My name is Princess Tarin. 31 yrs old a single mom of twin girls. May 12 2015 my usual check up turn into stat CS. Finally i will meet my daughters but that excitement turns into a nightmare sophia was the 1st one who got out due to cord coil but olivia didnt survive that doctors said that she was already gone 3 days ago they based it on her macerated skin. Sophia got infection in her blood she was in the nicu for 1 week and they released her but she has a heplock on her arm for the medication. We go to the ER during AM and PM for her medication to inject onto her that was our routine for 2 weeks until she was cleared from infection. I thought that was the end but i was wrong from 2nd month up to 6 mos of her life was good. Until i saw her jerking i thought it was a simple movement but when i saw her hands where shaking i know something was wrong but i didnt mind it because maybe she was shock or terrified to the sounds. As weeks goes by she was like that then i realized all the milestone that she has from 1st months up to 6 mos were suddenly gone. She was unable to grab her toys, look at me when i called her name, wasnt smiling, her head were lagging, unable to roll like she used to. I decided to brought her to the gen. Pedia and they referred us to neuropedia that was the time the doctor said that she has Cerebral palsy, epilepsy. We've done series of test, doctor hopping and many more.. most of the doctor said that she was not able to survive 1yr of age. I was so broken that day but i had to fight for my daughter i will prove to them that she will conquer all these challenges.. she starts therapy 8mos pt ot visual therapy. That was our routine for 4 yrs now. Her final diagnosis are CEREBRAL PALSY, EPILEPSY, CORTICAL BLINDNESS, MICROCEPHALY. I know strugglea is real for us but i will fight for my daughter and now she was able to sit on her own, pull herself to sit, stands with support, grabs her toys again, grabs her bottle to feed herself, she was able to smile, have an eye contact with me. My only wish for her is to continue her therapies i hope that someone might help me to raise a fund for my daughter for her therapies and laboratories for her to achieve full development and recovery.