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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
08-28-14  →  Yesterday my husband was diagnosed with ALS (50 views, 5 replies)
08-28-14  →  Just diagnosed (46 views, 8 replies)
08-28-14  →  Hospital (60 views, 2 replies)
08-28-14  →  Weakness versus Soreness (117 views, 3 replies)
08-28-14  →  I need your thoughs (100 views, 2 replies)
08-28-14  →  Worrisome EMG (129 views, 3 replies)
08-28-14  →  ALSA Ice Bucket Windfall (94 views, 1 replies)
08-28-14  →  Difficult to eat..could it be ALS? (151 views, 4 replies)
08-27-14  →  strange smell (263 views, 4 replies)
08-27-14  →  WalkAide System Foot Drop System LOT Of 2 Model 20-0100 (84 views, 0 replies)
08-27-14  →  so thankful for millenium (152 views, 3 replies)
08-27-14  →  Is this anxiety or AlS? (207 views, 6 replies)
08-27-14  →  Are you here because of the Ice Bucket challenge? (280 views, 11 replies)
08-27-14  →  Ants crawling on my spine (175 views, 8 replies)
08-27-14  →  I am pretty scared (158 views, 5 replies)
08-27-14  →  Has anyone heard about or tried Simplesa? (47 views, 0 replies)
08-27-14  →  Contagious Patterns in ALS? (238 views, 12 replies)
08-27-14  →  Als (236 views, 9 replies)
08-27-14  →  Two new potential drugs out of Harvard (163 views, 0 replies)
08-27-14  →  Do i have ALS? (225 views, 3 replies)
08-26-14  →  Young 24 years Extremely worried....please help (392 views, 7 replies)
08-26-14  →  Somewhat diappointing news... (192 views, 0 replies)
08-26-14  →  Do I have als (349 views, 7 replies)
08-26-14  →  cbd's (204 views, 13 replies)
08-26-14  →  Turmeric (248 views, 8 replies)
08-26-14  →  ALS update topic on Aug. 27th 700 Club tv show (158 views, 3 replies)
08-26-14  →  als patient from indiana (228 views, 6 replies)
08-26-14  →  Questions about Mefloquine toxcicity and dual diagnosis (194 views, 3 replies)
08-26-14  →  Help from a Veteran please (206 views, 13 replies)
08-26-14  →  Tired (249 views, 5 replies)
08-26-14  →  sore throat and phlegm (152 views, 3 replies)
08-26-14  →  Any sugguestions to help with hydration/ (219 views, 14 replies)
08-26-14  →  Anxiety or cause for worry? (357 views, 10 replies)
08-26-14  →  Adjusting to Bipap (258 views, 12 replies)
08-26-14  →  team minzey (119 views, 0 replies)
08-26-14  →  For everyone worried about twitching (290 views, 0 replies)
08-26-14  →  I have been diagnosed with ALS for 2.5 years and I am 73 years old (267 views, 7 replies)
08-26-14  →  Progressed...ugh! (264 views, 2 replies)
08-25-14  →  Twitching with ALS (305 views, 3 replies)
08-25-14  →  Weakness on right side of body (344 views, 5 replies)
08-25-14  →  So I see this facebook post on my feed today... (472 views, 20 replies)
08-25-14  →  need information (229 views, 4 replies)
08-25-14  →  you are all my family (344 views, 17 replies)
08-25-14  →  Max will be at Houston ALS clinic sept 4 (319 views, 9 replies)
08-25-14  →  Why people go away... (393 views, 14 replies)
08-25-14  →  a nightmare (399 views, 7 replies)
08-25-14  →  Adaptive clothing (201 views, 4 replies)
08-25-14  →  Anxiety meds (249 views, 6 replies)
08-25-14  →  Urgent!!! Deadline 8/27 (341 views, 14 replies)
08-25-14  →  Normal NCS, and some issue on EMG (352 views, 10 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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