Thursday, February 16, 2012

Frustrated, In Pain and Exhausted...

Written by

Miriam36

Miriam36

Thu, March 13, 2008

  Posted document.write(''+ myTimeZone('Wed, 12 Mar 2008 00:00:11 GMT-0700', '03-12-2008 12:00 AM')+''); 03-12-2008 12:00 AM I always feel like I am defending myself to my My Nurse Practioner (my Neurologist only can see me once a year...so I get stuck seeing the NP) I see her every month and I keep a migraine diary. It is SO frustrating to explain everything to her and then she doesn't even remember 2 days later. Isn't it her job to write everything down and remember??!!!

I called last week to tell her I was tested for influenza and I ended up having it. She didn't want me to come to my appt. because I would just be spreading my illness....plus I was super sick. Anyway, when I talked to her today about the migraine I got last night, she asked why I wasn't at my appt. last week. I told her because of influenza...remember??? She then asked me how I got better so fast....what did she think I was lying about the flu??!! I was sick a week before I was diagnosed and it's almost another week since I was diagnosed (2 weeks!!) I'm much better but I still have the cough. Why do I have to defend myself to her? I am an honest person!

I am still waiting for the Keppra to kick in and I can't take triptans because of my risk of stroke. I also take atenolol and celexa. I take every prophylaxis meds they ask me to take. Why do they make me feel like a drug-seeker when I need pain meds??!! If I'm doing everything they want me to do...and I still have EXTREME pain...am I supposed to just live with it?! I had visual aura, numb face, weak hand and confusion yesterday...the pain came later and it was as bad as it gets. I took the butalbital and Naproxen and it did not work. That is why I called the next morning. I wanted to know what I should do. She told me that a patient was waitng for her and she had already wasted too much time talking to me. She then wrote a prescription for 20 percocet and told me someone had to pick it up. My sister did....and the NP was very upset and said that it looked like I had taken this before. She also said that I needed preventative drugs to work. I realize this...that's why I am on keppra, atenolol andd celexa. I did take percocet before. It was 8 years ago when I delivered my second child and she was 10 pounds 1 ounce. I was given 3 doses in the hospital and sent home with some pills in a bottle. I never even took those pills...they expired and I actually found them way back in my cupboard about 4 years ago and threw them away. If I told my NP this....she probably wouldn't believe me. WHY? I am completely telling the truth.

Two years ago I was given an MRI/MRA. I was given 10 mg of valium because I was so scared to go in the tube. I almost didn't make it through the test....but I prayed and prayed and just made it without having a panic attack. That was the 1st time I EVER had valium and it didn't seem to make me calm down. I told my NP this and she said it was probably because I had taken it a lot and built up a tolerance to it. I told her I had never taken it...not even once, prior to that MRI. She just looked at me like...yeah right! WHY??
3/14/08 11:09am

Hello, and welcome to MyMigraineConnection.com!

If we don't have a good relationship with our medical team, it can really play havoc with our well being and treatment plan. It sounds like it may be time to look for a new doctor who is willing to work with you, treat you like a partner in your health care. We have a quiz that might help you decide if you doctor is right for you. You can find that HERE.  

 

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3/17/08 1:47pm

Dear Miriam,

So sorry for you that you have had to go through such a hard time.  Sounds like you need a new Dr. who has more time to see you, not schedule you with an overworked NP who clearly does not understand Migraines.  I am curious as how they determined you could not take triptons because of stroke risks.  I have taken them for 10 years even though my mother,died at 62 of stroke, brother at 56, another brother at 61 of strokes and I have had blood clots myself years ago. At times there is chest pain but that usually is only after a few days of tripton use.  My neurologist is great and I believe we are only 2 hours away from you (Gundersen Clinic LaCrosse, WI. Dr. Hutter) They also have open MRI's and give you a choice as to which one you can tolerate. They were so thoughtful to me and kept asking if I was okay. Good luck, All the best to you,

Trish

3/17/08 5:40pm

Hi!  The reason I don't take triptans is because my neurologist said they are contraindicated in people who get hemiplegic migraines.  I get blindness, numbness, confusion, etc.....I guess we have a greater risk of stroke.  Maybe other neurologist feel differently.  My OBGN said he would never take a triptan because he feels he thinks they're very dangerous....as far as stroke goes. 

 

I lived in Onalaska for 3 years and I worked in Lacrosse.  I saw a neurologist at Gunderson Lutheran for 3 years....I can't remember his name (it was between '95-'98)

and I had my first baby at Franciscan-Skemp. I live in the Twin Cities now.  Big Smile

3/18/08 10:23am

Hi Miriam,

Thanks for the reply.  I am curious about the triptans because for the first few years of migraines I thought I was having a stroke or brain aneurysm.  I went numb on my left side, lost my vision, can't speak well ect.. this happens still at times.  Sometimes I get the aura prior to a migraine, most times I do not. I have lost my vision up to 15 minutes in one eye.  At first they told my it was a panic attack, I am like, what? Then after about a year they finally figured out it was migraine.  I resisted taking triptans because of stroke risk and took nothing for 2 years.  My quality of life was not good so I tried many preventatives which did not work & gave Zomig a try.  The chest pain scares me alot!  I try not to take it unless I know I am going to have a week of migraines(female related :) It does abort an attack most of the time but is scary! I read about a new abortive coming out that does not constrict the blood vessels so I am looking forward to that.  I am from LaCrosse and live in Onalaska so maybe we have metBig Smile

Trish

Anonymous
Bonnie Sweeney
3/28/08 5:35pm
Hi Miriam- After reading your letter I want to punch your NP. I think you need to get rid of her, can you? I too am a sufferer of Migranes. I am currently on a washout program for ten weeks. That means no drugs for ten weeks because the doctor thinks all the drugs I tak e for my migranes are now causing them. He told me I could take them in an emergency. So I have been but its hard to suffer when I have a pill that works. Have you tried Relpax. Its the only thing so far that works for me. My migrane is gone within an hour. Big Smile

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