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Optical nerve block steroid injections in head, side effects
Hi all, A week ago I had my first steroid injections in my head for my chronic headaches and dizziness. I was told about possible side effects, but this is beyond what I anticipated: 1. Two days after the injections i started having severe headache (literally 9,5/10) where I ended up in bed for 2 full
Hi all, A week ago I had my first steroid injections in my head for my chronic headaches and dizziness. I was told about possible side effects, but this is beyond what I anticipated: 1. Two days after the injections i started having severe headache (literally 9,5/10) where I ended up in bed for 2 full
spruce002
in
Pain Concern
3 years ago
I’m pretty sure the new spike was caused by painkillers
Hello all….about 3 weeks ago I had sciatica so initially I took lots of ibuprofen,I was fine at that point but then I received naxproxen from my GP and having only taken 3 tablets I noticed a spike in my tinnitus which was worse than the previous spike.I’ve had tinnitus for many years but it’s never
Hello all….about 3 weeks ago I had sciatica so initially I took lots of ibuprofen,I was fine at that point but then I received naxproxen from my GP and having only taken 3 tablets I noticed a spike in my tinnitus which was worse than the previous spike.I’ve had tinnitus for many years but it’s never
Bowler200
in
British Tinnitus Association
3 years ago
PMR OR OTHER !
Hi all. I have appreciated input on this site before, here goes;. First diagnosed with PMR in 2017, put on pred which had defo positive effect on my neck, shoulder, back and arm pain. Starting I think 15-20mg pred. Over time i reduced my pred, had several flareups, upped again which had the desired effect
Hi all. I have appreciated input on this site before, here goes;. First diagnosed with PMR in 2017, put on pred which had defo positive effect on my neck, shoulder, back and arm pain. Starting I think 15-20mg pred. Over time i reduced my pred, had several flareups, upped again which had the desired effect
SRIXON
in
PMRGCAuk
3 years ago
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Struggling to get any doctors to listen to me.
I’m having an extremely difficult time getting any doctors to listen to me. I have been struggling with my joints now for around 6-7 years. I have been seeing GPs and the like for all of this time and the answers have always been the same, there’s a potential I have arthritis but because my Rheumatoid
I’m having an extremely difficult time getting any doctors to listen to me. I have been struggling with my joints now for around 6-7 years. I have been seeing GPs and the like for all of this time and the answers have always been the same, there’s a potential I have arthritis but because my Rheumatoid
SadGirlRaceClub
in
LUPUS UK
3 years ago
Help with endometriosis
Hi all Can anyone help me ive been diagnosed with endometriosis and just found out I have it on my tubes my ovaries and my bowel I am in constant pain on a daily basic with my stomach, back and legs and my stomach as never been so big! I cannot take the contraception pill as they don't agree with me
Hi all Can anyone help me ive been diagnosed with endometriosis and just found out I have it on my tubes my ovaries and my bowel I am in constant pain on a daily basic with my stomach, back and legs and my stomach as never been so big! I cannot take the contraception pill as they don't agree with me
Jenna1985
in
Endometriosis UK
3 years ago
Changing medication to zomorph
I have chronic pain , Chrons and stage 3 kidney disease as well as other issues. I use fentanyl patch 37 strength and my gp has just changed my tablet pain medication from OxyContin 5mg to zomorph 10mg as they are trying to cut my opioids down. could anyone please tell me if they have used this and
I have chronic pain , Chrons and stage 3 kidney disease as well as other issues. I use fentanyl patch 37 strength and my gp has just changed my tablet pain medication from OxyContin 5mg to zomorph 10mg as they are trying to cut my opioids down. could anyone please tell me if they have used this and
Mimbabe
in
Crohn's and Colitis Support
3 years ago
Where do I go from here?
Hi everyone, this is my 1st post for which I will apologise for in advance….it’s going to be a long one. Everything started for me in December with severe pain in my right side and under my right rib cage. After several visits to A&E the pain was being looked at as gallbladder issues, however after numerous
Hi everyone, this is my 1st post for which I will apologise for in advance….it’s going to be a long one. Everything started for me in December with severe pain in my right side and under my right rib cage. After several visits to A&E the pain was being looked at as gallbladder issues, however after numerous
Reemy
in
Thyroid UK
3 years ago
Pain relief
Hi can anyone say what type of painkillers they use to help with polymyalgia. Thanks
Hi can anyone say what type of painkillers they use to help with polymyalgia. Thanks
Uglow
in
PMRGCAuk
3 years ago
Is this normal?
Hey everyone. My doctor has said after speaking with a gynaecologist that I have endo - I haven’t had a scan and finding it impossible to get one. I’ve been in agony for two weeks now, started during my period and still here afterwards - at first the pain was in the middle and now it’s moved to the right
Hey everyone. My doctor has said after speaking with a gynaecologist that I have endo - I haven’t had a scan and finding it impossible to get one. I’ve been in agony for two weeks now, started during my period and still here afterwards - at first the pain was in the middle and now it’s moved to the right
abbiecx_
in
Endometriosis UK
3 years ago
Flare or not
I reduced prednisone on 2/11 now 11:11 and my hips don’t lie lol I’m not sure if I’m having a flare or just in pain. But painkillers not shifting. I hate the idea of going up on pred again but will follow your advice. 14to 13 mg It’s really restricted my walking. Thank you folks
I reduced prednisone on 2/11 now 11:11 and my hips don’t lie lol I’m not sure if I’m having a flare or just in pain. But painkillers not shifting. I hate the idea of going up on pred again but will follow your advice. 14to 13 mg It’s really restricted my walking. Thank you folks
Uglow
in
PMRGCAuk
3 years ago
Pain advice
Hey guys Any advice on pain killers to take or any sort of therapy to relief pain n stiffness in top of back neck and shoulders
Hey guys Any advice on pain killers to take or any sort of therapy to relief pain n stiffness in top of back neck and shoulders
Chocolate-lady
in
Fibromyalgia Action UK
3 years ago
Temperature during Endo flare
Hi all, I am hoping that someone is awake and more knowledgeable than me about this. Today my flare up has well and truly arrived, I have had a worse build up in respect of migraines disturbing vision, nausea and muscular pain from my neck all down my back and now tonight the pain is really awful, I
Hi all, I am hoping that someone is awake and more knowledgeable than me about this. Today my flare up has well and truly arrived, I have had a worse build up in respect of migraines disturbing vision, nausea and muscular pain from my neck all down my back and now tonight the pain is really awful, I
HolsBamboozledwomb
in
Endometriosis UK
3 years ago
Insane lower back, buttock
Hi. From 3 nights ago, I was perfectly fine, I did some cleaning up about 4 hours before bed and layed on my back watching something on my phone, had to go toilet and realized severe lower pack pain that seems to be affecting both sides but mostly left side. I don't have any other symptoms or problems
Hi. From 3 nights ago, I was perfectly fine, I did some cleaning up about 4 hours before bed and layed on my back watching something on my phone, had to go toilet and realized severe lower pack pain that seems to be affecting both sides but mostly left side. I don't have any other symptoms or problems
Marot
in
Pain Concern
3 years ago
Bit of a setback after last chemo
Last chemo was on Friday October 29th. Usual after effects - i.e. OK Friday and Saturday up to the evening; not too bad Sunday until the afternoon. As usual started to feel yukky and went to bed. Had a bit of cornflakes Monday morning and then nothing and off to bed again. Taking anti sickness pills
Last chemo was on Friday October 29th. Usual after effects - i.e. OK Friday and Saturday up to the evening; not too bad Sunday until the afternoon. As usual started to feel yukky and went to bed. Had a bit of cornflakes Monday morning and then nothing and off to bed again. Taking anti sickness pills
magstherunner
in
The Roy Castle Lung Cancer Foundation
3 years ago
Should I be worried?
Hi all, So im new here but I have a few concerns that I was hoping to get some clarification on, so here goes……. Some time ago i was taken to hospital with a suspected PE (blood clot), I had some scans done and thankfully no blood clot was found. A few weeks later and I was looking over my medical records
Hi all, So im new here but I have a few concerns that I was hoping to get some clarification on, so here goes……. Some time ago i was taken to hospital with a suspected PE (blood clot), I had some scans done and thankfully no blood clot was found. A few weeks later and I was looking over my medical records
MRSB18
in
HFI Connect - Hepatitis
3 years ago
Endometriosis, adhesions and struggling to work.
Hi everyone, I’ve been off work sick for the last week with constant abdominal and lower back pain made worse when sitting. I suffer with my bowels and long periods and have spent the past two years trying different ways of resolving my issues. My job involves me spending hours on the phone so no alternative
Hi everyone, I’ve been off work sick for the last week with constant abdominal and lower back pain made worse when sitting. I suffer with my bowels and long periods and have spent the past two years trying different ways of resolving my issues. My job involves me spending hours on the phone so no alternative
Las20
in
Endometriosis UK
3 years ago
Castle Walt Disney designed the castle he built at Disney Land. This castle welcomes you to the outskirts of the diamond village of Toledo.
My name is Anna, I was officially diagnosed by BMB of a Myeloproliferative Neoplasm, Essential Thrombocytosis in December 2011. I have been aware of the condition due to the consistently high platelets counts since I got a DVT while travelling in 1999. I have also been informed over the years and
My name is Anna, I was officially diagnosed by BMB of a Myeloproliferative Neoplasm, Essential Thrombocytosis in December 2011. I have been aware of the condition due to the consistently high platelets counts since I got a DVT while travelling in 1999. I have also been informed over the years and
Gordito
in
MPN Voice
3 years ago
GP rant🥲
I had to se my GP following receiving a letter from my neurologist advising about the MSA & medication will be needed to be prescribed by them. It was 10 mins I won’t forget, he read the letter and then said ‘ I don’t know why they send you a copy, so misleading ‘probable’ might mean you don’t have
I had to se my GP following receiving a letter from my neurologist advising about the MSA & medication will be needed to be prescribed by them. It was 10 mins I won’t forget, he read the letter and then said ‘ I don’t know why they send you a copy, so misleading ‘probable’ might mean you don’t have
Bizzyissy
in
Multiple System Atrophy Trust
3 years ago
Mysterious chest pain
Hoping for someone experiencing similar issues. I have had excruciating upper left chest pain for over 5 weeks. My Gp has sent me to a and e twice because the symptoms match a heart attack. ECG bloods and chest X-ray all normal. Diagnosed first with Costochondritis and then Bornholm disease. No painkillers
Hoping for someone experiencing similar issues. I have had excruciating upper left chest pain for over 5 weeks. My Gp has sent me to a and e twice because the symptoms match a heart attack. ECG bloods and chest X-ray all normal. Diagnosed first with Costochondritis and then Bornholm disease. No painkillers
Ponkysue
in
Thyroid UK
3 years ago
LIDOCAINE 5% PAIN PATCHES
My sister-in-law has these patches for her back pain (she has a steel rod for a back), and one day at her house she gave me a few for my muscle spasms and nerve pain. They are miracle workers! I asked my doctor for a prescription. He said FDA only recognized them for permanent Shingle nerve pain. My
My sister-in-law has these patches for her back pain (she has a steel rod for a back), and one day at her house she gave me a few for my muscle spasms and nerve pain. They are miracle workers! I asked my doctor for a prescription. He said FDA only recognized them for permanent Shingle nerve pain. My
agapepilgrim
in
My MSAA Community
3 years ago
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