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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.
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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
02-12-16  →  Medical alert for Vets (35 views, 2 replies)
02-12-16  →  Adoption - trying to find out birth family information (72 views, 3 replies)
02-11-16  →  Feeding tube recipes (56 views, 1 replies)
02-11-16  →  used equipment accounted for. (70 views, 1 replies)
02-11-16  →  My elderly uncle has been diagnosed with unusual form of ALS, we're puzzled (162 views, 5 replies)
02-11-16  →  just officially diagnosed with FALS (184 views, 7 replies)
02-11-16  →  Last One (175 views, 1 replies)
02-10-16  →  Wednesday again already? (160 views, 7 replies)
02-10-16  →  Advocacy Conference 2016 (132 views, 6 replies)
02-10-16  →  In the process of a diagnosis (151 views, 2 replies)
02-10-16  →  Does bulbar present swelling sensation in throat (88 views, 1 replies)
02-10-16  →  Part 2 of Sleep Study (139 views, 4 replies)
02-10-16  →  Thinking I may have onset of bulbar als (319 views, 11 replies)
02-10-16  →  rib pain (140 views, 7 replies)
02-10-16  →  Is this als - pleas help (213 views, 5 replies)
02-10-16  →  symptoms move quickly (334 views, 5 replies)
02-09-16  →  Tizanidine- night time dizziness? (133 views, 7 replies)
02-09-16  →  5 months in... (234 views, 15 replies)
02-09-16  →  Symptoms .. and scared (214 views, 3 replies)
02-09-16  →  Ongoing Testing for MND (237 views, 6 replies)
02-09-16  →  Mouth open (224 views, 7 replies)
02-09-16  →  Fvc (347 views, 19 replies)
02-09-16  →  EMG sound at muscle rest - please advise (378 views, 15 replies)
02-09-16  →  localized twitching (320 views, 10 replies)
02-09-16  →  Max's Birthday (323 views, 29 replies)
02-08-16  →  Soft Palate doesn't rise Symmetrically (171 views, 1 replies)
02-08-16  →  SAH grant (142 views, 5 replies)
02-08-16  →  Supplement Laminine (156 views, 2 replies)
02-08-16  →  Don't know what to do anymore.. (339 views, 8 replies)
02-08-16  →  I have no where else to turn (211 views, 7 replies)
02-08-16  →  My neurologist cannot rule out als (176 views, 1 replies)
02-07-16  →  Cluster of symptoms (269 views, 4 replies)
02-07-16  →  Contractor's Near The Villages FL. (126 views, 5 replies)
02-06-16  →  New member with many questions. (458 views, 13 replies)
02-06-16  →  No definite diagnosis of ALS yet (460 views, 13 replies)
02-06-16  →  Tongue is going crazy (304 views, 7 replies)
02-06-16  →  Hospital bed (278 views, 9 replies)
02-06-16  →  What happens with No interventions? (450 views, 12 replies)
02-06-16  →  Peg tube bumper rising (248 views, 7 replies)
02-06-16  →  finally at peace (280 views, 7 replies)
02-05-16  →  Symptoms (262 views, 6 replies)
02-05-16  →  Breathing Percent (532 views, 18 replies)
02-05-16  →  Voice Banking Question (259 views, 13 replies)
02-05-16  →  Way too worried about ALS (195 views, 2 replies)
02-05-16  →  Second opinion (357 views, 8 replies)
02-05-16  →  Als symptoms (470 views, 9 replies)
02-05-16  →  High ck . Continued facics further weakness . (209 views, 1 replies)
02-05-16  →  Questions about early nocturnal breathing symptoms (370 views, 20 replies)
02-05-16  →  Worried (295 views, 8 replies)
02-04-16  →  Project on ALS.. Looking for information. (295 views, 9 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)
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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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