LymeNet Home LymeNet Home Page LymeNet Flash Discussion LymeNet Support Group Database LymeNet Literature Library LymeNet Legal Resources LymeNet Medical & Scientific Abstract Database LymeNet Newsletter Home Page LymeNet Recommended Books LymeNet Tick Pictures Search The LymeNet Site LymeNet Links LymeNet Frequently Asked Questions About The Lyme Disease Network LymeNet Menu

LymeNet on Facebook

LymeNet on Twitter




The Lyme Disease Network receives a commission from Amazon.com for each purchase originating from this site.

When purchasing from Amazon.com, please
click here first.

Thank you.

LymeNet Flash Discussion
Dedicated to the Bachmann Family

LymeNet needs your help:
LymeNet 2020 fund drive


The Lyme Disease Network is a non-profit organization funded by individual donations.

LymeNet Flash Post New Topic  New Poll  Post A Reply
my profile | directory login | register | search | faq | forum home

  next oldest topic   next newest topic
» LymeNet Flash » Questions and Discussion » Medical Questions » Lyme Connection? Lou Gehrig's

 - UBBFriend: Email this page to someone!    
Author Topic: Lyme Connection? Lou Gehrig's
hurtingramma
LymeNet Contributor
Member # 7770

Icon 1 posted      Profile for hurtingramma     Send New Private Message       Edit/Delete Post   Reply With Quote 
Lou Gehrig's Disease Linked to Algae?
Featured Videos
Lou Gehrig's Disease Linked to Algae?

Researchers at Dartmouth-Hitchcock Medical Center have been looking into Lou Gehrig's disease and a potential link to the illness nearby. Nine people living near Mascoma Lake in Enfield, N.H., have been diagnosed with the illness in the past 20 years. But more research is needed to know whether a disease cluster really exists.

Roger Barnes grew up in Enfield spending his summers on Mascoma Lake. For two decades it's been a special place for him.

"You know it's got the mountains, Shaker Mountain on the western side, plenty of places to hike. Especially with the lake there is plenty of fishing," Barnes said.

But what else may be in the water besides fish has caught the attention of researchers at Dartmouth-Hitchcock Medical Center who are mapping out clusters of ALS-- or Lou Gehrig's disease-- a disease that attacks nerve cells in the brain and spinal cord.

"In mapping out the patients we noticed that there appeared to be a fairly high density of ALS patients around water bodies," explained Dr. Elijah Stommel, a neurologist.

Stommel says certain algae blooms produce a neurotoxin that may trigger the disease. The blue-green algae can be fatal to animals and should be avoided.

"If you see an active bloom in the water, which is like a green scum of the surface of the water or you hear of one, swimming in the water is probably not a good idea," Stommel advised.

According to Enfield's Health Inspector, no blue-green algae blooms have been spotted on Mascoma Lake this year.

Statistics show that the prevalence of ALS here is about 25 times greater than national norms. However, according to Dr. Stommel, there is no direct link between the disease and the lake, and there is no cause for public alarm.

"We certainly were not looking to scare anyone who lives near water and there is probably some necessity to have a genetic predisposition," Stommel said.

Back at the Barnes summer home, this native Granite Stater is worried more about milfoil in the water than anything else.

"I don't think people should panic. I think more information is obviously needed," Barnes said.

Neurologists agree even with the summer swimming season right around the corner.

This appeared on the WCAX TV news

Dartmouth is noted for it's denial of LD

[ 06-12-2009, 09:40 AM: Message edited by: hurtingramma ]

--------------------
"Few of us can do great things, but all of us can do small things with great love". Mother Theresa

http://www.facebook.com/profile.php?id=1629665573&ref=name

Posts: 938 | From Northeast Kingdom Vermont | Registered: Aug 2005  |  IP: Logged | Report this post to a Moderator
bettyg
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
on page 2; suggest you add ALS or lou gehrig's to subject line ....

just click on pencil to open up subject line .... might be moer readers/replies [Smile] good luck.

IP: Logged | Report this post to a Moderator
Keebler
Honored Contributor (25K+ posts)
Member # 12673

Icon 1 posted      Profile for Keebler     Send New Private Message       Edit/Delete Post   Reply With Quote 
-

Dr Martz's recovery from paralyzing misdiagnosed "ALS" that turned out to be tick-borne infection:


http://www.dreamdoctor.com/radio/battle.shtml

-

Posts: 48021 | From Tree House | Registered: Jul 2007  |  IP: Logged | Report this post to a Moderator
Kerryblue
LymeNet Contributor
Member # 4077

Icon 1 posted      Profile for Kerryblue     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi, I feel after much research Parkinson`s, along with FM(think is worst co-infection,ME/Cfids/+++ many co-infections, or what ever not co-infection but take entity of their. No diff than cancer has way over 100 names.
I am in Late stage with treated too late unfortunately recent picc (so expense).
In hopes to halt it some put road block up so to speak.
Was not enough med. to really try a reversal of my Lyme.Have NO doubt all of us (If able). After 20+yrs.Very ill went from 1 day,good to 7daysbad.

Not going to get cure over night doc say admitted also & that I knew more about Lyme than he doe`s. So need to get more antibiotic`s on ID doc, just came on my HMO, Finally doc would do some treatment.
.
Mine leaning toward ALS upset me so I found my paperwork (his blood work no neg).
Yrs, back Kaiser filtered through all 100`s of paper work they sent.
Found paperwork with all positive across board,elisa,bart,babs,Plus anti bodies. Finally someone took me seriously. Lymie Tony came & there is a diff. how woman get treated.

Posts: 746 | From Clearwater/fl/Pinellas | Registered: Jun 2003  |  IP: Logged | Report this post to a Moderator
   

Quick Reply
Message:

HTML is not enabled.
UBB Code� is enabled.

Instant Graemlins
   


Post New Topic  New Poll  Post A Reply Close Topic   Feature Topic   Move Topic   Delete Topic next oldest topic   next newest topic
 - Printer-friendly view of this topic
Hop To:


Contact Us | LymeNet home page | Privacy Statement

Powered by UBB.classic™ 6.7.3


The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:

The Lyme Disease Network of New Jersey
907 Pebble Creek Court, Pennington, NJ 08534 USA


| Flash Discussion | Support Groups | On-Line Library
Legal Resources | Medical Abstracts | Newsletter | Books
Pictures | Site Search | Links | Help/Questions
About LymeNet | Contact Us

© 1993-2020 The Lyme Disease Network of New Jersey, Inc.
All Rights Reserved.
Use of the LymeNet Site is subject to Terms and Conditions.