ALSforums is an open support community for individuals affected MND and ALS.  We encourage you to join our support group to ask questions and to share your experiences with ALS and MND.  We offer tips about ALS, help, care, support and friendship - join today.
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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?
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.

To browse the discussions click any link below:


  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 rose
Today 02:35 AM Go to last post
2,425 22,201
Stories of Hope (1 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.
08-18-2008 12:22 AM Go to last post
38 501
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.
Today 12:16 AM Go to last post
779 7,764
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 rose
Today 01:55 AM Go to last post
478 5,054
ALS/MND Caregivers are welcome to share experiences, answer questions, discuss topics of interest and provide help to people affected by motor neuron disease.
537 5,804
Event Announcements (1 Viewing)
Post your event information for all to see. Feel free to post your questions and thoughts about an ALS fundraising event.
08-11-2008 03:03 PM Go to last post
99 565
ALS/MND Research News (3 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 Al
08-02-2008 12:22 PM Go to last post
101 817
Healthcare professionals can meet and discuss current issues or gain insight and knowledge from other individuals affect by Lou Gehrig's disease.
08-11-2008 10:15 AM Go to last post
24 242
A place for CALS to remember their beloved PALS. Please use this forum to inform us of a loved one's passing.
08-13-2008 06:57 PM Go to last post
59 783
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 CindyM
08-18-2008 09:23 AM Go to last post
52 176
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 Peg B
08-07-2008 09:37 PM Go to last post
7 68
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 Al
Yesterday 02:06 PM Go to last post
207 1,954
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.
08-05-2008 08:08 PM Go to last post
68 522
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.
pma
by jean
08-06-2008 07:53 PM Go to last post
25 319
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.
141 1,614
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.
06-25-2008 03:17 PM Go to last post
37 258

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