 ALS/MND Support Group Forums | | | 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?
ALSforums.com 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 panguinjen
Today 02:04 AM | 5,485 | 60,054 | | 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 kiwisally
Today 01:57 AM | 3,233 | 38,283 | | 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 panguinjen
Today 01:48 AM | 1,565 | 22,085 | | 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 Ms. Pie
Yesterday 11:29 PM | 311 | 4,576 | | 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 Peacola
05-13-2012 11:51 PM | 333 | 3,298 | | 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 pearshoot
05-10-2012 01:55 PM | 389 | 3,215 | | 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). | | 76 | 1,232 | | 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 Cereus
05-10-2012 10:29 PM | 36 | 416 | | Healthcare professionals can meet and discuss current issues or gain insight and knowledge from other individuals affect by Lou Gehrig's disease. |
by themommy
05-03-2012 06:38 AM | 46 | 587 | | A place for CALS to remember their beloved PALS. Please use this forum to inform us of a loved one's passing. |
by cervus
Yesterday 11:29 AM | 416 | 9,897 | | Post your event information for all to see.
Feel free to post your questions and thoughts about an ALS fundraising event. |
by momap53
Yesterday 03:46 PM | 291 | 2,353 | | 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 caldona
05-11-2012 03:07 PM | 438 | 1,547 | | 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 Pandora
Today 03:13 AM | 1,891 | 25,811 | | This forum is for people that have provided care to someone with ALS that they have since lost to ALS. |
by LizT
Yesterday 10:58 PM | 55 | 945 | | Off Topic This forum is for off topic conversations, stories, and other unrelated ALS topics of interest. | | Stories, other diseases, off topic discussions and general off topic conversations. |
by arkallen
Yesterday 07:21 AM | 318 | 7,889 | | |
by BrianD
05-15-2012 09:42 AM | 129 | 2,615 | | |
by peter57
Yesterday 09:38 PM | 57 | 1,218 | | |
by LizT
Yesterday 10:47 PM | 3 | 2,574 | | |
by Annie's Phil
Yesterday 07:27 PM | 17 | 4,750 | | |
by panguinjen
Today 01:57 AM | 4 | 13,294 | | |
by tammyg
05-06-2012 11:28 AM | 8 | 903 | | |
by panguinjen
04-18-2012 10:58 PM | 20 | 591 | 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 Brother Rock
Yesterday 04:55 PM | 629 | 7,788 | 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 panguinjen
05-08-2012 10:17 PM | 163 | 1,400 | 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. | | |
by mrd1956
02-14-2012 11:11 AM | 57 | 549 | | 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 butlertl
03-19-2012 08:35 PM | 47 | 363 | | 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 KITT
04-17-2012 05:32 PM | 47 | 372 | | Chat about whether your symptoms sound like Fibromyalgia, or discover Fibromyalgia symptoms. |
by munecagirl22
08-17-2011 04:28 PM | 20 | 188 | | 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 notme
06-08-2011 02:38 PM | 5 | 13 | | |
by notme
06-22-2011 11:21 AM | 15 | 171 | | 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 Toto's Dorothy
04-29-2012 02:54 PM | 265 | 3,965 | | 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 Ms. Pie
04-28-2012 12:54 PM | 142 | 1,182 | | What's Going On? |  Currently Active Users: 651 (11 members and 640 guests)
|  | Most users ever online was 5,802, 03-07-2012 at 03:46 PM. kiwisally, hke2000, arialB, glupavomomiche, karma898, Pandora, hkmke, Jellycat, trfogey, nikejersey34, fivebucks | |
ALS/MND Support Group Forums Statistics
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Threads: 16,791,
Posts: 226,974,
Members: 18,385
Please give a warm welcome to nikejersey34, our newest member! |  | Forum Contains New Posts |  | Forum Contains No New Posts | | Forum is Closed for Posting | |
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