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Tendonitis
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GVHD and skin dryness.
Unfortunately I have chronic graft versus host desiese of the skin and have controlled it with a steroid cream since my ASCT a year and a half ago. My only issue currently is that I find it hard to look after the skin on my hands and feet that are dry and chapped. I have used quite a few emoluments
Unfortunately I have chronic graft versus host desiese of the skin and have controlled it with a steroid cream since my ASCT a year and a half ago. My only issue currently is that I find it hard to look after the skin on my hands and feet that are dry and chapped. I have used quite a few emoluments
Kraskie1915
in
CLL Support
5 months ago
Heart meds and sunlight sensitivity
I am currently taking these post cardioversion (procedure successful early November 2022) meds: morning: Entresto sacubitril/valsartan 24mg/26mg Apixiban 5mg Bisoprolol Fumarate 5 mg Spironolactone 25mg Dapagliflozin 10mg evening: Entresto sacubitril/valsartan 24mg/26mg Apixiban 5mg Bisoprolol
I am currently taking these post cardioversion (procedure successful early November 2022) meds: morning: Entresto sacubitril/valsartan 24mg/26mg Apixiban 5mg Bisoprolol Fumarate 5 mg Spironolactone 25mg Dapagliflozin 10mg evening: Entresto sacubitril/valsartan 24mg/26mg Apixiban 5mg Bisoprolol
thurstonloveseva
in
AF Association
5 months ago
Severe Dilated Cardiomyopathy with heart failure - and now AF - anyone else out there like me?
I have severe dilated cardiomyopathy and heart failure but had been doing well despite the inner chaos. I played tennis 5 times a week, kicked a football with my children, took long walks, and was able to run up the stairs to my flat. After the metapneumovirus triggered AF 6 weeks ago I stopped being
I have severe dilated cardiomyopathy and heart failure but had been doing well despite the inner chaos. I played tennis 5 times a week, kicked a football with my children, took long walks, and was able to run up the stairs to my flat. After the metapneumovirus triggered AF 6 weeks ago I stopped being
Jishuang44
in
AF Association
5 months ago
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T3 side effects
Feels more like
tendonitis
than arthritis type pain. I have a blood test booked in 2 days time so interested to see my results. Definitely not feeling the benefits yet.
Feels more like
tendonitis
than arthritis type pain. I have a blood test booked in 2 days time so interested to see my results. Definitely not feeling the benefits yet.
Flamingo60
in
Thyroid UK
29 days ago
🎖️🏃🏃♀️⭐️⭐️⭐️ JANUARY 2024 GRADUATION BADGES HERE ⭐️⭐️⭐️🎖️🏃🏃♀️
Woooo hooooo!!! You’re here!! You’ve made it and your smile is infectious!!! Welcome to my new years post…who’s badge is going to be the first one I pin on this year?? You must be so so proud of yourself & rightly so…we’re extremely proud of you, you have come such a long way since those first, sometimes
Woooo hooooo!!! You’re here!! You’ve made it and your smile is infectious!!! Welcome to my new years post…who’s badge is going to be the first one I pin on this year?? You must be so so proud of yourself & rightly so…we’re extremely proud of you, you have come such a long way since those first, sometimes
Mummycav
Administrator
in
Couch to 5K
5 months ago
Sprinter returning after THR
Has anyone returned to sprinting (60m, 100m, 200m) after a total hip replacement. I am 69 and just over 2 years since the operation and wondering if anyone has or knows of experience in returning to sprinting after a THR ? I have just over a year before going into the 70-74 age group and potentially
Has anyone returned to sprinting (60m, 100m, 200m) after a total hip replacement. I am 69 and just over 2 years since the operation and wondering if anyone has or knows of experience in returning to sprinting after a THR ? I have just over a year before going into the 70-74 age group and potentially
oldspeed
in
Couch to 5K
5 months ago
Catching a cold when you have fibro - turns out it’s COVID fml
Do you find that when you catch a cold you are affected much worse than other people around you? I never get ‘just a sniffle’. I always say I’m a woman who gets man flu. My partner went to work right through his cold even though he felt quite rough. I just got up to make a drink and dragging my body
Do you find that when you catch a cold you are affected much worse than other people around you? I never get ‘just a sniffle’. I always say I’m a woman who gets man flu. My partner went to work right through his cold even though he felt quite rough. I just got up to make a drink and dragging my body
Brigga
in
Fibromyalgia Action UK
6 months ago
central sensitivity syndrome
Has anyone heard of CSS. My dr said this can cause restless legs and stems from childhood trauma. Sort of crappy to think that yes, my childhood was super traumatic and potentially from that I still need to suffer.
Has anyone heard of CSS. My dr said this can cause restless legs and stems from childhood trauma. Sort of crappy to think that yes, my childhood was super traumatic and potentially from that I still need to suffer.
Jenevewill
in
Restless Legs Syndrome
6 months ago
Not been here for a while but I need help....
I've been running for quite a while after completing the C25K course. I've suffered many injuries which are so frustrating but I've tried to be sensible and thankfully I've always recovered. I'm a casual runner, not really interested in races or PB,s but run for weight control and because I enjoy it.
I've been running for quite a while after completing the C25K course. I've suffered many injuries which are so frustrating but I've tried to be sensible and thankfully I've always recovered. I'm a casual runner, not really interested in races or PB,s but run for weight control and because I enjoy it.
Pete1w
Graduate
in
Couch to 5K
6 months ago
learning to live with GCA/PMR
Hi everyone I've never joined an online forum before but the PMRGCAuk helpline said this was a good one so here goes. I was diagnosed with GCA and PMR in late August this year and am just about starting to feel more like myself now that the symptoms are being controlled with steroids. So I'm starting
Hi everyone I've never joined an online forum before but the PMRGCAuk helpline said this was a good one so here goes. I was diagnosed with GCA and PMR in late August this year and am just about starting to feel more like myself now that the symptoms are being controlled with steroids. So I'm starting
bookbear68
in
PMRGCAuk
6 months ago
Stay on the IC extended😬
This time, it's peroneal
tendonitis
(no, me neither 🤔😏). Hi gang, those who know my history will know that I've spent a lot of time unable to run with one thing and another - breaking my ankle in the first lockdown being the most dramatic event.
This time, it's peroneal
tendonitis
(no, me neither 🤔😏). Hi gang, those who know my history will know that I've spent a lot of time unable to run with one thing and another - breaking my ankle in the first lockdown being the most dramatic event.
grumpyoldgirl
Graduate
in
Couch to 5K
1 year ago
Is this chronic tendonitis or chronic repetitive strain injury in wrists or is it My CRPS/RSD?
I've had an EMG which tested positive for mild carpal tunnel in both wrists and I even had an MRI on one of my wrists and it did not show up any kind of
tendonitis
or
tendonitis
or any breaks or anything.
I've had an EMG which tested positive for mild carpal tunnel in both wrists and I even had an MRI on one of my wrists and it did not show up any kind of
tendonitis
or
tendonitis
or any breaks or anything.
Hidden
in
Pain Concern
7 months ago
How much pred to take?
On pred since then, started at 15mg and the lowest I've ever manage to taper to is 3mg.2023 was a very stressful year and I needed extra pred for trochanteric bursitis &
tendonitis
. In November, I was in hospital with sepsis 😳, lucky to have survived.
On pred since then, started at 15mg and the lowest I've ever manage to taper to is 3mg.2023 was a very stressful year and I needed extra pred for trochanteric bursitis &
tendonitis
. In November, I was in hospital with sepsis 😳, lucky to have survived.
SQQQ
in
PMRGCAuk
4 months ago
R-alpha Lipoic Acid
I read in the Autumn 2023 ME Association magazine that R-Alpha Lipoic Acid could be helpful for someone with ME. I use Methotrexate for my RA. Has anyone used this supplement with Methotrexate?
I read in the Autumn 2023 ME Association magazine that R-Alpha Lipoic Acid could be helpful for someone with ME. I use Methotrexate for my RA. Has anyone used this supplement with Methotrexate?
64notout
in
NRAS
7 months ago
What could be causing pain in the testicle?
Share you with my opinions. There are many reasons for testicular pain, the most common reason is chronic prostatitis, epididymitis and varicocele. Testicular pain is one of the main symptoms of chronic prostatitis. The main symptom of acute epididymitis is also testicular pain. If not treated for a
Share you with my opinions. There are many reasons for testicular pain, the most common reason is chronic prostatitis, epididymitis and varicocele. Testicular pain is one of the main symptoms of chronic prostatitis. The main symptom of acute epididymitis is also testicular pain. If not treated for a
Henry0831
in
Pain Concern
7 months ago
Vagus Nerve Stimulation for RLS
https://pubmed.ncbi.nlm.nih.gov/37846650/ An interesting study on Vagus Nerve Stumulation on 15 drug resistant RLS patients showed significant improvements in quality of life scale and that 2 of the 15 reduced their IRLSS below 5. The study doesn't say what meds the patients were taking. Sadly, they
https://pubmed.ncbi.nlm.nih.gov/37846650/ An interesting study on Vagus Nerve Stumulation on 15 drug resistant RLS patients showed significant improvements in quality of life scale and that 2 of the 15 reduced their IRLSS below 5. The study doesn't say what meds the patients were taking. Sadly, they
Joolsg
in
Restless Legs Syndrome
7 months ago
Moving to MTX after 9 years of prednisolone?
The last year has been very stressful (bereavements, sepsis, house move) and I have had 3 episodes of joint pain - trochanteric bursitis x 1 and two episodes of
tendonitis
/ psoriatic arthropathy in my hand/ finger joints.
The last year has been very stressful (bereavements, sepsis, house move) and I have had 3 episodes of joint pain - trochanteric bursitis x 1 and two episodes of
tendonitis
/ psoriatic arthropathy in my hand/ finger joints.
SQQQ
in
PMRGCAuk
3 months ago
I would like to ask…
More recently, before increasing my dose to 87.5mcg, I had severe and sudden-onset elbow pain/
tendonitis
in both arms and weakness in my arms (with no obvious cause/injury) that made them feel like there was no power or strength in them. This has now also resolved completely.
More recently, before increasing my dose to 87.5mcg, I had severe and sudden-onset elbow pain/
tendonitis
in both arms and weakness in my arms (with no obvious cause/injury) that made them feel like there was no power or strength in them. This has now also resolved completely.
JoJoloveschocolate
in
Thyroid UK
6 days ago
PA, or just getting older?
I wonder if I can blame my B12 deficiency for my sciatica and wrist
tendonitis
? I had thought of them as unrelated. In a way this would be good news as it means they might improve as I get my B12 levels back up.
I wonder if I can blame my B12 deficiency for my sciatica and wrist
tendonitis
? I had thought of them as unrelated. In a way this would be good news as it means they might improve as I get my B12 levels back up.
Permexpi
in
Pernicious Anaemia Society
7 months ago
Out of action and a bit gutted...
Went to see a physio yesterday who said it was
tendonitis
but was confident it would improve if I did the exercises and looked after my back. So, my question is: has anyone had a similar injury but made a full recovery?
Went to see a physio yesterday who said it was
tendonitis
but was confident it would improve if I did the exercises and looked after my back. So, my question is: has anyone had a similar injury but made a full recovery?
Neonlemon1950
in
Bridge to 10K
27 days ago
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