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Limbo
It feels like I'm in limbo at the moment. I'm stuck in my flat and living a sort of non-existence at the moment, waiting for the council to finish assessing my housing application so I can be moved and waiting for my GP to find some way of sourcing me a wheelchair that has some sort of stabiliser to
It feels like I'm in limbo at the moment. I'm stuck in my flat and living a sort of non-existence at the moment, waiting for the council to finish assessing my housing application so I can be moved and waiting for my GP to find some way of sourcing me a wheelchair that has some sort of stabiliser to
alexfrombath
in
Tourettes Action
11 years ago
Asthma and Pain
Sorry if this ends up being a duplicate post, I wrote it this morning but not sure if I deleted it or it was referred, so Im rewriting it. Does anyone else find that pain plays a big part in their asthma? Increasingly Im finding my chest and back are really painful, not just after acute attacks where
Sorry if this ends up being a duplicate post, I wrote it this morning but not sure if I deleted it or it was referred, so Im rewriting it. Does anyone else find that pain plays a big part in their asthma? Increasingly Im finding my chest and back are really painful, not just after acute attacks where
Hidden
in
Asthma Community Forum
11 years ago
I have been asked to share my story. Make yourself comfy and I will begin .......
In 1988 I went to my G.P. with joint pains which fluctuated around my body. When I booked the appointment I had pain in my neck and shoulders, by the time I saw him it was in my knees and wrists! The pain was put down to my being pregnant (with my second child), hormones etc. - advice, take pain killers
In 1988 I went to my G.P. with joint pains which fluctuated around my body. When I booked the appointment I had pain in my neck and shoulders, by the time I saw him it was in my knees and wrists! The pain was put down to my being pregnant (with my second child), hormones etc. - advice, take pain killers
Moley1
in
Vasculitis UK
11 years ago
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Chronic back Pain
Hello, just found this forum, and im hoping I can get some advice or help. 3 years ago last month my back decided it would give me jip and also give me sciatica down my left leg (due to the disc being on it). The following May 2011, I had surgery to remove most of once of my discs, with the 3 under
Hello, just found this forum, and im hoping I can get some advice or help. 3 years ago last month my back decided it would give me jip and also give me sciatica down my left leg (due to the disc being on it). The following May 2011, I had surgery to remove most of once of my discs, with the 3 under
katwilson04
in
Pain Concern
11 years ago
Hi - have very extensive adhesions, following multiple surgeries, and Ovarian Remnant Syndrome. Need advice on pain relief
My pain issue is that my GP seems to be incredibly reluctant to prescribe any opiate-based pain relief, and is constantly on at me about the risk of addiction and trying to get me to reduce my usage, at one point reducing my prescription by 75% and leaving me virtually suicidal with the pain. Yet I have
My pain issue is that my GP seems to be incredibly reluctant to prescribe any opiate-based pain relief, and is constantly on at me about the risk of addiction and trying to get me to reduce my usage, at one point reducing my prescription by 75% and leaving me virtually suicidal with the pain. Yet I have
housebythesea
in
Pelvic Pain Support Network
11 years ago
Hip Bursitis and sciatica do they go hand in hand and are the treatments and physio for these, similar for each ailment ?
Also is there "really" no cure , I am going into my 3rd month & doesn't seem to be getting better or going away , does this indicate that I am stuck with it and therefore will never be pain free again & always dosed up on Co Codamol & feeling nauseous, ... I am seeing a Physio tomorrow, what is it
Also is there "really" no cure , I am going into my 3rd month & doesn't seem to be getting better or going away , does this indicate that I am stuck with it and therefore will never be pain free again & always dosed up on Co Codamol & feeling nauseous, ... I am seeing a Physio tomorrow, what is it
cazzz
in
Pain Concern
11 years ago
Hi everyone , im new to this wonderful site , was diagnosed 13 months ago with seron neg RA , After 6yrs of symptoms im having worst ever
Symptoms , in so much pain cant do much at all . Ie walk or get in /out of a chair .having neuro symptoms numbness jerking etc waiting to see neuro in 4 weeks . On methotrexate , hydroxqloriquine sulphalazine gabapentin . Tramadol co codamol . Im in tears last day or so and this morning got letter saying
Symptoms , in so much pain cant do much at all . Ie walk or get in /out of a chair .having neuro symptoms numbness jerking etc waiting to see neuro in 4 weeks . On methotrexate , hydroxqloriquine sulphalazine gabapentin . Tramadol co codamol . Im in tears last day or so and this morning got letter saying
Hidden
in
NRAS
11 years ago
Hip and groin pain-advice?
This is a new one for me! Horrible groin and outer hip pain. Does anyone else wake up with this.It's just on the left side and it's tender to touch. The pain is hard to ignore! Hasn't got any better all morning despite Co-codamol. 30/500. It feels like a straight line of pain running through from the
This is a new one for me! Horrible groin and outer hip pain. Does anyone else wake up with this.It's just on the left side and it's tender to touch. The pain is hard to ignore! Hasn't got any better all morning despite Co-codamol. 30/500. It feels like a straight line of pain running through from the
hev53
in
NRAS
11 years ago
Severe constipation and bowel problems, can this be thyroid related ? Recommended pain relief !
I was diagnosed with IBS several years ago before I knew anything about my thyroid problems (Hypo and Hashi's), for the past two months though the constipation has been horrific, I have had severe itching, pain and bleeding when going to the toilet, even though I take the maximum amount of lactulose
I was diagnosed with IBS several years ago before I knew anything about my thyroid problems (Hypo and Hashi's), for the past two months though the constipation has been horrific, I have had severe itching, pain and bleeding when going to the toilet, even though I take the maximum amount of lactulose
itchyinsomniac
in
Thyroid UK
11 years ago
maths solution according to the chemist.
The chemist told me that the difference with separating the drugs into their own tablets is that I can control what I am taking according to the pain. She said she thinks the GP is trying to get me off the codeine. I am baffled as the pain level has increased and the co codamol are not working and between
The chemist told me that the difference with separating the drugs into their own tablets is that I can control what I am taking according to the pain. She said she thinks the GP is trying to get me off the codeine. I am baffled as the pain level has increased and the co codamol are not working and between
superannie
in
Pain Concern
11 years ago
Maths help needed re meds. Hi all, between my chemist and GP we have changed my meds which were co codamol 30/500 . Taken two ,three times
a day To a single tablet of codeine 60mg and 500mg paracetamol two tablets , taken four times a day. I don't know if I am wrong but it seems like it amounts to the same dosage? I can see that I am taking the new dosage once more a day but I used to take the old dosage four times anyway. Is it me or can
a day To a single tablet of codeine 60mg and 500mg paracetamol two tablets , taken four times a day. I don't know if I am wrong but it seems like it amounts to the same dosage? I can see that I am taking the new dosage once more a day but I used to take the old dosage four times anyway. Is it me or can
superannie
in
Pain Concern
11 years ago
HSG caused me so much pain!
So i had a hysterosalpingogram on 5th November the procedure itself was uncomfy but i got through it. When i got home i was in so much pain in my stomach , back , shoulders the stomach pain is the same as the endometriosis (ive had endometriosis since i was 14 diagnosed in 2011 im now 22) I went to
So i had a hysterosalpingogram on 5th November the procedure itself was uncomfy but i got through it. When i got home i was in so much pain in my stomach , back , shoulders the stomach pain is the same as the endometriosis (ive had endometriosis since i was 14 diagnosed in 2011 im now 22) I went to
Hidden
in
Endometriosis UK
11 years ago
Please help - advice needed!! What happens when you go to A and E??
Hi all, I haven't posted for a while, probably since had my ovaries out back in June. Haven't had the best of recoveries as had HRT implant fitted during surgery, and for around 6/7 weeks, I had no menopause symptoms. Which they explained was good as meant HRT dose was right. Anyway then started having
Hi all, I haven't posted for a while, probably since had my ovaries out back in June. Haven't had the best of recoveries as had HRT implant fitted during surgery, and for around 6/7 weeks, I had no menopause symptoms. Which they explained was good as meant HRT dose was right. Anyway then started having
ClareLouise1980
in
Endometriosis UK
11 years ago
Hi all new to this site! but not new to RA :(
Hi all, I have had RA now for 18 months, I went to my GP march 2012, to see about my hands and feet & my lower back as they had been hurting me for some time, i had put it down to work and the fact i was in the TA at the time, anyway i go see him and he takes some blood tests, 1 week later i get
Hi all, I have had RA now for 18 months, I went to my GP march 2012, to see about my hands and feet & my lower back as they had been hurting me for some time, i had put it down to work and the fact i was in the TA at the time, anyway i go see him and he takes some blood tests, 1 week later i get
marcus6
in
NRAS
11 years ago
High BP for over a week. also changed meds.
Hi all, I have changed from co codamol 30/500 to a single tablet of 60mg codeine and two x 500mg paracetomol four times a day. Not related to the meds , I was found to have bp of over 200/98 The doc made me wait 20 mins and redid it and it was the same. He has asked me to come back this Tuesday when
Hi all, I have changed from co codamol 30/500 to a single tablet of 60mg codeine and two x 500mg paracetomol four times a day. Not related to the meds , I was found to have bp of over 200/98 The doc made me wait 20 mins and redid it and it was the same. He has asked me to come back this Tuesday when
superannie
in
Pain Concern
11 years ago
Morphine patches
Hi everyone, what is anyone's opinion on morphine patches y doctr has asked my to give thm a try, those of you that have could you plzz tll me a little about them, I have to give y doctor an answer on Thursday, I already take tramadol, gabapentin, and hv co-codamol as a back up, gentle hus to all.
Hi everyone, what is anyone's opinion on morphine patches y doctr has asked my to give thm a try, those of you that have could you plzz tll me a little about them, I have to give y doctor an answer on Thursday, I already take tramadol, gabapentin, and hv co-codamol as a back up, gentle hus to all.
Cookie72
in
Fibromyalgia Action UK
11 years ago
Proper grown up flare!?
Hello everyone, I've been hijacking Tilda's blog ( thank you ;) so thought I would write my own for some advice? I was diagnosed earlier in the year after two years of constant stiffness and pain, i was diagnosed as Sero-negative and the RA was mainly affecting my hands but also my knees, ankles, shoulder
Hello everyone, I've been hijacking Tilda's blog ( thank you ;) so thought I would write my own for some advice? I was diagnosed earlier in the year after two years of constant stiffness and pain, i was diagnosed as Sero-negative and the RA was mainly affecting my hands but also my knees, ankles, shoulder
Hidden
in
NRAS
11 years ago
Knee pain
Hi all, Pretty much unable to walk without an aid since Saturday, in unbearable pain, been put on co-codamol by GP but they are having no effect, been signed off of work for a week, awaiting blood test results to see if its a lupus flare. Any suggestions on what could help would be very much appreciated
Hi all, Pretty much unable to walk without an aid since Saturday, in unbearable pain, been put on co-codamol by GP but they are having no effect, been signed off of work for a week, awaiting blood test results to see if its a lupus flare. Any suggestions on what could help would be very much appreciated
March2012
in
LUPUS UK
11 years ago
Urgent advise. Can Pregavalin be the cause suddenly with painful, swollen knees Aquiles tendonitis, and other tendons. Also put on weight.
I am really worried about loosing a lot of movement and increased pain. Restless Legs are not too bad. But since I have to hide at work that I have RL, fibromyalgia , pain it has become impossible to pretend that all is well. Having no support makes it more difficult. I had a more understanding boss
I am really worried about loosing a lot of movement and increased pain. Restless Legs are not too bad. But since I have to hide at work that I have RL, fibromyalgia , pain it has become impossible to pretend that all is well. Having no support makes it more difficult. I had a more understanding boss
Mispiernas
in
Restless Legs Syndrome
11 years ago
Feeling left high and dry to suffer alone...
So sorry, I only seem to post when I am feeling down! Am having the worst flare I have ever experienced, 5 days so far and no sign of a reprieve. My lower back pain is immense, as is my neck pain and tingling hands and feet. Bad arthritis is causing havoc in my hands and elbows, and Raynauds is bad
So sorry, I only seem to post when I am feeling down! Am having the worst flare I have ever experienced, 5 days so far and no sign of a reprieve. My lower back pain is immense, as is my neck pain and tingling hands and feet. Bad arthritis is causing havoc in my hands and elbows, and Raynauds is bad
sparkle247
in
LUPUS UK
11 years ago
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