Career change due to AEDs

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RanMan

Too Much Experience with Epilepsy
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My name is Randy, I'm Canadian. Music runs in my family and starting from age 9, I was playing drums and guitar with proffesional bands. Up until age 21 (1979) I was a singer/songwriter, music teacher. My only dream in life was to make a good living with my music. (I also developed Ulcerative Colitis at the same time as the "seizure condition" (notice I didn't say epilepsy), the Docs. say the two conditions are connected)

Well, all that had to come to a stop. I was sitting at my desk at my P/T job when I had my first seizure. (Oct./1979) All I remember from that point on was waking up in the ambulance on the way to the hosp. After going through several tests and then seeing a neurologist, the tests showed that there was seizure activity in my lower tempral lobe. He then persribed Dilantin and Pheonobarb (still on today) and the seizures were under control. I was even able to keep my drivers licence.

One major problem though, the pills were severely messing up my co-ordination. I walked like a drunk, slurred my speech, my own family was embarassed to be seen with me.

Since my co-ordination was so bad, I could no longer play guitar or drums and I had to give up teaching.

I was so depressed, I could no longer fulfill my dream, now what was I going to do.
I had to make a career change. I was putting in job applications all over but I had no other experience.

Finally I got hired on by the Federal Government as a courier and mail clerk. I worked my way up to Administraion Manager for the Unemployment Insurance Office for 21 years and then 9 years with Veterans Affairs.
My condition was getting worse with age, no seizures but the meds were blocking my learning ability so I couldn't take on extra duties.
As a result of this, my employer(The Government of Canada) offered me an early retirement package for medical reasons and also counselled me to apply for disability insurance.

I had to learn to live with my disability and work around it.

Randy


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Diagnosed with epilepsy and ulcerative colitis in 1979,
 
career

Randy:

Part of this condition is regrouping every so often, and the loss list can add up. I am sorry to hear of your lost dream in the music field. Sounds like you rebounded and found something else suitable. Not what you had planned. I worked in a law office for over a decade, and then my brain abandoned me. Now, I am 52 and looking for work with no experience. I think I will start doing volunteer work, since I do not seem to be employable, and there is so much competition out there. Staying at home is driving me nuts!! Life is trying, especially with this condition. What are you doing while retired?
 
Randy:

Part of this condition is regrouping every so often, and the loss list can add up. I am sorry to hear of your lost dream in the music field. Sounds like you rebounded and found something else suitable. Not what you had planned. I worked in a law office for over a decade, and then my brain abandoned me. Now, I am 52 and looking for work with no experience. I think I will start doing volunteer work, since I do not seem to be employable, and there is so much competition out there. Staying at home is driving me nuts!! Life is trying, especially with this condition. What are you doing while retired?

Gigi,
My long term use of AEDs combined with my age has caused a bit of a learning disability so I am unemployable.
I live in the suberbs so there's not much around for volunteer work as well as not having a drivers license so I do absolutely nothing.
 
How about a re-assessment of your meds? I know that Dilantin and Pheonobarb, messed me up big time...I was literally a zombie. Maybe you can switch and feel more coherent and balanced.
 
Hey Randy!

You might want to get your dilantin levels checked...quickly! The stumbling and lack of coordination are classic symptoms of toxic levels of dilantin!
 
Hi Skillefer.

I also have Ulcerative Colitis which I also take meds for and dilantin is the only AED that doesn't react to it.
I don't have those symptoms all the time ~ only when I have a UC flare up at which time I have to double up on the UC meds, causing the dilantin to go toxic for only a couple of days but it's better than having a seizure.
 
Can someone please tell me where to find or get a job where all I have to do is answer the phone? This is what my doctor has restricted me to...no multi-tasking, answering the phone only. Our job services angency thought I was kidding or not quite playing with a full deck when I told them that. I'm also restricted to only working part-time so that widened the eyes a bit further. I haven't received any referral letters from them yet. This would definitely be a career shift for me!
 
Zoofemme -- There are agencies that do telephone polls -- don't know if you'd be up for that, that's a bit more than just answering phones.
 
I did telemarketing for Time-Life books, once upon a time. (That was before I became a full-time writer.) It was pretty tedious.

But there's a guy at our local EFA who's photosensitive and he phones around looking for EFA speaking and educational opportunities. And he does manage to book quite a few dates. He finds it very fulfilling. But he does NOT get paid. :-(
 
I think this is the hardest part of the whole E game for me :( I had finally clawed my way back into the work force and was making a decent wage, I was getting ready to go off of disabilaty and everything went to hell in a hand basket. I'm angry that the doc has limited me in what I can do yet, when I look at the work that I use to do....one of the things involved teaching others, to include individuals for whom English was not their native language and who did not learn well through verbal instruction. The lesson plans perplex me :crying: I have a difficult time following them or comprehending the processes theyy refer to, yet I know that at one time i knew the stuff like the back of my hand...I was the expert to whom even the government and military came to for advice or assistance. Now, I can answer the phone.
 
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