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Untitled Comment
Nan from the Dunes
Wednesday, October 28, 2009 at 06:42 PMre: Untitled Comment
Linda
Thursday, October 29, 2009 at 02:22 AMhi nan, thanks for writing,, i am no longer taking the cymbalta,, actually, i am taking 30 mgs a day in the morning until i see the doctor this friday, thirty doesnt do anything, my p.c.p asked me not to take myself off of it totaly (was suppose to work my way up to ninety mgs), i was taking it in the morning,, falling asleep on the way home from work and everywhere else, go to bed usually around eleven pm, (except for tonight, working on a resume),, so i took it in the morning,, still couldnt sleep at night, i tried every thing,, mylegs were flying all over the place too,, i never had that before.
hmmmmmmmmmmmm what was that all about any clue? thank you, linda
re: re: Untitled Comment
Nan from the Dunes
Thursday, October 29, 2009 at 07:06 AMLinda:
Take it at nite, max dose is 60 mg and you shouldn't fall asleep. I have no problem with it and have had it work wonders when I needed it fpr several years, infact since it came out. Although, because I feel I am taking to many meds, and have to go on medicare part D in december (I have come to the end of my employer coverage, after 4 1/2 years) I am titrating myself off of several meds and switching a couple of others. I also found savella worked wonders for the aches, but caused excessive sweating. I wish you luck. I think the most important thing when dealing with chronic pain and a new dx, is to not overreact. Provide your supervisor, and human resources with information from your doc and they really can't harm you. Do the best you can, and perhaps work a different shift (you did say medical field right?) People will be trying to look for an excuse to do whatever to you, or they might be completely understanding. Don't make your dx the excuse, just explain you need their help in working out the ability of your body as it becomes adjusted to new meds . Make adjustment yourself to help, take copius amounts of notes if necessary, to make sure you do everything your supposed to do, find different ways to learn to adjust.
Good Luck and God Bless
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Untitled Comment
Karen Lee Richards
Saturday, October 31, 2009 at 11:06 PMHi Linda,
I can empathize with what you're going through. Years ago, shortly after I was diagnosed, I had to sit down with my boss and explain what was going on with me. Thankfully, he was understanding and patient.
Recently I wrote an open letter that FM patients can give to friends and family to explain what fibromyalgia is and what they can do to help. Please feel free to send the link or print it out and share it with whomever you need to. Here's the link: Understanding Fibromyalgia
I hope your friend and co-workers are as receptive as mine were. – Karen
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Cymbalta
Saraboo
Sunday, November 01, 2009 at 01:59 PMHi Linda,
I heard about Lyrica from another friend with FM, I'm not sure how drug coverage works in the US, but if you have coverage, ask your MD what he thinks. It was a life saver for her and has made a huge difference in my life dealing with neurological pain. It is a really strong drug, but once you get used to it (it took me about a week each time the dosage was raised) - it makes a huge difference over time. I'm not pain free, but in my case after spending 30+ years on getting on average 2 to 4 hours sleep a night due to pain, I now sleep soundly through the night. This has an amazing impact on pain levels and energy. Chronic pain really affects energy levels tremendously, the pain itself can affect our boundaries during conversations, and FM sufferers also have to deal with brain fog. So it can be really difficult to convey the issues you are dealing with. Lyrica will cause memory issues in large doses, your doctor should know what will work for you. Hope this helps. Saraboo
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Hi and welcome
I am sorry to hear of your problems. One question, when are you taking the cymbalta?
What time of day? Are you taking it at nite?