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Experiences with
Muscle pain
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Zoladex and HRT
I was diagnosed with endo in 2021, it was removed from my abdominal wall but my pain never fully left. Just 4 months later my symptoms returned and the pain was as bad as it was pre-op. Here I am, 19 months later in significant daily pain. I am signed off sick from work for the 3rd week, and it seems
I was diagnosed with endo in 2021, it was removed from my abdominal wall but my pain never fully left. Just 4 months later my symptoms returned and the pain was as bad as it was pre-op. Here I am, 19 months later in significant daily pain. I am signed off sick from work for the 3rd week, and it seems
Ccn2018
in
Endometriosis UK
1 year ago
Flare up
Hi, I have had lupus for 7 years now and feel I've been very lucky as meds have controlled it really well , until now. I have continued to go on holiday and wear solbari clothing and 50 factor sun screen . I have been able to sit in shaded places . However this time had a really bad flare in my ankles
Hi, I have had lupus for 7 years now and feel I've been very lucky as meds have controlled it really well , until now. I have continued to go on holiday and wear solbari clothing and 50 factor sun screen . I have been able to sit in shaded places . However this time had a really bad flare in my ankles
Waxed
in
LUPUS UK
1 year ago
Only Right side back pain after Fet
Hi all Ladies.Dies anyone felt the same as Iam🥲😢..i have severe back pain started last friday..a sharp back pain and and 2 days now. It hurt so much. Does this cause by stimulation and progesteron, is it ok to drink pain reliever. Im going also to call my clinic i necer ezperience this before, i felt
Hi all Ladies.Dies anyone felt the same as Iam🥲😢..i have severe back pain started last friday..a sharp back pain and and 2 days now. It hurt so much. Does this cause by stimulation and progesteron, is it ok to drink pain reliever. Im going also to call my clinic i necer ezperience this before, i felt
PrayingforMyBaby
in
Fertility Network UK
1 year ago
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Feeling woefully undermedicated……
Would this account for my symptoms, which include joint and
muscle
pain
/weakness, exhaustion, inertia, brain fog, swollen tongue, puffy eyes? Ferritin continues to be inadequate 42 ug/L [23.0 - 300.0] and I’ve ordered a full iron panel.
Would this account for my symptoms, which include joint and
muscle
pain
/weakness, exhaustion, inertia, brain fog, swollen tongue, puffy eyes? Ferritin continues to be inadequate 42 ug/L [23.0 - 300.0] and I’ve ordered a full iron panel.
J972
in
Thyroid UK
1 year ago
Enlarged Prostate Medication
Good afternoon. I’ve been recently diagnosed with enlarged prostate. My general health is not good as I had a Triple Bypass and Mitral Valve Repair and also, last year was diagnosed with Heart Failure. I’ve also got Severe Spinal Stenosis which has returned following a Failed Laminectomy Spine Operation
Good afternoon. I’ve been recently diagnosed with enlarged prostate. My general health is not good as I had a Triple Bypass and Mitral Valve Repair and also, last year was diagnosed with Heart Failure. I’ve also got Severe Spinal Stenosis which has returned following a Failed Laminectomy Spine Operation
Davewm
in
Men's Health Forum
1 year ago
Possible hypothyroidism?
Chest tremors/
pain
. Joint
pain
.
Muscle
pain
. Very stiff after waking up. Hip pain. Lower back pain (probably from pelvic floor issues and diastasis recti). I now have a goiter showing a small cyst and nodule on my thyroid per ultrasound that showed up recently.
Chest tremors/
pain
. Joint
pain
.
Muscle
pain
. Very stiff after waking up. Hip pain. Lower back pain (probably from pelvic floor issues and diastasis recti). I now have a goiter showing a small cyst and nodule on my thyroid per ultrasound that showed up recently.
Mama-ash0619
in
Thyroid UK
8 months ago
T3 monotherapy - different brands
Since being on it my symptoms have changed - fatigue and brain fog for 2 days, followed by fatigue,
muscle
pain
, headaches, knee pain, Plantar Fasciitis flare up, now that's all gone, and I have a familiar symptom of a sinus soreness and fatigue.
Since being on it my symptoms have changed - fatigue and brain fog for 2 days, followed by fatigue,
muscle
pain
, headaches, knee pain, Plantar Fasciitis flare up, now that's all gone, and I have a familiar symptom of a sinus soreness and fatigue.
Agapanthus
in
Thyroid UK
8 months ago
Not tolerating thyroid medications , tried t4 , t3 and ndt as well as cow thyroid , ready to give up completely
I recently had and increase of ndt and the
muscle
pain
and joint pain are hiddeous, doesn't matter which meds I try none of them work, cant get within range without terrible side effects.
I recently had and increase of ndt and the
muscle
pain
and joint pain are hiddeous, doesn't matter which meds I try none of them work, cant get within range without terrible side effects.
Rhannii7
in
Thyroid UK
1 year ago
Nerve compression after surgery for Cauda Equina
Ho- just wondered if anyone had been through a similar thing. A relative had surgery for Cauda Equina which failed. She had had a new nerve compression- due to pressure from centralised disc - but she has been refused surgery despite the excruciating pain. She has tried several neuropathic painkillers
Ho- just wondered if anyone had been through a similar thing. A relative had surgery for Cauda Equina which failed. She had had a new nerve compression- due to pressure from centralised disc - but she has been refused surgery despite the excruciating pain. She has tried several neuropathic painkillers
Mymysonlyone
in
Pain Concern
1 year ago
GP says results are fine
Fatigue, brainfog,
muscle
aches, joint
pain
, and other various symptoms. Below are my blood test results. The GP stated there is nothing of concern. He seemed more focused on mental health issues. Is there anything obvious below? Someone said to post here.
Fatigue, brainfog,
muscle
aches, joint
pain
, and other various symptoms. Below are my blood test results. The GP stated there is nothing of concern. He seemed more focused on mental health issues. Is there anything obvious below? Someone said to post here.
ArinEla
in
Thyroid UK
2 months ago
ARRRGH !
Hi all, I live in Tasmania, Australia and do not have private health cover. I am 60 years old and have had rls since I was 21, that I know of. I have also been on antidepressants since 1980... I realky believe that they have caused the rls as no one in my family had it. Anyway, it became absolutely
Hi all, I live in Tasmania, Australia and do not have private health cover. I am 60 years old and have had rls since I was 21, that I know of. I have also been on antidepressants since 1980... I realky believe that they have caused the rls as no one in my family had it. Anyway, it became absolutely
Oscarcat63
in
Restless Legs Syndrome
1 year ago
Flaring up after Booster
Good morning all,I hope everyone is well as can be given their conditions. I read everyone's messages but rarely post. I had my fourth Covid vaccination yesterday morning. It should be my fifth but I didn't take the previous one. By late afternoon/evening, my shoulder was hurting and my hand and some
Good morning all,I hope everyone is well as can be given their conditions. I read everyone's messages but rarely post. I had my fourth Covid vaccination yesterday morning. It should be my fifth but I didn't take the previous one. By late afternoon/evening, my shoulder was hurting and my hand and some
Choccy23
in
NRAS
1 year ago
Pain that effects my life
Last 2 days had pain right side wrist leg and shoulder . Previously to this for years I had back ache and shoulder . I know think it could be possibly fibromeliga and will keep going back with a pain log . I went today but the doctor said I come to early and implying I am wasting there time . I did
Last 2 days had pain right side wrist leg and shoulder . Previously to this for years I had back ache and shoulder . I know think it could be possibly fibromeliga and will keep going back with a pain log . I went today but the doctor said I come to early and implying I am wasting there time . I did
Amanda556
in
Borders Pain Management
1 year ago
Hi Penny
I was on pred for 3 years for p m a.I reduced very slowly but it was extremely difficult once I hit 5mgms I then reduced by half a mgm every 2 months.At each reduction I experienced break through pain .When I finally stopped I was in severe pain but I persevered with the help of pain killers heat bags
I was on pred for 3 years for p m a.I reduced very slowly but it was extremely difficult once I hit 5mgms I then reduced by half a mgm every 2 months.At each reduction I experienced break through pain .When I finally stopped I was in severe pain but I persevered with the help of pain killers heat bags
Whist
in
NRAS
1 year ago
New here Hi
Hello everyone- I’ve been suffering with extreme fatigue
muscle
aches inc knee
pain
for 2years rheumatologist done X-ray on my knees and hips 2021 and showed mild OA but shouldn’t be causing so much pain.
Hello everyone- I’ve been suffering with extreme fatigue
muscle
aches inc knee
pain
for 2years rheumatologist done X-ray on my knees and hips 2021 and showed mild OA but shouldn’t be causing so much pain.
Glutusmaximus
in
PMRGCAuk
9 months ago
ibs-d and facing surgery
I’m having a knee replacement on Wednesday and worried about my ibs-d as bad at the mo. I’m taking loperamide but worried that if I take too many with the combination of strong painkillers I’ll end up constipated. Also concerned that as im having an epidural I wont be able to feel if I need to go😩
I’m having a knee replacement on Wednesday and worried about my ibs-d as bad at the mo. I’m taking loperamide but worried that if I take too many with the combination of strong painkillers I’ll end up constipated. Also concerned that as im having an epidural I wont be able to feel if I need to go😩
BasilG
in
IBS Network
1 year ago
Is codeine ok with prednisolone.
Foolishly went mad digging garden couple of weeks ago and upset my back....past slipped disc. Seeing pysio and doing all the right things and keeping pain killers to a minimum as even the paracetamol make me feel strange, light headed and upset digestive system. I am on omeprazole. Would codeine be a
Foolishly went mad digging garden couple of weeks ago and upset my back....past slipped disc. Seeing pysio and doing all the right things and keeping pain killers to a minimum as even the paracetamol make me feel strange, light headed and upset digestive system. I am on omeprazole. Would codeine be a
Ebiker
in
PMRGCAuk
1 year ago
More surgery....
So I finally got to see the endometriosis specialist again after screaming and shouting yet again, they told me they will finally take out my overies away and put me on prostap injections up until this surgery I really hope it helps, this is my last resort it's been years of pain pills injections and
So I finally got to see the endometriosis specialist again after screaming and shouting yet again, they told me they will finally take out my overies away and put me on prostap injections up until this surgery I really hope it helps, this is my last resort it's been years of pain pills injections and
Bubblepoppy
in
Endometriosis UK
1 year ago
PMR flare, muscle pain or side effects of medication?
I thought it was a
muscle
problem initially and have been taking paracetamol but the
pain
is still there so I am now wondering whether it is a flare and whether I should try increasing the steroids. Tapering had been going well. My starting dose was 20mg in June 2022.
I thought it was a
muscle
problem initially and have been taking paracetamol but the
pain
is still there so I am now wondering whether it is a flare and whether I should try increasing the steroids. Tapering had been going well. My starting dose was 20mg in June 2022.
sewinggranny
in
PMRGCAuk
1 year ago
Hi I’m dory10. I was diagnosed inDec2019 but had it for 27 years. I fall over a lot now I’m having tests to find out why.
She was fine a genius infact but I was left in
muscle
spasms and so much
pain
. I was told I was so close to being a paraplegic. I put up with all the little things that went wrong, I was fortunate not to be paraplegic.
She was fine a genius infact but I was left in
muscle
spasms and so much
pain
. I was told I was so close to being a paraplegic. I put up with all the little things that went wrong, I was fortunate not to be paraplegic.
Dory10
in
Fibromyalgia Action UK
5 months ago
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