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Restless arm syndrome
Hi ive been on clonazepan now for a few months for restless arms , no problem with any other part of my body . My doc is just tresting symptons and this drug does reduce the awful sensation of wanting to keep moving it although doesnt stop it. My problem is all day not so much at night. Ive had mri on
Hi ive been on clonazepan now for a few months for restless arms , no problem with any other part of my body . My doc is just tresting symptons and this drug does reduce the awful sensation of wanting to keep moving it although doesnt stop it. My problem is all day not so much at night. Ive had mri on
Halfpint1234
in
Restless Legs Syndrome
3 years ago
Still low
Good morning peeps I've got no idea what's going on with me it's been 11 weeks since I had a heart attack and I still can't stop crying, im still in pain even tho my gp stopped the statins to see if they were the cause I'm now paying for physio because I've got no idea where I am on my recovery,I feel
Good morning peeps I've got no idea what's going on with me it's been 11 weeks since I had a heart attack and I still can't stop crying, im still in pain even tho my gp stopped the statins to see if they were the cause I'm now paying for physio because I've got no idea where I am on my recovery,I feel
Emcd8477
in
British Heart Foundation
3 years ago
Base of skull pain
I’m new to the group and was wondering if anyone has experienced cervicogenic headaches. I have an appointment with physio in 2 months time to get diagnosed for certain
I’m new to the group and was wondering if anyone has experienced cervicogenic headaches. I have an appointment with physio in 2 months time to get diagnosed for certain
Janie03
in
NRAS
3 years ago
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Sorry for the moan
Oh dear well after my last post I seem to have lost my mojo and I was so elated at running for 40 mins. Everything is against us at the moment on the house hunting front, I'm feeling a little bewildered weepy and miserable. I now have a pinched tendon in my shoulder the physio said so no more upper
Oh dear well after my last post I seem to have lost my mojo and I was so elated at running for 40 mins. Everything is against us at the moment on the house hunting front, I'm feeling a little bewildered weepy and miserable. I now have a pinched tendon in my shoulder the physio said so no more upper
doggytail
Graduate10
in
Bridge to 10K
3 years ago
Dysfunctional breathing training
Hi everyone just an update on my physio a week ago which I found interesting, I met with the physio and explained a bit about my self and she asked me what symptoms I was getting she had pen and paper at hand and she wrote down atleast 12 symptoms I was getting on a regular day to day basis from mouth
Hi everyone just an update on my physio a week ago which I found interesting, I met with the physio and explained a bit about my self and she asked me what symptoms I was getting she had pen and paper at hand and she wrote down atleast 12 symptoms I was getting on a regular day to day basis from mouth
bryan45735
in
Lung Conditions Community Forum
3 years ago
been to the gp, card carrying PMR now
hallo! well, forty five minutes with the gp. he's confident with pmr diagnosis, but slightly concerned that the corticoids will obscure the things we've been keeping an eye on for the past bunch of time, which is why he was hesitant, and hoping he could get a quick rheumy consult organized. he could
hallo! well, forty five minutes with the gp. he's confident with pmr diagnosis, but slightly concerned that the corticoids will obscure the things we've been keeping an eye on for the past bunch of time, which is why he was hesitant, and hoping he could get a quick rheumy consult organized. he could
hazmatrec
in
PMRGCAuk
3 years ago
Fed up/ angry 😡
So had my post op appointment today with my surgeon , who carried out my laparoscopy 3 months ago.. I tried to ask questions.. like why is my pain worse now than it was prior my op? .. his response was 'well I removed the Endo so you shouldn't be in pain' .. I then went on to express that I have to take
So had my post op appointment today with my surgeon , who carried out my laparoscopy 3 months ago.. I tried to ask questions.. like why is my pain worse now than it was prior my op? .. his response was 'well I removed the Endo so you shouldn't be in pain' .. I then went on to express that I have to take
Mummabear123
in
Endometriosis UK
3 years ago
Lung Physio
Has anyone bought one of these devices? If so, are they any good? Thanks.
Has anyone bought one of these devices? If so, are they any good? Thanks.
Grandjury
in
Lung Conditions Community Forum
3 years ago
10 years post-injury: lost confidence in physical ability, causing falls. Physio maybe?
I am wondering if anyone has experienced something similar and could give me some tips. My mother in law had a serious brain injury 10 years ago. Over time she has developed more low moods, negative or anxious attitudes to physical activity and has put on a lot of weight. She is not able to remember
I am wondering if anyone has experienced something similar and could give me some tips. My mother in law had a serious brain injury 10 years ago. Over time she has developed more low moods, negative or anxious attitudes to physical activity and has put on a lot of weight. She is not able to remember
Redscarf
in
Headway
3 years ago
Chronic pain with scleroderma?
Hi, I have suffered with debilitating pain that I had attributed solely to my scleroderma as that is how it all started - pain n joints n stiffness all over…but now roughly 9 years in I am beginning to wonder if it is more chronic pain syndrome as my consultant says bloods show no inflammation in muscles
Hi, I have suffered with debilitating pain that I had attributed solely to my scleroderma as that is how it all started - pain n joints n stiffness all over…but now roughly 9 years in I am beginning to wonder if it is more chronic pain syndrome as my consultant says bloods show no inflammation in muscles
momo17
in
Scleroderma & Raynaud's UK (SRUK)
3 years ago
Knuckle problem
Hi, Was wondering if anyone could help me please. So basically I think i`ve done something to my knuckle but no idea what. One idea I do have is that earlier this year I dislocated my thumb and whilst all it was being concentrated on the thumb, I was also getting pain on the side of the finger, the round
Hi, Was wondering if anyone could help me please. So basically I think i`ve done something to my knuckle but no idea what. One idea I do have is that earlier this year I dislocated my thumb and whilst all it was being concentrated on the thumb, I was also getting pain on the side of the finger, the round
emmaaaar18
in
NRAS
3 years ago
n00b
hello, everyone! just thought I'd do more than skulk and read the the read mees for a moment, as I'm likely to be asking for help at some point and it might be nice to have said hello already. the gp seemed very excited when i said i couldn't raise my arms and both hips were giving me new grief, neither
hello, everyone! just thought I'd do more than skulk and read the the read mees for a moment, as I'm likely to be asking for help at some point and it might be nice to have said hello already. the gp seemed very excited when i said i couldn't raise my arms and both hips were giving me new grief, neither
hazmatrec
in
PMRGCAuk
3 years ago
Piercing Left Chest and Shoulder Pain: Is it Osteoarthritis or Bronchitis ?
Three months ago I was exposed to cold after losing a loved one. Then this burning sensation started in my left shoulder through the chest radiating to the arm muscles. X-rays revealed bronchitis, and cervical wear. I was on meds for a whole month with physio. I would feel a tender lump in my left
Three months ago I was exposed to cold after losing a loved one. Then this burning sensation started in my left shoulder through the chest radiating to the arm muscles. X-rays revealed bronchitis, and cervical wear. I was on meds for a whole month with physio. I would feel a tender lump in my left
Lunje
in
Arthritis Action
3 years ago
Post Morton’s and ankle operation
Morning all , it’s been a while since I posted , but as it’s all been doom and gloom I didn’t think anyone would want to hear , but unfortunately I’m at the end of my tether . Back in July I had my first post op physio the other was done on the phone (don’t get me started) he wasn’t happy with the swelling
Morning all , it’s been a while since I posted , but as it’s all been doom and gloom I didn’t think anyone would want to hear , but unfortunately I’m at the end of my tether . Back in July I had my first post op physio the other was done on the phone (don’t get me started) he wasn’t happy with the swelling
Nessa28
in
NRAS
3 years ago
Advice please
After having PMR for 6 years I finally reduced to 0.5mg and then zero. I began to have discomfort again but didn’t know if It was OA as I also stopped taking naproxen following a total hip replacement. I have been seen by the physio at my GP surgery and he’s referred me to a rheumatologist with suspected
After having PMR for 6 years I finally reduced to 0.5mg and then zero. I began to have discomfort again but didn’t know if It was OA as I also stopped taking naproxen following a total hip replacement. I have been seen by the physio at my GP surgery and he’s referred me to a rheumatologist with suspected
margiebell4
in
PMRGCAuk
3 years ago
Physio
Applied for physio four months ago on my shoulder and managed to get telephone conversation today. Very nice lady Went through history etc then last lot of questions. What would you like to achieve by having physio ? Answer Being able to dress myself, wash my hair,doing the ironing and basically do normal
Applied for physio four months ago on my shoulder and managed to get telephone conversation today. Very nice lady Went through history etc then last lot of questions. What would you like to achieve by having physio ? Answer Being able to dress myself, wash my hair,doing the ironing and basically do normal
Hidden
in
Pernicious Anaemia Society
3 years ago
I'm New Here -- Living with CFS and my treatments
My Treatment I have had CFS and Fibromyalgia for 2, almost 3 years. I have been taking Celebrex and Amytriptaline for about the same years for the pain. I have also been taking D-Ribose (for energy), Ashwagandha, Vitamin D, Zinc, Magnesium, Calcium along with regular multivitamin gummies. I also use
My Treatment I have had CFS and Fibromyalgia for 2, almost 3 years. I have been taking Celebrex and Amytriptaline for about the same years for the pain. I have also been taking D-Ribose (for energy), Ashwagandha, Vitamin D, Zinc, Magnesium, Calcium along with regular multivitamin gummies. I also use
Jeanne30
in
Myalgic Encephalomyelitis Community
3 years ago
Pulled muscle treatment for those on multiple heart meds.
Does anyone have any experience of treating a very bad pulled muscle through sport - shoulder in my case from golf - and is on a cocktail of heart meds. In my case aspirin, tricagelor, Ramipril, Felodopine, atorovastatin. I've spoken to my pharmacist: I can't use heat treatment or ibuprofen or gels containing
Does anyone have any experience of treating a very bad pulled muscle through sport - shoulder in my case from golf - and is on a cocktail of heart meds. In my case aspirin, tricagelor, Ramipril, Felodopine, atorovastatin. I've spoken to my pharmacist: I can't use heat treatment or ibuprofen or gels containing
Heartattackvictim
in
British Heart Foundation
3 years ago
New member
Hi everyone , I'm New to the site and would like to share my experiences of fnd. I retired in 2015 and was looking forward to doing everything in retirement .In early 2016 I started with balance problems and a tremor in my left hand this escalated in to loss of speech severe weakness
Hi everyone , I'm New to the site and would like to share my experiences of fnd. I retired in 2015 and was looking forward to doing everything in retirement .In early 2016 I started with balance problems and a tremor in my left hand this escalated in to loss of speech severe weakness
Dave-147
in
Functional Neurological Disorder - FND Hope
3 years ago
Immunosuppressed
I had PMR 13 years ago which was diagnosed eventuallyby my physio daughter when I visited her in London. I had what I think of now as typica PMR . My GP was very hazy about PMR but after a blood test that I requested she phoned to say my ESR was 70 and she had left me out some tablets. So was started
I had PMR 13 years ago which was diagnosed eventuallyby my physio daughter when I visited her in London. I had what I think of now as typica PMR . My GP was very hazy about PMR but after a blood test that I requested she phoned to say my ESR was 70 and she had left me out some tablets. So was started
Booge_15
in
PMRGCAuk
3 years ago
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