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Bengi and your family is in my prayers............... Stay encouraged and strong.

Bengi and your family is in my prayers............... Stay encouraged and strong.

Bengi and your family is in my prayers............... Stay encouraged and strong.

Just keep the faith and everything will be o.k. I was new to it as well with my family being African American it is very rare for us and when they told me what the disease was I 'd never heard of it befor in my life. I looked through medical books to see exactly what it was and if the books...

Just keep the faith and everything will be o.k. I was new to it as well with my family being African American it is very rare for us and when they told me what the disease was I 'd never heard of it befor in my life. I looked through medical books to see exactly what it was and if the books...

Just keep the faith and everything will be o.k. I was new to it as well with my family being African American it is very rare for us and when they told me what the disease was I 'd never heard of it befor in my life. I looked through medical books to see exactly what it was and if the books...

I guess looking at my name you assume that I would be a gentleman but my name is short for Seanette, I am actually his mother. Thank you for all of your responses. Sean

I guess looking at my name you assume that I would be a gentleman but my name is short for Seanette, I am actually his mother. Thank you for all of your responses. Sean

I guess looking at my name you assume that I would be a gentleman but my name is short for Seanette, I am actually his mother. Thank you for all of your responses. Sean

I just wanted to give everyone a message of hope. My son is 10 years old and was diagnosed with cystic fibrosis when he was 5 months old. After diagnosis he hemmoraged on his brain due to lack of vitamin k from cf at 7 months. we had lots of hospitalizations for pneumonia and respiratory...

I just wanted to give everyone a message of hope. My son is 10 years old and was diagnosed with cystic fibrosis when he was 5 months old. After diagnosis he hemmoraged on his brain due to lack of vitamin k from cf at 7 months. we had lots of hospitalizations for pneumonia and respiratory...

I just wanted to give everyone a message of hope. My son is 10 years old and was diagnosed with cystic fibrosis when he was 5 months old. After diagnosis he hemmoraged on his brain due to lack of vitamin k from cf at 7 months. we had lots of hospitalizations for pneumonia and respiratory...