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Duloxetine no no....!
Nothing really bad but I haven't been able to go out unless it's doctors or hospital (for my
Depo
-
Medrone
jab). It's a big day tomorrow. 'The Day of the PIP Assessment' 😱😱😱 I just hope I can make it out of the house!
Nothing really bad but I haven't been able to go out unless it's doctors or hospital (for my
Depo
-
Medrone
jab). It's a big day tomorrow. 'The Day of the PIP Assessment' 😱😱😱 I just hope I can make it out of the house!
Blackwitch
in
Fibromyalgia Action UK
6 years ago
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
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
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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
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
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
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
Having PMR Is Like Dancing With A Gorilla……..
The dance isn’t over until the gorilla decides it’s over. 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
The dance isn’t over until the gorilla decides it’s over. 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
Admiral06
in
PMRGCAuk
6 years ago
Coming off Depo-Provera
Hey guys, 3 months ago I had my first injection of DP. However I don’t feel like it agreed with me and I chose to not get my second injection. However while on the injection I did see a relief of my symptoms, since I was meant to have my other injections a couple of days ago I have felt dreadful. I
Hey guys, 3 months ago I had my first injection of DP. However I don’t feel like it agreed with me and I chose to not get my second injection. However while on the injection I did see a relief of my symptoms, since I was meant to have my other injections a couple of days ago I have felt dreadful. I
Georgia6206
in
Endometriosis UK
6 years ago
Even more fed up..
I wrote a post on here a few days ago about my ongoing diagnosis - I was told IBS but after seeing people's experiences on here and with similar symptoms I thought I would go back to my GP for advice on endometriosis and push for this diagnosis. After my appointment today,I wish I never went as it has
I wrote a post on here a few days ago about my ongoing diagnosis - I was told IBS but after seeing people's experiences on here and with similar symptoms I thought I would go back to my GP for advice on endometriosis and push for this diagnosis. After my appointment today,I wish I never went as it has
MiaW1
in
Endometriosis UK
6 years ago
So fed up 😞
Hi everyone! I am in desperate need of some advice and just someone to talk to really. I apologise for the long post. 6 months ago I experienced some abdominal pain which came on suddenly accompanied with nausea, back and leg pain as well as this feeling that I could not empty my bladder fully. 5 years
Hi everyone! I am in desperate need of some advice and just someone to talk to really. I apologise for the long post. 6 months ago I experienced some abdominal pain which came on suddenly accompanied with nausea, back and leg pain as well as this feeling that I could not empty my bladder fully. 5 years
MiaW1
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
Big blood clot
I’m waiting for my laparoscopy to look for endo, meanwhile my GP put me on Depo Provera (I’ve been on it for a year before) to manage my pain for my periods. Ive still suffered the same daily sharp pains and dull aches. I’m currently on day 13 of my period. It’s acrually got heavier and more painful
I’m waiting for my laparoscopy to look for endo, meanwhile my GP put me on Depo Provera (I’ve been on it for a year before) to manage my pain for my periods. Ive still suffered the same daily sharp pains and dull aches. I’m currently on day 13 of my period. It’s acrually got heavier and more painful
Loulou1994
in
Endometriosis UK
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
Newbie...Possible Adenomyosis (or Endometriosis or Fibroids)!
Hello, I'm new here and wondering if there are any who have had a similar situation to me. I am 43, had severely painful and long and heavy periods in my teens and 20s. Went on Depo Provera in my 30s for 5 years which was amazing. No pain, no period, no migrained. Came off it and still no pain or migraines
Hello, I'm new here and wondering if there are any who have had a similar situation to me. I am 43, had severely painful and long and heavy periods in my teens and 20s. Went on Depo Provera in my 30s for 5 years which was amazing. No pain, no period, no migrained. Came off it and still no pain or migraines
ElizabethC
in
Adenomyosis Advice Association
6 years ago
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