Question: After browsing a plethora of narcolepsy related websites, I feel a desire to write about my experiences with the various symptoms and people’s reactions.
I am 21 years old, and (so far as we know) have had symptoms since I was about 11 or 12 years old, but was only diagnosed earlier this year. It has made such a profound impact on my life.I previously thought that I had experienced all of the classic symptoms of narcolepsy except Automatic Behavior, but just thought of an incident which may have actually been Automatic Behaviour, though I’m not actually sure. Once, on Facebook, a friend of mine replied to a comment I had apparently left on a status of his, but which I do not remember writing at all. It might have been someone else on my account but a few things make that unlikely 1) it sounded like how I would have worded it 2)the only computer I was logged onto Facebook on at the time was mine, which was in my possession when the comment was posted (I had it with me, but don’t remember getting on). So there you go, I might be a
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For about a year while my Dad was unemployed, I had no medical insurance and so went to the doctor much less often, and when I did, shied away from the more expensive blood tests, so that I probably ended up being checked for thyroid, glucose levels and who knows what all else many times. Then I went off to college, which made it even harder to get in to see my family doctor. And, once again, I was surrounded by peers who thought me lazy, a wuss, or who “taught” me all these things about good sleep hygiene that might have really helped, if I hadn’t already known all that. It was really hard to believe that my sleepiness was actually something more than just my imagination.
For the next few years, I would occasionally bring it up to the doctor, when I saw him and was in town. I ended up eventually dropping out of college- partly due to being unable to stay awake even in classes I really really enjoyed, and partly due to depression and I got a job at a fast-food restaurant here locally. Finally, earlier this year after my doctor said in my latest appointment with him that he had just reached the end of what he could think of/know to try, and with the exhaustion beginning to affect how well I did my job, I wrangled my way into an appointment at a sleep clinic (Thank goodness I live in a large city with almost half a dozen certified sleep clinics 🙂
I talked to the doctor there about my symptoms. After I was finished he looked at me and said two things : 1) You have narcolepsy and 2)Why did you wait so long to come in?
Over the next few months, I have found a combination of Vyvanse, Wellbutrin (the REM suppressant), caffeine and scheduled naps which has almost restored me to completely normal functioning; I wouldn’t presume to assign numbers or percentages to my functionality, but I usually only sleep at most 2 hours during the day (an average of about 50 minutes total) and have cut my caffeine intake to a fraction of what it was- and I am able to think more clearly and enjoy life more. Also, the Wellbutrin helps with the cataplexy to the point that even my face muscles don’t always sag.
However, sometimes people’s reactions (even if they mean well) is discouraging.
Like, right before the appointment with the sleep doctor, I and a friend of mine were having lunch, and I mentioned how I was going to see the doctor because I was so tired and she immediately responded with what she sincerely meant to be encouraging; “Well, I’m sure he’ll just tell you that you need to sleep better/more”
Shortly after my narcolepsy became common knowledge within my social circle, someone said to me “You know, I’d love to be able to fall asleep like you do” to which I replied “NO, no you really don’t”. I think I offended her. Whoopsâ¦
Some people’s reactions though, restored some of my faith in humanity.
My manager (the one who allowed me to work split-shifts) apparently thought of epilepsy when I originally tried to explain it to her, so then she asked me if I would explain it to her boss (who really did need to know). When I did, his first reaction (much like hers had been) was “Bless your heart! What can we do to help?”. Not “How will this affect your job performance?” or even “What does this mean for insurance/paperwork/etc?” but “What can we do to help?”
My family, as I mentioned previously, have been amazingly, wonderfully supportive of me. Even when I didn’t fully believe there was something wrong with me, they kept pushing me to get to the bottom of why I was so tired all the time. My brother in particular has been wonderful. He would help make sure I woke up in time to go to work and stuff if I fell asleep during the day, actually called me every day while I was in college to make sure I was up and heading to class, and has generally been there for me through it all. I am so grateful to him.
Now that I know, now that I am getting help, the narcolepsy no longer limits me the same ways it did before. I can drive by myself again without worrying about it. I can watch movies with friends without falling asleep (if I’m careful and/or it’s exciting). I can let myself let go and just laugh as hard as I want and not fear hitting my head on the floor.
In the end, I am able to control it, instead of it controlling me. And that is the best feeling of all.
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