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Hello everyone! I would like to ask for your help to raise an amount of money for my son's operation and medical expenses. This is my son, Joemel Shaun, he is now 1yr and 5months. I just want to share his journey for the past 1 year. When he was born, he was diagnosed with ruptured omphalocele with perforation (ileum), S/P reduction of perforated bowel, double barrel ileostomy, sepsis neonatorum, Congenital heart disease, pneumonia, S/P IJ cutdown, S/P insertion of PICC line, neonatal purpura fulminans, and hypothyroidism. He was admitted for almost 2months. His journey was a bumpy road, he was on the point that his life was on the 50/50 chance of survival. God made things possible for him, so he survived. But after how many months, he was diagnosed with a rare blood condition called protein s and c deficiency, 1 in a million can get this condition. There is no cure for it now according to his hematologist. Today, we are knocking into your hearts for any humble amount you can share with him for his operation the closure of intestine and for his medical expenses since his checkup and laboratory for his blood and thyroid glands are a bit expensive. May God bless all of you and thank you for sharing your blessings.
- Anna Lauren Pongos
Update Nov. 11Update posted by Anna Lauren Pongos at 10:03 am
Shaun will be admitted starting tomorrow Nov. 12 for his upcoming operation. He will have his laboratory work up.
Update for his operationUpdate posted by Anna Lauren Pongos at 05:10 pm
Hello everyone! We had been discharged from the hospital. Just an update: since Shaun had a pneumonia, he needs to recuperate first to proceed for the operation. Tentative date of operation will be on the third or fourth week of October. I would like to thank everyone who gave us. . . . .