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Be your own advocate

The best way to get the care you need is to be your own advocate. Living with epilepsy and taking medications that affect mood and thinking patterns, can degrade self esteem. This can take a toll on the willingness to speak up and say, “Hey, that’s not right!”, whatever ‘that’ may be.

There are times when it is important to let your doctor know about new side effects your medicine may be causing. Not only because it can negatively impact your quality of life but also those side effects can be doing more damage than you realize.

Then there are times when you may be having little seizures that seem like “nothing”. But since seizures beget seizures that means each seizure makes you more open to more seizures. It’s always worth mentioning.

Or it could be you just have a small question but you don’t want to “bother” the doctor between visits. Well, chances are you won’t. It may well be something that the administrative staff can handle and the doctor won’t even know you called.

Just think of it like going to a restaurant. You can go to the best restaurant in town, but if you don’t open your mouth and tell the staff what you want then you’ll be seated by the kitchen and wait for an hour to get cold food.

Silly analogy I know, but it can get that bad.

It just boils down to don’t feel bad about asking for what you want. Or for telling the doctor what you need. Remember you are paying for this service. If you keep that in mind it will help.


Follow Jessica K. Smith:


Founder and CEO Jessica brings a unique perspective to this leading epilepsy blog as she was diagnosed with epilepsy as a teen. She also brings 20+ years experience in marketing.

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