Living With Epilepsy
If you have epilepsy, you may
have questions regarding the condition and how it may effect your life.
Will having epilepsy affect the option of driving a car or continuing in
a job? Will having epilepsy affect your relationships? What are some of
the attitudes of society encountered by those with epilepsy.
For some individuals, having epilepsy will require few changes in
lifestyle. For others with uncontrolled seizures, their lives change
significantly.
Local epilepsy association can provide you with information regarding
your concerns. Most association have helpful resource materials as well
as a staff committed to answering questions and providing information.
Associations often offer in-services to worksites and schools in order
to educate others about he condition. Association may also be able to
link you with self-help and support groups, and with trained
professionals.
Living with epilepsy can result in personal challenges, but it does not
have to result in an inability to have a full and rewarding life.
Educating yourself and others about your condition, finding the
appropriate treatment, developing a support network, and continuing to
pursue what brings joy into your life are all important in achieving a
fulfilling quality of life.
Feelings
A range of emotions may accompany a diagnosis of epilepsy. You
may feel depressed, angry or frustrated. You may be concerned about your
plans for the future. You may find that family or friends respond
negatively to your condition out of fear or a lack of knowledge.
Depression is more common in individuals with epilepsy than it is in the
general population. This could be due to psychosocial factors, the
seizures themselves and/or anticonvulsant therapy. If you are struggling
with or thing you may have depression, contact your physician to obtain
support.
Assistance
For some individuals with epilepsy, little change in lifestyle
is necessary. For others, there may be significant change. Local
epilepsy associations have valuable resources on many aspects of
epilepsy and they may be able to link you with self-help and support
groups, and with trained professionals. Both of these services are
provided by the Edmonton Epilepsy Association, contact us for more
information.
Helpful Tools
There are many devices and items available to help manage
day-to-day concerns. Wearing an identification bracelet or necklace can
aid in assistance should a seizure happen. Carry a pre-programmed cell
phone or beeper in case you need help. If seizure medication or seizures
affect memory, using a watch with an alarm, a day-timer and a medication
dispenser may be helpful.
Sharing with Others
Consider carefully with whom your will discuss your epilepsy.
The decision involving who should be told may depend partially on the
type and frequency of your seizures. Sometimes the decision may be based
on how close you feel to the person. Do you spend a lot of time with
this person? Are you likely to have seizures with the person? Whether or
not people would know how to help if you have a seizure with them may be
a deciding factor. While it may not be necessary to discuss your
condition with everyone, it is important that those you are with
frequently know what to do if you have a seizure.
Be Positive
Living with epilepsy can result in personal challenges but it
does not have to result in an inability to have a rewarding and full
life. Learning about epilepsy and sharing that information with others,
finding the medical treatment that is best for you, developing a network
of family and friends who support and care about you, and pursuing what
matters in your life, are all important.
