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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.



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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
05-23-15  →  Nighttime: hot then cold then hot? (80 views, 4 replies)
05-23-15  →  Delicate question about a crappy subject... (99 views, 3 replies)
05-23-15  →  my crazy life.. (117 views, 5 replies)
05-23-15  →  Air mouse (88 views, 2 replies)
05-23-15  →  ALS, alcholism, and suffering (178 views, 5 replies)
05-22-15  →  No wheelchair with hospice (183 views, 8 replies)
05-22-15  →  Can one live on ensure plus or boost plus alone (225 views, 7 replies)
05-22-15  →  in ALS limbo (291 views, 7 replies)
05-22-15  →  How long does it take? (376 views, 11 replies)
05-22-15  →  Doctor concerned (269 views, 6 replies)
05-22-15  →  Bulbar palsy & odd tongue sensation (131 views, 2 replies)
05-21-15  →  Pain (216 views, 9 replies)
05-21-15  →  Diahrrea with peg formulas. (193 views, 8 replies)
05-21-15  →  Hand issues (522 views, 15 replies)
05-21-15  →  Anticipatory Grief and Death with Dignity (334 views, 14 replies)
05-20-15  →  One Year Update (266 views, 1 replies)
05-20-15  →  I am 18 (197 views, 3 replies)
05-20-15  →  Invacare Slings Only (126 views, 1 replies)
05-20-15  →  ALS? bulbar?lower motor? (450 views, 11 replies)
05-20-15  →  PBP and Social Security disability (146 views, 5 replies)
05-19-15  →  It's all starting to catch up with me (373 views, 9 replies)
05-19-15  →  New to Forum -Thankful for All of You (220 views, 6 replies)
05-19-15  →  How to locate members near me? (237 views, 7 replies)
05-19-15  →  ALS just shows up on list of diagnoses? (284 views, 4 replies)
05-19-15  →  Long time no see ... (189 views, 2 replies)
05-19-15  →  coughing up a little blood? (437 views, 25 replies)
05-19-15  →  trying to stay calm (403 views, 3 replies)
05-19-15  →  a little insight please (244 views, 3 replies)
05-19-15  →  Feeling at loose ends (256 views, 10 replies)
05-19-15  →  Augie Nieto's New Blog (179 views, 1 replies)
05-19-15  →  PBP with strange tongue sensation (128 views, 1 replies)
05-18-15  →  The worry (289 views, 2 replies)
05-18-15  →  Had my Second Opinion Today (370 views, 11 replies)
05-18-15  →  Very tired (830 views, 36 replies)
05-18-15  →  Eating/drinking. (319 views, 8 replies)
05-18-15  →  scared. (292 views, 5 replies)
05-18-15  →  Technology: Tobii eye-gaze (239 views, 9 replies)
05-18-15  →  Rare disease registry thread (163 views, 0 replies)
05-18-15  →  Rare disease registry (188 views, 1 replies)
05-18-15  →  Chasing Midnight (313 views, 13 replies)
05-18-15  →  Update. (276 views, 0 replies)
05-17-15  →  I just have to vent a little (311 views, 8 replies)
05-17-15  →  loss of muscle, bigger waist (681 views, 32 replies)
05-17-15  →  Question to CALS (511 views, 19 replies)
05-17-15  →  Riluzole and other therapies (236 views, 7 replies)
05-17-15  →  New to the ALS Forums (204 views, 4 replies)
05-17-15  →  My Brother newly diagnosed (415 views, 8 replies)
05-17-15  →  up.. down.. who knows anymore. (537 views, 20 replies)
05-16-15  →  Freaking out! (639 views, 20 replies)
05-16-15  →  Trilogy Mask Leaking (195 views, 2 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. ALSforums.com 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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