Parents wish for their children to be healthy and happy — to have lives without discomfort or loss — and hope to be able to protect them and keep them from harm. When a child is diagnosed with MS, the family's wishes remains the same, and the National MS Society is committed to helping ensure the very best.
Whether the diagnosis is relatively new, or you have been searching for answers for quite some time, the words “multiple sclerosis” can be very frightening. It is important to remember that:
- You are not alone — there are both social and clinical networks to support your child and family.
- Each person’s experience with MS is different.
- This is a hopeful time. While the cause of MS is unknown and there isn’t a cure yet, there are treatments available, and an increasing number of clinicians and researchers have taken a specific interest in better understanding diagnosis and treatment of children with MS and related disorders.
Read more about our focus on pediatric MS
and what that means for families.
Connect with other families
Online groups where you can share concerns and information:
Network of Pediatric MS Centers
In 2006, the National MS Society established a nationwide network of Pediatric MS Centers to provide comprehensive evaluation and care to children and teens (up to age 18) with MS and related central nervous system (CNS) demyelinating disorders.
Today, the network has evolved to include twelve centers engaged in research to better understand the cause(s) of MS, the characteristics of these disorders in children, and how best to treat children with MS. The centers offer evaluation, diagnosis, treatment and support to families with a child displaying symptoms suggestive of any CNS demyelinating disorder; a child does not need to have a definite diagnosis of MS in order to be evaluated.
Find a center near you.
Pediatric MS Newsletter: Read about current research happening throughout the pediatric focused network