Not gotten better and it's 2
months anyone else have the
Same experience?
Not gotten better and it's 2
months anyone else have the
Same experience?
Hi bwaite
I am so sorry to read that your flare up has not resided yet, and I genuinely hope that you can find some resolution and relief to the issue. I was wondering if your GP had given you any new medications because of how bad your flare is? This sort of information is always handy for members to know!
I have pasted you a web link to NICE and there are many links on this page to myofascial trigger points, so I hope that you find this useful:
evidence.nhs.uk/search?q=my...
I have also pasted you the FibroAction page for symptoms, and this has a write up on myofascial pains as well:
fibroaction.org/Pages/What-...
I want to wish you all the best of luck with getting some good useful answers to your question.
All my hopes and dreams for you
Ken
Thank you ken you our a very considerate person. He's just up my Butrans from
10 to 20mg. Just waiting till
my appt at pain clinic. But
I will look up the info you've
Given me.
Ken I see you are an author
what material have you written?
Hi bwaite
I am a parapsychologist, but under the guidelines of the forum I am not allowed to self advertise!
Didn't see that one coming
Hey? What? Who? Come again?
Yes beaite think this is all part of fibro really hope your flare lifts soon lots of rest needed . I am having Myofascia release massage it is really ihelping with the pain it makes it more bareable .anyone else tried this .
Sweetheart have you seen a pain specialist? If not, you should. It the only thing that keeps me going, Best of luck to you!!!!
Thank mizblue that's comforting
I am so depressed I've been on
the coach for a week know. I
really help they can help.
Hi Bwaite,
I'm really sorry that you are having such a bad flare. I have also been having my worst flare yet for the last 2 months. I'm not sure that it can be just cos your getting older as your doc says because I am only 29.
There could be a number of different triggers that have caused your flare. I have found that trying to do too much for long periods of time and not giving myself time to rest is my biggest problem. That and getting stressed about things - I am in my third and final year as a student nurse and have had to go on health interruption until I am well enough to continue.
I know it is so hard when you can't see any signs of the flare calming down! All I can suggest is that you go and have a chat with your doc to see if they can do something - change meds or referral to pain clinic. Also just look after yourself and try to rest and reduce stress.
I really hope you get some relief soon!
Gentle hugs to you
Becky xx
Also they might change your medication when you go to the pain clinic. I was on Butrans and when at the pain clinic they said to stop that right away because it does not work for fibro pain. I hope that your appt is soon
Xx
The Butrans seems to help a little. What other pain med.
Did they put you on at the
Pain clinic?
I have previously been on tramadol which gave me insomnia, gabapentin which made me really angry all the time, amitriptyline which made me really drowsy the next day, duloxetine and the butrans patch. I am currently taking pregabalin, co codamol 30/500 and nortriptyline. The pain clinic told me to stop using the patch and to stop taking duloxetine and replace that with the nortriptyline.
They also put me forward for the Glasgow pain management program. This is a 12 week program where you go once a week for 2.5 hours to a small group class. I have not started it yet but I have heard it is helpful.
I hope you find the pain clinic helpful
Xx
I will thank you xxx
Thank you xxx
Becky what is cotrmdole?