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ibuptofen?
I am about 10 weeks post aortic valve replacement. Prior to learning I had aortic valve stenosis earlier this year I always regarded ibuprofen as a superior pain killer to paracetamol. Might have something to do with a childhood in Nottingham where it was developed by Boots! Tended to use it for the
I am about 10 weeks post aortic valve replacement. Prior to learning I had aortic valve stenosis earlier this year I always regarded ibuprofen as a superior pain killer to paracetamol. Might have something to do with a childhood in Nottingham where it was developed by Boots! Tended to use it for the
Petitlady
in
British Heart Foundation
9 months ago
I stopped steroids rapidly and all PMR symptoms returned - HELP!
Hi, I have only found this group today so I am really pleased to find ANYONE else who has PMR! I have difficult situation as I was responding really well 25mg of steroids per day, when I developed a CSR in my eye. I have had one before from Stress a couple of years ago and knew this was a risk,
Hi, I have only found this group today so I am really pleased to find ANYONE else who has PMR! I have difficult situation as I was responding really well 25mg of steroids per day, when I developed a CSR in my eye. I have had one before from Stress a couple of years ago and knew this was a risk,
Megasorearms
in
PMRGCAuk
9 months ago
Osteochondral defect, loose bodies in the knee and Baker's cyst.
Hi everyone,Hope you are all managing. Since the beginning of the year, I have been experiencing tear sensation at the back of my right knee. When I told my mum she said it might be that I have added weight. That it would stop when I reduce some weight. In April, I experiened a locked knee. It was
Hi everyone,Hope you are all managing. Since the beginning of the year, I have been experiencing tear sensation at the back of my right knee. When I told my mum she said it might be that I have added weight. That it would stop when I reduce some weight. In April, I experiened a locked knee. It was
ijeasike
in
LUPUS UK
9 months ago
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Ampyra
I have been on Ampyra/Dalfampridine for about 4 years. I am thinking of stopping as it is expensive. What effect may it have on my MS? does anyone have any thoughts?
I have been on Ampyra/Dalfampridine for about 4 years. I am thinking of stopping as it is expensive. What effect may it have on my MS? does anyone have any thoughts?
whwiechm
in
My MSAA Community
11 months ago
Hope, perhaps?
Hi everyone, I just wanted to post a little positivity on here! I know how difficult it is to live with endo (of course), so I wanted to share any positive experiences to anyone who might need it.I had my first laparoscopy (both diagnostic and therapeutic, in the end), in July, so I'm about 6 weeks out
Hi everyone, I just wanted to post a little positivity on here! I know how difficult it is to live with endo (of course), so I wanted to share any positive experiences to anyone who might need it.I had my first laparoscopy (both diagnostic and therapeutic, in the end), in July, so I'm about 6 weeks out
CaffeineCat
in
Endometriosis UK
9 months ago
Pred and painkillers
Hi all Can you tell me what painkillers are safe to take with Pred. Is ibuprofen and aspirin off limits and if so what do you suggest for general aches and pains. Many thanks.
Hi all Can you tell me what painkillers are safe to take with Pred. Is ibuprofen and aspirin off limits and if so what do you suggest for general aches and pains. Many thanks.
Fredddie
in
PMRGCAuk
9 months ago
Increased bleeding after first scan…
hi everyone, this is my first post. First IVF cycle. I have PCOS and my bleeds are [u]extremely[/u] unpredictable. I started my current cycle with very light murky bleeding and because there was nothing else to go on and none of my bleeds are the same, we started the protocol given by our doctor.
hi everyone, this is my first post. First IVF cycle. I have PCOS and my bleeds are [u]extremely[/u] unpredictable. I started my current cycle with very light murky bleeding and because there was nothing else to go on and none of my bleeds are the same, we started the protocol given by our doctor.
IchigoKeikaku
in
Fertility Network UK
9 months ago
Urgent help needed. Extremely severe RLS, cannot identify cause.
It's so goddamn severe that at this point, I either have the most severe case of RLS in medical history or it's something else. I rate it 9 on the severity scale. Did every possible test related to RLS (iron, vitamin D, etc) except for for transferrin saturation and serum iron because it wasn't available
It's so goddamn severe that at this point, I either have the most severe case of RLS in medical history or it's something else. I rate it 9 on the severity scale. Did every possible test related to RLS (iron, vitamin D, etc) except for for transferrin saturation and serum iron because it wasn't available
RestlessDaily
in
Restless Legs Syndrome
9 months ago
Possible Outcome of Severe Spinal Stenosis
I had a Triple Bypass and Mitral Valve Repair and have now been diagnosed with heart failure so I’m not able to take any of the normal
pain
relief medication. I was referred to the
Pain
Management
Specialist. I’ve now had 3 lots of 6 Facet Joint Injections without any relief.
I had a Triple Bypass and Mitral Valve Repair and have now been diagnosed with heart failure so I’m not able to take any of the normal
pain
relief medication. I was referred to the
Pain
Management
Specialist. I’ve now had 3 lots of 6 Facet Joint Injections without any relief.
Davewm
in
Pain Concern
1 year ago
📣 Discussion Topic: What pancreatitis issue is most important to you and why?
- Access to treatments -
Pain
& Symptom
Management
- Education & Awareness - Challenging Stigmas - Research & Breakthroughs - Other Let us know in the replies!
- Access to treatments -
Pain
& Symptom
Management
- Education & Awareness - Challenging Stigmas - Research & Breakthroughs - Other Let us know in the replies!
Skye_MC
Administrator
in
Chronic Pancreatitis Support
1 year ago
Endo history lesson!!!!
On a bored afternoon today, i thought i'd look up when Endo was first diagnosed. It was about 1860, here in England. I wonder how women coped then???. Was it getting drunk that helped numb the pain, cos there were no painkillers like we have today i think. I have endo at the minute, it feels like
On a bored afternoon today, i thought i'd look up when Endo was first diagnosed. It was about 1860, here in England. I wonder how women coped then???. Was it getting drunk that helped numb the pain, cos there were no painkillers like we have today i think. I have endo at the minute, it feels like
valgal76
in
Endometriosis UK
9 months ago
37 M, Functional Tremor, with hyperreflexia, dysphagia, SBD, and urinary incontinence. All diagnosed.
How can I have so many positive neurological findings and tests and be told that all of the stiffness/rigid feeling that has slowly developed and worsened the past 3 years be entirely FND? I was under the impression that FND, not just functional tremor, required a lack of positive neurogenic findings
How can I have so many positive neurological findings and tests and be told that all of the stiffness/rigid feeling that has slowly developed and worsened the past 3 years be entirely FND? I was under the impression that FND, not just functional tremor, required a lack of positive neurogenic findings
Hidden
in
Functional Neurological Disorder - FND Hope
9 months ago
Into the 4th year, updates and next step
Continuing on abi + Zoladex • March 2023, new hip pain, new mets on pubic bone confirmed by CT/Bone scan,RT for
pain
management
, switched to Olaprid (full doze) + Zoladex Acceptable side effects, blood works fine.
Continuing on abi + Zoladex • March 2023, new hip pain, new mets on pubic bone confirmed by CT/Bone scan,RT for
pain
management
, switched to Olaprid (full doze) + Zoladex Acceptable side effects, blood works fine.
Juliane314
in
Advanced Prostate Cancer
9 months ago
Help me having internal scanning or an appointment from a gynecologist
management
form for hospital every three months explaining my worse situation every six months but no good reply from John Radcliffe Oxford hospital.
management
form for hospital every three months explaining my worse situation every six months but no good reply from John Radcliffe Oxford hospital.
Kamna1
in
Endometriosis UK
1 year ago
Recovery time
Hello folks, it's been a while since I posted, or had anything to post about. I have to retire to my bed or any horizontal surface these days as my fractured vertebrae are soon put to the test and become uncomfortable if I'm sitting or standing for a while. Speed bumps are a menace and I always have
Hello folks, it's been a while since I posted, or had anything to post about. I have to retire to my bed or any horizontal surface these days as my fractured vertebrae are soon put to the test and become uncomfortable if I'm sitting or standing for a while. Speed bumps are a menace and I always have
Gandalf2
in
Encephalitis Society
9 months ago
Ankle Fusion wahey
i am in hospital after an an ankle fusion yesterday. Great fun. Lovely nurses 🤪 just going home. And I've had my second Oxy pill. Oh my! Do watch Painkiller if you have Netflix. It's evil big pharma and so on. This was going on when I was living in California.... Awful sights... 9mg and I'm doing
i am in hospital after an an ankle fusion yesterday. Great fun. Lovely nurses 🤪 just going home. And I've had my second Oxy pill. Oh my! Do watch Painkiller if you have Netflix. It's evil big pharma and so on. This was going on when I was living in California.... Awful sights... 9mg and I'm doing
discoballs
in
PMRGCAuk
9 months ago
hand pain
the awful pain i had in my hands is just worse by the day, i thought it would go cos maybe gluten related but after setting doc she said she can see joints inflammation. nothing can be done except painkillers. now i’ve realised and admitted to myself that it is arthritis 😢 after all these years of
the awful pain i had in my hands is just worse by the day, i thought it would go cos maybe gluten related but after setting doc she said she can see joints inflammation. nothing can be done except painkillers. now i’ve realised and admitted to myself that it is arthritis 😢 after all these years of
Junny123
in
Gluten Free Guerrillas
9 months ago
post CRR-D procedure
I had a CRT-D procedure test yesterday and all went well the cardiologist and nurses were amazing. I feel as though I can actually breathe normally now which is amazing. My question is how long does the wound take for the pain to ease off where you don’t have to take painkillers? Thank you, Joy
I had a CRT-D procedure test yesterday and all went well the cardiologist and nurses were amazing. I feel as though I can actually breathe normally now which is amazing. My question is how long does the wound take for the pain to ease off where you don’t have to take painkillers? Thank you, Joy
honeybubs
in
British Heart Foundation
9 months ago
Journey Ditty
Twenty twenty was the year all went wrong that's crystal clear. Things had not been going well before that date, just to tell. Ailments I'd not had before taxed me like a plague of yore. Unknown this and unknown that caught me square and laid me flat. Muscles cramping so in pain no relief drove
Twenty twenty was the year all went wrong that's crystal clear. Things had not been going well before that date, just to tell. Ailments I'd not had before taxed me like a plague of yore. Unknown this and unknown that caught me square and laid me flat. Muscles cramping so in pain no relief drove
cycli
in
PMRGCAuk
9 months ago
Update- any hope for my reconsideration request?zero points for PIP and doesn’t tally with anything I said at interview.
Update: finally finished filling out reconsideration. It’s taken so long and has been making me really anxious. When I got the report from my assessment it seemed to hinge on a paragraph she had copied and pasted for each section stating I had no significant input for pain and mental health. I have provided
Update: finally finished filling out reconsideration. It’s taken so long and has been making me really anxious. When I got the report from my assessment it seemed to hinge on a paragraph she had copied and pasted for each section stating I had no significant input for pain and mental health. I have provided
Brigga
in
Fibromyalgia Action UK
9 months ago
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