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Tens machine
Dear all My physio suggests a tens machine on my cervical neck to try to help with chronic tinnitus I had an ablation for paf 18 months ago and all good. Any thoughts on usage of the machine Thanks Rod
Dear all My physio suggests a tens machine on my cervical neck to try to help with chronic tinnitus I had an ablation for paf 18 months ago and all good. Any thoughts on usage of the machine Thanks Rod
7164
in
AF Association
2 years ago
New Diagnosis
Not much of a purpose, just an update really. I recently got diagnosed by a GP and a rheumatologist with Fibromyalgia. Honestly, there's a mixture of feelings right now, I'm angry because I've been in pain for 8 years and told time and time again there isn't anything wrong with me, but now everything
Not much of a purpose, just an update really. I recently got diagnosed by a GP and a rheumatologist with Fibromyalgia. Honestly, there's a mixture of feelings right now, I'm angry because I've been in pain for 8 years and told time and time again there isn't anything wrong with me, but now everything
Cassi0
in
Fibromyalgia Action UK
2 years ago
NEW GFR POST TRANSPLANT
I was wondering how quickly after transplant the GFR starts showing some normalcy. From my blood test I had yesterday, thursday, I received the results and I was shocked to learn that the day of the surgery, my GFR was down to 8. So after the transplant on January 25th, my GFR is now 57! I am just
I was wondering how quickly after transplant the GFR starts showing some normalcy. From my blood test I had yesterday, thursday, I received the results and I was shocked to learn that the day of the surgery, my GFR was down to 8. So after the transplant on January 25th, my GFR is now 57! I am just
TaffyTwoshoes27
in
Kidney Dialysis
2 years ago
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Went to physio yesterday for first time she advised another X-ray before we proceed. Iv had this back pain for months and now worse than ever. Gp gave me some diazepam isn’t doing a thing. I take paracetamol and Oxycodone but that doesn’t touch it. If I’m sitting it’s ok as soon as I stand 😩😩😩 my
Went to physio yesterday for first time she advised another X-ray before we proceed. Iv had this back pain for months and now worse than ever. Gp gave me some diazepam isn’t doing a thing. I take paracetamol and Oxycodone but that doesn’t touch it. If I’m sitting it’s ok as soon as I stand 😩😩😩 my
Uglow
in
Bone Health and Osteoporosis UK
2 years ago
Hopeless?
I truly give up. Every time I see a doctor it's always 'go see a physio'. I've seen a physio, and because my shoulder doesn't hurt when move it in a certain way my pain was dismissed. I'm hopeless at this point, I give up. I am just expected to live the rest of my life in pain because nobody seems
I truly give up. Every time I see a doctor it's always 'go see a physio'. I've seen a physio, and because my shoulder doesn't hurt when move it in a certain way my pain was dismissed. I'm hopeless at this point, I give up. I am just expected to live the rest of my life in pain because nobody seems
Danceidol
in
Fibromyalgia Action UK
2 years ago
Plump up the cushions on the Injury Couch 🛋
Remember that ankle “twang” I posted about…..? Ended up in A&E after physio suspected a stress fracture. Fortunately it isn’t fractured, just a sprain, but (long story short) they were concerned about the residual lump/ strange tingly sensation on my foot left after an injury 2 years ago and further
Remember that ankle “twang” I posted about…..? Ended up in A&E after physio suspected a stress fracture. Fortunately it isn’t fractured, just a sprain, but (long story short) they were concerned about the residual lump/ strange tingly sensation on my foot left after an injury 2 years ago and further
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Graduate10
in
Bridge to 10K
2 years ago
new....well sort of ; )
hi. it feels strange to say i am ‘new’ here, having been a member since 2018. i have read your collective posts daily for over 3 years now and feel like i know a lot of you. and i have been saddened by those that have passed. but you all don’t even know i exist…lol. not really sure why i decided
hi. it feels strange to say i am ‘new’ here, having been a member since 2018. i have read your collective posts daily for over 3 years now and feel like i know a lot of you. and i have been saddened by those that have passed. but you all don’t even know i exist…lol. not really sure why i decided
kokopelli2017
in
SHARE Metastatic Breast Cancer
2 years ago
Be aware of high fevers
I just spent a week in the hospital. The prednisone caused me to become unaware of my surroundings. Fortunately my husband saw these changes and called an ambulance. My 105 degree fever was quite serious and I was on antibiotics of all kinds to stop cellulitis in my arm from reaching the point of death
I just spent a week in the hospital. The prednisone caused me to become unaware of my surroundings. Fortunately my husband saw these changes and called an ambulance. My 105 degree fever was quite serious and I was on antibiotics of all kinds to stop cellulitis in my arm from reaching the point of death
Ronswife
in
PMRGCAuk
2 years ago
Knocked out of marathon training (How to tell the children about BCR)
Proximal hamstring tendinopathy knocked me out of training for my second marathon. Physical therapy is helping me to conquer my overuse injury and dreams of hitting the magical four hour marathon finishing time seemed to have just been delayed until the fall. I even allowed myself to wonder if I could
Proximal hamstring tendinopathy knocked me out of training for my second marathon. Physical therapy is helping me to conquer my overuse injury and dreams of hitting the magical four hour marathon finishing time seemed to have just been delayed until the fall. I even allowed myself to wonder if I could
farmanerd
in
Advanced Prostate Cancer
2 years ago
Burning pain in spine
I pay privately for
physiotherapy
because the NHS only offer phone physio.. Today I saw a private orthopaedic consultant surgeon who wasn’t very helpful and barely laid a hand on my back, moreover, no investigations. He only wanted to push the services of his colleague who was a pain consultant.
I pay privately for
physiotherapy
because the NHS only offer phone physio.. Today I saw a private orthopaedic consultant surgeon who wasn’t very helpful and barely laid a hand on my back, moreover, no investigations. He only wanted to push the services of his colleague who was a pain consultant.
mauschen
in
Pain Concern
3 years ago
Sjogren's
Hello, I hope this post finds you all safe and well as you can be. I recently posted about just finding out that as a child I had been diagnosed with Larsen Syndrome. All of you lovely people pointed me in a direction to find out more. At the moment I am suffering with really quite bad arm weakness
Hello, I hope this post finds you all safe and well as you can be. I recently posted about just finding out that as a child I had been diagnosed with Larsen Syndrome. All of you lovely people pointed me in a direction to find out more. At the moment I am suffering with really quite bad arm weakness
Jinnty89
in
NRAS
2 years ago
Hi, I'm Laurelin & I'm new to the LSN!
Just joined today! Have Lymphoedema, Lymphedema, Overactive Bladder & Fecal Incontinence. Have an Osteopath for my Primary Care Physician, fortunately. Have a Urogynecologist too!! Would like to get a Lymphedema Physical Therapist to go to now that I know I have Lymphoedema. It's a drag having these
Just joined today! Have Lymphoedema, Lymphedema, Overactive Bladder & Fecal Incontinence. Have an Osteopath for my Primary Care Physician, fortunately. Have a Urogynecologist too!! Would like to get a Lymphedema Physical Therapist to go to now that I know I have Lymphoedema. It's a drag having these
Laurelin
in
LSN
2 years ago
Knee replacement in March
I am due to have a TKR on my right leg on 17th March and was hoping you lovely folk might help me get prepared. Given the huge waiting lists on NHS we are using a chunk of our savings to get it done at our local Nuffield hospital, but they don't link with occupational therapy so I have no idea what
I am due to have a TKR on my right leg on 17th March and was hoping you lovely folk might help me get prepared. Given the huge waiting lists on NHS we are using a chunk of our savings to get it done at our local Nuffield hospital, but they don't link with occupational therapy so I have no idea what
rounder
in
NRAS
2 years ago
What is the best pain relief for osteoarthritis?
Hi guys... I have had OA for a few years now and it's just getting progressively worse. I am also very overweight which doesn't help and have been battling with my weight all my life and I'm still trying everyday!!! The pain everyday is just chronic and has really taken a toll on my mental health as
Hi guys... I have had OA for a few years now and it's just getting progressively worse. I am also very overweight which doesn't help and have been battling with my weight all my life and I'm still trying everyday!!! The pain everyday is just chronic and has really taken a toll on my mental health as
fluffy10
in
Osteoarthritis Action
2 years ago
Managing pain and mobility
I have endo , pcos and adenmyosis. Currently I take metformin for the pcos and heat packs and pain killers when the pain is bad . My last period lasted 5 weeks and was heavy as I stopped the metformin due to side effects and have since restarted it . Had to take medication to stop my period . I’ve tried
I have endo , pcos and adenmyosis. Currently I take metformin for the pcos and heat packs and pain killers when the pain is bad . My last period lasted 5 weeks and was heavy as I stopped the metformin due to side effects and have since restarted it . Had to take medication to stop my period . I’ve tried
Redhen17
in
Endometriosis UK
2 years ago
Referral to a London hospital to investigate ulnar nerve compression
Hi all. I’ve been referred to Kings College Hospital as my Rheumy consultant thinks I may need surgery for nerve compression in my elbow. I’ve had lots of physio but it’s not really helped. Has anyone had this surgery? Also, I’m waiting for my PIP decision. I had my assessment 2 weeks ago, and I know
Hi all. I’ve been referred to Kings College Hospital as my Rheumy consultant thinks I may need surgery for nerve compression in my elbow. I’ve had lots of physio but it’s not really helped. Has anyone had this surgery? Also, I’m waiting for my PIP decision. I had my assessment 2 weeks ago, and I know
Pink75928
in
NRAS
2 years ago
aiming for diagnosis
I just had my appointment and they have said it could be fibro but because that diagnosis comes from the exclusion of others they cant be sure its not just intermittent yet, so im being referred back to msk for
physiotherapy
and ‘pain management’ as she found some hyper mobility in my joints, doesnt
I just had my appointment and they have said it could be fibro but because that diagnosis comes from the exclusion of others they cant be sure its not just intermittent yet, so im being referred back to msk for
physiotherapy
and ‘pain management’ as she found some hyper mobility in my joints, doesnt
aprilj15
in
Fibromyalgia Action UK
3 years ago
Update on my phone appt. with Neph. last Wed.
3 months ago myNeph. had said he may take me off Prednisone in Jan. as an experiment to see if my kidney numbers stayed up since when I started Pred. they jumped from eGFR of 28 up to 50. It had been 35 - 30 the previous 4 or 5 years. My Jan. labs showed I'd dropped to 42 which is still my best in 8
3 months ago myNeph. had said he may take me off Prednisone in Jan. as an experiment to see if my kidney numbers stayed up since when I started Pred. they jumped from eGFR of 28 up to 50. It had been 35 - 30 the previous 4 or 5 years. My Jan. labs showed I'd dropped to 42 which is still my best in 8
Sophiebun11
in
Kidney Disease
2 years ago
Muscle weakness… again.
So this is something I’ve struggled with for a long time now. It has disappeared at times, most recently when I was on 60mcg T3 only but after a few months that dose proved to be too high, and I was getting breathless, so I dropped it again to 57mcg. So now the muscle weakness is back, and I’m back
So this is something I’ve struggled with for a long time now. It has disappeared at times, most recently when I was on 60mcg T3 only but after a few months that dose proved to be too high, and I was getting breathless, so I dropped it again to 57mcg. So now the muscle weakness is back, and I’m back
Murphysmum
in
Thyroid UK
2 years ago
3K in 29 minutes.
I taken up running as recommended by my physiotherapist after many physio sessions from a serious leg injury. Can now do 3K in 29 minutes whereas 12 weeks ago when I started running I could only run slowly a few metres. Don't how to graduate on anything on this site but I am looking forward to trying
I taken up running as recommended by my physiotherapist after many physio sessions from a serious leg injury. Can now do 3K in 29 minutes whereas 12 weeks ago when I started running I could only run slowly a few metres. Don't how to graduate on anything on this site but I am looking forward to trying
Comte
Graduate
in
Couch to 5K
2 years ago
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