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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
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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
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
Rehab ramblings and thoughts.
EDIT: I decided to change the picture ! This was Misty doing her Meerkat impression yesterday . After several more kind messages asking how I am, thank you so much , they are very much appreciated! I thought I would post a quick update. As I think most here will know, I had a Heart attack on Monday
EDIT: I decided to change the picture ! This was Misty doing her Meerkat impression yesterday . After several more kind messages asking how I am, thank you so much , they are very much appreciated! I thought I would post a quick update. As I think most here will know, I had a Heart attack on Monday
Instructor57
Graduate10
in
Bridge to 10K
1 year ago
Follow on re groin and hip pains
Following on from another member's issues with groin and hip discomfort - here is my situation - very similar I have just had results for another hip xray and nothing more showing than over a year ago but the pain in my groin and top of my leg have increased so much in the last 3-6 months. I have
Following on from another member's issues with groin and hip discomfort - here is my situation - very similar I have just had results for another hip xray and nothing more showing than over a year ago but the pain in my groin and top of my leg have increased so much in the last 3-6 months. I have
LozzaSandstrom
in
PMRGCAuk
1 year ago
Suspected endo/fertility issues
Hi everyone ☺️ this is my first post and really just after some advice at this point. I started my periods age 10, had horrific cramps in my teenage years and hormonal migraines. Never considered at the time that this was anything other than 'bad periods'. I went on the mini pill age 17 for contraception
Hi everyone ☺️ this is my first post and really just after some advice at this point. I started my periods age 10, had horrific cramps in my teenage years and hormonal migraines. Never considered at the time that this was anything other than 'bad periods'. I went on the mini pill age 17 for contraception
Bluebells86
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
2 years ago
New to PMR and hopefully its on its way out!
I started suffering bad neck stiffness and then back and eventually hip stiffness about 6 weeks ago (early March 2023). I'm 56 and a very keen cyclist (normally 8-12 hours of cycling a week), and so am not used to feeling like an invalid! I find cycling OK, although my legs feel very heavy, but walking
I started suffering bad neck stiffness and then back and eventually hip stiffness about 6 weeks ago (early March 2023). I'm 56 and a very keen cyclist (normally 8-12 hours of cycling a week), and so am not used to feeling like an invalid! I find cycling OK, although my legs feel very heavy, but walking
fast_peddler
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
2 years ago
Why did my endometriosis pain get worse after taking progesterone birth control bills?
After I have been diagnosed with endometriosis, I have tried taking 2 different birth control bills (both of them are progesterone based and were prescribed by doctors). The first bill I took for 3 months and it did not help at all, it actually gave me weak pain from time to time which was not normal
After I have been diagnosed with endometriosis, I have tried taking 2 different birth control bills (both of them are progesterone based and were prescribed by doctors). The first bill I took for 3 months and it did not help at all, it actually gave me weak pain from time to time which was not normal
Zahraa2019
in
Endometriosis UK
1 year ago
Pain and sleep problems
Looking for advice my head / T is so loud at the moment it feel like my head is going to explode. Also painful but not sure what pain killers to take. It wakes me every night i then have to put sleep music on to block out the noise. Resorted to a shop brought sleeping tablet last night. Did sleep but
Looking for advice my head / T is so loud at the moment it feel like my head is going to explode. Also painful but not sure what pain killers to take. It wakes me every night i then have to put sleep music on to block out the noise. Resorted to a shop brought sleeping tablet last night. Did sleep but
Parrcj
in
Tinnitus UK
1 year ago
Ongoing Headaches/anxiety
Hey all, I have had Hippocampal Sclerosis since the age of 8 months and am now 41. I had surgery in 2017 to eradicate my seizures which were occurring on average 3 times a week. Since the operation, I have only had one due to being trialed off medication. Apart from escaping the ongoing seizures,
Hey all, I have had Hippocampal Sclerosis since the age of 8 months and am now 41. I had surgery in 2017 to eradicate my seizures which were occurring on average 3 times a week. Since the operation, I have only had one due to being trialed off medication. Apart from escaping the ongoing seizures,
sguthrie
in
Epilepsy Action
1 year ago
I've OHS in 10 days - tips and must haves?
Hello everyone, So, after the very unexpected heart attack (clot passing through the hole in my heart) 3 weeks ago, all of a sudden I have the date for my OHS to close the ASD (and maybe repair the stretched valves too). It's planned for 14 April. 10 days' time. I feel woefully unprepared. I need to
Hello everyone, So, after the very unexpected heart attack (clot passing through the hole in my heart) 3 weeks ago, all of a sudden I have the date for my OHS to close the ASD (and maybe repair the stretched valves too). It's planned for 14 April. 10 days' time. I feel woefully unprepared. I need to
LadyZ13
in
British Heart Foundation
1 year ago
Painkillers and Buserelin
Hi ladies Maybe a silly question - am day 6 into Buserelin injections and have had a splitting headache for the last 2 days Can I take any painkillers? Am worried I'll effect how the drugs will work if I take extra meds. Thanks a lot xx
Hi ladies Maybe a silly question - am day 6 into Buserelin injections and have had a splitting headache for the last 2 days Can I take any painkillers? Am worried I'll effect how the drugs will work if I take extra meds. Thanks a lot xx
Katieloulou1983
in
Fertility Network UK
1 year ago
Peginterferon side effects!
Hi all, I have ET Jak2+ since 2021 and have been injecting 45mg Peginterferon weekly for 6 months and doing relatively ok until just recently. I now am experiencing severe aching arms and legs radiating down from my neck to my knees. It is so bad that I have to take pain killers daily. My blood pressure
Hi all, I have ET Jak2+ since 2021 and have been injecting 45mg Peginterferon weekly for 6 months and doing relatively ok until just recently. I now am experiencing severe aching arms and legs radiating down from my neck to my knees. It is so bad that I have to take pain killers daily. My blood pressure
Fairbank
in
MPN Voice
1 year ago
Fatty pad atrophy (ball of foot)
Hello, I am hoping there might be someone here who has experience of coping with fatty pad atrophy. I have recently been told by a podiatrist that this is the cause of the pain in the balls of my feet. I feel like I'm walking on my bones and have nerve pain due to the reduction in the fatty pad.
Hello, I am hoping there might be someone here who has experience of coping with fatty pad atrophy. I have recently been told by a podiatrist that this is the cause of the pain in the balls of my feet. I feel like I'm walking on my bones and have nerve pain due to the reduction in the fatty pad.
Dorunrun61
Graduate
in
Couch to 5K
1 year ago
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