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ALSforums is an online support group that provides answers, tips, friendship, care and support to people affected by motor neuron disease, including, but not limited to ALS, PLS, PMA, PBP or any MND related disease.

Help ALSforums Grow Your support is greatly needed and greatly appreciated.

Welcome to the ALS support and help forum,

Click here to join the support forums.
Click here to view the support forums.
Click here to search the support forums.

The ALS support forum is an all-volunteer driven resource provided free of charge to help anyone directly or indirectly affected by ALS and MND (also known as Lou Gehrig's disease). We help individuals get support with ALS, as well as providing ALS caregiver support, and people affected by ALS with help, questions and answers, and private discussions; all under one roof.

The ALS support and MND help forums are here for individuals like yourself - people impacted by ALS and MND (motor neuron disease), whether you're a caregiver, patient, friend or family member.

Our community consists of individuals working together; exchanging information, providing moral support, caregiver support and general help with ALS - together we cope with ALS, make friends, and help one another support those with ALS.

We encourage you to join our support group to ask questions, get help with ALS, and to share experiences.

Remember, you're not alone, chat about your journey with ALS with people that understand and have experience with this deadly disease.

Together we provide hope, information, support, help, and friendship. ALS support staff, individuals, mothers, daughters, brothers, sisters, patients, caregivers and friends alike.

We've already made a big difference, help us do even better, join today to get help with ALS.

Please take a moment to join our support group, click here.
Registration takes less than five minutes

Searching for ALS information online?

Experience has shown that there are many individuals ready, willing, and actively taking advantage of people searching for information about ALS and MND. These individuals are shameless in their pursuits and often use spam e-mail tactics, or worse yet, false claims, promises of miracle cures, misleading leading information and fear tactics in order to profit from your situation.

Have something to add to our information about potential scams? Do you have a personal story to share? Please feel free to share it with us through our publicly available ALS support and help groups. Working together we can make the Internet a safer place for people affected by ALS/MND.

Join the ALS forum

ALSforum is a support group to help people deal with the daily living issues associated with ALS. The ALS forum will connect you with people that can provide answers, support and help with ALS.

We invite you to join the community.

ALS directory

Please take a moment to review our nonprofit directory. Our directory currently includes information and links to registered and recommended nonprofits.

Recent ALS chat and support group threads

Click a link below to view recent support group discussions and ALS information, or browse through our archives:

RSS Feed - ALS Support Group Forum - Subscribe to our RSS feed

DateThread Title / Views
01-30-15  →  Two beds (3 views, 0 replies)
01-30-15  →  Vitamins/Supplements (17 views, 0 replies)
01-30-15  →  pep talk (48 views, 6 replies)
01-30-15  →  Vote (55 views, 0 replies)
01-30-15  →  Spasticity (117 views, 1 replies)
01-30-15  →  Question (107 views, 1 replies)
01-29-15  →  Wife wont let me drive anymore (264 views, 17 replies)
01-29-15  →  ALS takes another thing away (247 views, 11 replies)
01-29-15  →  Anyone here with respiratory issues? (193 views, 8 replies)
01-29-15  →  On the outside looking in. (186 views, 6 replies)
01-29-15  →  Unsure and confused (283 views, 6 replies)
01-29-15  →  Sister given probable ALS diagnosis (260 views, 6 replies)
12-01-14  →  Updates and Concerns Re: Atrophy (824 views, 14 replies)
01-29-15  →  Peg? (109 views, 3 replies)
01-29-15  →  Not on BiPap but lots of mucus (172 views, 9 replies)
01-29-15  →  Webinar on Diaphragm Pacemaker (146 views, 10 replies)
01-29-15  →  Get me to the Church 'er to the Commode on time - ACK! (177 views, 8 replies)
01-29-15  →  Mayo Clinic and Medicare (172 views, 5 replies)
01-29-15  →  My & Gerard's oldest son... (244 views, 11 replies)
01-28-15  →  Caregiver for a mean person with als (154 views, 2 replies)
01-28-15  →  My first brush with ALS (285 views, 7 replies)
01-28-15  →  Info for patients to understanding caregiver needs (137 views, 2 replies)
01-28-15  →  Feeling guilty! (234 views, 10 replies)
01-28-15  →  Florida, flu,and strange diseases (189 views, 6 replies)
01-28-15  →  Really confused (238 views, 3 replies)
01-28-15  →  VA assessment (110 views, 3 replies)
01-28-15  →  My Mom is finally at peace (183 views, 10 replies)
01-28-15  →  Shoulder, arm and hand symptoms (254 views, 3 replies)
01-28-15  →  Local News Anchor Announces ALS Diagnosis and Retires in Touching Broadcast (205 views, 3 replies)
01-28-15  →  Clarification/Does this sound like ALS? (332 views, 3 replies)
01-27-15  →  Clinitron At-Home Air Fluidized Therapy Hospital Bed For Sale (90 views, 0 replies)
01-27-15  →  Threat to our social security disability (171 views, 1 replies)
01-27-15  →  Is cough syrup w/codeine safe? (142 views, 2 replies)
01-27-15  →  Sleeping in my Chair (332 views, 10 replies)
01-27-15  →  Definitely starting to feel him slipping away! (214 views, 6 replies)
01-27-15  →  What kind of pool lift? (118 views, 1 replies)
01-22-15  →  how does atrophy feel (745 views, 15 replies)
01-27-15  →  Not sure... (174 views, 4 replies)
01-27-15  →  A little concerned (174 views, 1 replies)
01-27-15  →  The dreaded twitch (285 views, 4 replies)
01-27-15  →  Worried due to parathesia (249 views, 2 replies)
01-27-15  →  My pals has left me. (453 views, 21 replies)
01-26-15  →  Handicap Van (115 views, 1 replies)
01-26-15  →  Pain meds question (240 views, 6 replies)
01-26-15  →  New peg tube (165 views, 5 replies)
01-26-15  →  Gallbladder issues/Removal? (164 views, 4 replies)
01-25-15  →  A Month or 2 with PLS (392 views, 7 replies)
01-25-15  →  Stumbling (226 views, 5 replies)
01-25-15  →  My journey to the new here... (559 views, 14 replies)
01-25-15  →  sensory loss (260 views, 4 replies)
03-31-06  →  Sporty Wheelchair? (sporty wheelchair for rough terrain)
03-31-06  →  Eric Edney and Even Better Now (important read for those affected by ALS)
Click to go back to the top of this page.

Sponsorship and thanks

A very special thank you goes out to Al Pettit (ALS forum moderator supreme). Al passed away in 2012 from ALS. It's with great joy that we know Al is watching us from above. Without Al Pettit's hardwork, kind nature, and thorough knowledge of ALS, this website would not be as important, or as helpful, as it is today.

A special thank you also goes to our web technology sponsor. benefits from non profit website design in Toronto, web development and web maintenance by the kind folks at Intrigue Design located in Toronto, Ontario. Without the generosity and sponsorship of Intrigue as well as the sponsored hosting, this P'ALS community would not be possible.

In lieu of the success of this site we've launched a similar moderated support forum in beta at Fibromyalgia Forums and Lyme Forums. Fibromyalgia Forums supports individuals with Fibromyalgia, and those that suffer from Chronic Fatigue Syndrome (CFS) and chronic pain related syndromes. Lyme Forums is for individuals and groups that are affected by Lyme disease, whether family members, friends or those infected with Lyme.

Most importantly, a very big thank you to all of our heroic members and daily visitors - if only we could have met on different terms - keep up the fight!

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