Myasthenia gravis (MG) is an autoimmune neuromuscular disorder that affects voluntary muscles. Common symptoms can include a drooping eyelid, blurred or double vision, slurred speech, difficulty chewing and swallowing, weakness in the arms and legs, chronic muscle fatigue and difficulty breathing. The weakness tends to increase with continued activity and can be improved with periods of rest. Not everyone will display all symptoms, and symptoms can fluctuate.
We can provide you with general information regarding MG, but you should consult with your doctor if you think you have MG. Request an information packet here.
The goal of MG treatment is to remove antibodies, reduce antibodies, and inhibit the binding of antibodies through the various medications and treatments available. (from Summer 2006 newsletter article by K. Sivakumar, MD)
There is no known cure for MG, but there are effective treatments that allow many people with MG to lead full lives. Common treatments include medications such as Mestinon® (pyridostigmine), prednisone, Cellcept® (mycophenolate mofetil), Imuran® (azathioprine), cyclosporine, and treatments such as thymectomy, plasmapheresis, and intravenous immunoglobulin (IvIg) infusions. Spontaneous improvement and even remission may occur without specific therapy. Rest and a well-balanced diet can help.
There are certain drugs that patients with MG should avoid or only use with caution. You should always discuss these concerns with your doctor or neurologist; make sure these professionals knows every drug you are taking, including ove-the-counter medications. You pharmacist may be another good resource. For more information on drugs MG patients should avoid or only use with caution you can see the following links: Emergency Alert Card 1, Emergency Alert Card 2, Medications and Myasthenia Gravis.
In some cases, MG may go into remission for a time, during which no treatment is necessary.
The generic form of Mestinon® has been on the market since February 2003 and to our knowledge no studies have been conducted as to the relative effectiveness of the medication in relation to the brand version. By law the generic medications must have the same active ingredients as the brand name medication; however, the “fillers” or excipients may differ.
Often, the cause of MG contraction is not known for the particular patient. It is possible to contract MG from Penicillamine, which is used to treat Wilson’s disease, rheumatoid arthritis, other chronic autoimmune diseases, and cystinuria. It is also possible to contract MG by being treated with interferon alpha, or through a bone marrow transplant. (From “Medication and Myasthenia Gravis”).
Researchers are uncertain of the cause of MG, but do not believe that it is hereditary. A genetic predisposition to autoimmune diseases can run in families, but MG is not thought to be directly hereditary.
Researchers are uncertain of the cause of MG, but do not believe that it is contagious.
Approximately 20 out of 100,000 individuals in the U.S. have been diagnosed with MG. However, MG is considered under-diagnosed and the prevalence is thought to be much higher.
The most common age at onset is the second and third decades in women and the seventh and eighth decades in men. As the population ages, the average age at onset increases correspondingly; now males are more often affected than females, and the onset of symptoms is usually after age 50.
Researchers are uncertain of the cause of MG, but do not believe that it is hereditary or contagious. A genetic predisposition to autoimmune diseases can run in families, but MG is not thought to be directly hereditary. There is a 12% to 20% incidence of neonatal myasthenia in infants born to mothers with MG. Neonatal myasthenia is a temporary condition of general weakness in a baby and usually occurs within the first 24 to 48 hours after birth and may last days or weeks. It is usually self-limited, lasting three to five weeks, but occasionally lasts longer.
This partially depends on the nature of your job and your MG, but most MG patients continue working successfully. You may wish to contact the Ticket for Work Program which is a self-sufficiency employment program for people with disabilities who are interested in going to work. 1-866-968-7842 or http://www.yourtickettowork.com/program_info.
MGFA cannot provide referrals for liability reasons. In general, we suggest that people see a neurologist who focuses on neuromuscular conditions at a university medical center. You may also wish to contact your local chapter, as they may have some ideas for you as well.
You or your doctor can request a professional packet for your doctor and we will send a packet via US Mail. Please allow two weeks for delivery. Click here to request the professional packet.
The Myasthenia Gravis Foundation of America (MGFA) produces and distributes informational pamphlets available to the general public. These materials describe various aspects of the illness, information on treatment programs and a number of other selected topics. You may download and print our materials. If you have difficulty downloading and printing, request a packet here and we will send it via US Mail. Please allow two weeks for delivery.
MGFA does not publish the Practical Guide or Survival Guide. If you would like copies of those publications, you can contact the Myasthenia Gravis Foundation of California at 800-574-7884 (if in California or Nevada) or 323-887-0056, or access www.myasthenia-ca.org for more information.
A research summary from our annual Scientific Session can be found on our Web site. Information of other research is also available here.
Yes. Foundation Focus is a quarterly publication that we distribute at no charge, although we do appreciate donations to help cover our expenses. We can send the newsletter by mail or e-mail. To subscribe, contact the national office.
MGFA newsletters from the past several years can be found on our Web site. Click here
We have 16 chapters throughout the country. You can check here to see if there is one in your area.
You should contact your area chapter to find out if there is a support group in your area. If there is not a chapter in your area you may wish to contact the North American Chapter here. To view a complete list of support groups click here.
You can donate online. You can also mail donations to:
Myasthenia Gravis Foundation of America, Inc.
355 Lexington Avenue, 15th Floor
New York, NY 10017-6603
If you’d like to donate in memory or in honor of an individual, we generally send an acknowledgement to your designee (with the dollar amount omitted), as well as a thank you note to the person who made the donation. Please include the person’s name and address that you’re honoring and we’ll promptly send the acknowledgement.
Thank you for your support of MGFA.
Information about Social Security Disability is available online at www.ssa.gov/disability or you can call 800-772-1213.
Our primary purpose is to provide information and promote awareness about myasthenia gravis, and unfortunately we do not have funds to assist with patient medical needs. You may want to contact your local United Way First Call For Help or another information and referral line in your area to determine whether there are any organizations in your area that offer low-cost medical services or other assistance. You may also wish to see our compiled list of patient assistance resources.
MGFA does not award scholarships. The Foundation offers research fellowships that are awarded annually. The Post-Doctoral Fellowship is a post-doctoral research fellowship.