My name is Dylan Samantha Souter and I am 7 years old. I have Rett Syndrome. This is a rare and very severe neurological disease which almost exclusively affects girls. I cannot walk, talk or use my hands. I will face many more problems in the future. But a cure is possible. Rett Syndrome has been reversed. The biggest obstacle standing in our way is money. Please help give Dylan a future. 2017 Event: Tickets on sale.
http://www.curefordylan.com/
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Marc Souter
Marc Souter
34 Brea●●●●●●●Gardens
Ric●●●ond , Surrey, TW10 7SQ
UNITED KINGDOM
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Marc Souter
Marc Souter
34 Brea●●●●●●●Gardens
Ric●●●ond , Surrey, TW10 7SQ
UNITED KINGDOM
View this contact
Marc Souter
Marc Souter
34 Brea●●●●●●●Gardens
Ric●●●ond , Surrey, TW10 7SQ
UNITED KINGDOM
View this contact
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Welcome | curefordylan.com Reviews
https://curefordylan.com
My name is Dylan Samantha Souter and I am 7 years old. I have Rett Syndrome. This is a rare and very severe neurological disease which almost exclusively affects girls. I cannot walk, talk or use my hands. I will face many more problems in the future. But a cure is possible. Rett Syndrome has been reversed. The biggest obstacle standing in our way is money. Please help give Dylan a future. 2017 Event: Tickets on sale.
Marc Souter is fundraising for Reverse Rett
https://www.justgiving.com/curefordylan
Fundraising on the go. Fundraising for Reverse Rett. Raised of £1,000,000. Funding research into curing Rett Syndrome for Reverse Rett. Because it is a REVERSIBLE disease. Raised of £1,000,000. Event: Raising awareness of Rett Syndrome and appealing directly to people for donations towards finding a cure for my daughter Dylan and the thousands of girls like her. We fund cutting edge research to reverse Rett Syndrome for good. Please help them to help us. Reverse Rett is a UK medical research charity work...
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Cure for Diseases
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My name is Dylan Samantha Souter and I am 7 years old. I have Rett Syndrome. This is a rare and very severe neurological disease which almost exclusively affects girls. I cannot walk, talk or use my hands. I will face many more problems in the future. But a cure is possible. Rett Syndrome has been reversed. The biggest obstacle standing in our way is money. Please help give Dylan a future. 2017 Event: Tickets on sale.
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Importance of balanced body structure. My view on FCST. My view on FCST. VIEW ON FCST FROM A NON-PHYSICIAN and PATIENT PERSPECTIVE. Cause of Dystonia (and other chronic disorders). Two subsections: my story. And diary during treatment. Explains concepts and theories behind FCST (Functional Cerebrospinal Therapy). It is recommended to read the subsections in chronological order. Explains all the available treatments at Dr Lee’s private medical practice (also known as FCST clinic). March 14, 2014 at 5:04 am.
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