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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
08-29-14  →  anxiety over ALS (19 views, 1 replies)
08-29-14  →  A little lost (24 views, 0 replies)
08-28-14  →  ALS like symptoms- Need advice (80 views, 2 replies)
08-28-14  →  Do I have ALS :((((( (104 views, 3 replies)
08-28-14  →  Yesterday my husband was diagnosed with ALS (171 views, 13 replies)
08-28-14  →  Just diagnosed (114 views, 9 replies)
08-28-14  →  Hospital (121 views, 2 replies)
08-28-14  →  Weakness versus Soreness (203 views, 6 replies)
08-28-14  →  I need your thoughs (123 views, 2 replies)
08-28-14  →  Worrisome EMG (173 views, 3 replies)
08-28-14  →  ALSA Ice Bucket Windfall (112 views, 1 replies)
08-28-14  →  Difficult to eat..could it be ALS? (202 views, 6 replies)
08-27-14  →  strange smell (311 views, 8 replies)
08-27-14  →  WalkAide System Foot Drop System LOT Of 2 Model 20-0100 (90 views, 0 replies)
08-27-14  →  so thankful for millenium (158 views, 3 replies)
08-27-14  →  Is this anxiety or AlS? (232 views, 6 replies)
08-27-14  →  Are you here because of the Ice Bucket challenge? (300 views, 11 replies)
08-27-14  →  Ants crawling on my spine (188 views, 8 replies)
08-27-14  →  I am pretty scared (179 views, 5 replies)
08-27-14  →  Has anyone heard about or tried Simplesa? (56 views, 0 replies)
08-27-14  →  Contagious Patterns in ALS? (244 views, 12 replies)
08-27-14  →  Als (247 views, 10 replies)
08-27-14  →  Two new potential drugs out of Harvard (195 views, 1 replies)
08-27-14  →  Do i have ALS? (240 views, 3 replies)
08-26-14  →  Young 24 years Extremely worried....please help (409 views, 7 replies)
08-26-14  →  Somewhat diappointing news... (201 views, 0 replies)
08-26-14  →  Do I have als (401 views, 9 replies)
08-26-14  →  cbd's (209 views, 13 replies)
08-26-14  →  Turmeric (257 views, 8 replies)
08-26-14  →  ALS update topic on Aug. 27th 700 Club tv show (160 views, 3 replies)
08-26-14  →  als patient from indiana (244 views, 7 replies)
08-26-14  →  Questions about Mefloquine toxcicity and dual diagnosis (201 views, 3 replies)
08-26-14  →  Help from a Veteran please (213 views, 13 replies)
08-26-14  →  Tired (254 views, 5 replies)
08-26-14  →  sore throat and phlegm (164 views, 3 replies)
08-26-14  →  Any sugguestions to help with hydration/ (224 views, 14 replies)
08-26-14  →  Anxiety or cause for worry? (370 views, 10 replies)
08-26-14  →  Adjusting to Bipap (273 views, 12 replies)
08-26-14  →  team minzey (122 views, 0 replies)
08-26-14  →  For everyone worried about twitching (299 views, 0 replies)
08-26-14  →  I have been diagnosed with ALS for 2.5 years and I am 73 years old (282 views, 7 replies)
08-26-14  →  Progressed...ugh! (272 views, 2 replies)
08-25-14  →  Twitching with ALS (318 views, 3 replies)
08-25-14  →  Weakness on right side of body (366 views, 5 replies)
08-25-14  →  So I see this facebook post on my feed today... (485 views, 20 replies)
08-25-14  →  need information (231 views, 4 replies)
08-25-14  →  you are all my family (364 views, 17 replies)
08-25-14  →  Max will be at Houston ALS clinic sept 4 (332 views, 9 replies)
08-25-14  →  Why people go away... (405 views, 14 replies)
08-25-14  →  a nightmare (437 views, 8 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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