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plantar fasciitis - corticosteroid
I have had plantar fasciitis for about 12 months and in that time have had one injection of a corticosteroid in the heal of the foot. The pain is now affecting quality of life, walking the dog just causes too much pain, therefore I am trying to obtain another corticosteroid injection. My GP is concerned
I have had plantar fasciitis for about 12 months and in that time have had one injection of a corticosteroid in the heal of the foot. The pain is now affecting quality of life, walking the dog just causes too much pain, therefore I am trying to obtain another corticosteroid injection. My GP is concerned
RobertCLL
in
CLL Support
4 years ago
Vertebral fractures
Hello everyone. I'm new here and am exploring help and advice for my 88 year old mum. Mum was diagnosed with RA about 6 years ago and has been taking Methotrexate for this. Mum was never able to come of prednisolone completely which she had to start when she was newly diagnosed and though her dose is
Hello everyone. I'm new here and am exploring help and advice for my 88 year old mum. Mum was diagnosed with RA about 6 years ago and has been taking Methotrexate for this. Mum was never able to come of prednisolone completely which she had to start when she was newly diagnosed and though her dose is
PaulaE
in
Bone Health and Osteoporosis UK
4 years ago
Temporal Arteritis
111 then a Visit to A&E I helped with the shopping yesterday at about 6 after cleaning and loading I started to get a severe headache which I thought was at first a migraine but then it all got a bit weird. The pain was on the outside of my head and very painful to touch as well? by 10 pm I was getting
111 then a Visit to A&E I helped with the shopping yesterday at about 6 after cleaning and loading I started to get a severe headache which I thought was at first a migraine but then it all got a bit weird. The pain was on the outside of my head and very painful to touch as well? by 10 pm I was getting
Offcut
in
Atrial Fibrillation Support
4 years ago
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First Post from a newbie
Hi all I was diagnosed with PMR a few weeks ago now after a trip to the walk in centre when, what they thought was an OA flare let me in severe pain and pretty much unable to walk or move. Hospital, actually , didn't get the diagnosis but my doctors did the following week. I was started on Prednisone
Hi all I was diagnosed with PMR a few weeks ago now after a trip to the walk in centre when, what they thought was an OA flare let me in severe pain and pretty much unable to walk or move. Hospital, actually , didn't get the diagnosis but my doctors did the following week. I was started on Prednisone
Bcol
in
PMRGCAuk
4 years ago
Help please
Hi iv suffered with lumber spinal stenosis for 15yrs and now been told iv bilateral avascular necrosis of the hip with secondary arthritis My doctor decided to put me on tramadol, what I need help with.. can anyone tell me if I can still take Gabapentin naproxen Co-codamol and sertaline (anti depressants
Hi iv suffered with lumber spinal stenosis for 15yrs and now been told iv bilateral avascular necrosis of the hip with secondary arthritis My doctor decided to put me on tramadol, what I need help with.. can anyone tell me if I can still take Gabapentin naproxen Co-codamol and sertaline (anti depressants
JEWEW
in
Pain Concern
4 years ago
PMR
I was diagnosed with PMR 3 years ago by GP. Blood test did not show PMR.I was Prescribed 15mg of Prednisilone and the pains in my shoulders and thighs disappeared. After 2 years my Blood pressure rose to 200/96 and was told to cut down the steroids gradually to zero. The pains returned. Rhematologist
I was diagnosed with PMR 3 years ago by GP. Blood test did not show PMR.I was Prescribed 15mg of Prednisilone and the pains in my shoulders and thighs disappeared. After 2 years my Blood pressure rose to 200/96 and was told to cut down the steroids gradually to zero. The pains returned. Rhematologist
sailboatstewart
in
PMRGCAuk
4 years ago
Update need my knowledgeable friends advice again 🙄
Hello well I've not posted for a while as I've been having blood tests and ferritin level tests for my RLS. Well on my first blood test gp forgot to test for the ferritin level. But gave me ferrous sulphate tablets 200mg 1 a day which gave me severe constipation (is this the same as iron?) and I put
Hello well I've not posted for a while as I've been having blood tests and ferritin level tests for my RLS. Well on my first blood test gp forgot to test for the ferritin level. But gave me ferrous sulphate tablets 200mg 1 a day which gave me severe constipation (is this the same as iron?) and I put
Netball-50
in
Restless Legs Syndrome
4 years ago
Co codamol and Afib
You’ve guessed it....can I take Co-codamol with Afib? I’m on Bisoprolol.
You’ve guessed it....can I take Co-codamol with Afib? I’m on Bisoprolol.
Julia7
in
AF Association
4 years ago
CLL & the Corona virus
I have been on the FLAIR drug trials for five years, taking Ibrutinib, plus
Co
-
Trimoxazole
and Aciclovir. My blood cancer has gone into remission, but there are still enough bad cells for me to continue on the drugs. Recently I developed a dry cough and inflamed vocal cords.
I have been on the FLAIR drug trials for five years, taking Ibrutinib, plus
Co
-
Trimoxazole
and Aciclovir. My blood cancer has gone into remission, but there are still enough bad cells for me to continue on the drugs. Recently I developed a dry cough and inflamed vocal cords.
hazelmark
in
CLL Support
4 years ago
What’s the reason for my pains?
New pains doc doesn’t think the PA causes and just says it must fibromyalgia I just don’t know Pain in hands in morning hurt to clench them, pain under soles of feet when get up struggle to walk, painful knees, pain on right in lower back/hip area any ideas please just tried two co codamol today Tracey
New pains doc doesn’t think the PA causes and just says it must fibromyalgia I just don’t know Pain in hands in morning hurt to clench them, pain under soles of feet when get up struggle to walk, painful knees, pain on right in lower back/hip area any ideas please just tried two co codamol today Tracey
Trace-67
in
Pernicious Anaemia Society
4 years ago
WEATHER IS CAUSING HAVOC TO BODY
Flippin weather. When the humidity started last week I could give Popeye a run for his money . Swelling more manageable but... yesterday with all the storms I became stiffer and this morning every joint and ligament is stiff and painful had to take co-codamol just to get out of bed. I can’t take any
Flippin weather. When the humidity started last week I could give Popeye a run for his money . Swelling more manageable but... yesterday with all the storms I became stiffer and this morning every joint and ligament is stiff and painful had to take co-codamol just to get out of bed. I can’t take any
Hidden
in
NRAS
4 years ago
GP Ignoring Me
I'm female mid 50s. I found out I had wildly fluctuating BP over 24 hours, a brain aneurysm, autoimmune thyroid disease, low Vit D (less than 20, UK measurements), raised parathyroid levels - all last year. I lost my 1st baby at week 17 due to placental abruption, 'severe' pre-eclampsia 2nd pregnancy
I'm female mid 50s. I found out I had wildly fluctuating BP over 24 hours, a brain aneurysm, autoimmune thyroid disease, low Vit D (less than 20, UK measurements), raised parathyroid levels - all last year. I lost my 1st baby at week 17 due to placental abruption, 'severe' pre-eclampsia 2nd pregnancy
RabbitMum_1965
in
Hughes Syndrome APS Forum
4 years ago
Can't honestly cope with the brokenness of me, completely and utterly at the end of my rope
Hi everyone, I have just joined this community. I have had M.E for 10 years now, and along with that comes the depression of having this debilitating illness steal my life, but these last three weeks have been just unbearable. I am so used to living with pain, and have also been suffering with PTSD
Hi everyone, I have just joined this community. I have had M.E for 10 years now, and along with that comes the depression of having this debilitating illness steal my life, but these last three weeks have been just unbearable. I am so used to living with pain, and have also been suffering with PTSD
Brandy4
in
Foggy's "Invisible Illness" Support
4 years ago
Pain a 1 year after surgery?
So I had my laparoscopic surgery to clear cysts for my stage 2/3 endometriosis. I had the mirena coil put in but I am still having to take co-codamol for prolonged and tiring pain in my pelvis and hips which makes the tops up r my legs ache. Anyone know if it’s worth going back to the gyne or if it’s
So I had my laparoscopic surgery to clear cysts for my stage 2/3 endometriosis. I had the mirena coil put in but I am still having to take co-codamol for prolonged and tiring pain in my pelvis and hips which makes the tops up r my legs ache. Anyone know if it’s worth going back to the gyne or if it’s
Runner365
in
Endometriosis UK
4 years ago
Removal of Opiod painkillersong term.
I was on Co-codamol for years for various conditions the main one being Tratatoric Bursitis. I was blantently told on collection of my prescription one day by "note" that i need to talk to my GP about long-term use. I made an appointment went to see my GP and in about a 10min consultation she asked me
I was on Co-codamol for years for various conditions the main one being Tratatoric Bursitis. I was blantently told on collection of my prescription one day by "note" that i need to talk to my GP about long-term use. I made an appointment went to see my GP and in about a 10min consultation she asked me
Ventorist11
in
Action on Pain
4 years ago
30+ years of worsening dysmenorrhea
Hi, I'm going to apologise in advance for the long one, but I guess I want to vent and see if anybody has experienced the same symptoms but had different treatment offered, or even a diagnosis? I half wonder if it's adenomyosis but until now just think it's "one of those things". What are my rights as
Hi, I'm going to apologise in advance for the long one, but I guess I want to vent and see if anybody has experienced the same symptoms but had different treatment offered, or even a diagnosis? I half wonder if it's adenomyosis but until now just think it's "one of those things". What are my rights as
Farleygirl
in
Pelvic Pain Support Network
4 years ago
My blood pressure varies enormously during the day, but nearly always in the normal zone of 120/80 to 90/60 is this anything to worry about?
My heart failure nurse has loaned me a blood pressure monitor so I can take my own blood pressure. I have been experiencing dizzy spells. I also have rheumatoid arthritis, this has flared up really badly during lockdown and I've not been able to access timely treatment. I've been in terrible pain
My heart failure nurse has loaned me a blood pressure monitor so I can take my own blood pressure. I have been experiencing dizzy spells. I also have rheumatoid arthritis, this has flared up really badly during lockdown and I've not been able to access timely treatment. I've been in terrible pain
GracieOS
in
British Heart Foundation
4 years ago
Back pain
Hi I have back pain long time ago 5 to 6 year I'm taken I take co codamol and not help me after one hour pain is back and chest pain same im waiting to reopen hospital again I cant sleep sametimes
Hi I have back pain long time ago 5 to 6 year I'm taken I take co codamol and not help me after one hour pain is back and chest pain same im waiting to reopen hospital again I cant sleep sametimes
Alios671
in
Pain Concern
4 years ago
Arm/wrist
I've got an apt 8the june with a rheumatologist. I've got a positive ana, raised esr, high rheumatoid factor and positive ccp. I'm petrified this pain is something like cancer. My right wrist started hurting and then left 2 lumps. Now I don't know if it's the lumps that are hurting or my actual wrist
I've got an apt 8the june with a rheumatologist. I've got a positive ana, raised esr, high rheumatoid factor and positive ccp. I'm petrified this pain is something like cancer. My right wrist started hurting and then left 2 lumps. Now I don't know if it's the lumps that are hurting or my actual wrist
Zipster369
in
NRAS
4 years ago
Mirapexin Prolonged-Release
I am back on the DA's. I have now been on Prolonged-Release Mirapexin (0.26mg) since 1st April and have been more or less RLS-free ever since! I hardly dare to say it. Before that I was on 1200 mg Gabapentin which did not work very well as I had to complement with Co-Dydramol every night. And before
I am back on the DA's. I have now been on Prolonged-Release Mirapexin (0.26mg) since 1st April and have been more or less RLS-free ever since! I hardly dare to say it. Before that I was on 1200 mg Gabapentin which did not work very well as I had to complement with Co-Dydramol every night. And before
Felicity21
in
Restless Legs Syndrome
4 years ago
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