2yr-old Gabby Fights Histiocytosis

This is Yosef Gabriel, turning 2 next month, is diagnosed with a very rare disease called Langerhans Cell Histiocytosis.

https://www.hopkinsmedicine.org/kimmel_cancer_center/centers/pediatric_oncology/becoming_our_patient/cancer_types/histiocytosis.html

His Mom, Josephine Borris, is a housewife and his father, Jameuel Pantujan, is working as a callcenter representative here in Dumaguete City, Negros Oriental, Philippines.

Gab-Gab was a healthy and energetic baby boy. There were no early signs of the disease except for a few bumps on his head which the doctors thought of as an allergy until last month (May 2019), when his appetite suddenly dropped and his skin including his eyes turned yellowish. He then was brought to Silliman Medical Center Hospital where a series of laboratory tests were performed. It was then that they found out that he has LCH and will need to undergo a chemotherapy as soon as possible to avoid the disease from spreading into his internal organs which can be fatal.

In connection, I am knocking at your kind hearts for any amount that could help further Gab-Gab’s treatment.

You may also send your donations through remittance centers (Palawan, Cebuana, ML, etc). You may contact Gab-Gab’s mom directly.

Josephine Borris https://m.facebook.com/josephine.borris?0955 336 1381

Thank you and may God bless us all.

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Updates:

Baby Gab will have a chemo once a week for 6 weeks, after that he will continue his chemo every 21st day of the month for 1 year.

He will have his 1st chemo this wednesday June 26, 2019 @ SUMC

🙏🙏🙏🙏🙏🙏