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TinkL *.
on 1/26/11 10:41 am - Columbia, SC
Topic: RE: People at work
Thanks!   I'm just trying to create boundries for what I can and cannot do.

12 hour work days just ain't happening anymore.   I'm trying to get my type A personality under control.  I'm the worker that always says yes, I'll do it.   Then I end of working 6 12's a week.

I'm sure that is why I took it badly.  I WANT to be working and accomplishing things.   It's KILLING me not to be in control.  I'm trying soooo hard to please the doctor and stop hurting.

Yoga does help.  I'm way down on vicodin.  Why is it that you try to do something for yourself (health) and no one else is supportive. 

Oh well, I'll just have to grow a thicker skin.
Hislady
on 1/26/11 7:24 am - Vancouver, WA
Topic: RE: People at work

You should have asked her when she got her medical degree! Some people just don't get it and never will. Sounds like prefers to be the center of attention and you're stealing her limelight. Poo on her I say! We loves ya and know you aren't a hypochondriac, I wish that's all it was with ALL of us. Deep breathewe're here for you!

marion6366
on 1/26/11 2:35 am - Hammond, WI
Topic: RE: Migraine Headaches
Well I've had migraines for the past 14 years and my Dr also had high hopes that WLS would help.....well, I'm now 19 months post RnY, down 90 lbs, no sleep apnea, no high blood pressure, but unfortunately - no change in my migraines.  At first we thought I wouldn't see a change until I was done losing all my weight, because during weight loss the body sees that as a "trauma"...but I have stayed the same now for about 5 months and still no change.

I get migraines about every other day - at least.  Headaches daily.  About every 3-4 months I end up in the hospital getting a shot of Toradal & Morphine, which knocks me out for 2 days straight (just happened on Monday).  I have been to the neurologist at the Mayo Clinic and they just can't seem to figure anything out.  I've been on every drug, herb, vitamin, you can think of at one point in time.  My insurance even approved Botox, but that only made things worse.  

Right now I have Relpax for my attacks, Vicodin for pain and Percocet for the BAD ones....for me it's just come to a point of making it through the day, hoping I don't get another one, & trying to make sure I don't have rebound headaches from all the meds I do take!!!

Hope things work out better for you......and let me know if you find something new that works for you!  I'm always on the look out!
            
Hit my 1st goal of 150 and on to my 2nd of 135!!
TinkL *.
on 1/26/11 1:21 am - Columbia, SC
Topic: People at work


So I find out today that some people at work think I'm a hypochondriac.   Just because I was dx'd with fibro and Graves disease in the same year.  

Just because I've had a few sick days out while I deal with what is happening to my body.
Just because the first meds I took were too strong and after giving it 6 weeks, had to change meds because it just made me too out of it.

So - all I have to do is have a great outlook on life and not eat and stop listening to the doctors.

So what if the doc tested me for a marker for heart attack and came up positive. 

So what if the doc tested me for a marker for high cholesterol and tri's and came up positive.
So what if I have diabetes in the family
All I have to do is believe I'm well and ignore the doctors and not be a hypochondriac.

So I guess to be acceptable to these people, I have to tell my endocronologist to stop treating my Graves, it's all in my head.

I guess I''ll have to tell my PCP that I have no need of the Cymbalta and Trazadone. Or the vicodin and calcitriol.   Because god knows everyone can will themselves better.   Just have a great outlook.

Coming from Ms this divorce is making me crazy and every dog is as important as a human being.

Vent over - but I'm still angry.   And you know what anger does.  Makes it all hurt worse. 

Lovely.

 

sleepyjules
on 1/26/11 1:04 am - Centrally located in, IL
Topic: RE: Can't believe I found this board...
I am so sorry you are going through this.  I know all to well what you are going through, and would not wi**** upon anyone!  In the last year I went from being a hard working, employed, home owner, and single mom to an unemployed, non-functioning, single mom who lost her home to foreclosure.  I am no longer able to work in my chosen field because it is too taxing on my body.  The exhaustion I have every single day prevents me from even searching for a job.  I struggle with filing for disability because in my head I feel like a 37 yr old woman should be able to work and provide for her family.   That, unfortunately, is not my reality.

I would highly recommend that you consider hiring a disability law firm to assist you in filing for your disability.  Best wishes to you! 

Julie     


MainePam
on 1/24/11 4:35 am - Bucksport, ME
Topic: RE: Sleep mask
Sue that is a good idea to get a twin heated blanket I might just do that !! If even I have to use 2 blankets it is hard to move them.. So one heated blanket might work. My arms are getting useless..My right one I had a total shoulder replacement,April of 2010. It still is not good. My left one has a lot of bone spurs he wanted to go in and clean that out. I do not want any nmore surgeries. So now my arms are both bad.
I never thought of my arms bad becuase I had my knees done and my back is bad. Oh well.....
Hislady
on 1/23/11 5:13 am - Vancouver, WA
Topic: RE: Can't believe I found this board...

Welcome, sorry you are having such a rough time. Stress of any kind will worsen our fibro, sadly, and who doesn't have stress these days. Thanks for the meds info, I take cymbalta plus morphine and oxycodone for pain but some of mine is from severe arthritis but it helps the fibro too of course. Please post often we can always use more input!

A. Player
on 1/23/11 5:01 am - Lansing Charter Township, MI
Topic: RE: Views who are ya all
Hi!  I had wls and have Fibro also.  I have been dealing with this disease for over 20 years.  My doctor sent me to many specialist for the horrible headaches and bodyaches.  I was diagnosed with Rheumatoid Arthritis, and Lupus.  The Fibro was diagnosed later after nothing helped me with the "sick spells".  Sick spells consisted of headaches that turned to throwiing up my guts all the way  to irregular heart beats which landed me in the hospital and on blood thinners!  I have since gotten off of the thinners but still have the headaches.  I had the surgery, got myself into classes in the local pool and took up scrapebooking, gardening and other things to fill my day. So far, I've chosen not to take the meds that have been prescribed (Lyrica).  I mainly take Ultram when needed because with the surgery I got off so many meds that going back that route is a problem for me.  I suppose that I will have to take those drugs in earnest at some point but for now I feel good most days and ride out the bad days with a few painkillers....Thanks for starting this post! 
"The task ahead of us is never as great as the power behind us."           
sillysue45
on 1/23/11 4:51 am
Topic: RE: Sleep mask
I've got a heated throw for when I'm out on my recliner couch.  I use it on my worst days.  They only stay on for 3 hours though so you might want to grab a twin but get it quick before they are out of the stores and you have to wait for next winter.
Will never get back to my right weight but I need to lose a lot....
    
adasha
on 1/23/11 4:44 am - Beaumont, TX
Topic: RE: interstitial cystitis?
I have FMS and IC.  The doctor I went to said I am just not emptying my bladder all the way.  He suggested Kiegel exercises and gave me (I think) Elavil.  I never took it.  My regular doctor told me to take Sudafed every day.  I have seen something about the histamine effect in the literature I've read. 

I have not fully done what is needed to manage it.  I've been too busy focusing on pain in my arms from the FMS.  But, since it's allergy season, and I'm taking Sudafed, I haven't noticed my IC.  So, may be a connection...

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Live life today like there is no tomorrow!!!!!

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