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Stopped Methotrexate being screened for Adalimumab
So after being on Methotrexate (injections) for 2 years since diagnosis and feeling dreadful on it (swollen fingers, nausea, constant headaches, depression) I last injected on 18th December 2023. Needless to say my RA is raging in every joint now! Just had a steroid injection and being screened for
So after being on Methotrexate (injections) for 2 years since diagnosis and feeling dreadful on it (swollen fingers, nausea, constant headaches, depression) I last injected on 18th December 2023. Needless to say my RA is raging in every joint now! Just had a steroid injection and being screened for
Amandaazz
in
NRAS
3 months ago
Paxlovid for “mild” COVID?
hello all. Just wondering what your experiences have been regarding taking Paxlovid. I realize you can’t advise but I would love to hear from fellow immune suppressed types like me. I have taken it before but when I had it last year I felt pretty bad and taking the Paxlovid was a no brainer. This time
hello all. Just wondering what your experiences have been regarding taking Paxlovid. I realize you can’t advise but I would love to hear from fellow immune suppressed types like me. I have taken it before but when I had it last year I felt pretty bad and taking the Paxlovid was a no brainer. This time
Bon1
in
NRAS
3 months ago
Back to square one
Hi, I first started having coughing problems back in November 2022 when I caught what I thought was just a bad cold or covid, I was getting phlegm stuck in my airways which was tough to get out when coughing, and sometimes I struggled to breath. Sometimes to the point where I actually cried because
Hi, I first started having coughing problems back in November 2022 when I caught what I thought was just a bad cold or covid, I was getting phlegm stuck in my airways which was tough to get out when coughing, and sometimes I struggled to breath. Sometimes to the point where I actually cried because
amygx25
in
Asthma Community Forum
3 months ago
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Septic Arthritis
Evening all, Has anyone experienced Septic Arthritis due to RA? What were your symptoms? I'm having the worst pain and swelling in my left knee that I've ever had. I had an emergency appt with Rheumatology this morning who drained fluid from my knee and sent off for testing as it was cloudy? They also
Evening all, Has anyone experienced Septic Arthritis due to RA? What were your symptoms? I'm having the worst pain and swelling in my left knee that I've ever had. I had an emergency appt with Rheumatology this morning who drained fluid from my knee and sent off for testing as it was cloudy? They also
Mummyto2x
in
NRAS
3 months ago
Septic Arthritis
Evening all, Has anyone experienced Septic Arthritis due to RA? What were your symptoms? I'm having the worst pain and swelling in my left knee that I've ever had. I had an emergency appt with Rheumatology this morning who drained fluid from my knee and sent off for testing as it was cloudy? They also
Evening all, Has anyone experienced Septic Arthritis due to RA? What were your symptoms? I'm having the worst pain and swelling in my left knee that I've ever had. I had an emergency appt with Rheumatology this morning who drained fluid from my knee and sent off for testing as it was cloudy? They also
Mummyto2x
in
FieryBones - RA Community
3 months ago
just to say thanks
thanks everyone who replied to me , about my Painful Knee, it’s lovely to know there’s help when u need it, still struggling, all over flare now , just come home from hospital after having all over steroid injection, hope it works, should be starting new drug soon, thank u all once again Kate x
thanks everyone who replied to me , about my Painful Knee, it’s lovely to know there’s help when u need it, still struggling, all over flare now , just come home from hospital after having all over steroid injection, hope it works, should be starting new drug soon, thank u all once again Kate x
Kate2628
in
NRAS
3 months ago
COVID-19
Been battling Covid for 17 days. I am negative but have a lot of physical issues achy big time. Always exhausted. No motivation. Starting to take a toll on me mentally. Doctor says that sometimes it takes weeks or months to get rid of everything. I hate feeling like this
Been battling Covid for 17 days. I am negative but have a lot of physical issues achy big time. Always exhausted. No motivation. Starting to take a toll on me mentally. Doctor says that sometimes it takes weeks or months to get rid of everything. I hate feeling like this
Trainchaser
in
Anxiety and Depression Support
3 months ago
Leg Pain pt 3
Writing again because one of you lovely people suggested I saw my MRI results for myself. She was right, my doctor said it was wear and tear in the back. Keep taking the painkillers and walk. But I did see the results and it is Grade 1 degenerative spondylolisthesis. He did not suggest physio. But
Writing again because one of you lovely people suggested I saw my MRI results for myself. She was right, my doctor said it was wear and tear in the back. Keep taking the painkillers and walk. But I did see the results and it is Grade 1 degenerative spondylolisthesis. He did not suggest physio. But
Alloagirl
in
Pain Concern
3 months ago
COVID & sulfasalazine?
After all these years hubby has passed COVID to me! Contacted GP, they have referred me to respiratory@home still waiting for them to call. Question is do I keep taking sulfasalazine.? I've called my Rheumy helpline but they've not got back to me and I've looked on here but can't find anything saying
After all these years hubby has passed COVID to me! Contacted GP, they have referred me to respiratory@home still waiting for them to call. Question is do I keep taking sulfasalazine.? I've called my Rheumy helpline but they've not got back to me and I've looked on here but can't find anything saying
Haz58
in
NRAS
3 months ago
COPD and Long Covid
Hi all, I've been ill for over three years with Long Covid and just last week diagnosed with COPD stage 2. Looking through my medical history COPD was mentioned back in 2005, but I was told it was Asthma! Just joined my local Breathe Easy group who are great and very supportive.
Hi all, I've been ill for over three years with Long Covid and just last week diagnosed with COPD stage 2. Looking through my medical history COPD was mentioned back in 2005, but I was told it was Asthma! Just joined my local Breathe Easy group who are great and very supportive.
SimonJJJ
in
Lung Conditions Community Forum
3 months ago
Covid - Reflux
Just out of interest has anyone's reflux problems come on after having Covid? I had it back in early December and got problems in middle of January. I have read somewhere that there could be a link .
Just out of interest has anyone's reflux problems come on after having Covid? I had it back in early December and got problems in middle of January. I have read somewhere that there could be a link .
Pinkcatfairy
in
Acid Reflux Support
3 months ago
What would be your Low Dose Naltrexone (LDN) dosing recommendation for long Covid and Mast Cell Activation?
What would be your Low Dose Naltrexone (LDN) dosing recommendation for long Covid and Mast Cell Activation? Answered by Sebastian Denison, RPh https://youtu.be/w5RLJy34ArU
What would be your Low Dose Naltrexone (LDN) dosing recommendation for long Covid and Mast Cell Activation? Answered by Sebastian Denison, RPh https://youtu.be/w5RLJy34ArU
Shewulf
Administrator
in
LDN Research Trust
3 months ago
Rash any advice?
I have noticed this rash over last 2 or 3 months. Its not itchy or raised. Any advice most welcome. Im taking 100mcg teva levo and 15mcg thybon henning. Vit d, magnesium glycinate. Any advice most welcome 🌸🌸🌸🌸🌸
I have noticed this rash over last 2 or 3 months. Its not itchy or raised. Any advice most welcome. Im taking 100mcg teva levo and 15mcg thybon henning. Vit d, magnesium glycinate. Any advice most welcome 🌸🌸🌸🌸🌸
Geegee777
in
Thyroid UK
5 months ago
chronic knee pain, can anyone help!
lve had knee pain before, lve had my knee drained , steroid injection s , but the last 2weeks have been chronic pain never had it this bad before, l dread going to bed trying to walk when l get out of bed is almost impossible, l need a chair with wheels on to get to bathroom, it’s okay when I’m sitting
lve had knee pain before, lve had my knee drained , steroid injection s , but the last 2weeks have been chronic pain never had it this bad before, l dread going to bed trying to walk when l get out of bed is almost impossible, l need a chair with wheels on to get to bathroom, it’s okay when I’m sitting
Kate2628
in
NRAS
3 months ago
sjogens?
I have post PV Myelofibrosis. When I was dx with PV I took Pegasys from April 22 @ 45mg then 60mg then 90mg fortnightly. (On Jakavi since August 23) So took Pegasys for about 16 months After a couple of months on Pegasys I started to experience close vision problems which could not be corrected with
I have post PV Myelofibrosis. When I was dx with PV I took Pegasys from April 22 @ 45mg then 60mg then 90mg fortnightly. (On Jakavi since August 23) So took Pegasys for about 16 months After a couple of months on Pegasys I started to experience close vision problems which could not be corrected with
Yanico
in
MPN Voice
5 months ago
shingles vaccine
Hi folks This is a brilliant site has keep me steady since my husband’s diagnosis of SLL now CLL. My Husband had been W&W for 6 years, now on acalabrutinib for two years with no side affect and doing well. He has been offered the shingles vaccine but he hasn’t had chickenpox’s, is it safe to get the
Hi folks This is a brilliant site has keep me steady since my husband’s diagnosis of SLL now CLL. My Husband had been W&W for 6 years, now on acalabrutinib for two years with no side affect and doing well. He has been offered the shingles vaccine but he hasn’t had chickenpox’s, is it safe to get the
Charles4
in
CLL Support
5 months ago
Raised Blood Pressure after Covid
Not sure if this is the right Forum to post this on but I wondered if anyone who has high blood pressure and has had Covid has found that their blood pressure readings have risen since having it. I had an appointment with my Cardiologist this morning and showed him my readings over the last month orso
Not sure if this is the right Forum to post this on but I wondered if anyone who has high blood pressure and has had Covid has found that their blood pressure readings have risen since having it. I had an appointment with my Cardiologist this morning and showed him my readings over the last month orso
Jomaur
in
AF Association
3 months ago
Finally, we may have found the smoking gun.
We had been able to put it aside, and the hospital agreed they had made a mistake when they said Margaret had Cirrhosis. And was, in fact, NASH with Grade 1 fibrosis. Still, NASH was a surprise, as Magaret was a nondrinker, not obese, and had no health conditions that would even be considered for
We had been able to put it aside, and the hospital agreed they had made a mistake when they said Margaret had Cirrhosis. And was, in fact, NASH with Grade 1 fibrosis. Still, NASH was a surprise, as Magaret was a nondrinker, not obese, and had no health conditions that would even be considered for
ceward204
in
British Liver Trust
3 months ago
still not 100%
I don’t have a fever and my throat only hurts when I first wake up. Then it goes away. I have so much post nasal drip so I think that’s what’s making it hurt. I was out of work for two days due to my colonoscopy, and tomorrow is looking like it’ll be a snow day due to a huge storm. I am going to try
I don’t have a fever and my throat only hurts when I first wake up. Then it goes away. I have so much post nasal drip so I think that’s what’s making it hurt. I was out of work for two days due to my colonoscopy, and tomorrow is looking like it’ll be a snow day due to a huge storm. I am going to try
Daisy425
in
Anxiety and Depression Support
3 months ago
Covid Vaccines - Can you still book them?
Hi all, something that has slipped my mind but it’s been 6 months since I had my last Covid Vaccine. Are the Immune Deficient still eligible? If so how do we do it, is it via 119, or do we go to a walk in or are we referred (I hope not GPs hopeless) the online service doesn't allow bookings any more
Hi all, something that has slipped my mind but it’s been 6 months since I had my last Covid Vaccine. Are the Immune Deficient still eligible? If so how do we do it, is it via 119, or do we go to a walk in or are we referred (I hope not GPs hopeless) the online service doesn't allow bookings any more
Investigator1
in
Vasculitis UK
3 months ago
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