find my family: Marilyn

November 12, 2014 by nohandsbutours Children Who Wait, GWCA 0 Comments

When the first thing someone say to describe you is that your “smile lights up a room” you must just radiate joy and that is how Marilyn is described by her current agency staff who recently met her. This shy and soft-spoken 8 year old has Down Syndrome and CHD (PDA). She does well at …Read More

find my family: sam

November 4, 2014 by nohandsbutours boys, Children Who Wait, GWCA 0 Comments

Little Sam is 3 years old! Sam has a few orthopedic conditions including Osteogenesis Imperfecta, scoliosis, and a difference of his right elbow and ankle joint. He is mobile and his file states he just can’t jump. People believe that he may be a little delayed compared to his peers but it may also be …Read More

Find My Family: Delilah

October 10, 2014 by nohandsbutours advocating, Children Who Wait, GWCA 0 Comments

Dainty Delilah! Little Delilah’s most favorite thing to do is play with dolls. While she has a few different medical needs, she is simply a sweet little two year old girl. She is a special child who is hoping for her very own special family to love and cherish her. She is post-operative for anal …Read More

Find my Family: Dexter

July 22, 2014 by nohandsbutours advocating, Children Who Wait, Family Found, GWCA 7 Comments

Update: My Family has found me! All it takes is one photo to cut you to your very core, and little Dexter’s photo has done just that for many. This photos, some of his newest, show a little boy whose round face has given way to noticeable weight loss, his kissable lips, dry and cracked …Read More

Find My Family: Hanson

June 28, 2014 by nohandsbutours advocating, Children Who Wait, epidermolysis bullosa, Family Found, girls, GWCA 0 Comments

Update: My family has found me! Hi! I’m Hanson! Due to my epidermolysis bullosa I see doctors and nurses a lot so I have a good relationship with them. Even though I get sores on my body, I rarely cry and I try to be very strong! I can be quiet but I love getting …Read More


October 20, 2008 by nohandsbutours birthmark, Family Stories, GWCA, Skin Conditions, Sturge Weber Syndrome, Vascular System 0 Comments

by Monica, big sister to Reese, from China, who has Sturge-Weber Syndrome We originally were aiming to go to China for a NSN girl, as young as possible. As we were gathering paperwork, some friends called us and said, “you have to look at these kids on your agency’s waiting list”. We did, and found …Read More