Teens with Spina Bifida face the same emotional roller coaster that other teens experience. Tears, moodiness, and occasional outbursts can be expected. It is always difficult to be an adolescent and an adolescent with Spina Bifida will have additional challenges to face. Some teens will balk at doing things they were doing so well a few years before. Although this period is known as a time of rebellion, your teen needs to realize that cathing and taking prescribed medications are mandatory, not optional. Serious consequences to their medical health are not worth the risks of a little freedom. Teens do need to feel, though, that they have some control over their lives. Give your teen lots of opportunities to make decisions about things that are not life-threatening.
Allow your teen to have fashion and hairstyle preferences, shut his or her bedroom door for privacy, and choose friends and activities (within reason). Be available to your teen for support and heart-to-heart talks, but let your teen decide when these chats will occur and how much to share. In other words, your involvement needs to be just as intense as it was when your child was younger, but somehow you have to figure out how to do it in a less direct way. Parents of teens walk a tricky path and often make mistakes. Sometimes parents may need to reach out for professional guidance.
Challenges during the teen years
There are many physical, mental, emotional, and social changes are associated with the adolescent and teen years. It is important that during these years, the teen become as independent as possible so they can reach their full potential.
Becoming independent means fully taking over the management of your care. This should include bowel and bladder care, moving independently, making doctor’s appointments, having and participating in a physical activity program, engaging in activities with friends, and more.
Transition to Adult Care
Transition is the process of moving from child-centered health care to adult-centered health care. It can be a time of great change, as the young adult often moves from their life-long pediatric health care providers to adult providers. It will take work to find a clinician to provide care. Please visit our clinic and provider list to locate a provider near year. If there is not a Spina Bifida specialist near you, please share the Guidelines for the Care of People with Spina Bifida with your primary care physician and any specialists you may see. Contact the National Resource Center if you need additional information.
Teens with spina bifida and their families should begin planning for life after high school. This includes:
- Looking for doctors that treat adults with SB.
- Deciding if the person affected by spina bifida will live outside of his or her parents’ home.
- Choosing work.
- Exploring college or vocational school opportunities.
- Being volunteers in the community.
- Having healthy relationships.
Planning early can help make the years ahead easier.
Resources for Teens & Transition
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