[News] Help Support Robert and Mabel William's son, John fight ALS

Anti-Imperialist News news at freedomarchives.org
Tue Mar 8 11:21:33 EST 2016


Dear friends, my good friend John Williams - son of Robert and Mabel 
Williams - needs support. Please help if you can and do spread the word.
claude

------------------------------------------------------------------------
Hello everyone.  I am sending this message today because my brother John 
Chalmers Williams (son of Robert & Mabel Williams) was recently 
diagnosed with having ALS or amyotrophic lateral sclerosis.  ALS is also 
known as Lou Gehrig's disease and it is a progressive neurodegenerative 
disease that affects nerve cells in the brain and the spinal cord.

Motor neurons reach from the brain to the spinal cord and from the 
spinal cord to the muscles throughout the body. The progressive 
degeneration of the motor neurons in ALS eventually leads to their 
demise. When the motor neurons die, the ability of the brain to initiate 
and control muscle movement is lost. With voluntary muscle action 
progressively affected, people may lose the ability to speak, eat, move 
and breathe. The motor nerves that are affected when you have ALS are 
the motor neurons that provide voluntary movements and muscle control. 
Examples of voluntary movements are making the effort to reach for a 
smart phone or step off a curb. These actions are controlled by the 
muscles in the arms and legs.

There are two different types of ALS, sporadic and familial. Sporadic 
which is the most common form of the disease in the U.S., is 90 – 95 
percent of all cases. It may affect anyone, anywhere. Familial ALS 
(FALS) accounts for 5 to 10 percent of all cases in the U.S. Familial 
ALS means the disease is inherited. In those families, there is a 50% 
chance each offspring will inherit the gene mutation and may develop the 
disease. French neurologist Jean-Martin Charcot discovered the disease 
in 1869.

While John's health insurance will cover traditional medical approaches 
that deal with ALS (none of these are geared towards a cure) they do not 
cover non-traditional or experimental approaches (such as various stem 
cell based treatments).  So in an effort to help raise funds to 
participate in those experimental treatments and cures, which cost many 
tens of thousands of dollars, the family and friends of John and his 
wife Lisa have setup two major fund raising initiatives.

The first initiative is a go fund me page which can be accessed using 
the following link:

https://www.gofundme.com/jwilliamslovegives

The second initiative is a tribute and dinner on May 7th from 4pm to 6pm 
and a panel discussion from 6pm to 8pm at the Charles Wright Museum of 
African American History at 315 East Warren Avenue, Detroit Michigan 
48201 (313) 494-5800.  The fund raising dinner will have a $50 cost.  
Please visit http://brotherjohnwilliams.weebly.com/  to purchase tickets 
and get general information.

Any help that you can provide will be greatly appreciated!!!

You can contact me at  Frank Williams at fhwdaman at hotmail.com 
<mailto:fhwdaman at hotmail.com>  (734) 751-9275, or Doreatha Ewald 
pdmewald at wowway.com <mailto:pdmewald at wowway.com>(586) 778-3617 if you 
have any questions.

/*Frank Williams*/*/
/*

-- 
Freedom Archives 522 Valencia Street San Francisco, CA 94110 415 
863.9977 www.freedomarchives.org


-------------- next part --------------
An HTML attachment was scrubbed...
URL: <http://freedomarchives.org/pipermail/news_freedomarchives.org/attachments/20160308/7a201375/attachment.html>


More information about the News mailing list