a smile for the camera.
Girl, born September 2002
Mild to moderate delays, Cerebral Palsy
Update June 2013:
Frieda is also very sweet but is delayed. She is shy when you meet her but she loves lollipops and will smile for one There is video also available with her in it, for interested families. She knew the words to the lyrics to the songs they performed and also tried to dance along to the music. She does like to rock a little bit when she sits more than likely to self-soothe.
Girl, born December 2004
Mild to moderate delays
Update June 2013:
She is delayed but she tries very hard to keep up with everything. She is super, super smiley- like she could not stop smiling and giggling. She loved singing and she also loved watching everyone else dance (she did not participate). She also rocks when she sits, but again probably to self-soothe. There is video available with her in it as well.
Girl, born December 2002
Mild to moderate delays
Another lovely young lady, still waiting for her forever family.
Update June 2013:
This picture does not show off her true beauty! She loved wearing this dress as when she danced the beads went flying. She has some pretty good dancing moves! I am not sure if she knew the words to the song but her mouth moved the entire time. She also rocks when she sits and does present as delayed. She has a very sweet, shy smile.
Girl, born October 2006
Mild to moderate delays
New picture (red stripes) from summer 2013.
Girl, born June 2005
Mild to moderate mental delays
This little peach is just waiting for a family of her own!
Update June 2013:
So disappointed her new picture is fuzzy. She is teeny-tiny and a very happy little girl!
Girl, born December 2004
Mild to moderate mental delays
Isn't she just the sweetest?
Update June 2013:
Coralina is also such a sweet girl! She loved the beach balls and was running around the room making sure they all stayed in one place. She is very small especially considering she is almost 9. She is in a video, available to interested families.
Ryan #6-14
Diagnosis: Down syndrome
Ryan is 11 years old. He has been in an institutionHis gross motor skills are well developed. He walks, runs, climbs and prefers physical activities. He exhibits some stereotypical movements. He plays with toys and attempts to manipulate them correctly. He requires 1:1 assistance for academic tasks. He is currently being instructed in how to trace letters, though he still requires assistance with this task. He tries to fit shapes into puzzles. He can arrange blocks and builds towers with them. He likes to arrange the chairs in stacks. He eats independently, though he's still working on hygiene in related to table skills. He does put away his own dishes once he's done eating. He can dress himself, but he does not undress himself independently. His personal hygiene skills are not built up at this time. During art class, he requires assistance with coloring and art projects. He can glue items onto paper if the items are pre-cut for him. His emotions and attention are unstable. He is hyperactive and doesn't always follow the rules. He exhibits difficult behaviors when he doesn't get his way or doesn't want to do something. He is sometimes aggressive with objects and with his peers. He enjoys dancing and prefers to participate in activities and play that involve a ball and interacting with children who are more physical.
Additional information: Ryan has been visited by an experienced adoptive family and members from an adoption team well experienced in observing children with special needs. During the visits, he exhibited aggression toward the adults and staff members from the institution. He had difficulty following basic instructions from the staff and often didn't respond to his name. He did seem to enjoy interacting in small amounts with the adults, though he wanted those interactions on his terms. He did not respond well to restrictions or being made to do things that he did not want to do. He will need a family willing to provide a lot of structure, routine and consistency in behavior management.
Additional photos and videos of Ryan from October 2012 are available.
Boy, born
November 2000
Down syndrome, neurodystrophy, psychological and motor development disorder, alalia
From someone who met Duane in 2012:
Sweet little Duane is the huggiest boy I've ever met! He is a determined, strong willed little guy and is up walking and chasing after balls despite some mild CP on his left side that causes his left knee to extend backwards in a painful looking manner. He has an amazing laugh, though it is sometimes a mischievous laugh. He sometimes feels the need to push boundaries, such as throwing balls at the other children, but he is a boy with a lot of love to give, both to the adults and the other kids in his group. He also sometimes gives massages. I feel he would especially thrive in a house where he is the youngest, or at least the smallest child in the home.
Duane's best friend is Isolde; they could be adopted together.
Boy, born 2008


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*A talking thermometer that gives, ear, forehead & room temperature readings*
Order today for Monday delivery
The Talking Thermometer is a high quality hand-held infrared thermometer that can read temperatures back to you in a human voice - an essential aid for the visually impaired.
Measurements are taken rapidly, within 1 second, from either the forehead or the ear. The unit has a washable sensor tip and can store up to 20 measurements. The thermometer has an LED torch, clock, calendar and also measures room temperature: handy for the nursery!
Excellent thermometer and the forehead adapter is much easier to use than an in ear one when you have a wriggling baby. Really pleased with this product.
The Thermometer takes temperatures of foreheads and ears in seconds and can read them to you in a human voice. It also plays a jingle for younger ones and also has a clock, torch and calendar so is great for any nursery.
These are exclusive customer reviews unless otherwise stated. Specifications of goods are subject to change.
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This product is available as a pre-order. This means that we do not currently have the item in stock but we are expecting it shortly. You can place an order for this product now your expected shipping date will be 25-04-2014
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