Thanks Missy! I checked on it however there's not much of information. I need help. seriously need help. my son is turning six.. I can't get him proper medication. I reached out to Boston Children's Hospital. Do you have any idea how can I raise fund for him?
Have you tried something like crowdfunding? Or gofundme.com?
I know that Dr. Levitin is planning to open an office in Guam. While I know it's a little closer to the philippines ... well, it's not as far away as Boston. Get in touch with Dr. Levitin at http://birthmarkcare.com
The Rotary Club of Makati West was helping families get treatments a few years ago. Have you contacted the Makati Medical Center? I bet they have a specialist on staff who can help you.
What did Dr. Levitin say? Did you send your photo to him his website?
An international charitable
organization that networks families affected by a vascular birthmark, tumor, or syndrome to the appropriate medical professionals for evaluation and/or treatment,
provides informational resources as well as sponsors physician education, mobilizes medical missions trips, and supports research and programs that promote acceptance
for individuals with birthmarks.
Here you will find information and resources for patients and families affected by hemangioma, port wine stain,
arteriovenous malformation, capillary malformation, lymphatic malformation, Sturge Weber syndrome, Klippel-Trenaunay syndrome, and any other type of vascular birthmark
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in order to impart general information relating to the diagnosis
and treatment of vascular birthmarks. Such information is not complete
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care related questions regarding this matter, please see your physician
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