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Welcome to Winning The Fight

View studies in world renowned scientific journals confirming the effectiveness of the Deanna ProtocolTM therapy for ALS!

What is Winning the Fight

Winning the Fight against Neurodegenerative Diseases, otherwise known as Winning the Fight (WFND), is a mostly volunteer 501(c)3 non-profit organization. We focus on designing and studying nutritional therapies for Amyotrophic Lateral Sclerosis, otherwise known as Lou Gherig’s Disease. We developed a therapy for ALS called the Deanna Protocol TM  and scientific studies show that the therapy is indeed effective! We do not directly sell the nutritional supplements involved in the Deanna Protocol and we make very little money when individuals purchase them. The money we do make is donated directly toward research to improve the Deanna ProtocolTM  nutritional therapy. In addition to improving the Deanna ProtocolTM for ALS, we also hope to eventually optimize it to target other neurodegenerative diseases (NDs) such as Alzhiemer's Disease, Parkinson's Disease, and Multiple Sclerosis. If you would like to support our research, please donate today! Even one cent will help!

In addition to designing and funding research, we also spend a great deal of time providing information and support to the ALS community and to those who are taking the Deanna ProtocolTM. We answer questions about the therapy and the supplements and assist PALS with finding retailers from which they can purchase the supplements. We also assist PALS in finding strength trainers, physical therapists, speech therapists, and any other types of medical professionals who work with individuals who have ALS. PALS have a lot of questions for us and we are here to help via email or Facebook!

      Video Made January, 2013

NOTE: The mouse studies referenced in the video are now     finished. Research concluded that the Deanna Protocol is effective. 

 Organizational Structure: Volunteers and Paid Personnel

Our organization consist of a board of nine directors, a medical liaison, and several experts in the fields of neurology, all of whom are volunteers. The only individuals paid for their work for WFND are the scientists who conduct our research, one part time administrative assistant, and one part time freelance web developer who helps us resolve technical issues as-needed. If you donate to our organization, you can rest assured that the vast majority of your money will fund research to improve the Deanna Protocol TM! This research will help us lengthen and improve the lives of those with ALS!

Video made April 18, 2013 - New video & updated information coming soon


Why do we work for free?

We believe in this cause! Our board members all have one or more loved ones with ALS. Two of our board members have ALS. We found something, the Deanna ProtocolTM, that allows us and our loved ones to fight ALS and actually have a chance at winning. We devote our free-time to sharing this with the world so that other PALS and their loved ones can have the same hope that we do. Some people spread hope by volunteering at homeless shelters, hospitals, soup kitchens, etc. We choose to spread hope by spending our evenings and weekends working for Winning the Fight and helping individuals with ALS fight the disease.


 

 

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News

CBN Article on Deanna Protocol Therapy for ALS - Tuesday, September 2, 2014
CBN published an article on Winning the Fight's Deanna Protocol therapy for ALS.
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Examiner Article - Thursday, July 31, 2014
The Examiner published an article on the Deanna Protocol and explained the studies that prove its effectiveness.
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ALS Untangled wrote an article evaluating the Deanna Protocol - Sunday, August 4, 2013
ALS Untangled wrote an article evaluating the Deanna Protocol and addressed several concerns. WFND has responded and answered ALS Untangled's concerns in a separate article. Please see ALS Untangled's article and WFND's responding article.
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