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Depo-Medrol
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I’d like to introduce myself
New here and want to share my history with you. On Dec 2015 went to primary doctor due to sore throat and while there told him “oh by the way, my index finger is swollen and really hurts.” Sent me to a rheumatologist who thought I had psoriatic arthritis ( I have2 brothers with that) and started me
New here and want to share my history with you. On Dec 2015 went to primary doctor due to sore throat and while there told him “oh by the way, my index finger is swollen and really hurts.” Sent me to a rheumatologist who thought I had psoriatic arthritis ( I have2 brothers with that) and started me
sara1215
in
NRAS
6 years ago
HOT FLASHES – Why? What to do?
We often hear prostate cancer patients recommending to other prostate cancer patients regarding hot flashes: get “MEGACE!” – NOT for prostate cancer patients, my friends! Medical Oncologist Stephen B. Strum, M.D., FACP – renowned for his experience and expertise in the treatment of recurring and advanced
We often hear prostate cancer patients recommending to other prostate cancer patients regarding hot flashes: get “MEGACE!” – NOT for prostate cancer patients, my friends! Medical Oncologist Stephen B. Strum, M.D., FACP – renowned for his experience and expertise in the treatment of recurring and advanced
maack1
in
Advanced Prostate Cancer
6 years ago
Can prednisone cause hives.
A few days ago when taking my daily dose of 25 mg prednisone I started to feel panicky, complete with the feeling of chest tightness and some difficulty swallowing. At first I dismissed it, knowing prednisone can cause panic attacks and I am prone to them. Next day same symptoms, but noticed hives in
A few days ago when taking my daily dose of 25 mg prednisone I started to feel panicky, complete with the feeling of chest tightness and some difficulty swallowing. At first I dismissed it, knowing prednisone can cause panic attacks and I am prone to them. Next day same symptoms, but noticed hives in
Skenjin
in
NRAS
6 years ago
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Finally
No lupus RRMS had my fst series of solumedrol it's kicking my ass with late side effects but at least I know what expect next time. This will explain all the problems I've been experiencing. Good luck to all of you and thanks for the support.
No lupus RRMS had my fst series of solumedrol it's kicking my ass with late side effects but at least I know what expect next time. This will explain all the problems I've been experiencing. Good luck to all of you and thanks for the support.
I814u24u
in
LUPUS UK
6 years ago
Medication experiences ?!?
Hello hope all is as well as can be... I'm wondering about my pain meds like if I'm on the right ones I have been on quite a few over the years but ATM for my pain I'm on gabapentin which has benn upped an upped over the years and Marol... they do help I just feel drained even more which I feel I don't
Hello hope all is as well as can be... I'm wondering about my pain meds like if I'm on the right ones I have been on quite a few over the years but ATM for my pain I'm on gabapentin which has benn upped an upped over the years and Marol... they do help I just feel drained even more which I feel I don't
Hidden
in
Fibromyalgia Action UK
6 years ago
Finally
After almost three years and multiple doctors I finally have a diagnoses of RRMS. Now they want do genetic testing for what I don't know, it's expensive and I'm not going to pay for it. I get my first round of solumedrol Monday. Wish me luck. It's got allot of side effects. I'm very apprehensive
After almost three years and multiple doctors I finally have a diagnoses of RRMS. Now they want do genetic testing for what I don't know, it's expensive and I'm not going to pay for it. I get my first round of solumedrol Monday. Wish me luck. It's got allot of side effects. I'm very apprehensive
I814u24u
in
LUPUS UK
6 years ago
Lots of veins
I've been on medrol for over a year. I've noticed the skin on my hands has thi nes and my veins now show. My hands appear older than the rest of me. Also lots of spider veins on my face and legs. I'm hoping to get off medrol at some point. Will the spider veins on my face disappear after I'm off
I've been on medrol for over a year. I've noticed the skin on my hands has thi nes and my veins now show. My hands appear older than the rest of me. Also lots of spider veins on my face and legs. I'm hoping to get off medrol at some point. Will the spider veins on my face disappear after I'm off
Kdbarnes
in
NRAS
6 years ago
Exacerbation
I know there are many knowledgable people on this site so I'm hoping somebody can help. I have stage 4 emphysema. Cutting a long story short grandson came over with bad cough and 4 days later I develop a cough and the next day I was so sob I could hardly talk. Went to local GP who said chest infection
I know there are many knowledgable people on this site so I'm hoping somebody can help. I have stage 4 emphysema. Cutting a long story short grandson came over with bad cough and 4 days later I develop a cough and the next day I was so sob I could hardly talk. Went to local GP who said chest infection
CyprusPat
in
Lung Conditions Community Forum
6 years ago
LUNG INVOLEMENT IN CFS/FIBRO
Hi, My name is Nancy and I am new here. Have had fibro/cfs for 30 yrs Things have changed … Now I am having swallowing disorder. Had barium swallow/ manometry...all tests show that my esophagus has little motility. So I cough to the point of going to ER, and prednisone and IV solumedrol help to stop
Hi, My name is Nancy and I am new here. Have had fibro/cfs for 30 yrs Things have changed … Now I am having swallowing disorder. Had barium swallow/ manometry...all tests show that my esophagus has little motility. So I cough to the point of going to ER, and prednisone and IV solumedrol help to stop
JChris
in
Fibromyalgia Action UK
6 years ago
asking for help finding a doctor in Reading
Good day! I have lupus Nephritis. I have plans on visiting UK this coming July, I just wanted to know if you guys have idea how much this medicines will cost in UK? I am taking Cycloposporine, medrol, and hydroxycloquine, and I wanted to ask if you can recommend where I can see a doctor for Lupus in
Good day! I have lupus Nephritis. I have plans on visiting UK this coming July, I just wanted to know if you guys have idea how much this medicines will cost in UK? I am taking Cycloposporine, medrol, and hydroxycloquine, and I wanted to ask if you can recommend where I can see a doctor for Lupus in
jessa08
in
LUPUS UK
6 years ago
Having PMR Is Like Dancing With A Gorilla……..
On August 25, 2017, I began a treatment regimen which included weekly injections of
depo
-
medrol
that provided me with an average of 11.4 mg per day. Ten months later, I had tapered my daily dose to approximately 3.3 mg and switched over to 4.0 mg of oral medrol.
On August 25, 2017, I began a treatment regimen which included weekly injections of
depo
-
medrol
that provided me with an average of 11.4 mg per day. Ten months later, I had tapered my daily dose to approximately 3.3 mg and switched over to 4.0 mg of oral medrol.
Admiral06
in
PMRGCAuk
6 years ago
GETTING BETTER ALL THE TIME! TOO GOOD TO BE TRUE? VACULITIS, PMR/GCA??
Hi to All, My diagnosis has never been entirely clear. Antibodies to PR3 at 1.6 in September, 2016; given diagnosis of C- ANCA vasculitis, but no lung or kidney involvement that I could feel or see. I have always thought symptoms were PMR, (with family history of my maternal grandmother having had it
Hi to All, My diagnosis has never been entirely clear. Antibodies to PR3 at 1.6 in September, 2016; given diagnosis of C- ANCA vasculitis, but no lung or kidney involvement that I could feel or see. I have always thought symptoms were PMR, (with family history of my maternal grandmother having had it
Christophene47
in
Vasculitis UK
6 years ago
Mycophenolate and periods
I wonder if anyone has experienced a change in their cycle after starting mycophenolate. I have had troublesome periods for years, more so in the last two years as disease activity increased prior to diagnosis. I've had 6 months of depo provera injections which helped initially for a few weeks but
I wonder if anyone has experienced a change in their cycle after starting mycophenolate. I have had troublesome periods for years, more so in the last two years as disease activity increased prior to diagnosis. I've had 6 months of depo provera injections which helped initially for a few weeks but
flap7
in
LUPUS UK
6 years ago
Duloxetine no no....!
Well, I tried it and really didn't realise how depressed and anxious it made me until my husband mentioned it! I stuck with it for 3 weeks and that was it. I phoned the hospital and they noted yet another medication I've had a bad reaction to. The trouble is that the anxiety has hung on to the point
Well, I tried it and really didn't realise how depressed and anxious it made me until my husband mentioned it! I stuck with it for 3 weeks and that was it. I phoned the hospital and they noted yet another medication I've had a bad reaction to. The trouble is that the anxiety has hung on to the point
Blackwitch
in
Fibromyalgia Action UK
6 years ago
I can’t get relief from costochondritis
can’t take nsaids . I’m on tramadol (already on it for fibromyalgia) muscle relaxants and now gabapentin and lidocaine patches. I want to die ! This is terrible pain I get severe sternal chest tightness abs then my back feels like it will collapse. I was initially diagnosed with pericarditis ( now resolved
can’t take nsaids . I’m on tramadol (already on it for fibromyalgia) muscle relaxants and now gabapentin and lidocaine patches. I want to die ! This is terrible pain I get severe sternal chest tightness abs then my back feels like it will collapse. I was initially diagnosed with pericarditis ( now resolved
Nickel38
in
Fibromyalgia Action UK
6 years ago
I can’t get relief from costochondritis
. I can’t take nsaids . I’m on tramadol (already on it for fibromyalgia) muscle relaxants and now gabapentin and lidocaine patches. I want to die ! This is terrible pain I get severe sternal chest tightness abs then my back feels like it will collapse. I was initially diagnosed with pericarditis ( now
. I can’t take nsaids . I’m on tramadol (already on it for fibromyalgia) muscle relaxants and now gabapentin and lidocaine patches. I want to die ! This is terrible pain I get severe sternal chest tightness abs then my back feels like it will collapse. I was initially diagnosed with pericarditis ( now
Nickel38
in
My Fibro Community
6 years ago
PolyBursitis Rheumatica & Bacon Sandwiches
She gave me a
Depo
Medrol
shot and said not to taper for at least 2 months until I see her again. Unfortunately the
Depo
Medrol
shot that normally really helps was awful this time around. Jitters, sweats, nausea, weepy ect. NO MORE for me. I think too much too soon.
She gave me a
Depo
Medrol
shot and said not to taper for at least 2 months until I see her again. Unfortunately the
Depo
Medrol
shot that normally really helps was awful this time around. Jitters, sweats, nausea, weepy ect. NO MORE for me. I think too much too soon.
Marie1479
in
PMRGCAuk
6 years ago
Depo-provera shots/Tramadol/Hysterectomy
I had 2 depo-provera shots and scan after 5 months showed ovary stuck to uterus. For 3 weeks prior to scan had bleeding, severe pelvic, back & neck pain, no sex drive, stressed, anxiety attacks, pain when breathing, pressure in bowels, bloating and nausea. I would like to know why this occurred while
I had 2 depo-provera shots and scan after 5 months showed ovary stuck to uterus. For 3 weeks prior to scan had bleeding, severe pelvic, back & neck pain, no sex drive, stressed, anxiety attacks, pain when breathing, pressure in bowels, bloating and nausea. I would like to know why this occurred while
slindo19
in
Endometriosis UK
6 years ago
MS giving flu like symptoms
Hi everyone, I was wondering if anyone ever feels like they have the flu but really don’t? In the past I’ve realized that I start to have flu like symptoms prior & during a relapse which is not fun at all. The last several days my head feel heavy, I have a constant headache or dull pain behind my eyes
Hi everyone, I was wondering if anyone ever feels like they have the flu but really don’t? In the past I’ve realized that I start to have flu like symptoms prior & during a relapse which is not fun at all. The last several days my head feel heavy, I have a constant headache or dull pain behind my eyes
Eveliz
in
My MSAA Community
6 years ago
i was admitted with 4000 platelet count!!!
2 years back 2016 jaundice hepatatis A striked me den through it the bilribrium level reached to 51 count and then my haemglobin level came down to 4 frm 13 or 11. i was admitted and transfused blood twice.and was given treatment for autoimmuno disease and jaundice i was given predinasolone from 60mg
2 years back 2016 jaundice hepatatis A striked me den through it the bilribrium level reached to 51 count and then my haemglobin level came down to 4 frm 13 or 11. i was admitted and transfused blood twice.and was given treatment for autoimmuno disease and jaundice i was given predinasolone from 60mg
Platelet4000
in
ITP Support Association
6 years ago
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