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heart palpitations anxiety
hey guys. Me again, sorry to bother and ramble on, the past 3 days I’ve been having a few heart palpitations a day. Now I did phone my doctors and they told me this didn’t sound serious and it was normal. They said if the palpitations were regular every few minutes it would be a concern. I get 2 or 3
hey guys. Me again, sorry to bother and ramble on, the past 3 days I’ve been having a few heart palpitations a day. Now I did phone my doctors and they told me this didn’t sound serious and it was normal. They said if the palpitations were regular every few minutes it would be a concern. I get 2 or 3
Littlechopsxo
in
Anxiety and Depression Support
1 year ago
RA reaction to medication would like general advice on how to manage RA
Hello, I’ve had a reaction to medication I was on for an over active thyroid, which has given me RA symtoms, came on very suddenly so hoping it will eventually clear (have read can take 3/4 weeks). Have been referred to a rheumatoid specialist but apparently it might take months for an appointment. I
Hello, I’ve had a reaction to medication I was on for an over active thyroid, which has given me RA symtoms, came on very suddenly so hoping it will eventually clear (have read can take 3/4 weeks). Have been referred to a rheumatoid specialist but apparently it might take months for an appointment. I
Abimilne
in
NRAS
1 year ago
Seeking some advice [Had numerous tests]
Hi, 48yr old male, not overweight, eat relatively healthy, but due to a back issue, limited exercise. Take no meds other than painkillers from time to time for my back. But wasn't taking them during these episodes. My issues began a week today exactly. Got up for the loo around 4am, and went back to
Hi, 48yr old male, not overweight, eat relatively healthy, but due to a back issue, limited exercise. Take no meds other than painkillers from time to time for my back. But wasn't taking them during these episodes. My issues began a week today exactly. Got up for the loo around 4am, and went back to
ProfBaw
in
British Heart Foundation
1 year ago
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liver and pain relief medication
I take pregabalin and cocodamol for neuropathic pain relief plus cervical spondylosis pain relief but I was given a blood test last week and the do raid there was a problem with my liver and I’m to have another blood test Monday but I’m wondering if it’s the pain reliever meds I take that has caused
I take pregabalin and cocodamol for neuropathic pain relief plus cervical spondylosis pain relief but I was given a blood test last week and the do raid there was a problem with my liver and I’m to have another blood test Monday but I’m wondering if it’s the pain reliever meds I take that has caused
Pearce1940oscar
in
Pain Concern
1 year ago
Going on Holiday???
Hi All, Only my second post as am techno moron, so hope it all works and it posts ok. - Would like to ask for help here because I really want to get back into taking proper holidays as so tired. Am growing nice little cataracts and get leg cramps, so have guilt that I'm so dependent on hubs and son for
Hi All, Only my second post as am techno moron, so hope it all works and it posts ok. - Would like to ask for help here because I really want to get back into taking proper holidays as so tired. Am growing nice little cataracts and get leg cramps, so have guilt that I'm so dependent on hubs and son for
KimiJay
in
Fibromyalgia Action UK
1 year ago
paracetamol
Not sure if it’s a bad cold or flu I have . I know NSAIDs are a very bad idea ( my first episode was triggered by Celebrex). Has anyone been triggered by Paracetamol ? Are there any safe pain killers ? Thanks
Not sure if it’s a bad cold or flu I have . I know NSAIDs are a very bad idea ( my first episode was triggered by Celebrex). Has anyone been triggered by Paracetamol ? Are there any safe pain killers ? Thanks
Peony4575
in
AF Association
1 year ago
TB testing before starting a biologic.
Hi everyone, hope your all well as can be.I'm to start a biologic soon, so had my bloods done, (microbiology) bloods for TB has come back positive, I've been referred to a respiratory specialist for further testing. I'm not doing very well at all at the moment, im in a massive flaire, and currently
Hi everyone, hope your all well as can be.I'm to start a biologic soon, so had my bloods done, (microbiology) bloods for TB has come back positive, I've been referred to a respiratory specialist for further testing. I'm not doing very well at all at the moment, im in a massive flaire, and currently
jojoishere
in
NRAS
1 year ago
EXTEND - Addition of Metastasis-Directed Therapy to Intermittent Hormone Therapy for Oligometastatic Prostate Cancer
The results of the EXTEND [EXTernal beam radiation to Eliminate Nominal metastatic Disease] Phase II Trial were published in JAMA Oncology this month [1]. {However, many will have seen the results, as presented at ASTRO 2022, & posted by Fish, 6 months ago [2].}
Results
"The study included
The results of the EXTEND [EXTernal beam radiation to Eliminate Nominal metastatic Disease] Phase II Trial were published in JAMA Oncology this month [1]. {However, many will have seen the results, as presented at ASTRO 2022, & posted by Fish, 6 months ago [2].}
Results
"The study included
pjoshea13
in
Fight Prostate Cancer
1 year ago
Ibuprofen
Ive just realised my tinnitus gets worse after I've taken ibuprofen. Just googled this and seen that it can happen. Has anyone else noticed this and if so have you found a relatively strong painkiller that doesn't affect it
Ive just realised my tinnitus gets worse after I've taken ibuprofen. Just googled this and seen that it can happen. Has anyone else noticed this and if so have you found a relatively strong painkiller that doesn't affect it
marigold60
in
Tinnitus UK
1 year ago
Which is the worst - Prednisolone or Methatrexate?
I’ve mentioned my position in reply to other’s posts, but briefly, Jan 2023 - having been convinced the MTX wasn’t making any difference, I asked to stop it but my Rheumy said no, but you can half your dose to 10mg (once a week). I was also on 1.5mg Pred with Rhuemy pushing me to reduce by .5 for
I’ve mentioned my position in reply to other’s posts, but briefly, Jan 2023 - having been convinced the MTX wasn’t making any difference, I asked to stop it but my Rheumy said no, but you can half your dose to 10mg (once a week). I was also on 1.5mg Pred with Rhuemy pushing me to reduce by .5 for
Prof99
in
PMRGCAuk
1 year ago
Chances of getting a hysterectomy on the nhs aged 30?
Anyone had any success getting a hysterectomy at aged 30 ? If so what did you have to do to persuade your gp it was right for you ? After 12 yrs of back and forth with no progress, I want to be able to make a choice myself. Finally a gp suggested endo in 2021 but nothing is confirmed. My ovaries
Anyone had any success getting a hysterectomy at aged 30 ? If so what did you have to do to persuade your gp it was right for you ? After 12 yrs of back and forth with no progress, I want to be able to make a choice myself. Finally a gp suggested endo in 2021 but nothing is confirmed. My ovaries
Hidden
in
Endometriosis UK
1 year ago
Raynaud’s Pain
Has anyone been prescribed pain medication for Raynaud’s pain when the spasms occur. Tylenol and Advil helps a little bit.
Has anyone been prescribed pain medication for Raynaud’s pain when the spasms occur. Tylenol and Advil helps a little bit.
Dermatray15
in
Scleroderma & Raynaud's UK (SRUK)
1 year ago
Pain Medication after Laparoscopy
Hi all, Can anyone offer advice on which medication they used after surgery for pain management? Due to my other medical issues I can’t take any NSIADS including: ibuprofen, naproxen, diclofenac, celecoxib, mefenamic acid, etoricoxib & indomethacin. I normally take just cocodamol and rest when
Hi all, Can anyone offer advice on which medication they used after surgery for pain management? Due to my other medical issues I can’t take any NSIADS including: ibuprofen, naproxen, diclofenac, celecoxib, mefenamic acid, etoricoxib & indomethacin. I normally take just cocodamol and rest when
Cats1311
in
Endometriosis UK
1 year ago
Back pain/clicking and how to stay positive
Hi everyone Looking for tips on pain management/positivity and also to see if anyone experiences the same types of pain/clicking in joints. I've been suffering with back pain (as well as pelvis, abdomen, hips, neck etc) for around 2 years now, alongside a huge number of other symptoms as I'm sure
Hi everyone Looking for tips on pain management/positivity and also to see if anyone experiences the same types of pain/clicking in joints. I've been suffering with back pain (as well as pelvis, abdomen, hips, neck etc) for around 2 years now, alongside a huge number of other symptoms as I'm sure
Lauren_0203
in
Endometriosis UK
1 year ago
Letterbox.
I do find this condition puzzling, you think you are getting a handle on it and then it jumps on you from another angle. Most of my difficulties with Osteoradionecrosis were associated with the right hand side of my jaw which I was finally starting to manage to a reasonable level of discomfort (I also
I do find this condition puzzling, you think you are getting a handle on it and then it jumps on you from another angle. Most of my difficulties with Osteoradionecrosis were associated with the right hand side of my jaw which I was finally starting to manage to a reasonable level of discomfort (I also
AncientMariner
in
PMRGCAuk
1 year ago
Visceral hypersensitivity
You know those films where someone is strapped to a chair and the torturer is holding a syringe and says: 'I'm just going to give you something to enhance the pain; you'll feel everything much more'. No wait! I already have IBS, thanks all the same. I feel everything in my guts, multiplied. Solids
You know those films where someone is strapped to a chair and the torturer is holding a syringe and says: 'I'm just going to give you something to enhance the pain; you'll feel everything much more'. No wait! I already have IBS, thanks all the same. I feel everything in my guts, multiplied. Solids
XDjames
in
IBS Network
1 year ago
Never ending problems
I am going to moan - big time - because I am getting to the point where I don't know which way to turn. I have Hashimotos Thyroiditis, Arthritis, Pernicious Anaemia, Hypertension, Coeliac disease and now some unexplained kidney problem. I have had an MRI which has shown a problem but I don't know what
I am going to moan - big time - because I am getting to the point where I don't know which way to turn. I have Hashimotos Thyroiditis, Arthritis, Pernicious Anaemia, Hypertension, Coeliac disease and now some unexplained kidney problem. I have had an MRI which has shown a problem but I don't know what
Loobs39
in
Kidney Disease
1 year ago
Question about reducing Pred
The last six weeks I have been reducing very slowly by .5mg from 4mg to 3.5mg. I have done this a few times without success ending in a flare. This time I am at the moment totally free in the upper half of my body from pain or stiffness, but have been getting what I think is withdrawal symptoms around
The last six weeks I have been reducing very slowly by .5mg from 4mg to 3.5mg. I have done this a few times without success ending in a flare. This time I am at the moment totally free in the upper half of my body from pain or stiffness, but have been getting what I think is withdrawal symptoms around
Purplegloss
in
PMRGCAuk
1 year ago
Magnesium salts and RLS: malate, glycinate or citrate
Just following up on a recent post recommending magnesium malate for RLS, quoting recommendations made by Californian company Pure Biogenics in promoting their RLS supplement Seratame. Looking into this, experiments on rats suggested that malate may be the most bio-available form of magnesium; there
Just following up on a recent post recommending magnesium malate for RLS, quoting recommendations made by Californian company Pure Biogenics in promoting their RLS supplement Seratame. Looking into this, experiments on rats suggested that malate may be the most bio-available form of magnesium; there
ChrisColumbus
in
Restless Legs Syndrome
1 year ago
Might blood be good news?
Before chemo started, I was getting pains in the
rectal
wall, sharp bladder discomfort and
pain
on urination - along with blood in the urine.
Before chemo started, I was getting pains in the
rectal
wall, sharp bladder discomfort and
pain
on urination - along with blood in the urine.
CrocodileShoes
in
Advanced Prostate Cancer
11 months ago
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