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06/20/2008 19:05
nhlflagg
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Posts: 248
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What about muscle relaxer? I went to the Rhemu and she put me on 2 different ones. I have only been on them a week and they don't seem to be doing much. My family doctor has given a oxycodone. I have only started the rollcoaster of meds, I think. Imitrex work for me when I get a migraine but not for a regular headache.
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06/20/2008 19:13
tdecker68
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I am going to a new doctor and I am making a list of some meds I would like to ask about...muscle relaxers are on my list. Let me know if they start to help at all.. My appointment is in July and I want to be prepared...
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07/05/2008 20:39
eve
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I understand completely where you are coming from. I'm 33 I have an 8 yr old and a 9 yr old. It breaks my heart when I have to tell them not lean on me or hug me to tightly because "mommy's skin hurts". They try to understand . . . but how can they really. I have been sick since I was 21 ... it was quite sudden ... first it was the chronic endometriosis that I battled with for 10 years . . . and then I was diagnosed almost 2 years ago with fibromyalgia and restless leg syndrome, after a surgery I had had for the endometriosis. FOr the last 12 years I have been the one that has led the doctors to the correct diagnosis and trying different meds in hope of some relief . . . after i ran out of ideas i finally caved and went to pain managment . . . that i avoided for years . . . but i was at my wits end. they gave me 13 shots in one treatment . . . ofcours i felt nothing . . . and then they said the same thing that they told you . . . up to 3 weeks . . . that relief never came . . . and then they said they could not help me so I went back to my trusty doctor. I have a problem that has progressvily gotten worse not only do I metabolize meds quickly but I have developed an allergy to opiates that has gets worse as I increase the dose . . . all I really want is a med that I can take at the end of the day or when it is really bad . . . that can just take me away for a little while . . . i want to fall asleep not in pain. I often feel that I should put all my surgeries and meds that I have taken and I am currently taking in resume format . . . do you feel that way?

for pain I've taken vicodin (very allergic to), darvocet, tramadol, percocet (took a lot of that for the endo pain until I became allergic to it),oxycontin, hydromorphon, methadone and fentanly . . . i am now allergic to all of them . . . i get very, very itchy for days, only to be relieved by very high doses of benadrly that reder me unconcious and useless for days.

nsaids are out of the question . . . they created an ulcer . . . after over using them for my endo pain (i wanted to be concious for my childen).

so I am currently taking:

1200 mg 3x neurontin

90 mg cymbalta

600 mg 2x lodine

.5mg estradial (hormone replacent)

protonix for the occasional ulcer flareup

phentermine (for energy, which really, I haven't seen a difference, so I need to reconsider that one)

I always hope that it will get better . . . with the endo . . . I had years in between the surgeries that I was well . . . and was the person I wanted to be . . . but this fibro thing . . . has thrown me for a loop . . . there's no surgery or surgen that can make it better.

My family keeps me going . . . they believe that I will get better . . . so I try for them. I keep involved in their lives . . . I volunteered as much I can at their school . . . I led the art program for the entire school. This year I will be homeschooling, so will see how that goes. They know I must take a nap and are understanding that sometimes we I need to take it a little slower.

how are things with your family (if you don't mind me asking?)

take care

eve


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07/10/2008 16:02
lil12
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As far as muscle relaxers go I've taken Skelaxin in the past and had quite a bit of relief from it. I felt a lot less nerve pain and my muscles, especially my back, were much looser.
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07/22/2008 18:37
Leonardy
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Hi Jamie,I am currently in that 10 day lapse period between meds-I take 10mg Lorcet 3x day and Soma 350 mg a day at the same frequency. Of course, some days are worse than others and and I have to take at least double that for relief.So, of course I run out. I have a question or two- I am on CYmbalta, about a month now.For breakthrough pain I have ultram. What are the side effects of these drugs and how much is too much of ultram.

Thanks!

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08/08/2008 11:39
loril
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[color=#0000FF][/color

I am so glad that you mentioned the stomach hernia .... I have one and am worried. I spoke to my gastroendrologist who told me not to worry, but I have noticed that whenever I "bear" down, I have a spot about a couple of inches above my belly button that comes out... and from what I read on the internet, they require surgery. It does go away when I lay down.

But, obviously I am on narcotics and have IBS, so with consitipation always at my door, and now this alien trying to pop out of my stomach, doe anyone have any suggestions? I'll be so upset to know that this could have been prevented!!

Really worried...


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08/08/2008 14:15
Debi
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leonardy- the one caution I would give with cymbalta and ultram is that they both increase the seratonin levels in your brain. I was on both and had severe pain and the md at that time kept increasing my ultram. I had a terrible reaction to it. The md that I see now took me off the ultram all together. I was on wellbutrin for years for migraines and I had a terrible reaction to it as well and had to be started on the cymbalta. I am very sensitive to any ssri's and nssri's. I don't even take cymbalta now. Just make sure that you don't go over what you md tells you is safe.

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08/24/2008 00:42
Kittield
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I am just diagnosed with Fibro this year and I have finally run the guantlet that is ruling out everything else, including depression since I have been on prozac (at my request) since college.

I go to see my rhuem. this week, but in the mean time I was having some exceptional pain that I am not used to...up to this point the pain has been barable and my major complaint was the fibro fog and lack of sleep.

So after a night of crazy amounts of pain and restless legs and all the other wonderful things that go along with Fibro I finally went to raid my medicine cabinet and found an old bottle of Hydrocodine that I had from an old surgery. It was expired (I DONT RECOMMEND EVER TAKING EXPIRED DRUGS, but I was at my wits end) but I took it anyway figuring it would work, not work, or land me in the hospital where I could get something that would take care of the pain...I was lucky...it actually made a dent in the pain and put me right to sleep, and since I didnt experience any adverse effects I have been slowly working my way through the bottle. I only take it at night as that is when the pain is the worst, but I found that about 2pm the next day I ended up with a horrible headache.

Anyone else taking this med? Anyone else had similar symptoms?

Lori
I'M NOT CRAZY, FIBRO IS!!
(A little hint from my doctor to help keep me sane even on those days when I feel a little crazy...feel free to steal this for your sanity!!)
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08/27/2008 20:20
clovergirly
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I have tennis elbow and golfers elbow in both arms for about a year now.My pain in my arms in CHRONIC. It will not go away and it just keeps getting worse. The doctor has me on 20 mg of oxy twice a day and up to 4 percocets for breakthrough a day. Now i find the oxy and percs give me a little bit of energy, numb the pain, but does not take the pain away. Im just glad i can function during the day with these meds. At this time with the pain never getting better and my life limited on what i can do(because i can no longer straighten my arms) thank god for medications like these. Now with being narcotics i am somewhat concerned about the addiction factor but i try not to worry about that right now. I believe the doctor is starting to lean towards fibromyalgia only because my arms will not heal and i have had 5 cortizone shots. So if the oxy works for any of you..take one day at a time. xoxo

Post edited by: clovergirly, at: 08/27/2008 20:24

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08/27/2008 21:02
Sistrozzie
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I have had that in both of my elbows so I know the pain you are dealing with. I've said on the forum before that I have a chiropractor who deals in fibro and works on the tender points every other week for me. You might consider finding a chiro who works with fibro and see if he or she can fix that pain for you. I never had any cortizone shots for my elbows.
PatOsborn
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