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pregabalin
Hi it has been a good couple of years since I was last on here . I suffered terribly from RLS . It had got to the stage where it seemed all over my body too . It was horrendous and I was finding it so hard to cope . I was prescribed pregabalin- 50 mg - 3 times a day. Manerva kindly suggested taking the
Hi it has been a good couple of years since I was last on here . I suffered terribly from RLS . It had got to the stage where it seemed all over my body too . It was horrendous and I was finding it so hard to cope . I was prescribed pregabalin- 50 mg - 3 times a day. Manerva kindly suggested taking the
Esme2007
in
Restless Legs Syndrome
2 years ago
Day 1 Lap Recovery
Hi everyone, I had my first laparoscopy yesterday and as suspected they found endometriosis. I’ve been waiting a long time for this diagnosis so I’m really pleased that I have an answer. I’m participating in a blind clinical trial that hopes to understand endo pain better so I have no idea if they
Hi everyone, I had my first laparoscopy yesterday and as suspected they found endometriosis. I’ve been waiting a long time for this diagnosis so I’m really pleased that I have an answer. I’m participating in a blind clinical trial that hopes to understand endo pain better so I have no idea if they
Coco1860
in
Endometriosis UK
2 years ago
My rectrum pain
I was diagnosed with IBS two years ago, but I have always had my doubts, so have one or two doctors whom I have visited in the past, I was literally told to get on with it, and offered no medication at all what so ever, my symptoms have slowly got worse over the months, and now I am in chronic pain constantly
I was diagnosed with IBS two years ago, but I have always had my doubts, so have one or two doctors whom I have visited in the past, I was literally told to get on with it, and offered no medication at all what so ever, my symptoms have slowly got worse over the months, and now I am in chronic pain constantly
Lamly
in
IBS Network
2 years ago
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Hi everyone!
Hi everyone! I hope you are as well as can be. After having covid for the 2nd time in June, I've now been diagnosed with Fibromyalgia. I already have CFS so this is a double whammy. I cannot seem to get the pain under control especially in my legs. I seem to live on painkillers but they don't seem to
Hi everyone! I hope you are as well as can be. After having covid for the 2nd time in June, I've now been diagnosed with Fibromyalgia. I already have CFS so this is a double whammy. I cannot seem to get the pain under control especially in my legs. I seem to live on painkillers but they don't seem to
Torti68
in
Fibromyalgia Action UK
2 years ago
Update - methotrexte liver test
https://healthunlocked.com/nras/posts/148494355/liver-test-results-methotrexate?responses=148576780 Since the last post ive had one test come back at 73 and then the latest back up to 170. Ive not drank in months, i dont take a single pain killer, i take prednisolone, hydroxychloroquine, sertraline
https://healthunlocked.com/nras/posts/148494355/liver-test-results-methotrexate?responses=148576780 Since the last post ive had one test come back at 73 and then the latest back up to 170. Ive not drank in months, i dont take a single pain killer, i take prednisolone, hydroxychloroquine, sertraline
Nelliekel
in
NRAS
2 years ago
Very last stage
hi everyone, Colin has been put on “end of life” drugs now via a syringe driver, he stopped eating last Wednesday, although he hadnt eaten or had anything to drink much for while, as he is now unable to open his mouth. He has lost so much weight so quickly. Getting him to take his painkillers was a nightmare
hi everyone, Colin has been put on “end of life” drugs now via a syringe driver, he stopped eating last Wednesday, although he hadnt eaten or had anything to drink much for while, as he is now unable to open his mouth. He has lost so much weight so quickly. Getting him to take his painkillers was a nightmare
Helen119
in
PSP Association
2 years ago
toothache
it’s been a month now since my tooth nightmare happened. Now my dad’s turn 🙈. He’s in so much pain, had to go into emergency but useless. They said no infection or anything. Just gingivitis. Dads insisting something has to be wrong. Painkillers aren’t helping. Hope he can sleep tonight 😥
it’s been a month now since my tooth nightmare happened. Now my dad’s turn 🙈. He’s in so much pain, had to go into emergency but useless. They said no infection or anything. Just gingivitis. Dads insisting something has to be wrong. Painkillers aren’t helping. Hope he can sleep tonight 😥
Junny123
in
Pain Concern
2 years ago
Sunday’s poem Timothy Winters - Charles Causley
Charles Causley – 1917 to 2003) Timothy Winters comes to school With eyes as wide as a football pool, Ears like bombs and teeth like splinters: A blitz of a boy is Timothy Winters. His belly is white, his neck is dark, And his hair is an exclamation mark. His clothes are enough to scare a crow
Charles Causley – 1917 to 2003) Timothy Winters comes to school With eyes as wide as a football pool, Ears like bombs and teeth like splinters: A blitz of a boy is Timothy Winters. His belly is white, his neck is dark, And his hair is an exclamation mark. His clothes are enough to scare a crow
Lyd12
in
Lung Conditions Community Forum
2 years ago
Please help
I am 53 and have been struggling with illness for about 8 years now, have bloods and appointment with GP in the next week and due to see my rheumatologist this week too. I have Hashimotos and primary Sjögrens or a Lupus/Sjögrens overlap depending on the day it seems. I take T3, hydroxychloroquine and
I am 53 and have been struggling with illness for about 8 years now, have bloods and appointment with GP in the next week and due to see my rheumatologist this week too. I have Hashimotos and primary Sjögrens or a Lupus/Sjögrens overlap depending on the day it seems. I take T3, hydroxychloroquine and
puffyface
in
Fibromyalgia Action UK
2 years ago
ProRenal + D kidney health multivitamins
hello everyone. Recently saw a vitamin on Amazon created by Nephrologists (I think). Lots of reviews on Amazon and other sources mention that it lowered their creatinine. Anyone else heard of these renal vitamins and benefits before?? I have my dad (testing) whose creatinine went from less
hello everyone. Recently saw a vitamin on Amazon created by Nephrologists (I think). Lots of reviews on Amazon and other sources mention that it lowered their creatinine. Anyone else heard of these renal vitamins and benefits before?? I have my dad (testing) whose creatinine went from less
Dna4christ
in
Kidney Transplant
2 years ago
Struggling
Cant even stand for 5 mins without crying the pain alo g to bottom of my back and down mmy legs is unreal taking every painkiller u can think of but nothing helps
Cant even stand for 5 mins without crying the pain alo g to bottom of my back and down mmy legs is unreal taking every painkiller u can think of but nothing helps
Djemima
in
Fibromyalgia Action UK
2 years ago
Meeting with a new EP/Cardiologist
Since my last procedure the end of April I have been doing poorly. Unfortunately I cannot seem to get the attention of my EP who not only did the procedure VOM but is the pioneer of it. I liked the doctor however it appears that I am being ostracized. He has a medical secretary Who is not only inept
Since my last procedure the end of April I have been doing poorly. Unfortunately I cannot seem to get the attention of my EP who not only did the procedure VOM but is the pioneer of it. I liked the doctor however it appears that I am being ostracized. He has a medical secretary Who is not only inept
DawnTX
in
AF Association
2 years ago
Ketamine?
Levodopa, a standard Parkinson’s therapy, is a precursor molecule that is converted to dopamine in the brain. It is well-known for controlling Parkinson’s disease symptoms such as rigidity and slowness of movement. However, prolonged use of levodopa may result in spontaneous involuntary movements
Levodopa, a standard Parkinson’s therapy, is a precursor molecule that is converted to dopamine in the brain. It is well-known for controlling Parkinson’s disease symptoms such as rigidity and slowness of movement. However, prolonged use of levodopa may result in spontaneous involuntary movements
kaypeeoh
in
Cure Parkinson's
2 years ago
PMR returns, probably never away
Hi, I haven’t posted for a while, brief history I was diagnosed with PMR about a year ago, although my markers were normal, seen a Rheumatologist and my two GPs decided it wasn’t PMR, I was on about 10 mg of prednisolone at the time. I still had severe back and leg pain, was put on every painkiller
Hi, I haven’t posted for a while, brief history I was diagnosed with PMR about a year ago, although my markers were normal, seen a Rheumatologist and my two GPs decided it wasn’t PMR, I was on about 10 mg of prednisolone at the time. I still had severe back and leg pain, was put on every painkiller
Carathedog
in
PMRGCAuk
2 years ago
My IBS lasting over a couple of weeks. Worried.
Hi everyone. Just need to talk to someone who understands. Ive had IBS since my 20s and I’m 84 now. On and off over the years mostly caused by stress. This latest attack started with really bad Diarrhea and then days of no BM . Saw Dr and was given macrogol sachets which worked over the next few days
Hi everyone. Just need to talk to someone who understands. Ive had IBS since my 20s and I’m 84 now. On and off over the years mostly caused by stress. This latest attack started with really bad Diarrhea and then days of no BM . Saw Dr and was given macrogol sachets which worked over the next few days
gloden
in
IBS Network
2 years ago
giving up 😭
im giving up, from loving happy i get to depressed and giving up as theres bo help ! had appendix surgery 12.2020, 6 months later pain and lump like hernia after appendix removed. january 2022 pain was so bad i went to a&e then been signed off from work ( next momth im back to work ) and then many trips
im giving up, from loving happy i get to depressed and giving up as theres bo help ! had appendix surgery 12.2020, 6 months later pain and lump like hernia after appendix removed. january 2022 pain was so bad i went to a&e then been signed off from work ( next momth im back to work ) and then many trips
sweet_lily
in
Endometriosis UK
2 years ago
giving up
im giving up, from loving happy i get to depressed and giving up as theres bo help ! had appendix surgery 12.2020, 6 months later pain and lump like hernia after appendix removed. january 2022 pain was so bad i went to a&e then been signed off from work ( next momth im back to work ) and then many trips
im giving up, from loving happy i get to depressed and giving up as theres bo help ! had appendix surgery 12.2020, 6 months later pain and lump like hernia after appendix removed. january 2022 pain was so bad i went to a&e then been signed off from work ( next momth im back to work ) and then many trips
sweet_lily
in
The Endometriosis Foundation
2 years ago
Bilateral rotary cuff in shoulders after coming off pred....
After 3.5 years tapering pred I have been left with bilateral rotary cuff which is excruciating. I have had it a year now and finally have an MRI Monday. Apart from an ultra sound scan which confirmed it I have been taking anti inflammatory meds (Nurofen/ Naproxen) and exercising. It has not got any
After 3.5 years tapering pred I have been left with bilateral rotary cuff which is excruciating. I have had it a year now and finally have an MRI Monday. Apart from an ultra sound scan which confirmed it I have been taking anti inflammatory meds (Nurofen/ Naproxen) and exercising. It has not got any
Seriola
in
PMRGCAuk
2 years ago
Painkiller
What are the best painkillers.Tried tramadol n has a bad effect on me.Looking for things inbetween paracetamol n tramadol worth a try.
What are the best painkillers.Tried tramadol n has a bad effect on me.Looking for things inbetween paracetamol n tramadol worth a try.
versa2508
in
Headway
2 years ago
I am tired of being Poorly
hi, this is my first post on here. I am 30 years old in the UK, recently diagnosed with fibromyalgia. struggling with it for about 1-2 years. Doctors are upping my painkillers etc but I’m in constant agony, I have flare up minimum for every 2 weeks, for 3/4 days at a time. work have redeployed
hi, this is my first post on here. I am 30 years old in the UK, recently diagnosed with fibromyalgia. struggling with it for about 1-2 years. Doctors are upping my painkillers etc but I’m in constant agony, I have flare up minimum for every 2 weeks, for 3/4 days at a time. work have redeployed
NewToFibrox
in
Fibromyalgia Action UK
2 years ago
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