This is topic Literatures about connection of Lyme and ALS please? in forum Medical Questions at LymeNet Flash.


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Posted by wtl (Member # 19883) on :
 
I just talked to someone whose whole family of 7 have ALS. I am smelling something terribly wrong but I can't find any specific articles to raise their awareness on this subject. A quick search here revealed nothing.

Any link to the topic will be greatly appreciated.
 
Posted by Dekrator48 (Member # 18239) on :
 
http://www.canlyme.com/gazette_martz_2006.html


http://www.canlyme.com/NFLALS2004.html


http://www.canlyme.com/martz.html


http://www.canlyme.com/als0503.html


http://www.drgregorybach.com/74/2622.html
 
Posted by wtl (Member # 19883) on :
 
Thank you. These are great.
 
Posted by TF (Member # 14183) on :
 
http://www.canlyme.com/phys.html

At the bottom of this page are a number of links regarding the connection between ALS and Lyme. Also, links between alzheimers and lyme, etc.

Also,

ttp://www.wellsphere.com/lyme-disease-article/als-caused-by-lyme-disease-with-babesia-co-infection/733679
 
Posted by asummers (Member # 18068) on :
 
Wow -- what great stories and just what I needed.

I grew up in the suburbs of Philly. I can't tell you HOW MANY of my friends parents (ages 55-65) have a dx of Parkinson/ALS/MS -- it is crazy! And how many friends/family have lyme symptoms and are suffering...

And being a lymie -- I don't believe in these diagnosis'. I know my family and friends think I 'over dx' lyme, but we live in an epidemic area and these people have no family hx of these dx's (parkinson/als/ms).

MAYBE they NOW have parkinson's/als/ms b/c the lyme has gotten so out of control, but I do believe that it was lyme first.
 
Posted by wtl (Member # 19883) on :
 
Great page. TF. I was just about to ask for Alzheimer's.

asummers - I know. I was attending an event at my daughter's day care and saw this family of "ALS". It was a heartbreaking site to see, with several of them together. You just kind of know something is wrong the way they all turned out to have ALS. I promised them to forward these articles to them and I will also drop off my UOS DVD for them this evening.
 
Posted by nefferdun (Member # 20157) on :
 
Please update us on what happens to them. I hope they see an LLMD. That is so tragic. I don't know how anyone could diagnose them all with such a rare disease that is not considered to be contagious. Seems crazy.

I have an acquaintance whose husband died of ALS. I remember when she first said he had it I was so concerned I researched the internet and it kept coming up lyme disease so I told her to have him checked out for it. She said the doctors told her there is no lyme in Montana and he had not been out of the state, so it was impossible for him to have it. Not true of course but I did not have it then.
 
Posted by massman (Member # 18116) on :
 
I was taught in 2005 that ALS is a stage of Lyme.
 


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