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Muscle pain
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‘They thought I had cancer’: painkiller banned in UK linked to Britons’ deaths in Spain
Just want to make sure anyone with access to metamizole is aware of these possible issues. It is NOT available in the UK. [i]
‘They thought I had cancer’: painkiller banned in UK linked to Britons’ deaths in Spain
[/i] [i]Patients’ group says reactions to metamizole can cause sepsis and organ
Just want to make sure anyone with access to metamizole is aware of these possible issues. It is NOT available in the UK. [i]
‘They thought I had cancer’: painkiller banned in UK linked to Britons’ deaths in Spain
[/i] [i]Patients’ group says reactions to metamizole can cause sepsis and organ
helvella
Thyroid UK
in
Thyroid UK
7 months ago
7 weeks on and a million questions sorry
hi and good morning all, well I’m 7 weeks after icu ventilation and I have a million questions I’m hoping people could shed some light on so I don’t dr google everything and think I have every illness known to man!! I was on ventilation for 9 days in icu and I still have health issues popping up here
hi and good morning all, well I’m 7 weeks after icu ventilation and I have a million questions I’m hoping people could shed some light on so I don’t dr google everything and think I have every illness known to man!! I was on ventilation for 9 days in icu and I still have health issues popping up here
Alfiedude99
in
ICUsteps
7 months ago
Sacral Insufficiency Fractures
Hi, I've just joined this online community, which feels like a good start! I was diagnosed with sacral insufficiency fractures following a scan in February of this year. My symptoms - excruciating pain and limited mobility - started in September 2022 only 3 months after the finish of my pelvic radiotherapy
Hi, I've just joined this online community, which feels like a good start! I was diagnosed with sacral insufficiency fractures following a scan in February of this year. My symptoms - excruciating pain and limited mobility - started in September 2022 only 3 months after the finish of my pelvic radiotherapy
Poir
in
Pelvic Radiation Disease Association
7 months ago
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SIDE EFFECTS FROM HYPO MEDS
The only thing the meds help with is taking away my
muscle
ache and joint
pain
. They also help with constipation. I’ve tried taking different doasages and experimented with the times day I’m taking them.
The only thing the meds help with is taking away my
muscle
ache and joint
pain
. They also help with constipation. I’ve tried taking different doasages and experimented with the times day I’m taking them.
Fairydancer
in
Thyroid UK
5 months ago
I didn’t know if I’d be able to come back…..
Hello It’s been months since I posted to all the lovely supportive people here. I’m very sorry but I couldn’t face it as I had an injury, which a physio said meant that I might not be able to run again. I was devastated. But the amazing news is after nearly 4 months of not running I started very slowly
Hello It’s been months since I posted to all the lovely supportive people here. I’m very sorry but I couldn’t face it as I had an injury, which a physio said meant that I might not be able to run again. I was devastated. But the amazing news is after nearly 4 months of not running I started very slowly
LindySearle
Graduate10
in
Bridge to 10K
7 months ago
Back and hips - is this a Flare??
Hi wonderful people, When I first had PMR and at each previous flare, the pain has been across my shoulders and down the backs of my legs. I am currently feeling it badly in my lower back and pelvic girdle and am not sure if it is a flare or summat else. I am somewhat stressed and know that this
Hi wonderful people, When I first had PMR and at each previous flare, the pain has been across my shoulders and down the backs of my legs. I am currently feeling it badly in my lower back and pelvic girdle and am not sure if it is a flare or summat else. I am somewhat stressed and know that this
MDT1
in
PMRGCAuk
7 months ago
Edinburgh Endo Clinic
Hello! Just wondering if anyone has been on a loooong waiting list to be seen by an Endo specialist for the first time since diagnosis? Currently, it's an 80-week waiting time in Edinburgh. I know there is an option to go privately but I am just totally shocked that someone has to suffer from pain etc
Hello! Just wondering if anyone has been on a loooong waiting list to be seen by an Endo specialist for the first time since diagnosis? Currently, it's an 80-week waiting time in Edinburgh. I know there is an option to go privately but I am just totally shocked that someone has to suffer from pain etc
Axolotl23
in
Endometriosis UK
7 months ago
Anticoagulant users
G'day, Just after some input from NOAC and Warfarin users. I use Warfarin and have done so for nearly 14 years. No sweat ! Never had bleed problems but have had an assortment of bruising problems in that time usually from DIY mishaps. All sorts of pretty colours of blues, greens, yellows and purples
G'day, Just after some input from NOAC and Warfarin users. I use Warfarin and have done so for nearly 14 years. No sweat ! Never had bleed problems but have had an assortment of bruising problems in that time usually from DIY mishaps. All sorts of pretty colours of blues, greens, yellows and purples
BenHall1
in
Atrial Fibrillation Support
7 months ago
U.S. Gov't to Negotiate Prices for Ibrutinib
https://www.cnn.com/2023/08/29/politics/medicare-drug-price-negotiations/index.html#:~:text=Medicare%20will%20soon%20start%20negotiating%20the%20prices%20of%2010%20drugs%20with%20manufacturers.&text=The%20Biden%20administration%20unveiled%20Tuesday,blood%20thinners%20and%20diabetes%20medications.
https://www.cnn.com/2023/08/29/politics/medicare-drug-price-negotiations/index.html#:~:text=Medicare%20will%20soon%20start%20negotiating%20the%20prices%20of%2010%20drugs%20with%20manufacturers.&text=The%20Biden%20administration%20unveiled%20Tuesday,blood%20thinners%20and%20diabetes%20medications.
michaeledward
in
CLL Support
10 months ago
T4 to T3 conversion.
For the past couple of months my
muscle
pain
/joint pain has been getting steadily worse. Also numbness and tingling in my thighs. I would like to try a t3/t4 regimen but I can't seem to source T3 here in the UK. Can anyone let me know a reliable source. Also can a private gp prescribe T3.
For the past couple of months my
muscle
pain
/joint pain has been getting steadily worse. Also numbness and tingling in my thighs. I would like to try a t3/t4 regimen but I can't seem to source T3 here in the UK. Can anyone let me know a reliable source. Also can a private gp prescribe T3.
miravet
in
Thyroid UK
11 months ago
Laparoscopy found nothing - symptoms all point to endometriosis
I don’t suppose anyone has been in the same situation as me and can help? I have suffered from a range of issues from 15 with periods; bleeding and pain with intercourse, severe leg pain, always bleeding/spotting outside of periods, bad period pains, UTI like symptoms and odd bowel movements around
I don’t suppose anyone has been in the same situation as me and can help? I have suffered from a range of issues from 15 with periods; bleeding and pain with intercourse, severe leg pain, always bleeding/spotting outside of periods, bad period pains, UTI like symptoms and odd bowel movements around
puddl0503
in
Endometriosis UK
7 months ago
Endo on the bladder
Anyone else have the bladder and bowel endo? Willing to try anything, for any kind of relief. I have endo on and going into my bladder and now also effecting my bowel. It's triggered normally about day 3 of my period and last for a good 3 weeks. The first few days I just have to be near a toilet, when
Anyone else have the bladder and bowel endo? Willing to try anything, for any kind of relief. I have endo on and going into my bladder and now also effecting my bowel. It's triggered normally about day 3 of my period and last for a good 3 weeks. The first few days I just have to be near a toilet, when
Country-Girl100
in
Endometriosis UK
7 months ago
arthritis
having cervicogenic headaches from arthritis in neck. Any painkillers better than paracetamol that we can safely take? Thanks again.
having cervicogenic headaches from arthritis in neck. Any painkillers better than paracetamol that we can safely take? Thanks again.
Lindaj754
in
AF Association
7 months ago
How to deal with side effect of hot flashes and feeling hot all the time from pain meds?
How do you deal with the side effect of hot flashes and feeling hot all the time that is being caused from your pain medicine or antidepressants used for pain? I take Tramadol at the highest dosage everyday for my severe nerve pain from CRPS because it's the only thing that works for me. However it makes
How do you deal with the side effect of hot flashes and feeling hot all the time that is being caused from your pain medicine or antidepressants used for pain? I take Tramadol at the highest dosage everyday for my severe nerve pain from CRPS because it's the only thing that works for me. However it makes
Hidden
in
Neuro Support
7 months ago
How to deal with side effects of feeling hot from pain meds and antidepressants for pain?
How do you deal with the side effect of feeling hot all the time and having hot flashes that are caused from your pain medicine or your antidepressant used for pain? I take Tramadol at the highest dosage for my severe nerve pain from CRPS because it's the only thing that works for me however I find that
How do you deal with the side effect of feeling hot all the time and having hot flashes that are caused from your pain medicine or your antidepressant used for pain? I take Tramadol at the highest dosage for my severe nerve pain from CRPS because it's the only thing that works for me however I find that
Hidden
in
Neuropathy Support
7 months ago
RSV and Flare
hi everyone, I seem to be in the wars a bit at the moment and need some advice: - diagnosed PMR and RA April 23 - dosage of 30mg pred and 20 mg methotrexate - gradually reduced pred to 10.5 as per Rhumetologist instructions - had a flare in calf muscles, increased pred to 12.5 - travelled to NYC
hi everyone, I seem to be in the wars a bit at the moment and need some advice: - diagnosed PMR and RA April 23 - dosage of 30mg pred and 20 mg methotrexate - gradually reduced pred to 10.5 as per Rhumetologist instructions - had a flare in calf muscles, increased pred to 12.5 - travelled to NYC
MegfromOz
in
PMRGCAuk
7 months ago
Oh well, it was inevitable I suppose!
One of the side effects of both drugs is
muscle
pain
. So far, I’ve been spared this but I suppose it may start later. I have managed runs even in this very cold weather (-6°c ) on Monday and Wednesday so again, I may see how the medicines affect me in more normal weather.
One of the side effects of both drugs is
muscle
pain
. So far, I’ve been spared this but I suppose it may start later. I have managed runs even in this very cold weather (-6°c ) on Monday and Wednesday so again, I may see how the medicines affect me in more normal weather.
Vragtes
Graduate10
in
Bridge to 10K
5 months ago
compressed vertebrae, i asked dr about stronger pain medication and they said no -- i wonder why?
Mum's got probably vertebral pain, is on an otc pain tablet, plus a step up from that, the prescription version. a dr friend of mine said she should be on something stronger like oxycodone. i asked specialist if Mum could have a stronger pain medication, and was told no. why's that? maybe cause elderly
Mum's got probably vertebral pain, is on an otc pain tablet, plus a step up from that, the prescription version. a dr friend of mine said she should be on something stronger like oxycodone. i asked specialist if Mum could have a stronger pain medication, and was told no. why's that? maybe cause elderly
MayGodBlessYou
in
Bone Health and Osteoporosis UK
7 months ago
muscle aches and pains
I have been taking thyroxine for over 20 years over the last 2 years I have had bad
muscle
aches in both my hips and also
muscle
pain
in my arms. GP has done test and X-rays which have all been clear.
I have been taking thyroxine for over 20 years over the last 2 years I have had bad
muscle
aches in both my hips and also
muscle
pain
in my arms. GP has done test and X-rays which have all been clear.
Na68
in
Thyroid UK
1 year ago
Adenomyosis/Endometriosis Pain Management
Hi All, Just looking for a bit of advice. I was diagnosed with Adenomyosis and Fibroids at 38. Its only been a year and a half but Im struggling hugely. I am very depressed and cant motivate myself day to day. I have constant pain in my lower abdomen, tailbone and Left bum. My pain has progressed
Hi All, Just looking for a bit of advice. I was diagnosed with Adenomyosis and Fibroids at 38. Its only been a year and a half but Im struggling hugely. I am very depressed and cant motivate myself day to day. I have constant pain in my lower abdomen, tailbone and Left bum. My pain has progressed
ABFr23
in
Endometriosis UK
8 months ago
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