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Leg pain
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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
5 months ago
Collapsed vein -another thing to fret about?
I do have Peripheral Artery Disease in my left
leg
but no
pain
or restrictions in my arms. She did manage to take blood from my left arm. Is this something to worry about? oh, I’m taking Clopidogrel, Atorvastatin and Famotidine.
I do have Peripheral Artery Disease in my left
leg
but no
pain
or restrictions in my arms. She did manage to take blood from my left arm. Is this something to worry about? oh, I’m taking Clopidogrel, Atorvastatin and Famotidine.
Ladylovesmilktray
in
British Heart Foundation
20 days 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
6 months ago
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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
6 months ago
Anti-epileptic drug
Hi! I have epilepsy since 2002. I use anti-epileptic drugs. I have T too for 3 years. Sometimes it is better sometimes worse. The interesting thing is that it is far better when I take in the "Cosim" (lacosamide). Do anybody have experience like this? The bad thing is that it's effect is lower now..
Hi! I have epilepsy since 2002. I use anti-epileptic drugs. I have T too for 3 years. Sometimes it is better sometimes worse. The interesting thing is that it is far better when I take in the "Cosim" (lacosamide). Do anybody have experience like this? The bad thing is that it's effect is lower now..
kchrisX
in
Tinnitus UK
4 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
6 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
6 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
6 months ago
lap is booked and i'm nervous
,
leg
pain
and vertigo associated with extreme pain and pms. it's also been difficult getting help without a diagnosis. what's worse is i'm only 22!
,
leg
pain
and vertigo associated with extreme pain and pms. it's also been difficult getting help without a diagnosis. what's worse is i'm only 22!
VioletCoffee
in
Endometriosis UK
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
6 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
6 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
6 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
6 months ago
New Blood in Stool
The only other issues I have are lower back and
leg
pain
. I already had a colonoscopy scheduled for October, but I’m thinking this warrants a more urgent look. I’ve been informing my GI about these sightings. Since it’s the weekend, I haven’t heard back since Friday.
The only other issues I have are lower back and
leg
pain
. I already had a colonoscopy scheduled for October, but I’m thinking this warrants a more urgent look. I’ve been informing my GI about these sightings. Since it’s the weekend, I haven’t heard back since Friday.
E08109
in
Colon Cancer Connected
10 months ago
Sciatic endo symptoms & waiting for surgery
Recently I had to visit my GP (she's defo sick of me😅) because during my last few flare ups I have had awful
leg
pain
and lost the ability to walk a few times which is concerning.
Recently I had to visit my GP (she's defo sick of me😅) because during my last few flare ups I have had awful
leg
pain
and lost the ability to walk a few times which is concerning.
endo_the_stigma
in
Endometriosis UK
4 months ago
Leg neuropathy after induced coma
After eight weeks in icu in a induced coma, I awake being paralised from the waist down, oh bugger I thought.After four months I have relearned to walk and speak again(love those traciotomies) but am left with severe nerve damage to my perinial nerves and am in constant
leg
pain
, even with a boat load
After eight weeks in icu in a induced coma, I awake being paralised from the waist down, oh bugger I thought.After four months I have relearned to walk and speak again(love those traciotomies) but am left with severe nerve damage to my perinial nerves and am in constant
leg
pain
, even with a boat load
Misterpaulwood
in
ICUsteps
11 months 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
6 months ago
Airing Pain 140: Out now!
[i]
Airing Pain
[/i] edition 140: Childhood Pain - Adverse Experiences and Parental Relationships is now available to listen to here: https://painconcern.org.uk/airing-pain-140-childhood-experiences/ Full transcript is available online and to download, as well as a captioned video on YouTube.
[i]
Airing Pain
[/i] edition 140: Childhood Pain - Adverse Experiences and Parental Relationships is now available to listen to here: https://painconcern.org.uk/airing-pain-140-childhood-experiences/ Full transcript is available online and to download, as well as a captioned video on YouTube.
PainConcernHelpline
Pain Concern
in
Pain Concern
6 months ago
constipation from panadeine, or vertebra nerves, or both?
so docs have said constipation can be caused by pain medication and by the nerves of the vertebra, what's your experience, thanks any pain medication comments welcomed, i think. a dr friend of mine has used patches.
so docs have said constipation can be caused by pain medication and by the nerves of the vertebra, what's your experience, thanks any pain medication comments welcomed, i think. a dr friend of mine has used patches.
MayGodBlessYou
in
Bone Health and Osteoporosis UK
6 months ago
Pelvic Pain Worse at Night
Hi all. Currently undiagnosed/suspected endo. Trying to document when I get flare ups of pelvic pain/cramping and notice any links/triggers. I don’t have periods due to having the coil (used to have incredibly painful periods/heavy periods) but still suffering from pelvic pain. If I get any spotting
Hi all. Currently undiagnosed/suspected endo. Trying to document when I get flare ups of pelvic pain/cramping and notice any links/triggers. I don’t have periods due to having the coil (used to have incredibly painful periods/heavy periods) but still suffering from pelvic pain. If I get any spotting
PBGV24
in
Endometriosis UK
6 months ago
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