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Physiotherapy/Acupuncture
After a move to Wiltshire I found a Physiotherapist who isn't near based but has helped people with Parkinson's. Treatment was mainly nerve/muscle stimulation but a year ago I also tried acupuncture. I am an engineer (well, used to be) and I can't understand how this treatment works but it is helping
After a move to Wiltshire I found a Physiotherapist who isn't near based but has helped people with Parkinson's. Treatment was mainly nerve/muscle stimulation but a year ago I also tried acupuncture. I am an engineer (well, used to be) and I can't understand how this treatment works but it is helping
CrazyHarry
in
Ataxia UK
10 months ago
Hip Bursitis and Thyroid Link
My consultant is not going to treat this as he says it is a hormonal issue (thyroid) and will right itself at some point and continue with
physiotherapy
. I have been researching this topic and it does say that the thyroid can cause bursitis in the hip.
My consultant is not going to treat this as he says it is a hormonal issue (thyroid) and will right itself at some point and continue with
physiotherapy
. I have been researching this topic and it does say that the thyroid can cause bursitis in the hip.
kaz90
in
Thyroid UK
2 months ago
Ankle manipulation and RLS/PLMD jerking
Has anyone else suffered like this from either MLD or
physiotherapy
on their ankle? Can anyone tell me why and how this RLS/PLMD jerking might be triggered? Should I continue with the therapy to reduce the lymphodema swelling? Or stop because it is triggering PLMD jerking?
Has anyone else suffered like this from either MLD or
physiotherapy
on their ankle? Can anyone tell me why and how this RLS/PLMD jerking might be triggered? Should I continue with the therapy to reduce the lymphodema swelling? Or stop because it is triggering PLMD jerking?
thorp
in
Restless Legs Syndrome
5 days ago
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Pelvic Floor Physiotherapy website with information about incontinence
Hello, My Physiotherapist gave me the name of this Australian Pelvic Floor
Physiotherapy
website that some here may find interesting or helpful.
Hello, My Physiotherapist gave me the name of this Australian Pelvic Floor
Physiotherapy
website that some here may find interesting or helpful.
Rebas
in
Pelvic Radiation Disease Association
9 months ago
Insurance & Pilates
Does anyone know whether insurance companies that cover '
physiotherapy
' include Pilates?
Does anyone know whether insurance companies that cover '
physiotherapy
' include Pilates?
rwlmartin1
in
Bone Health and Osteoporosis UK
10 months ago
Is this a lupus rash
Discharged from rhumatology and now just under
physiotherapy
. They are looking to put me into a spinal pain clinic. My question is I've started to come out in rashes the last few months. I thought it was an allergy but I'm not allergic to anything. Also it looks like a butterfly rash.
Discharged from rhumatology and now just under
physiotherapy
. They are looking to put me into a spinal pain clinic. My question is I've started to come out in rashes the last few months. I thought it was an allergy but I'm not allergic to anything. Also it looks like a butterfly rash.
Peppermints
in
LUPUS UK
7 months ago
Painkillers stopped working
I do
physiotherapy
for an hour in the morning and evening. I also work 40 hours. It's getting harder and harder to exist. What options are there for me?
I do
physiotherapy
for an hour in the morning and evening. I also work 40 hours. It's getting harder and harder to exist. What options are there for me?
Madhu5
in
Fibromyalgia Action UK
8 months ago
Introduction
Three months into chemo I developed septicemia & spent 12 days in ICU followed by 3 months on the cancer ward receiving intensive
physiotherapy
.
Three months into chemo I developed septicemia & spent 12 days in ICU followed by 3 months on the cancer ward receiving intensive
physiotherapy
.
Ildivolover
in
Scleroderma & Raynaud's UK (SRUK)
3 months ago
Physiotherapy
Has anyone had any experience of having
physiotherapy
, either NHS or private? I have had RA for 6 months now and although the methotrexate and hydroxychloroquine are bringing down the swelling it is painful to raise my arms above my head or reach behind my back.
Has anyone had any experience of having
physiotherapy
, either NHS or private? I have had RA for 6 months now and although the methotrexate and hydroxychloroquine are bringing down the swelling it is painful to raise my arms above my head or reach behind my back.
spartacus101
in
NRAS
1 year ago
First day Rehab
I am attending
physiotherapy
tomorrow. Again thank you .
I am attending
physiotherapy
tomorrow. Again thank you .
4stentstemi
in
British Heart Foundation
9 months ago
arthritis
Firstly I am type 2 Diabetic but that is by the by I was referred to the Orthopaedic clinic in 2013 with arthritis in the left knee at that time I was given
physiotherapy
which only exascipated the pain however this was defined as surgery was not essential, plus I was having gall Bladder problems and
Firstly I am type 2 Diabetic but that is by the by I was referred to the Orthopaedic clinic in 2013 with arthritis in the left knee at that time I was given
physiotherapy
which only exascipated the pain however this was defined as surgery was not essential, plus I was having gall Bladder problems and
Trina
in
Thyroid UK
5 months ago
How Do you Know When You're On Enough B12?
I've tried vestibular
physiotherapy
, pretty much anything I can think of including seeing a chiropractor. I stopped the latest migraine in January and I'm no worse not being on it. I'm not dizzy but unbalanced when I walk.
I've tried vestibular
physiotherapy
, pretty much anything I can think of including seeing a chiropractor. I stopped the latest migraine in January and I'm no worse not being on it. I'm not dizzy but unbalanced when I walk.
Sparklingsunshine
in
Pernicious Anaemia Society
4 months ago
Seronegative RA with OA in the Lumbar and Cervical Spine
My question is one of exercise - The GP has made a referral to
Physiotherapy
- I'm expecting that this will take a while for an appointment to come through, in the meantime I'd love some pointers re moderate exercise - I have some pretty decent exercise equipment that I have used historically up until
My question is one of exercise - The GP has made a referral to
Physiotherapy
- I'm expecting that this will take a while for an appointment to come through, in the meantime I'd love some pointers re moderate exercise - I have some pretty decent exercise equipment that I have used historically up until
Hopeful66
in
NRAS
7 months ago
Physiotherapy helping T
Hi not been on here for a while but wanted to give you an update on my T.After an ear infection, or what I thought was an infection, rendered me deaf for 3 weeks in my right ear, I saw my GP, went to A&E and saw 2 specialists. Whilst some antibiotics gave temporary relief, nothing resolved the deafness
Hi not been on here for a while but wanted to give you an update on my T.After an ear infection, or what I thought was an infection, rendered me deaf for 3 weeks in my right ear, I saw my GP, went to A&E and saw 2 specialists. Whilst some antibiotics gave temporary relief, nothing resolved the deafness
TurboTrace
in
Tinnitus UK
11 months ago
Finally got some information on the treatment for FND
I have requested
physiotherapy
, CBT (cognitive behavioral therapy), EEG (electroencephalogram), and fMRI (Functional Magnetic Resonance Imaging). I will keep everyone updated and let know how it goes. This is my last hope in the medical world before I go to a natural approach. Wish me good luck.
I have requested
physiotherapy
, CBT (cognitive behavioral therapy), EEG (electroencephalogram), and fMRI (Functional Magnetic Resonance Imaging). I will keep everyone updated and let know how it goes. This is my last hope in the medical world before I go to a natural approach. Wish me good luck.
BossStateofMind
in
Functional Neurological Disorder - FND Hope
8 months ago
Curious about my experiance. Interested in what others think?
Here in Wales Drs do not prescribe
physiotherapy
, we have to do it ourselves. Usually takes about about 12 weeks to be seen. However my disabled partner was in hospital with 2 osteoporotic vertebral fractures and was due home in a few days with a back brace and they saw me in 5 days.
Here in Wales Drs do not prescribe
physiotherapy
, we have to do it ourselves. Usually takes about about 12 weeks to be seen. However my disabled partner was in hospital with 2 osteoporotic vertebral fractures and was due home in a few days with a back brace and they saw me in 5 days.
LindyMc
in
PMRGCAuk
8 months ago
Anticoagulant users
No bruising at all, injury checked by Minor Injuries Unit, X-Rays and
Physiotherapy
. No bruising observed. So, my question is .... anyone wanna suggest any reason for no visible bruising. Is it possible that the bone joint took the full smash impact and that the bone itself was bruised.
No bruising at all, injury checked by Minor Injuries Unit, X-Rays and
Physiotherapy
. No bruising observed. So, my question is .... anyone wanna suggest any reason for no visible bruising. Is it possible that the bone joint took the full smash impact and that the bone itself was bruised.
BenHall1
in
Atrial Fibrillation Support
9 months ago
Unreal letter from the hospital!
I've been waiting to hear if they'll give me
physiotherapy
or mental health care or pain management... just something! And all the letter says is 'we are aware you are an out patient in this department. If you wish to stay on our list you must phone the number in the next 14 days.
I've been waiting to hear if they'll give me
physiotherapy
or mental health care or pain management... just something! And all the letter says is 'we are aware you are an out patient in this department. If you wish to stay on our list you must phone the number in the next 14 days.
SavageGold
in
Endometriosis UK
8 months ago
questions
Since then I have seen 2 Ent doctors, have tried
physiotherapy
, a chiropractor, B 12. I find when I do saline rinses my ears seem more sensitive. I was recently told it might be Eustachian tube dysfunction or blockage due to persistent sinus infections and a recent bout of Covid.
Since then I have seen 2 Ent doctors, have tried
physiotherapy
, a chiropractor, B 12. I find when I do saline rinses my ears seem more sensitive. I was recently told it might be Eustachian tube dysfunction or blockage due to persistent sinus infections and a recent bout of Covid.
Healthymetoday
in
Tinnitus UK
7 months ago
Meningioma !!
Still in recovery after complete removal(02/11/22), I feel lucky as it has only effected my right shoulder/arm and hand .I am still receiving
physiotherapy
for my shoulder/arm and hand. Getting better everyday.
Still in recovery after complete removal(02/11/22), I feel lucky as it has only effected my right shoulder/arm and hand .I am still receiving
physiotherapy
for my shoulder/arm and hand. Getting better everyday.
MadTrucker
in
Meningioma Support
11 months ago
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