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Physiotherapy
I was diagnosed in October last year and treatment (cyclophosphamide) was going well. No symptoms. I have finished that course and am now on mycophenolate tablets. I have severe lower back pain and am getting no where trying to get a physio referral. Does anyone think that this may work or do i need
I was diagnosed in October last year and treatment (cyclophosphamide) was going well. No symptoms. I have finished that course and am now on mycophenolate tablets. I have severe lower back pain and am getting no where trying to get a physio referral. Does anyone think that this may work or do i need
CotswoldOx
in
Myositis UK
2 months ago
Physiotherapy
I'm 15 weeks pregnant and I wanted to know, are all physios trained in antenatal
physiotherapy
? Or do you have to specifically have to ask? I can book a number of appointments for tomorrow but don't know whether I should. Many thanks Karla
I'm 15 weeks pregnant and I wanted to know, are all physios trained in antenatal
physiotherapy
? Or do you have to specifically have to ask? I can book a number of appointments for tomorrow but don't know whether I should. Many thanks Karla
Blackmito
in
Fertility Network UK - Pregnancy Support
2 months ago
Does physiotherapy help?
So I've had a pretty "hard" manual lifestyle and have arthritis in both shoulders, already had cortisone injections in both shoulders, so that tells me I have worn out my joints, also to throw into the mix I've now got chronic back ache,and my left hip is "twinging " I can't sleep with my back properly
So I've had a pretty "hard" manual lifestyle and have arthritis in both shoulders, already had cortisone injections in both shoulders, so that tells me I have worn out my joints, also to throw into the mix I've now got chronic back ache,and my left hip is "twinging " I can't sleep with my back properly
Cb1963
in
Anxiety and Depression Support
2 months ago
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Specialist private physio for FND
For more info about the
physiotherapy
offered by this provider in Burton on Trent see link. below FND is their speciality. info@pathwaysphysio.co.uk
For more info about the
physiotherapy
offered by this provider in Burton on Trent see link. below FND is their speciality. info@pathwaysphysio.co.uk
Shimmyaway
in
Functional Neurological Disorder - FND Hope
2 months ago
Physio option PCS
Does anyone know about
physiotherapy
regarding headaches..From what ive researched in the USA this has been treated successfully with neck/ head massage...If anyone has had this..is it available on NHS or privately Thanks
Does anyone know about
physiotherapy
regarding headaches..From what ive researched in the USA this has been treated successfully with neck/ head massage...If anyone has had this..is it available on NHS or privately Thanks
Muzzyfoxster
in
Headway
3 months ago
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
6 months ago
Bit of advice and support
I have a review next week with the
physiotherapy
and also the pain clinic. When it was first checked with blood tests my infection markers were slightly raised. Am in so much widespread pain, stiffness. Currently only taking paracetamol for the pain, which at times isn't enough.
I have a review next week with the
physiotherapy
and also the pain clinic. When it was first checked with blood tests my infection markers were slightly raised. Am in so much widespread pain, stiffness. Currently only taking paracetamol for the pain, which at times isn't enough.
Kat32A
in
Fibromyalgia Action UK
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
8 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
7 months ago
more bruising
I had lots of pain and soreness along with a neck injury,
physiotherapy
is helping. A&E did some x-rays which were good. Last week a strange feeling like a pressing happened over my eye and a new bruise and black eye is happening.
I had lots of pain and soreness along with a neck injury,
physiotherapy
is helping. A&E did some x-rays which were good. Last week a strange feeling like a pressing happened over my eye and a new bruise and black eye is happening.
bethmoggie
in
Headway
3 months ago
Excessive Sleeping
The decline was rapid - he is now on PEG for feeds, intermittent urine catheter, flatus tube for bowel movement, and a tracheotomy with ventilator on at night He has speech therapy,
physiotherapy
, occupational therapy that fills up his days However in the past week, he has had very few waking hours
The decline was rapid - he is now on PEG for feeds, intermittent urine catheter, flatus tube for bowel movement, and a tracheotomy with ventilator on at night He has speech therapy,
physiotherapy
, occupational therapy that fills up his days However in the past week, he has had very few waking hours
binnyrox
in
Multiple System Atrophy Trust
26 days ago
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
6 months ago
Advice on pain relief
After several years of blood tests, scans,
physiotherapy
treatment, carpel tunnel operations and in constant pain l was put on amatryptilin. This resulted in an acute allergic reaction resulting in chronic urticaria a over my body. I had 4 weeks of hell !!
After several years of blood tests, scans,
physiotherapy
treatment, carpel tunnel operations and in constant pain l was put on amatryptilin. This resulted in an acute allergic reaction resulting in chronic urticaria a over my body. I had 4 weeks of hell !!
Diy2
in
Fibromyalgia Action UK
2 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
8 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
5 months ago
OPEP therapy for bronchiectasis
Physiotherapy
(mucus clearing breathing exercises) worked a little bit. I've taken expensive herbal remedies none of which has had any impact.
Physiotherapy
(mucus clearing breathing exercises) worked a little bit. I've taken expensive herbal remedies none of which has had any impact.
Stormfever
in
COPD Friends
27 days ago
IC and pelvic pain
I also have regular
physiotherapy
and do gentle exercise (yoga, swimming). I started taking Desert Harvest Aloe Vera about a year ago and it has helped me get rid of the stinging feeling when emptying my bladder.
I also have regular
physiotherapy
and do gentle exercise (yoga, swimming). I started taking Desert Harvest Aloe Vera about a year ago and it has helped me get rid of the stinging feeling when emptying my bladder.
Salmonfishing
in
Pelvic Pain Support Network
3 days 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
5 months ago
physiotherapy
I got a neuro physio after 1 year waiting list. I’ve just had 4th session and she has discharged me saying my balance won’t improve. I can do the basic balance exercises she gave me and the basic hand ones. My goals were to be able to walk on beach and a way of dealing with a few steps without rails.
I got a neuro physio after 1 year waiting list. I’ve just had 4th session and she has discharged me saying my balance won’t improve. I can do the basic balance exercises she gave me and the basic hand ones. My goals were to be able to walk on beach and a way of dealing with a few steps without rails.
Sea_
in
Ataxia 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
3 months ago
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