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This page is a collection of useful sites and articles aimed specifically at children and teenagers with Multiple Sclerosis, and, also for their friends and family to help them understand the condition, and also to let them know they are not alone. Although thought to be relatively uncommon, it is fast becoming clear that there is a gathering number of children and teenagers being diagnosed with Multiple Sclerosis around the world. We hope to bring you as much information as possible with regards Paediatric MS. If you are the parent of a child who has been diagnosed with MS, or a child/teen with MS we would like to hear from you. Further Information © Multiple Sclerosis Resource Centre
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| Young Persons with MS: A Network for Families with a Child or Teen with MS | |
| The National Multiple Sclerosis Society and the Multiple Sclerosis Society of Canada have come together to offer “Young Persons with MS: A Network for Families with a Child or Teen with MS.” in North America. The network provides families living with a child or teen that has been diagnosed with MS the opportunity to connect with other families by offering multiple program options. The network targets two distinct populations: Children with MS (18 or younger) residing in the home of their parents or guardian. Parents of a child or teen with MS The network provides a variety of programs to meet the needs of these families. Education: Information and Referral: Emotional Support: Connecting Families: For more information or to register for the Network for Families, please call
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| For teens (ages 13 to 17) who have MS, or who have a parent or guardian with MS. We encourage you to invite your parents to participate here, too. How to register:
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