Profile
Name:
Helen
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3,935
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Joined:
Jul 3, 2008
Latest Activity:
1 year ago
Subscribers:
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Website:
RP International seeks to fund and develop the Institute for Degenerative Eye Disease. The Institute will be responsible for the funding and coordination of global research into degenerative blindness, and collection, evaluation and dissemination of information regarding its caused, treatment and availability of services.
Helen Harris is the founder of RPI and also a longtime activist for the blind and vision impaired. Years ago, Helen Harris, then a housewife, painter, and young mother, learned that she was slowly going blind from the degenerative blinding disease, retinitis pigmentosa. She soon learned that two of her three sons had inherited her disease. In 1973, she began RP International to provide support and counsel to those who suffer from retinitis pigmentosa and other degenerative eye diseases, and to find a cure for those diseases.
If you want any information, please give us your contact information so that we can provide you with what is needed.
Helen Harris is the founder of RPI and also a longtime activist for the blind and vision impaired. Years ago, Helen Harris, then a housewife, painter, and young mother, learned that she was slowly going blind from the degenerative blinding disease, retinitis pigmentosa. She soon learned that two of her three sons had inherited her disease. In 1973, she began RP International to provide support and counsel to those who suffer from retinitis pigmentosa and other degenerative eye diseases, and to find a cure for those diseases.
If you want any information, please give us your contact information so that we can provide you with what is needed.
Country:
United States
Occupation:
President/Founder
Companies:
RP International
Channel Comments
is this also an solution for her? pls tell me how and if this is the sollution, she will be really realy happy, it is soo sad to see her crying because the problem of RP you never know when you will completly blind.
pls let me know how and what, and for wich person theStem Cell Restores Sight will work
gr
What does a person with RP should stop straining their eyes looking at the computer , books and tv? What vitams and herbs should he be taking? Is there a cure at Cuba???? What about Canada wellspring clinic for holistic medicine???? Help!!
I just dont want to get blind T_T
please.. what can I do?
im 17 years old and i suffer from rp but im in reasonably early stages (cant see much at night etc) but it is noticably progressing and i was wondering what forms of rp this stem cell jazz can help cure? how long do you think it will take for this treatment to be available for people that dont get millions of dollars from abc?
also, only vitamin A can help and only with certain types of rp.
anyway, awesome page and keep up the god work.
thanks
and I hope this could be the answer to his prayers...
So I wonder how much the treatment cost? I would be very glad to get your response.Thank you so much
sincerely,
Queen
a page for blindness. my mom has RP. she has a guide dog, and is doing really well with her ^^
anyways, i just think its really cool you made this page. [=
one more thing, how can you "fight against blindness"?
Just want to get this comment board started. RP International's main goal is to make this channel a place people can go and share their feelings about Retinitis Pigmentosa and to make it the one place stop to view videos of inspiration, entertainment, goodwill, stories, etc. about people who have the condition or are already blind. We are very excited about the launch of the channel and hope you guys are too!
RP International Team.