This post is
part of the Epilepsy Blog Relay™ which will run from November 1st through
November 30th.
You could say I have evolved in my beliefs about
alternative medicine and epilepsy. I used to be dead set against it. I thought
it was too dangerous. Since it was unregulated, you didn’t know what effect the
chemicals would have on your body and how they would interact with your other medications.
Now however, since Epidiolex has been approved for two
types of epilepsy (Dravet Syndrome and Lennox-Gastaut Syndrome), doctors are
slowly warming up to using it.
A big concern that doctors have about products sold by
dispensaries is that they are all different and it’s hard to know what you’re
getting.
It wasn’t until I was at my wit’s end, still trying to
reduce my seizures, that my doctor actually brought up CBD as an option. Since
other medications hadn’t worked and my VNS was minimally helping, I decided to
give it a try. Surprisingly, it helped when I took a relatively low dose.
However, when I reached the “therapeutic level” for people with epilepsy, the
CBD lowered the levels of my other medications, causing more seizures.
This is not to say this is the wrong choice for other
people. I believe you should evaluate your own situation and see what the risks
and benefits are. Then, you can make an informed decision, whether it be a
traditional or an alternative treatment, or a combination of the two.
And, as Tevye on Fiddler
on the Roof said, “Our old ways were once new, weren’t they?” So who’s to
say that new and different types of treatments should be disregarded?
NEXT UP: Be sure to check out the next post tomorrow by Michael McKenna
at https://livingwellwithepilepsy.com for
more on epilepsy awareness. For the full schedule of
bloggers visit https://livingwellwithepilepsy.com/epilepsy-blog-relay/november-2018-participants.
TWITTER
CHAT: And don’t miss your chance to connect with bloggers on the
#LivingWellChat on December 6 at Noon ET.
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