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Families with multiple sclerosis can be
reassured that the risk of their children
acquiring MS at any age is low, varying from
about 1 in 100 if an aunt or uncle has MS to
approximately 1 in 40 if a parent has MS. This
compares to a 1 in 750 chance of a child getting
MS over a lifetime in the general population. |
Multiple sclerosis (MS) historically has been viewed as
an adult-onset disease and the majority of research and
support programs have targeted adults. Since 1980,
however, over 400 cases of childhood MS have been
recorded in over 25 medical publications. Initial
symptoms have been seen as early as 13 months old, with
diagnosis as young as 2 years of age. Largely because of
new technology, the numbers of children and adolescents
diagnosed with MS are steadily growing.
An estimated 400,000 Americans have MS, and of these,
8-10,000 are children or adolescents. However, an
additional 10-15,000 have experienced at least one
symptom suggestive of MS. Some of these will go on to
develop MS, although in most cases, they will not
actually be diagnosed until they are adults. The advent
of the MRI and other new ways of detecting MS lesions in
the brain and spinal cord have resulted in numerous
articles in the MS literature citing case after case of
pediatric MS across the country. Because neurologists so
rarely encounter childhood MS, diagnosis may be delayed
or more difficult than for adult-onset disease.
Today, childhood MS is often treated in the same way as
adult MS. In addition to a range of interventions to
treat the various symptoms that can occur, there are
four injectable disease-modifying drugs that have been
shown to alter the course of the disease. These drugs
have dosing schedules ranging from once a week to every
day. The medications have been tested and approved for
use by adults, but have not been systematically studied
for children.
Although consensus guidelines exist for diagnosis and
treatment of adult MS, none have been developed for
children and adolescents—largely because little is known
about the impact of MS on this young population.
Neurologists who treat children with MS have reported,
however, that some children present with cognitive
difficulties that may impact academic achievement. Some
studies also indicate that more young girls are
diagnosed with MS than young boys, mirroring a gender
imbalance also seen in adults with the disease.
MS is a disease that affects the whole family. Its
impact is felt throughout the entire family system,
affecting communication, relationships, and daily
functioning. Symptoms such as extreme fatigue, weakness,
bladder problems, and cognitive changes may alter the
child's ability to participate in normal childhood
activities. Children may also exhibit a range of
emotions and behaviors—such as aggression, chronic
depression and generalized anxiety—as a secondary
consequence of diagnosis.
Parents have valid concerns about their child's
health, education, and future, and the National
MS Society has established a broad range of
initiatives to help families with a child or
teen with MS.
As the leading private funder of MS research,
and because of the critical need to better
understand childhood MS, the National MS Society
established the first-of-its kind network of
Pediatric MS Centers of Excellence. The
centers were established in geographically
diverse areas so that they can serve as regional
centers for as many children and families living
with MS as possible. They are staffed by teams
of pediatric and adult MS experts who lead the
field in MS diagnosis and treatment. The Center
locations are:
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Center for Pediatric-Onset Demyelinating
Disease at the Children's Hospital of
Alabama, University of Alabama at Birmingham
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Pediatric MS Center of the Jacobs
Neurological Institute, State University of
New York at Buffalo
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Mayo Clinic T. Denny Sanford Pediatric
Outpatient Center, Rochester, MN
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National Pediatric MS Center at Stony Brook
University Hospital, Long Island
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Partners Pediatric MS Center at the
Massachusetts General Hospital for Children
in Boston
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University of California, San Francisco
Regional Pediatric MS Center
Get more information on the Pediatric MS
Centers of Excellence
For more information...
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Young Persons with MS: A Network for
Families with a Child or Teen with MS
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Pediatric MS Study Group
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MS Under 21 (InsideMS article)
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Teen InsideMS
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Young Persons with MS: A Network
for Families with a Child or Teen with
MS
Contact the Program Coordinator
Toll free:
1-866-KIDS W MS
(1-866-543-7967)
or send an e-mail to
childhoodms@nmss.org.
U.S. residents can also
contact
your Society chapter.
Toll-free: 1-800-344-4867
Find out more about the Network

Pediatric MS Centers of Excellence

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Kaley Zeitouni, founder of
YAMS (Youth Against MS) |

Pediatric MS
Study Group
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Increase knowledge of pediatric MS
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Increase awareness of pediatric MS
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Provide increased services for
children and parents
Read more about the Pediatric MS Study
Group

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Webcast
(transcript available) |
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Helping Kids with MS
featuring Dr. Lauren Krupp
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The Wall Street Journal—
Feb. 28, 2006: "The New Face of
Multiple Sclerosis: Doctors Increasingly
Detect The Disorder in Children"
Download PDF of article
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