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Welcome to the ALS/MND Support Group Forums.

If this is your first visit we would like to give you a warm welcome and thank you for taking the time to browse our ALS/MND/PLS and Lou Gehrig disease forums. If you have any questions, would like to join, or have interest about these diseases we encourage you to get involved.

How do I contact members?
Before you are able to participate in the conversations you will need to register for a forum account. Accounts are completely free and signing up takes less than five minutes. You will need a registered email account, we apologize if this is an inconvenience be we have had problems in the past when our forum allowed annonymous posts.

What does this website do? provides a free service in the form of this Internet support group. Our community consists of individuals working together to exchange information, and to offer moral support. We encourage you to join our community to learn about motor neuron disease, or to share your experiences with motor neuron disease (ALS/MND and PLS).

To view messages select the forum you would like to visit from the links below. If you prefer to search for ALS/MND/Lou Gehrig Disease information you can click the 'Search' link above, or click here.

  Forum Last Post Threads Posts
ALS and MND Support Group
Our support group is for ALL persons that have been affected by amyotrophic lateral sclerosis and motor neuron disease. This includes people afflicted with motor neuron disease, their friends, families, and loved ones. ALSforums is a community where you can ask questions, discuss concerns, voice your thoughts and experiences.
Please use this forum for any general discussions about Lou Gehrig disease, and inquiries or questions you may have regarding ALS/MND.
by Nikki J
Today 04:26 PM
7,317 82,471
Newly Diagnosed (28 Viewing)
Please use this forum for any discussions related to being newly diagnosed with ALS and MND. This may include questions about your diagnosis, or concerns with being newly diagnosed with ALS.
by GregK
Today 12:07 PM
372 6,113
Have symptoms? Not sure if you have ALS, or what ALS is? Would you like to ask a general question about ALS symptoms? Please post all related questions to this forum.
by Nuts
Today 04:06 PM
5,298 60,144
This forum was created to give individuals with ALS an opportunity to meet and discuss topics of interest. Individuals recently diagnosed with ALS can feel free to ask other members questions they may have.
by Green Queen
Today 09:24 AM
2,206 32,805
ALS that runs in the family is known as familial ALS (or fALS). ALS that doesnít run in families is called sporadic ALS. Familial ALS is very rare with only about one in ten of all ALS cases being familial.
by affected
06-17-2015 02:38 AM
38 292
Stories of Hope (24 Viewing)
Please place your stories of hope, and reasons to look forward to the future in this forum. Much of what we read about ALS is sad and depressing, this forum is not the place for those threads.
by caro
Today 02:09 PM
403 8,466
ALS Tips, Tricks, and Gadgets you have found useful for people affected by ALS/MND. Post items that you have invented, adapted, found or made usable for PALS.
by Mtzu
Yesterday 05:00 PM
562 5,258
ALS Research News (18 Viewing)
Post and read about interesting ALS related research news. Keep everyone updated, post your updates about Lou Gehrig's disease and ALS research news.
by Sjm16
Today 10:20 AM
568 4,820
ALS Drug Trials (6 Viewing)
Modern medicine is making great leaps and bounds; if you have any information about recent drug trials, clinical trials, post the information here. Drug trials and clinical trials are conducted to allow safety and efficacy data to be collected for health interventions (e.g., drugs, devices, therapy protocols, etc).
by LeprechaunSean
Today 02:09 PM
160 2,317
Frontotemporal dementia (FTD) is a clinical syndrome caused by degeneration of the frontal lobe of the brain and may extend back to the temporal lobe.
by affected
03-21-2015 02:05 PM
89 1,094
Healthcare professionals can meet and discuss current issues or gain insight and knowledge from other individuals affect by Lou Gehrig's disease.
by affected
09-08-2015 11:11 PM
51 534
A place for CALS to remember their beloved PALS. Please use this forum to inform us of a loved one's passing.
by cheerleader
Today 02:20 PM
578 13,477
Event Announcements (3 Viewing)
Post your event information for all to see. Feel free to post your questions and thoughts about an ALS fundraising event.
by MaxEidswick
10-08-2014 02:29 AM
324 2,460
This forum is for ALS related equipment sales. Any items that are no longer needed may be of great use to others affected by ALS.
by beccasom
09-30-2015 12:07 PM
732 2,198
PEG Feeding Tube
Percutaneous endoscopic gastrostomy (PEG), or feeding tube, is an essential element of care when ALS has progressed to the point where it interferes with a personís ability to swallow food and fluids. A feeding tube can reduce the stress and exhaustion of trying to swallow when swallowing becomes too difficult.
PEG feeding tubes supplement eating, or if swallowing is causing choking, may be used to replace eating. Ask your general questions about PEG tubes in this forum.
by dougieconnor
10-02-2015 04:58 AM
150 1,672
Please add your tips, tricks or information regarding frequently asked questions regarding PEG feeding tubes to this forum.
by Janie H
02-22-2014 09:44 AM
4 21
Discuss PEG care such as flushing, connecting and disconnecting as well as other general care and maintenance instructions.
by rosec
11-25-2013 05:32 PM
62 679
PEG Recipes (3 Viewing)
PEG feeding tube recipes can be shared and discussed in this forum.
by texastracy
06-16-2015 09:05 PM
16 204
Support for Caregivers of ALS (CALS)
This forum, inspired by the member jellycat, is for caregivers of people with ALS, both past and present.
This forum is for people that are currently providing caregiver support. People that have provided support can give support to those that are currently providing support.
by lgelb
Today 04:05 PM
2,481 37,543
This forum is for people that have provided care to someone with ALS that they have since lost to ALS.
by Atsugi
Yesterday 04:32 PM
164 2,663
Off Topic
This forum is for off topic conversations, stories, and other unrelated ALS topics of interest.
Other (9 Viewing)
Stories, other diseases, off topic discussions and general off topic conversations.
by chally
Today 08:47 AM
692 13,310
Rants & Raves (3 Viewing)
by DreamsEnd
08-24-2015 11:28 AM
252 5,472
Come For Tea (2 Viewing)
by texastracy
06-16-2015 10:58 AM
21 17,881
Birthdays (20 Viewing)
by Green Queen
08-30-2015 10:30 AM
36 1,217
by MaxEidswick
04-21-2015 05:47 PM
30 655
Primary Lateral Sclerosis Support Group
Our PLS forums are available to individuals affected by primary lateral sclerosis. The PLS support group is for PLS or disease related information, treatments, tips, caregiver and patient discussions.
Please use this support forum for questions, answers and discussions relating to Primary Lateral Sclerosis (PLS).
by lgelb
Today 02:30 PM
1,044 13,196
Progressive Bulbar Palsy Support Group
Please use this support forum for conversations relating to progressive bulbar palsy. Progressive bulbar palsy is a form of ALS that primarily affects both upper and lower motor neurons, but primarily motor neurons involved with controlling muscles in the neck, face, tongue and throat. Individuals diagnosed with PBP most frequently have difficulties with speech and swallowing.
Please use this forum for discussions about progressive bulbar palsy, PBP diagnosis, care, or to have any questions related to bulbar palsy answered.
by Jeanau
09-14-2015 05:57 PM
219 2,035
Progressive Muscular Atrophy Support Group
Please use this support forum for conversations relating to progressive muscular atrophy (PMA). Patients with PMA often survive longer than patients with ALS and in some cases symptoms can be restricted to the arms or legs for a long time before spreading elsewhere in the body.
Please use this forum for discussions about progressive muscular atrophy, diagnosis, care, questions and help related to PMA.
by Mike29
08-24-2015 03:43 PM
64 583
Multifocal Motor Neuropathy Support Group
Multifocal motor neuropathy is a progressive muscle disorder characterized by muscle weakness in the hands and differences from one side of the body to the other; affecting men much more often than women. Symptoms also include muscle wasting, cramping, and involuntary contractions or twitching of the leg muscles. MMN is mistaken for amyotrophic laterial sclerosis (ALS, or Lou Gehrig's disease) but unlike ALS, it is treatable. Early accurate diagnosis provides patients the ability recover quickly.
Our MMN forums are available to individuals affected by multifocal motor neuropathy . The MMN support group is for MMN related information, treatments and tips.
by Vincent
04-06-2015 04:27 PM
57 399
Fibromyalgia Support Group
This forum is intended for Fibromyalgia support, Fibromyalgia tips, sufferers of chronic fatigue and chronic pain.
Please discuss general topics about Fibromyalgia, Chronic Fatigue, or Chronic Pain.
by olly
01-03-2013 03:28 PM
67 591
Chat about whether your symptoms sound like Fibromyalgia, or discover Fibromyalgia symptoms.
by notme
12-29-2012 12:24 PM
28 240
Fibromyalgia is accompanied by chronic pain as a part of the syndrome and is usually widespread and the pain can occur anywhere at any time.
by MommyRissa
11-20-2012 09:48 PM
20 152
by lotusbri
11-26-2012 03:04 AM
32 362
Lyme Disease Support Group
This forum is intended for Lyme disease support and tips.
Please discuss general topics about Lyme disease.
by Lalebot
05-30-2015 08:08 PM
22 215
Information and discussions about Lyme diagnosis or being diagnosed with Lyme disease.
by lgelb
09-19-2015 02:02 AM
16 272
Discuss your thoughts, help, support or advice for people that are diagnosed and living with Lyme disease.
by NotALS!
10-08-2010 10:15 PM
2 25
Chat about whether your symptoms sound like Lyme disease, Lyme like symptoms.
by Tokahfang
11-02-2012 06:57 AM
4 62
Website Feedback and New Members
Please use this section of the forum if you are a new user, we'd love to have the opportunity to say hello. Post a quick greeting in the "Welcome New Members" forum. If you have feeback about the website, the forums, or the content, please post it in the "Problems/Bugs" forum.
We are very pleased you have found our online support group. If you are new, please take a moment to register and then post a message saying Hi to the members of the site.
by SanNicolas
08-11-2015 04:17 AM
348 4,543
If you encounter a problem with the forums please post it here and someone might be able to help. This forum is not monitored by any specific user.
by Nuts
Today 03:57 PM
175 1,495

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