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Coming off tramadol
On the 18th June I severely injured my foot fracturing my 2nd 3rd and 4th metatarsal and what's called a lisfranc injury where the mid foot is fractured and the ligament is damaged.I was prescribed co codmaol and tramadol both of these I worked my way up to maximum dose. I am not fully recovered but
On the 18th June I severely injured my foot fracturing my 2nd 3rd and 4th metatarsal and what's called a lisfranc injury where the mid foot is fractured and the ligament is damaged.I was prescribed co codmaol and tramadol both of these I worked my way up to maximum dose. I am not fully recovered but
Cornishlamp
in
Pain Concern
11 months ago
Hip pain
I have severe OP, had 5 compression fractures, 2 years of teriparatide, now on Raloxifene. Over the last week I’ve had nasty hip pain, much worse at night. It eases with exercise, is worse with sitting and standing. I’m generally quite active, I walk the dog every day and I’ve been doing standing and
I have severe OP, had 5 compression fractures, 2 years of teriparatide, now on Raloxifene. Over the last week I’ve had nasty hip pain, much worse at night. It eases with exercise, is worse with sitting and standing. I’m generally quite active, I walk the dog every day and I’ve been doing standing and
Nuthatch
in
Bone Health and Osteoporosis UK
11 months ago
Aviv HBOT
Well it looks impressive…but the cost OMG! “ Thank you for reaching out and expressing interest in Aviv Clinics. We’re excited for the opportunity to get to know you a little bit better. Aviv is a leader in brain and body performance. We treat a variety of conditions through the Aviv Medical Program
Well it looks impressive…but the cost OMG! “ Thank you for reaching out and expressing interest in Aviv Clinics. We’re excited for the opportunity to get to know you a little bit better. Aviv is a leader in brain and body performance. We treat a variety of conditions through the Aviv Medical Program
LeharLover62
in
Cure Parkinson's
11 months ago
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FREE 10 DAY ENDOMETRIOSIS EMPOWERMENT SUMMIT
I’ve just been sent this by one of the guest speakers, a US based pelvic health specialist. Thought it might be worth a look so I thought I’d share it with you all. FREE 10 DAY ENDOMETRIOSIS EMPOWERMENT SUMMIT Putting you in the driver's seat of endometriosis, so that you’re no longer hiding in
I’ve just been sent this by one of the guest speakers, a US based pelvic health specialist. Thought it might be worth a look so I thought I’d share it with you all. FREE 10 DAY ENDOMETRIOSIS EMPOWERMENT SUMMIT Putting you in the driver's seat of endometriosis, so that you’re no longer hiding in
Username12345678
in
Endometriosis UK
11 months ago
Cambridge area OP exercise class?
I have osteoporosis and would love to find a fun, regular, class run locally in the Cambridge area, which involves suitable weight resistance/core strength exercises and is aimed particularly at patients with OP (and run by a physio or someone who is knowledgeable about OP). Has anyone heard of such
I have osteoporosis and would love to find a fun, regular, class run locally in the Cambridge area, which involves suitable weight resistance/core strength exercises and is aimed particularly at patients with OP (and run by a physio or someone who is knowledgeable about OP). Has anyone heard of such
ranne21
in
Bone Health and Osteoporosis UK
11 months ago
Support: Anxiety about having a baby
Hello everyone, I've been suffering from chronic pain for about fifteen years now (half of my life) and it's really taken its toll. My wife is currently pregnant and I fluctuate between knowing I'm going to love this little bundle of joy as much as I can to feeling drained and terrified about failing
Hello everyone, I've been suffering from chronic pain for about fifteen years now (half of my life) and it's really taken its toll. My wife is currently pregnant and I fluctuate between knowing I'm going to love this little bundle of joy as much as I can to feeling drained and terrified about failing
Resqc
in
Pain Concern
11 months ago
Doing what is necessary....skipping Actemra
I just thought I'd share this experience in case others have to make the same decisions. I'd had shoulder surgery, replacement, on July 10th and had to wear what they call an immobilizer to keep my arms close to my body. The only way I could sleep at all was in a recliner. Next 6 weeks I spent most
I just thought I'd share this experience in case others have to make the same decisions. I'd had shoulder surgery, replacement, on July 10th and had to wear what they call an immobilizer to keep my arms close to my body. The only way I could sleep at all was in a recliner. Next 6 weeks I spent most
Grammy80
in
PMRGCAuk
11 months ago
Cortisone Injections?
Hi Does anyone have information on whether one can receive cortisone shots for various injuries unrelated to PC without adversely impacting one’s ADT treatment? I am in physical therapy for an injured shoulder and recently had a cortisone shot and forgot to consult my MO before receiving it. I was
Hi Does anyone have information on whether one can receive cortisone shots for various injuries unrelated to PC without adversely impacting one’s ADT treatment? I am in physical therapy for an injured shoulder and recently had a cortisone shot and forgot to consult my MO before receiving it. I was
jfoesq
in
Advanced Prostate Cancer
11 months ago
Finally some progress
Those who followed our Journey, know this is such a painful process of grief. Two weeks ago, the hospital wrote it would not change the factual information in my wife's chart. In her chart it had been written she had Biopys proven Nash Cirrhosis, which led doctors looking at ultrasounds that said
Those who followed our Journey, know this is such a painful process of grief. Two weeks ago, the hospital wrote it would not change the factual information in my wife's chart. In her chart it had been written she had Biopys proven Nash Cirrhosis, which led doctors looking at ultrasounds that said
Wolivere
in
British Liver Trust
11 months ago
Angian
Hi I am new to this group a little worried confused by the diagnosis, I was encouraged by my physio therapist about strange chest pains I was having for more than a decade thinking it was something else relating too fibromyalgia thanks too her insistence it helped a lot as we have such limited times
Hi I am new to this group a little worried confused by the diagnosis, I was encouraged by my physio therapist about strange chest pains I was having for more than a decade thinking it was something else relating too fibromyalgia thanks too her insistence it helped a lot as we have such limited times
Hel52
in
British Heart Foundation
11 months ago
sleepless nights
Hello🙋♀️. This is my first posting. Can I say how very informative I think this site is and I do hope someone can help me with my problem of not sleeping well at night…. I have had PMR for 5 years through this journey I’ve been prescribed Pred/MTX/& now anti-inflammatories. I am not on any medication
Hello🙋♀️. This is my first posting. Can I say how very informative I think this site is and I do hope someone can help me with my problem of not sleeping well at night…. I have had PMR for 5 years through this journey I’ve been prescribed Pred/MTX/& now anti-inflammatories. I am not on any medication
Suffolkpolly
in
PMRGCAuk
11 months ago
Cryotherapy
Has anyone tried cryotherapy for PMR? I’d be interested to know as it’s supposed to be reduce inflammation (as well as other benefits) . I am embedded in the football world and the physio of a club suggested it to me saying he thought it might help. Any thoughts?
Has anyone tried cryotherapy for PMR? I’d be interested to know as it’s supposed to be reduce inflammation (as well as other benefits) . I am embedded in the football world and the physio of a club suggested it to me saying he thought it might help. Any thoughts?
Windy183
in
PMRGCAuk
1 year ago
Inspirational old post on exercise
Gang. I’ve been a bit down recently. Post operative blues maybe but I think my belief that I’m too poorly to exercise has contributed. I can maybe mange 10? Good minutes on the bike and feel worse than I did before upon finishing. Then I read through my old posts and found this gem from member Bert
Gang. I’ve been a bit down recently. Post operative blues maybe but I think my belief that I’m too poorly to exercise has contributed. I can maybe mange 10? Good minutes on the bike and feel worse than I did before upon finishing. Then I read through my old posts and found this gem from member Bert
jeeves19
in
Cure Parkinson's
1 year ago
PIP Reconsideration
I am so angry at the moment, i put an application in for change of circumstances at the beginning of the year because i had got so much worse, i filled in the form and had the telephone assessment, they then sent me a letter stating that amongst other things, that 'ON THE BASIS OF PROBABILITY' i was
I am so angry at the moment, i put an application in for change of circumstances at the beginning of the year because i had got so much worse, i filled in the form and had the telephone assessment, they then sent me a letter stating that amongst other things, that 'ON THE BASIS OF PROBABILITY' i was
catherine19611
in
Fibromyalgia Action UK
1 year ago
Another curved ball 😐
Things had been going well !I was at the gym 2x a week for strength and Cardio ( also included a 30 minute treadmill run) But I have hurt my back again . I think this is the 3rd of 4th time now since my heart attack in February. It's quite painful at the moment and I have needed to add co codamol to
Things had been going well !I was at the gym 2x a week for strength and Cardio ( also included a 30 minute treadmill run) But I have hurt my back again . I think this is the 3rd of 4th time now since my heart attack in February. It's quite painful at the moment and I have needed to add co codamol to
Instructor57
in
Strength & Flex
1 year ago
Doctor won't diagnose PMR
I'm absolutely certain that I have PMR. But my blood tests all came back normal, including the erythrocyte sedimentation rate and the inflammatory marker test, and I'm only 56. My GP has just left me on NSAIDS and paracetamol with physio. It's not working. How common is it to have PMR with no obvious
I'm absolutely certain that I have PMR. But my blood tests all came back normal, including the erythrocyte sedimentation rate and the inflammatory marker test, and I'm only 56. My GP has just left me on NSAIDS and paracetamol with physio. It's not working. How common is it to have PMR with no obvious
Creas
in
PMRGCAuk
1 year ago
PMR and Covid vaccine
Hello. I was diagnosed with PMR in March 2023 but had pain from October 2022 which GP put down to deferred pain from hip problem which I had seen a physio who gave me excercises which with hindsight cured the hip pain. I had Covid vaccine in early October and I didn’t make the connection at the time
Hello. I was diagnosed with PMR in March 2023 but had pain from October 2022 which GP put down to deferred pain from hip problem which I had seen a physio who gave me excercises which with hindsight cured the hip pain. I had Covid vaccine in early October and I didn’t make the connection at the time
Richard170356
in
PMRGCAuk
1 year ago
Words of hope for the newly diagnosed
I was diagnosed with asthma in 2001, then COPD in about 2010. About 4 years later, I was diagnosed with Bronchiectasis. Recently, my diagnosis has changed to Chronic Asthma with mild fixed airways disease and Bronchiectasis. I am writing this to let you know that such diagnoses don't mean everything
I was diagnosed with asthma in 2001, then COPD in about 2010. About 4 years later, I was diagnosed with Bronchiectasis. Recently, my diagnosis has changed to Chronic Asthma with mild fixed airways disease and Bronchiectasis. I am writing this to let you know that such diagnoses don't mean everything
MoyB
in
Lung Conditions Community Forum
1 year ago
Atypical meningioma 2
I was diagnosed with atypical meningioma on the 25th May 23 got it removed 31st May was on my right front lobe after operation face was swollen and weakness in left leg and arm was transferred back to other hospital for physio after one month I returned home and since my quality of life poor I have extreme
I was diagnosed with atypical meningioma on the 25th May 23 got it removed 31st May was on my right front lobe after operation face was swollen and weakness in left leg and arm was transferred back to other hospital for physio after one month I returned home and since my quality of life poor I have extreme
Clayden
in
Meningioma Support
1 year ago
mood supplement Advice
I am long term Hashis suffer. I was for years on thyroid s. But due to supply problems and the stress of sourcing meds getting some thyroid s that was not up to scratch led my levels to go out of whack. for a while I tied synthetic t3 but I felt that aggravated some one term joint pain issues. I suffer
I am long term Hashis suffer. I was for years on thyroid s. But due to supply problems and the stress of sourcing meds getting some thyroid s that was not up to scratch led my levels to go out of whack. for a while I tied synthetic t3 but I felt that aggravated some one term joint pain issues. I suffer
redjay999
in
Thyroid UK
1 year ago
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