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Intramuscular Steroid injections
I suffer from Psoriatic Arthritis with flare ups normally occurring only once a year, although they now seem to be increasing in frequency. I am not currently on any regular meds for this because of the infrequency of flare ups, although I have in the past had intramuscular injections of kenalog. So
I suffer from Psoriatic Arthritis with flare ups normally occurring only once a year, although they now seem to be increasing in frequency. I am not currently on any regular meds for this because of the infrequency of flare ups, although I have in the past had intramuscular injections of kenalog. So
Soreknees2016
in
NRAS
7 years ago
steroid injection
hi im going for steroid injection in my spin in weeks time, but its all the way in sheffield, i am worried its only natural but also its so far away, if i book hospital transport home as my daughter will be with me can she come in hospital transport anyone no plz ?
hi im going for steroid injection in my spin in weeks time, but its all the way in sheffield, i am worried its only natural but also its so far away, if i book hospital transport home as my daughter will be with me can she come in hospital transport anyone no plz ?
jackie40luke
in
Fibromyalgia Action UK
7 years ago
Steroid injections in knees
Hello everyone hope you are all well. Billypam hope you are feeling a little better. I went to my 4 monthly rheumatology appt with the consultant. Basically I had to have steroid injections in both knees. Also a steroid injection I think depomedrone, for the whole body. Then my methotrexate has been
Hello everyone hope you are all well. Billypam hope you are feeling a little better. I went to my 4 monthly rheumatology appt with the consultant. Basically I had to have steroid injections in both knees. Also a steroid injection I think depomedrone, for the whole body. Then my methotrexate has been
rokia
in
NRAS
7 years ago
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Is this normal
Hi, I have been diagnosed with endometriosis about 10 years ago.. I suffer from chronic pain, but over past few years I am unable to sit for long on a chair due to incredible pain in my coccyx and just recently I have terrible pain down both my legs and Into feet.. I have had numerous MRIs and steroid
Hi, I have been diagnosed with endometriosis about 10 years ago.. I suffer from chronic pain, but over past few years I am unable to sit for long on a chair due to incredible pain in my coccyx and just recently I have terrible pain down both my legs and Into feet.. I have had numerous MRIs and steroid
Rachiedw
in
Endometriosis UK
7 years ago
UPDATE
Hi everybody, well 2 weeks ago had a hospital appt with my consultant who gave me news that my lungs are stabilised at the moment, although transference is running at 63 %, I know that's not going to improve but at least it is stabilised!! Had a pelvic x-ray because of pain in hips and groin, oh and
Hi everybody, well 2 weeks ago had a hospital appt with my consultant who gave me news that my lungs are stabilised at the moment, although transference is running at 63 %, I know that's not going to improve but at least it is stabilised!! Had a pelvic x-ray because of pain in hips and groin, oh and
fairy56
in
Scleroderma & Raynaud's UK (SRUK)
7 years ago
Injections
Hi I am due to have a steroid injection in my shoulder don't normally worrie about injections but relly nervous about this one has have heard and know people like my sister who had the same in the same place and said it's relly painfull relly worried any answers would be appreciated
Hi I am due to have a steroid injection in my shoulder don't normally worrie about injections but relly nervous about this one has have heard and know people like my sister who had the same in the same place and said it's relly painfull relly worried any answers would be appreciated
Dave0410
in
NRAS
7 years ago
Legs
I have written before about my legs but I am still non the wiser. Diagnosed with pmr in 2014, diagnosed with seronegative RA, then Inflammatory arthritis in the months following. They seem to have dismissed the pmr at rheumatology and the last man I saw decided it is all OA. I know that is ridiculous
I have written before about my legs but I am still non the wiser. Diagnosed with pmr in 2014, diagnosed with seronegative RA, then Inflammatory arthritis in the months following. They seem to have dismissed the pmr at rheumatology and the last man I saw decided it is all OA. I know that is ridiculous
Bailybiscuit
in
PMRGCAuk
7 years ago
Just seen lupus specialist prescribed new tablets
Hey all I have not improved since my last review in Nov, in fact as well as my voice being strained and chest pains, I now have protein in my urine. The specialist has prescribed me Mycophenolate mofetil tablets to take as well as Hydrox and steroid. I also had a high dose steroid injections. May I
Hey all I have not improved since my last review in Nov, in fact as well as my voice being strained and chest pains, I now have protein in my urine. The specialist has prescribed me Mycophenolate mofetil tablets to take as well as Hydrox and steroid. I also had a high dose steroid injections. May I
LSurtees
in
LUPUS UK
7 years ago
Spinal fusion L5 S1
Hi I am new here and wanted to see if I could get some more info. I have had severe continued pain in my lower pack for over 2 years now. I have tried steroid injections, nerve blocks, PT, pain meds, nerve meds, tens unit etc and no relief. I had my MRI and Dr thinks if the pain is this bad and nothing
Hi I am new here and wanted to see if I could get some more info. I have had severe continued pain in my lower pack for over 2 years now. I have tried steroid injections, nerve blocks, PT, pain meds, nerve meds, tens unit etc and no relief. I had my MRI and Dr thinks if the pain is this bad and nothing
jennwalton73
in
Pain Concern
7 years ago
Still in pain
Hi everyone I am still in pain after being on my current medication for almost 12 months. Having another steroid injection on Thursday. When I tell my consultant I am still in lots of pain he just says my inflammation is down and we have to give the medication time to work and doesn't explain anything
Hi everyone I am still in pain after being on my current medication for almost 12 months. Having another steroid injection on Thursday. When I tell my consultant I am still in lots of pain he just says my inflammation is down and we have to give the medication time to work and doesn't explain anything
Lomo1964
in
NRAS
7 years ago
Doctor at Pain Clinic
I hope everyone is feeling as well as can be. I went to see the doctor after he did the burning of the nerves that was done on the 1st Nov 16. When I was called in it was by a doctor I had not seen before and he had no Idea about me. He kept looking at the notes and writing things down and said very
I hope everyone is feeling as well as can be. I went to see the doctor after he did the burning of the nerves that was done on the 1st Nov 16. When I was called in it was by a doctor I had not seen before and he had no Idea about me. He kept looking at the notes and writing things down and said very
Jan101
in
NRAS
7 years ago
Need Help & Assistance
Hi! I know I don't answer posts much lately because of family needs and then school started and it's kicking my butt!!!!!! Sorry it will be long to read but had to write background so you can understand my questions. Thanks!! For a few weeks I have had swelling in my left leg and foot but ironically
Hi! I know I don't answer posts much lately because of family needs and then school started and it's kicking my butt!!!!!! Sorry it will be long to read but had to write background so you can understand my questions. Thanks!! For a few weeks I have had swelling in my left leg and foot but ironically
KATC1972
in
My MSAA Community
7 years ago
Newbie update
Hi All 😘 I do hope you are all comfortable and not bothered too much by the pain. Well, just wanted to thank you all for your kind words and for all the useful advice in this thread and in the community overall... my update: After my initial consultation with my Rheumatologist Mr Wright (Wed 1 Feb
Hi All 😘 I do hope you are all comfortable and not bothered too much by the pain. Well, just wanted to thank you all for your kind words and for all the useful advice in this thread and in the community overall... my update: After my initial consultation with my Rheumatologist Mr Wright (Wed 1 Feb
Stats12
in
NRAS
7 years ago
Steroid Injections
Hi I hope everyone is in a good place. Just a quick question for anyone who has had a steroid injection (in the buttock not into a joint). How long did the benefits of the jab last? I had one 3 weeks ago but pain / stiffness / swelling and fatigue are making an unwelcome return already. Has the steroid
Hi I hope everyone is in a good place. Just a quick question for anyone who has had a steroid injection (in the buttock not into a joint). How long did the benefits of the jab last? I had one 3 weeks ago but pain / stiffness / swelling and fatigue are making an unwelcome return already. Has the steroid
TTCC
in
NRAS
7 years ago
Shingles
My partner has been diagnosed with shingles today. Is there any risk to myself , I have lupus Hughes and raynauds. I had a steroid injection 3 weeks ago and I have had chicken pox as a child
My partner has been diagnosed with shingles today. Is there any risk to myself , I have lupus Hughes and raynauds. I had a steroid injection 3 weeks ago and I have had chicken pox as a child
clova
in
LUPUS UK
7 years ago
Methotrexate and painkillers
So my regular methotrexate query for those with more experience - I'm struggling a bit this evening with really painful tendons/joints especially in my hips and elbows. It's that really annoying pain where no matter what you do you just can't get comfortable and my shoulders are quite sharp pain. I don't
So my regular methotrexate query for those with more experience - I'm struggling a bit this evening with really painful tendons/joints especially in my hips and elbows. It's that really annoying pain where no matter what you do you just can't get comfortable and my shoulders are quite sharp pain. I don't
Mifford
in
LUPUS UK
7 years ago
Casey09
Hi I've had bac probs for almost 7yrs ,I've had al the treatment s ,4 steroid injections ,physio ,I'm on pregablin an morphine ,my pains are realy bad my joints are sore ,keep goin bac to my GP an no help at all ,I'm at my wit's end ,bein referred bac to pain clinic ,they won't do anything ,
Hi I've had bac probs for almost 7yrs ,I've had al the treatment s ,4 steroid injections ,physio ,I'm on pregablin an morphine ,my pains are realy bad my joints are sore ,keep goin bac to my GP an no help at all ,I'm at my wit's end ,bein referred bac to pain clinic ,they won't do anything ,
Casey09_
in
Pain Concern
7 years ago
SPINE PROCEDURE
I went to see my spine specialist on Tuesday and he has offered to do steroid injections in my spine. This will be the 4th procedure on my spine. I have had vertbroplasty, lazor to my nerves and steroids injections to the bottom of my spine. I would prefer this to the lazor of the nerves as I will only
I went to see my spine specialist on Tuesday and he has offered to do steroid injections in my spine. This will be the 4th procedure on my spine. I have had vertbroplasty, lazor to my nerves and steroids injections to the bottom of my spine. I would prefer this to the lazor of the nerves as I will only
Jan101
in
Fibromyalgia Action UK
7 years ago
Anyone else get weakness/heaviness in legs and arms when flaring???
The main characteristic of my major flares seems to be weakness and heaviness of my limbs, to the point that all my movements and walking pace slow down to the speed of a 90 year old (I'm 35). It's an effort to stay standing up or walk further than my kitchen. Does anyone else get this? I have UCTD
The main characteristic of my major flares seems to be weakness and heaviness of my limbs, to the point that all my movements and walking pace slow down to the speed of a 90 year old (I'm 35). It's an effort to stay standing up or walk further than my kitchen. Does anyone else get this? I have UCTD
LuckyJC
in
LUPUS UK
7 years ago
Rheumy keeps saying everything is due to fibromyligia not my RA & I don't think I even have fibromyligia
Been diagnosed with RA just over a year but I had symptoms for at least 2 years previously. 4 years ago had diagnosis of underactive thyroid and docs made me believe all symptoms were due to that. The RA is everywhere, no joint has been missed!!! I'm on leflunomide (off MTX as awful side effects). My
Been diagnosed with RA just over a year but I had symptoms for at least 2 years previously. 4 years ago had diagnosis of underactive thyroid and docs made me believe all symptoms were due to that. The RA is everywhere, no joint has been missed!!! I'm on leflunomide (off MTX as awful side effects). My
RAgemz81
in
NRAS
7 years ago
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