Recent Posts
I was on 300mg of Lyrica twice a day. 60 mg of Cymbalta twice a day. I have gained back 40 pounds. When I was taking the Lyrica I had a lot of short term memory loss. I am known for being able to be give a single word topic and I can recite conversations about it from months ago.
This severly impaired my ability to continue my job. One day the doc took me off the Lyrica and put me on Trazadone 50 mg at night only.
I now have a bit more pain. But I also have my memory back and I don't feel as though I am moving through a fog all the time.
Honestly I aged 20 years in brain power in 2 months of Lyrica.
All of the above isn't solely Lyrica, but I'm doing better on other meds
Pre op I was dx'd with polymyalgia. Just the hips and shoulders.
Pre op I had low thyroid levels and was taking 88mcg of synthroid.
Post op - at 4 years - full blown fibro. Vicodin is the only drug that touches the pain.
Post op - I have been dx'd with Graves disease. The meds they are using to control this are also wreaking havoc with my white blood cells. I am currently in my 3rd week of a cold that has left me weak, hoarse, coughing 24/7. The doc is calling in a 2nd script of something else to ease the cough but still viral so no antibiotics will work.
Vicodin use has been upped to 2 x a day from 1 time a day. Because I work full time, I only take my pain meds at night.
I think I would look at a surgery that does not create malabsorption. I am also protein deficient, and take mega doses of Vit C and D3 (dry D)
Iron is low side of normal.
Do a lot of research - I don't know that the surgery made it worse, but it is very hard to deal with both pain meds and deficiencies since we don't eat much.
Tink
Steroid injections have worked very well for mine, although I'm not sure if we can have them post op...?
I agree with the others. Thank your lucky stars that it's probably not Fibro.
I hurt all over. With the weather changing, mine has flared, and the worst of it is in my shoulders, and radiates down my arms and up my neck.
I have had a headache for weeks. When the headache first hit me, I thought I would die. It really was debilitating. It hurt so bad...I cried.
I hurt all over all the time, but when I say I have a flare....I still hurt all over, but it gets really bad in certain parts of my body. I have not had a pain free day in so long, I couldn't tell you when. When mine first started I would have some pain free days, but not anymore.
I sure hope you get this figured out, and I sure hope it's not Fibro. I don't think it is, but I'm not a doctor.
Take Care,
~Amy~
All the best on your upcoming surgery ~
Anne
She's started me on Savella. Way too early to notice a difference yet, but here's hoping!