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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
06-30-15  →  I wonder if there are windows in Heaven? (74 views, 4 replies)
06-30-15  →  need some perspective... (69 views, 3 replies)
06-30-15  →  had a dream last night (82 views, 4 replies)
06-30-15  →  Aid started today (54 views, 4 replies)
06-30-15  →  Concerned (152 views, 6 replies)
06-29-15  →  I've been looking for answers (195 views, 2 replies)
06-29-15  →  Got my ramp today! (159 views, 8 replies)
06-29-15  →  Need all my options (177 views, 5 replies)
06-29-15  →  Standard Do I have ALS - Please help if you can (249 views, 8 replies)
06-29-15  →  Tub to shower remodel ? (123 views, 7 replies)
06-29-15  →  weight of my body compresses (pinches) nerves (165 views, 5 replies)
06-29-15  →  Update - need all the help I can get (214 views, 5 replies)
06-28-15  →  finger tips hurt and tingle (160 views, 5 replies)
06-28-15  →  Progression faster in older pals? (222 views, 8 replies)
06-28-15  →  surprise party ... (317 views, 22 replies)
06-28-15  →  am confused (175 views, 4 replies)
06-28-15  →  Tongue Twitch is the Final Straw (233 views, 3 replies)
06-28-15  →  I call it early retirement and beyond.. (447 views, 19 replies)
06-27-15  →  Exercise- yes or no? (293 views, 14 replies)
06-27-15  →  Suddenly, heart rate in low 30's (261 views, 9 replies)
06-27-15  →  What type of AlS is this? (211 views, 6 replies)
06-27-15  →  Where did u work (570 views, 34 replies)
06-27-15  →  Just need your opinion (163 views, 2 replies)
06-27-15  →  Tobii I15 with gaze interaction for sale (78 views, 0 replies)
06-27-15  →  I am glad I got my.... (317 views, 14 replies)
06-27-15  →  PEG tube update + question (169 views, 9 replies)
06-26-15  →  Q Therapeutics Announces FDA Clearance of Its Stem Cell Therapy Q-Cells for Human Tri (201 views, 4 replies)
06-26-15  →  What do I do? (355 views, 15 replies)
06-26-15  →  Any advice on pain medication? (184 views, 9 replies)
06-26-15  →  PEG tube today (165 views, 8 replies)
06-26-15  →  Just had my first home support shower... (248 views, 9 replies)
06-26-15  →  Weird symptoms, do i have ALS? (269 views, 2 replies)
06-26-15  →  Going for a second visit (316 views, 9 replies)
06-26-15  →  DPS - PEG Seurgon (195 views, 10 replies)
06-26-15  →  I should have let everyone know earlier but... (360 views, 18 replies)
06-26-15  →  Frustrated (282 views, 9 replies)
06-26-15  →  Getting the lingo right (269 views, 9 replies)
06-26-15  →  Question on Nasal Pillows (123 views, 2 replies)
06-26-15  →  From Bathurst to Bridgetown (234 views, 25 replies)
06-26-15  →  New kid (419 views, 15 replies)
06-26-15  →  My Worst Nightmare, By beloved Brother has ALS (360 views, 14 replies)
06-25-15  →  Peg and breathing issues (184 views, 6 replies)
06-25-15  →  Robert Morse (329 views, 19 replies)
06-25-15  →  Quick-Fix Cold/Chest Infection Remedy? Ideas welcome (275 views, 19 replies)
06-25-15  →  Question (142 views, 1 replies)
06-25-15  →  DIHALS? will I? (361 views, 10 replies)
06-25-15  →  Palm Atrophy (284 views, 4 replies)
06-25-15  →  Adapted first pairs of shorts... (154 views, 3 replies)
06-25-15  →  saliva management (94 views, 0 replies)
06-25-15  →  Riluzole question (125 views, 3 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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