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living-with-als
3334 Members,
Archives:
Membership required
An avenue for persons living with ALS and their caregivers to communicate with the ALS community immediately, to share information, ideas, support and fellowship. All posts sent to this ...( more)
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PLS-FRIENDS
1284 Members,
Archives:
Membership required
PLS-Friends seeks to foster support and an exchange of ideas among Primary Lateral Sclerosis (PLS) and Hereditary Spastic paraplegia (HSP) patients, relatives...
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ozpals
246 Members,
Archives:
Membership required
Motor Neurone Disease Support Group for people by people with MND/ALS who live in Australia and New Zealand.
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Power4PALS
42 Members,
Archives:
Membership required
A local forum for discussion about ALS (Lou Gehrig's disease), its progression, and symptom management. A safe arena for caregivers, family members, friends, and persons with ALS to ...( more)
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Wisconsin-ALS
< 5 Members,
Archives:
Membership required
The purpose is to provide a forum for the Wisconsin ALS community to ask questions, exchange information, share experiences, feelings, emotions, etc. in the support of all affected by ...( more)
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paulspals2
Pauls Pals honors Lou Gehrig and Welcomes All who Are Looking For Chat, Useful Links Or Would Just Like To Post a Photo or...
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alslyme
344 Members,
Archives:
Membership required
An information- sharing resource for PALS (People with ALS) who have also tested positive for chronic Lyme and related infections, and for their caregivers, friends and health-care ...(more)
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PLSers-NEWS
309 Members,
Archives:
Membership required
PLSers from all over the world that have joined us will be able to read the NEWS, quickly too! The PLS News was started in 1999 by Frank Reyerse. The PLS Web Site at: http://www.geociti ...( more)
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alsormnd
This is a club for PALS/Caregivers to talk.
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alsalternativemedicine
I have been diagnosed with ALS and have tried many alternate medicines. Let's share what is available, what works and what doesn't. Let's find a common denominator to lead to a cure.
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