Have You...
- Downloaded the latest volume of "Antiphospho...What?"?
- Checked out our links page?
- Joined our online support forum?
- Shopped in our Cafepress* and Zazzle* stores for APS, Lupus, Infant Loss (& many more!) awareness items?
- Sent a family member or loved one flowers through our FlowerPetal* shop?
- Watched the videos on our YouTube page?
- Joined our mailing list to receive our newsletters and updates?
- Read how you can help the APSFA?
- Joined us on Facebook or Twitter?
- Submitted your patient story for our quarterly newsletter?
- Seen our segment on "Mystery Diagnosis"? You can buy it now on iTunes!
*APSFA ADVERTISEMENTS
Multiple Sclerosis Information Page
Since APS is commonly misdiagnosed as Multiple Sclerosis, we decided to provide a short informational page on MS. For a more in depth page on MS click here.
Table of Contents (click to jump to sections)
What is Multiple Sclerosis?
An unpredictable disease of the central nervous system, multiple sclerosis (MS) can range from relatively benign to somewhat disabling to devastating, as communication between the brain and other parts of the body is disrupted. Many investigators believe MS to be an autoimmune disease -- one in which the body, through its immune system, launches a defensive attack against its own tissues. In the case of MS, it is the nerve-insulating myelin that comes under assault. Such assaults may be linked to an unknown environmental trigger, perhaps a virus.
Most people experience their first symptoms of MS between the ages of 20 and 40; the initial symptom of MS is often blurred or double vision, red-green color distortion, or even blindness in one eye. Most MS patients experience muscle weakness in their extremities and difficulty with coordination and balance. These symptoms may be severe enough to impair walking or even standing. In the worst cases, MS can produce partial or complete paralysis. Most people with MS also exhibit paresthesias, transitory abnormal sensory feelings such as numbness, prickling, or "pins and needles" sensations. Some may also experience pain. Speech impediments, tremors, and dizziness are other frequent complaints. Occasionally, people with MS have hearing loss. Approximately half of all people with MS experience cognitive impairments such as difficulties with concentration, attention, memory, and poor judgment, but such symptoms are usually mild and are frequently overlooked. Depression is another common feature of MS.
Is there any treatment?
There is as yet no cure for MS. Many patients do well with no therapy at all, especially since many medications have serious side effects and some carry significant risks. However, three forms of beta interferon (Avonex, Betaseron, and Rebif) have now been approved by the Food and Drug Administration for treatment of relapsing-remitting MS. Beta interferon has been shown to reduce the number of exacerbations and may slow the progression of physical disability. When attacks do occur, they tend to be shorter and less severe. The FDA also has approved a synthetic form of myelin basic protein, called copolymer I (Copaxone), for the treatment of relapsing-remitting MS. Copolymer I has few side effects, and studies indicate that the agent can reduce the relapse rate by almost one third. An immunosuppressant treatment, Novantrone (mitoxantrone ), is approved by the FDA for the treatment of advanced or chronic MS.
While steroids do not affect the course of MS over time, they can reduce the duration and severity of attacks in some patients. Spasticity, which can occur either as a sustained stiffness caused by increased muscle tone or as spasms that come and go, is usually treated with muscle relaxants and tranquilizers such as baclofen, tizanidine, diazepam, clonazepam, and dantrolene. Physical therapy and exercise can help preserve remaining function, and patients may find that various aids -- such as foot braces, canes, and walkers -- can help them remain independent and mobile. Avoiding excessive activity and avoiding heat are probably the most important measures patients can take to counter physiological fatigue. If psychological symptoms of fatigue such as depression or apathy are evident, antidepressant medications may help. Other drugs that may reduce fatigue in some, but not all, patients include amantadine (Symmetrel), pemoline (Cylert), and the still-experimental drug aminopyridine. Although improvement of optic symptoms usually occurs even without treatment, a short course of treatment with intravenous methylprednisolone (Solu-Medrol) followed by treatment with oral steroids is sometimes used.
What is the prognosis?
A physician may diagnose MS in some patients soon after the onset of the illness. In others, however, doctors may not be able to readily identify the cause of the symptoms, leading to years of uncertainty and multiple diagnoses punctuated by baffling symptoms that mysteriously wax and wane. The vast majority of patients are mildly affected, but in the worst cases, MS can render a person unable to write, speak, or walk. MS is a disease with a natural tendency to remit spontaneously, for which there is no universally effective treatment.
What research is being done?
The National Institute of Neurological Disorders and Stroke (NINDS) and other institutes of the National Institutes of Health (NIH) conduct research in laboratories at the NIH and also support additional research through grants to major medical institutions across the country. Scientists continue their extensive efforts to create new and better therapies for MS. One of the most promising MS research areas involves naturally occurring antiviral proteins known as interferons. Beta interferon has been shown to reduce the number of exacerbations and may slow the progression of physical disability. When attacks do occur, they tend to be shorter and less severe. In addition, there are a number of treatments under investigation that may curtail attacks or improve function. Over a dozen clinical trials testing potential therapies are underway, and additional new treatments are being devised and tested in animal models.
In 2001, the National Academies/Institute of Medicine, a Federal technical and scientific advisory agency, prepared a strategic review of MS research. To read or download the National Academies/Institute of Medicine report, go to: "Multiple Sclerosis: Current Status and Strategies for the Future."
Select this link to view a list of studies currently seeking patients.
| Clearinghouse on Disability
Information Special Education & Rehabilitative Services Communications & Customer Service Team 550 12th Street, SW, Rm. 5133 Washington, DC 20202-2550 http://www.ed.gov/about/offices/list/osers Tel: 202-245-7307 202-205-5637 (TTD) Fax: 292024507636 |
International Essential Tremor
Foundation P.O. Box 14005 Lenexa, KS 66285-4005 http://www.essentialtremor.org Tel: 913-341-3880 888-387-3667 Fax: 913-341-1296 |
| Multiple Sclerosis Association
of America 706 Haddonfield Road Cherry Hill, NJ 08002 msaa@msaa.com http://www.msaa.com Tel: 856-488-4500 800-532-7667 Fax: 856-661-9797 |
Multiple Sclerosis Foundation 6350 North Andrews Avenue Ft. Lauderdale, FL 33309-2130 support@msfocus.org http://www.msfocus.org Tel: 954-776-6805 888-MSFOCUS (673-6287) Fax: 954-351-0630 |
| National Rehabilitation
Information Center (NARIC) 4200 Forbes Boulevard Suite 202 Lanham, MD 20706-4829 naricinfo@heitechservices.com http://www.naric.com Tel: 301-459-5900/301-459-5984 (TTY) 800-346-2742 Fax: 301-562-2401 |
National Ataxia Foundation (NAF) 2600 Fernbrook Lane North Suite 119 Minneapolis, MN 55447-4752 naf@ataxia.org http://www.ataxia.org Tel: 763-553-0020 Fax: 763-553-0167 |
| National Multiple Sclerosis
Society 733 Third Avenue 6th Floor New York, NY 10017-3288 nat@nmss.org http://www.nationalmssociety.org Tel: 212-986-3240 800-344-4867 (FIGHTMS) Fax: 212-986-7981 |
American Autoimmune Related
Diseases Association 22100 Gratiot Avenue Eastpointe East Detroit, MI 48201-2227 aarda@aarda.org http://www.aarda.org Tel: 586-776-3900 800-598-4668 Fax: 586-776-3903 |
| National Organization for Rare
Disorders (NORD) P.O. Box 1968 (55 Kenosia Avenue) Danbury, CT 06813-1968 orphan@rarediseases.org http://www.rarediseases.org Tel: 203-744-0100 Voice Mail 800-999-NORD (6673) Fax: 203-798-2291 |
Well Spouse Association 63 West Main Street Suite H Freehold, NJ 07728 info@wellspouse.org http://www.wellspouse.org Tel: 800-838-0879 732-577-8899 Fax: 732-577-8644 |
| Paralyzed Veterans of America (PVA) 801 18th Street, NW Washington, DC 20006-3517 info@pva.org http://www.pva.org Tel: 202-USA-1300 (872-1300) 800-424-8200 Fax: 202-785-4452 |
Accelerated Cure Project for
Multiple Sclerosis 300 Fifth Avenue Waltham, MA 02451 info@acceleratedcure.org http://www.acceleratedcure.org Tel: 781-487-0008 Fax: 781-487-0009 |
Related NINDS Publications and
Information
-
Multiple Sclerosis: Hope Through Research
Multiple Sclerosis (MS) information sheet compiled by the National Institute of Neurological Disorders and Stroke (NINDS). -
Neurological Diagnostic Tests and Procedures
Fact sheet on neurological diagnosis and testing, prepared by the National Institute of Neurological Disorders and Stroke (NINDS). -
Small Trial Shows Daclizumab Add-On Therapy Improves Multiple Sclerosis Outcome
May 2004 press release on a clinical trial showing improved patient outcome after use of the drug daclizumab. -
Old Drug, New Use: New Research Shows Common Cholesterol-Lowering Drug Reduces Multiple Sclerosis Symptoms in Mice
January 2003 news summary on studies suggesting that statin drugs may be useful for multiple sclerosis. -
Brain Produces New Cells in Multiple Sclerosis
February 2002 news summary on brain repair in multiple sclerosis. -
Biomarkers in Multiple Sclerosis - Workshop Summary
Biomarkers in Multiple Sclerosis - Workshop Summary -
Genetics and Multiple Sclerosis: Future Prospects Workshop
Genetics and Multiple Sclerosis: Future Prospects Workshop -
Multiple Sclerosis and Chemokines: Prospects for Therapeutic and Prophylactic Intervention
Health Disparities Working Group Meeting: Cognitive and Emotional Health Multiple Sclerosis and Chemokines: Prospects for Therapeutic and Prophylactic Intervention -
NINDS Seeks Patients with Multiple Sclerosis
Lay-language descriptions of new program announcements and clinical trials seeking patient volunteers. -
NINDS Accepts Organ Donations for Multiple Sclerosis Research
Lay-language descriptions of new program announcements and clinical trials seeking patient volunteers.
Publicaciones en Español
-
Esclerosis Múltiple: Esperanza en la Investigacion
A Spanish-language public information booklet on multiple sclerosis/Informacion de la Enfermadad de Esclerosis
Condensed from Multiple Sclerosis: Hope Through Research
Prepared by:
Office of Communications and Public Liaison
National Institute of Neurological Disorders and Stroke
National Institutes of Health
Bethesda, MD 20892
NINDS health-related material is provided for information purposes only and does not necessarily represent endorsement by or an official position of the National Institute of Neurological Disorders and Stroke or any other Federal agency. Advice on the treatment or care of an individual patient should be obtained through consultation with a physician who has examined that patient or is familiar with that patient's medical history.
All NINDS-prepared information is in the public domain and may be freely copied. Credit to the NINDS or the NIH is appreciated.
Last updated January 24, 2006
Page last update: 11/13/10
![]() |
|
![]() |
|
![]() |
|
|
![]() |
![]() |
![]() |
The APS Foundation of America, Inc. website and forums are both volunteer run and funded by donations to the APSFA.
Website hosted by Dreamhost. Website created and maintained by Heidi P.
DISCLAIMER: APS Foundation of America, Inc. website is not intended to replace standard doctor-patient visits, physical examination, and medical testing. Information given to members is only an opinion. All information should be confirmed with your personal doctor. Always seek the advice of a trained physician in person before seeking any new treatment regarding your medical diagnosis or condition. Any information received from APS Foundation of America, Inc. website is not intended to diagnose, treat, or cure. This site is for informational purposes only. Please note that we will be listing all donor or purchaser's names on the Donor page of our foundation site. If you do not want your name listed, please contact us to opt out. If you think you may have a medical emergency, call your doctor or 911 immediately.
APS Foundation of America, Inc. will be building a database with your email, name and address information for future mailings. Your information will be kept confidential and not sold to any third parties. You may opt out at anytime by emailing us.
APSFA ©2005-2013 | APSFA Privacy Policy | APSFA Advertising Policy | 501(c)3 Public Charity EIN #203085295






