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Leg pain
So a couple of years ago I started to get IBS
pain
low on the right side. Had scans etc, to check ovaries. Turns out it was definitely IBS
pain
. I have had it again since. I'm currently in a flare up with low abdo
pain
, this right sided
pain
is back as well. But also it goes into the top of my leg?
So a couple of years ago I started to get IBS
pain
low on the right side. Had scans etc, to check ovaries. Turns out it was definitely IBS
pain
. I have had it again since. I'm currently in a flare up with low abdo
pain
, this right sided
pain
is back as well. But also it goes into the top of my leg?
mithical
in
IBS Network
3 months ago
Lupus pain
I was diagnosed over23yrs ago i am now 64 and struggling quite alot with muscle and joint pains i am due ultrasound scans on both hips plus my right shoulder this month i cant sleep due to
pain
sick of feeling exhausted and downhearted i have severe acid reflux and ibs so cant take antinflamatory medications
I was diagnosed over23yrs ago i am now 64 and struggling quite alot with muscle and joint pains i am due ultrasound scans on both hips plus my right shoulder this month i cant sleep due to
pain
sick of feeling exhausted and downhearted i have severe acid reflux and ibs so cant take antinflamatory medications
LUPUSLADY60
in
NRAS
3 months ago
How long for Leflunomide to work?
I have a follow up F2F on 10 Jan with rheumy nurse, and know I have to bear this
pain
out while the drugs work (if they work) but just wondered if anyway could share their experiences of when it started to make a difference.. thank you
I have a follow up F2F on 10 Jan with rheumy nurse, and know I have to bear this
pain
out while the drugs work (if they work) but just wondered if anyway could share their experiences of when it started to make a difference.. thank you
Sapphire1701
in
NRAS
9 months ago
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Unusual pain
Been in perm AF for two years now so dont have to worry although did have a
pain
in middle of chest at the weekend which could have been caused by large glass of red went to hosp everything normal apart from heart rate up BP up and palpys
pain
was mainly when breathing deeply anyone else get this?
Been in perm AF for two years now so dont have to worry although did have a
pain
in middle of chest at the weekend which could have been caused by large glass of red went to hosp everything normal apart from heart rate up BP up and palpys
pain
was mainly when breathing deeply anyone else get this?
Robertmacintyre
in
Atrial Fibrillation Support
3 months ago
leg pain
pain
in hands arms neck ext brain fog I’m a 52 year old women TIA
pain
in hands arms neck ext brain fog I’m a 52 year old women TIA
Paula1jj
in
Fibromyalgia Action UK
3 months ago
Pelvic Pain Worse at Night
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 that brings on intense pelvic
pain
.
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 that brings on intense pelvic
pain
.
PBGV24
in
Endometriosis UK
11 months ago
Stopping Kevzara
I still have the
pain
and take my painkillers, but I feel more awake and less lethargic. It's not the first bio I have tried and the others have been the same. Does anyone have experience of this?
I still have the
pain
and take my painkillers, but I feel more awake and less lethargic. It's not the first bio I have tried and the others have been the same. Does anyone have experience of this?
tazman3
in
NRAS
8 months ago
daily pain
My MS affect my feet and ankles with constant
pain
. How am I supposed to lead a productive life I am fatigued with the disease, the Rx, the heat, and age. My grand baby is accustomed to the two of us running, walking, skating, and jumping together and now we can not. I'm letting her down.
My MS affect my feet and ankles with constant
pain
. How am I supposed to lead a productive life I am fatigued with the disease, the Rx, the heat, and age. My grand baby is accustomed to the two of us running, walking, skating, and jumping together and now we can not. I'm letting her down.
AllDayPain
in
My MSAA Community
3 months ago
New Rheumatology Referral - hope it comes through quickly!
Hello folks, I’ve had fairly mild Reynaud’s for a long time and have more recently been diagnosed with fibromyalgia due to ongoing raised glands,
pain
& fatigue without infection/ inflammation.
Hello folks, I’ve had fairly mild Reynaud’s for a long time and have more recently been diagnosed with fibromyalgia due to ongoing raised glands,
pain
& fatigue without infection/ inflammation.
Purple_Badgers
in
Scleroderma & Raynaud's UK (SRUK)
7 months ago
Walking Speed
I know our bodies are different, but we all have something in common. Has anyone done or tried something besides ampyra that increased the speed that you walk? I've tried ampyra, dysport and I'm still moving like a turtle. My legs still feel very heavy! I'm still hoping to be walking normal again!
I know our bodies are different, but we all have something in common. Has anyone done or tried something besides ampyra that increased the speed that you walk? I've tried ampyra, dysport and I'm still moving like a turtle. My legs still feel very heavy! I'm still hoping to be walking normal again!
Diva1976
in
My MSAA Community
6 months ago
Pain clinic
How many different
Pain
Clinics is it necessary to attend before they realise it doesn’t help someone with multiple health conditions? Eg - RA with secondary Sjögrens, Fibromyalgia, FND, severely degenerative disc disease with kyphosis/ rotational scoliosis, ME/CFS.
How many different
Pain
Clinics is it necessary to attend before they realise it doesn’t help someone with multiple health conditions? Eg - RA with secondary Sjögrens, Fibromyalgia, FND, severely degenerative disc disease with kyphosis/ rotational scoliosis, ME/CFS.
Blackwitch
in
Pain Concern
3 months ago
NHS Rheumatology Appointment
Update on my trials and tribulations regarding a diagnosis for my bilateral shoulder and hip
pain
...... Still haven't had any treatment or been given any medication bar
pain
killers and NSAIDs.... Got my referral letter for the NHS Rheumatology referral......Feb 24th 2024.....
Update on my trials and tribulations regarding a diagnosis for my bilateral shoulder and hip
pain
...... Still haven't had any treatment or been given any medication bar
pain
killers and NSAIDs.... Got my referral letter for the NHS Rheumatology referral......Feb 24th 2024.....
Paulx222
in
PMRGCAuk
10 months ago
Foot pain
Last night, the
pain
over the tarsal bones was enough to make it difficult to sleep. I've not changed shoes or been more active so I'm perplexed. Does this look like a pattern of RA type inflammation? Could compression help?...
Last night, the
pain
over the tarsal bones was enough to make it difficult to sleep. I've not changed shoes or been more active so I'm perplexed. Does this look like a pattern of RA type inflammation? Could compression help?...
Gottarelax
in
NRAS
3 months ago
SE from ADT and two natural remedies I always use. Anger=kava kava, insomnia=wild lettuce.
I also use this for sny
pain
anywhere in my body including headaches. This is my go to
pain
medicine. Don’t get me wrong oxycodone works better and longer for accute or severe
pain
. Kava kava i have used since college when i had anxiety block during calculus tests and it is AMAZING.
I also use this for sny
pain
anywhere in my body including headaches. This is my go to
pain
medicine. Don’t get me wrong oxycodone works better and longer for accute or severe
pain
. Kava kava i have used since college when i had anxiety block during calculus tests and it is AMAZING.
KocoPr
in
Fight Prostate Cancer
10 months ago
Pain increasing
I thought I was doing ok with 9 mg of pred since June 1. But it seems my hips and low back are hurting more lately. Walking is very painful and I’m slowing down each day. My neck has also started hurting, which is a new problem for me. I’ve had to lie on the heating pad for the last 2 days,for my neck
I thought I was doing ok with 9 mg of pred since June 1. But it seems my hips and low back are hurting more lately. Walking is very painful and I’m slowing down each day. My neck has also started hurting, which is a new problem for me. I’ve had to lie on the heating pad for the last 2 days,for my neck
Aqua47
in
PMRGCAuk
3 months ago
Magnesium Supplements to reduce frequency of migraines
They used to cause me to be sick but I have now learnt to control this and instead, when I have a migraine, I need to close myself in a dark room, avoid sound, and apply heat to my neck/ traps, trying to sleep it off with some strong
pain
killers (900mg of dispersible aspirin sometimes does the trick
They used to cause me to be sick but I have now learnt to control this and instead, when I have a migraine, I need to close myself in a dark room, avoid sound, and apply heat to my neck/ traps, trying to sleep it off with some strong
pain
killers (900mg of dispersible aspirin sometimes does the trick
MollyPigs
in
National Migraine Centre
6 months ago
Magnesium Supplements
They used to cause me to be sick but I have now learnt to control this and instead, when I have a migraine, I need to close myself in a dark room, avoid sound, and apply heat to my neck/ traps, trying to sleep it off with some strong
pain
killers (900mg of dispersible aspirin sometimes does the trick
They used to cause me to be sick but I have now learnt to control this and instead, when I have a migraine, I need to close myself in a dark room, avoid sound, and apply heat to my neck/ traps, trying to sleep it off with some strong
pain
killers (900mg of dispersible aspirin sometimes does the trick
MollyPigs
in
Migraine Support
6 months ago
Leg pain
Does anyone ever get leg
pain
, in there lower leg? Hard to describe but feels like like knocked my leg on something If yes, how do you manage the
pain
Does anyone ever get leg
pain
, in there lower leg? Hard to describe but feels like like knocked my leg on something If yes, how do you manage the
pain
Pulp88
in
Thyroid UK
3 months ago
Two Years On - What Treatment?
My
pain
levels are an average of 7/10, but I'm not allowed painkillers because the UK doesn't treat chronic
pain
with painkillers anymore [because they're not a solution, therefore not allowed - which is BS, but that's politics stepping into medicine for ya].
My
pain
levels are an average of 7/10, but I'm not allowed painkillers because the UK doesn't treat chronic
pain
with painkillers anymore [because they're not a solution, therefore not allowed - which is BS, but that's politics stepping into medicine for ya].
LilyMarshell
in
Functional Neurological Disorder - FND Hope
8 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
?
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
?
Hidden
in
Neuropathy Support
10 months ago
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