When our children enter their teen years a whole new set of questions
begin to flood our minds as parents. Their bodies, both mentally and
physically go through so many different changes. It can be a roller
coaster ride just as it is with many teenagers. They not only have to deal
with the everyday changes every teen goes through, they also have to deal
with their disability.
Physically they may experience dramatic growth spurts and it seems as
if this can happen overnight. You may notice a gait change; maybe their
hand seems to tighten up more so than normal. If your child has seizures
you may notice a change in the activity; if your child has been seizure
free it is possible that seizures may reappear at the onset of puberty.
Mentally they are trying to become young adults just like every other
teenager.
They are looking into the future and trying to figure out what that
holds. They probably have so many questions floating around in their minds
which may seem trivial, but to them these are very important. Many of
these questions will not be the typical question asked by many teens.
Raising a teen with hemiplegia may be a little different than raising
your "average teenager". Many things come up that are related to
their disability and often, the answers aren't readily available.
Finding solutions can take lots of brainstorming, patience, and many heart
to heart talks as the teen begins to understand and deal with themselves
as young adults with a disability. Some things that may work are:
- trying to deal with all of the issues together,
- keeping an open line of communication, and,
- through trial and error, learning together.
Many of the subjects in the "For Teens" section of the
website will be written from the personal experiences of CHASA families,
so please keep this in mind when reading the articles. Every child
is different and hemiplegia affects every child differently. We hope you
find the information helpful; it may not specifically relate to your teen,
but it may help you along the journey.