Today was an amazing day. ABC 15 News came to our house to interview us for Jasmins' story. I think I cried more than talked. All I could think about is my baby talking and asking for hugs, and I cried more. We (my family and I) were so happy about sharing our story to give hope to other families.
THERE IS HOPE!
Parents of children with disabilites understand that life can be hard, but we make the best of each day. We love our children and try to provide what we can to meet their needs. If there is a chance that a treatment for Cerabral Pasly is found then
I believe we need to take that chance.
Our children did not have a choice, but with new medicine we can give them a chance for a future.
My son Joseph (Jasmins' twin brother) prays every night for "OH GOD sissy walk and talk, go school, go college". That is the longest sentence he has ever spoken.I hope that with this stem cell transplant his prayer and ours comes true.
Jasmins' mom
About Me
- Jasmins Cause
- Jasmin is a beautiful little girl who is full of life, love, and laughter. She was born prematurly at 26 weeks and had a severe brain bleed. Because of the difficulties after birth Jasmin is unable to walk or talk. You can see that she has a personality,an inner being that is full of light. She laughs and cries. Many doctors told us that she would never feel- but she does. She feels when her brother or sister are ill- she cries when they do and laughs when they do. The most amazing thing is that inside the body is a little girl who is trying to come out. Her personality shines and draws people to her.
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