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Breathless ,mucus
Hi its Alice I have been away from this comuity for a good while been dealing with rheaumatiod
arthritis
, polymyligia reaumatica ,and sciatica lick
pain
,feel as though I've been in the wars ,what it is though since been on continual prednisalone (down to 11mgs now) and hydroxychloroquine given for
Hi its Alice I have been away from this comuity for a good while been dealing with rheaumatiod
arthritis
, polymyligia reaumatica ,and sciatica lick
pain
,feel as though I've been in the wars ,what it is though since been on continual prednisalone (down to 11mgs now) and hydroxychloroquine given for
Alice70
in
Lung Conditions Community Forum
1 year ago
Rheumatoid Arthritis
Just diagnosed, lucky second Doctor spot on. Had appointment with PhysioJo , only gave me exercises to do. Doctor has now prescribed 30mg Naproxen which has given me pain relief and helped with sleep
Just diagnosed, lucky second Doctor spot on. Had appointment with PhysioJo , only gave me exercises to do. Doctor has now prescribed 30mg Naproxen which has given me pain relief and helped with sleep
Firefighter1962
in
Arthritis Action
1 year ago
How to escape Augmentation?
I only learnt about Health Unlocked and its efforts on RLS through RLS -UK and this is my first post. I have suffered from RLS for several years and various doctors have prescribed all the general medicines starting with antidepressants (amitriptyline, mirtazapine, imipramine, and citralopram), dopramine
I only learnt about Health Unlocked and its efforts on RLS through RLS -UK and this is my first post. I have suffered from RLS for several years and various doctors have prescribed all the general medicines starting with antidepressants (amitriptyline, mirtazapine, imipramine, and citralopram), dopramine
davchar23
in
Restless Legs Syndrome
10 months ago
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confused diagnosis
I was diagnosed with Fibromyalgia in 2019 by a Reumotologist whom during my appointment when through in detail with the symptoms and suggested treatments medically and non medical. But in 2023 I saw another Reumotologist who told me that it wasn’t fibromyalgia but low grade Rheumatoid arthritis because
I was diagnosed with Fibromyalgia in 2019 by a Reumotologist whom during my appointment when through in detail with the symptoms and suggested treatments medically and non medical. But in 2023 I saw another Reumotologist who told me that it wasn’t fibromyalgia but low grade Rheumatoid arthritis because
healingspirit
in
Fibromyalgia Action UK
1 year ago
how to improve appetite/consume more calories. Pls help!
My heart is broken. My dad’s cancer had progressed, he has started chemo but overall is very unwell. He’s lost almost 30 pounds in the last few months and is having a lot of pain. We have to help him with getting out of the bed and at times putting on his shoes and clothes. All the pain medicine he used
My heart is broken. My dad’s cancer had progressed, he has started chemo but overall is very unwell. He’s lost almost 30 pounds in the last few months and is having a lot of pain. We have to help him with getting out of the bed and at times putting on his shoes and clothes. All the pain medicine he used
StayingSTRNG
in
Advanced Prostate Cancer
10 months ago
good morning
I am currently being treated for latent TB with Rifampin and on prednisone 6mg. I was doing so so well before this new med and it seems rifampin decreases the effects of prednisone which I’ve noticed so much lately! Ugh! I feel as if I’m back to square 1 with the PMR. Is anyone aware of how much I
I am currently being treated for latent TB with Rifampin and on prednisone 6mg. I was doing so so well before this new med and it seems rifampin decreases the effects of prednisone which I’ve noticed so much lately! Ugh! I feel as if I’m back to square 1 with the PMR. Is anyone aware of how much I
Curry_girl
in
PMRGCAuk
1 year ago
Unexplained headaches
Had to see a private rheumie earlier this year for PMR diagnosis as nhs rheumie and GP were trying to say I had fibromyalgia. Was told to start on 10mgs of pred for one week and if that didn’t help was to increase to 15mgs and start on usual nhs method of tapering. I did have to go to the 15 mgs and
Had to see a private rheumie earlier this year for PMR diagnosis as nhs rheumie and GP were trying to say I had fibromyalgia. Was told to start on 10mgs of pred for one week and if that didn’t help was to increase to 15mgs and start on usual nhs method of tapering. I did have to go to the 15 mgs and
Paul76
in
PMRGCAuk
10 months ago
gallbladder post surgery
I’m recovering from gallbladder surgery, the op was a breeze and no more pain, I’ve stopped with the painkillers as they just made me dizzy , my bowels have been a bit all over but seem to be settling down and hope it was just down to anesthetic. My bellybutton wound is taking longer to heal but the
I’m recovering from gallbladder surgery, the op was a breeze and no more pain, I’ve stopped with the painkillers as they just made me dizzy , my bowels have been a bit all over but seem to be settling down and hope it was just down to anesthetic. My bellybutton wound is taking longer to heal but the
JudJud
in
Pelvic Pain Support Network
10 months ago
Low heart rate
Hi has anyone had or got any issues with being like me at present in bradycardia resting heart rate of 55-58 recently had severe chest pains went to hospital sent home all tests done ECG bloods etc and nothing showing of concern but here's the thing I have heart heart failure cardiomyopathy and AF and
Hi has anyone had or got any issues with being like me at present in bradycardia resting heart rate of 55-58 recently had severe chest pains went to hospital sent home all tests done ECG bloods etc and nothing showing of concern but here's the thing I have heart heart failure cardiomyopathy and AF and
Clarkee73
in
British Heart Foundation
10 months ago
Gemcitibane/intravenous zoledronic acid
I was diagnosed stage 4b in January 2018, had debulking surgery, no adjuvant chemo, then two rounds of carboplatin about 18 months apart followed by Niraparib for 8 months, but no further treatment for the last 18 months.Then 3 weeks ago I needed treatment for hypercalcemia (which I didn't know I
I was diagnosed stage 4b in January 2018, had debulking surgery, no adjuvant chemo, then two rounds of carboplatin about 18 months apart followed by Niraparib for 8 months, but no further treatment for the last 18 months.Then 3 weeks ago I needed treatment for hypercalcemia (which I didn't know I
bamboo89
in
My Ovacome
10 months ago
Just diagnosed
Hi all. I have just been diagnosed with fibromyalgia along with Tendinopathy(bit like tendonitis) having previously been suspected to have Rheumatoid Arthritis. This new diagnosis makes more sense. Would the Fibromyalgia have come on recently, or could I have had it for years and not realised? I've always
Hi all. I have just been diagnosed with fibromyalgia along with Tendinopathy(bit like tendonitis) having previously been suspected to have Rheumatoid Arthritis. This new diagnosis makes more sense. Would the Fibromyalgia have come on recently, or could I have had it for years and not realised? I've always
BakerTom
in
Fibromyalgia Action UK
1 year ago
Problems with neck causing shoulder and arm pains
I have been back and forwards to the doctors over the past couple of years with a suspected torn rotator cuff in my right shoulder. I had a ultrasound on shoulder 2 months ago and was told my shoulder is fine and I probably have a neck problem which is causing the pain. Contacted doctors again and was
I have been back and forwards to the doctors over the past couple of years with a suspected torn rotator cuff in my right shoulder. I had a ultrasound on shoulder 2 months ago and was told my shoulder is fine and I probably have a neck problem which is causing the pain. Contacted doctors again and was
Papareaps
in
Pain Concern
10 months ago
PEG/RIG feeding tubes
Hi chaps, question for you. My wife has now had MSA since 2016 so is a fair way into it. She has the usual problems and is now too late for PEG tubes, however, it still might be possible for a RIG set up. She no longer eats much so I make her diet high in calories etc, drinking is sort of ok for now.
Hi chaps, question for you. My wife has now had MSA since 2016 so is a fair way into it. She has the usual problems and is now too late for PEG tubes, however, it still might be possible for a RIG set up. She no longer eats much so I make her diet high in calories etc, drinking is sort of ok for now.
Oliverwindsor
in
Multiple System Atrophy Trust
10 months ago
Pain in hip
Xray notes report subcondral sclerosis in both hips, prior xrays noted same
pain
was due to SI joint
arthritis
that supposedly disappeared? Anyone have any thoughts on this? Can one radiologist interpret images differently than another?
Xray notes report subcondral sclerosis in both hips, prior xrays noted same
pain
was due to SI joint
arthritis
that supposedly disappeared? Anyone have any thoughts on this? Can one radiologist interpret images differently than another?
Jeaniem130
in
Osteoarthritis Action
2 months ago
Benefits of knowing your illness/condition/disease to help others as well as yourself
It’s about time I posted that a couple of months ago my husband was diagnosed with Giant Cell Arteritis. I was somewhat overwhelmed by the diagnosis having had PMR, GCA/LVV myself over the past 5 and a half years and haven’t, until now, felt ready to share his story on the forum.
It’s about time I posted that a couple of months ago my husband was diagnosed with Giant Cell Arteritis. I was somewhat overwhelmed by the diagnosis having had PMR, GCA/LVV myself over the past 5 and a half years and haven’t, until now, felt ready to share his story on the forum.
123-go
in
PMRGCAuk
10 months ago
I’m currently having investigations into Endo-sorry long post but need some advice or any reassurance:)
Hi I’m Sara and I’ve just turned 22, this month, and over the last 3 years I have symptoms (similar to the ones listed for endometriosis) and they have become more severe or more frequent/longer episodes that have been stopping me from working or functioning properly (exercise, sex, going out); it has
Hi I’m Sara and I’ve just turned 22, this month, and over the last 3 years I have symptoms (similar to the ones listed for endometriosis) and they have become more severe or more frequent/longer episodes that have been stopping me from working or functioning properly (exercise, sex, going out); it has
Butterfly0509
in
Endometriosis UK
10 months ago
Pain and rheumatoid arthritis
Has anyone had a stiff neck wih rheumatoid arthritis for the last week my neck has been stiff at the moment I have a flare in my hands and shoulders,
Has anyone had a stiff neck wih rheumatoid arthritis for the last week my neck has been stiff at the moment I have a flare in my hands and shoulders,
Indersisive71
in
NRAS
1 year ago
Gastric sleeve op
Greetings to my HealthUnblocked friends! I thought I'd update you on what's been going on for me the last few weeks. Well, my gastric sleeve op was booked in for 30th September and my consultant talked about the diet I'd need to be on for the two weeks beforehand. The reason for it was that when they
Greetings to my HealthUnblocked friends! I thought I'd update you on what's been going on for me the last few weeks. Well, my gastric sleeve op was booked in for 30th September and my consultant talked about the diet I'd need to be on for the two weeks beforehand. The reason for it was that when they
saville75
in
Headway
11 months ago
NEWBIE
I have chronic myeloproliferative disease - between ET & prefibrotic myelofibrosis, on HU 500mg per day and 1000mg on Sundays, plus 75mg Aspirin. This is of course on top of all my usual pain medication. I was undiagnosed for 5years until this year in May, my high platelet levels were picked up by chance
I have chronic myeloproliferative disease - between ET & prefibrotic myelofibrosis, on HU 500mg per day and 1000mg on Sundays, plus 75mg Aspirin. This is of course on top of all my usual pain medication. I was undiagnosed for 5years until this year in May, my high platelet levels were picked up by chance
JOL13
in
MPN Voice
11 months ago
💥coping with chronic pain and fatigue💥
💥hi everyone! I’ve recently been diagnosed with fibro and I’m looking for ways to cope with the pain and fatigue. Does anyone have any advice they could offer me please? Anything from your experiences with medication and assistive devices, to the things you do to make daily living a bit more comfortable
💥hi everyone! I’ve recently been diagnosed with fibro and I’m looking for ways to cope with the pain and fatigue. Does anyone have any advice they could offer me please? Anything from your experiences with medication and assistive devices, to the things you do to make daily living a bit more comfortable
RatArt
in
Fibromyalgia Action UK
11 months ago
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