Hi everyone! Well, I actually wrote this on Saturday, but sent it to the
wrong place. I was wondering why nobody was responding to me!! I introduced
myself previously, but didn't have time to talk about my headaches. Plus,
I've read a few posts & have a couple responses. I'm sorry, but I've already
forgotten the name of the woman who lost her dog - my prayers are with you.
I love animals & I couldn't imagine having a beloved die in my arms!
To begin with - my ha's are not usually SEVERE, as I'm sure most of yours
are. I get them ALOT, but I don't get much of an aura & they don't usually
debilitate me. I guess I'm lucky for that because I am a stay at home mom &
when I get a headache, I can't climb in bed. When I talk about no aura, I
mean I don't get the flashing lights, etc. But I often just know when one is
coming even though it isn't truly here yet??? Does that make any sense to
anyone?? I was getting them almost daily (4-6 days/week). I sought
treatment at a headach clinic in Minneapolis (I am in Duluth, MN) & was first
put on Zoloft daily & Imitrix (abortive). The Zoloft didn't help but loved
the Imitrix because it helped & there were no side effects for me. Then she
switched me to Prozac & also gave me Zomig for the ones the Imitrix didn't
help. The Prozac didn't help. Eventually the Imitrix quit working for me &
have been mostly using the Zomig since. I used to love the Zomig because it
usually helped & also I had no side effects, but it seems that lately when I
take it, I feel horrible. I'm finding it makes me feel kind of out of it, I
don't feel comfortable driving anymore & it just makes the back of my neck
feel like it's in a vice grip. I had an ha a while back that nothing would
help & my local GP gave me Maxalt (which someone mentioned today), but I
didn't end up using it yet. Now, I'm kind of nervous to.
I went off daily meds back in October, because I was frustrated & sick of
taking something everyday when it wasn't helping. But things got stressful &
I was popping Zomig 6 X week (didn't find out until I called the dr about new
anti-depressent that that could have killed me!), so I got another daily,
Effexor, which, again, didn't help. Now I am on Wellbutrin and I am finally
gettin SOME relief. I get about 1-2 ha's/week on average.
We have horrible Medical insurance, so all of this has come out of our
pockets. So, needless to say, it was hard to keep travelling to an out of
town dr & all that when I wasn't getting relief. So, I quit going there.
Lately I have just been dealing with my gp, but she doesn't seem to have a
clue about migraines. I am considering going back to Minneapolis for
treatment by headache specialists. But, I am wondering what kind of docs you
all see. There are regular neurologists in my city, but I read that it was
better to see one that specializes in headache. Do you agree??
I am sorry for the length of this, but I felt it was necessary to give my
details. Thanks for listening & your help, in advance. I look forward to
hearing from you!
God Bless,
Sue