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Juvenile idiopathic arthritis
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pip for fibromyalgia
has anyone been successful in getting pip for for fibromyalgia? I have this also arthritis in both knees I work 32hrs a week and do take a lot of medication for my conditions but wondered if anyone had any issues or success in applying for this?
has anyone been successful in getting pip for for fibromyalgia? I have this also arthritis in both knees I work 32hrs a week and do take a lot of medication for my conditions but wondered if anyone had any issues or success in applying for this?
abichesh101
in
Fibromyalgia Action UK
7 months ago
atypical trigeminal neuralgia
Recently diagnosed with atypical trigeminal neuralgia, pain on left side of face/eye/head. I also have rheumatoid arthritis which I take methotrexate 20mg once per week for. Does anyone else know anything about this, or what helps, in a lot of pain.
Recently diagnosed with atypical trigeminal neuralgia, pain on left side of face/eye/head. I also have rheumatoid arthritis which I take methotrexate 20mg once per week for. Does anyone else know anything about this, or what helps, in a lot of pain.
PurpleDuckie
in
PMRGCAuk
7 months ago
Hello everyone!
I'm new here and I have never spoken about this since I live a sheltered life but I wanted to know how others cope with having Psoriasis Arthritis for a long period now?
I'm new here and I have never spoken about this since I live a sheltered life but I wanted to know how others cope with having Psoriasis Arthritis for a long period now?
Hidden
in
Beyond Psoriasis
7 months ago
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Thigh pain
I've had PMR for 8 years and then GCA. And came off steroids because I was up and down, then I developed osteoarthritis in last 2 years.in my back, neck and hips.While walking up a hil I developed thigh pain, thought it was a hamstring injury, I have had it for 3 months, but its quiet unbearable, I've
I've had PMR for 8 years and then GCA. And came off steroids because I was up and down, then I developed osteoarthritis in last 2 years.in my back, neck and hips.While walking up a hil I developed thigh pain, thought it was a hamstring injury, I have had it for 3 months, but its quiet unbearable, I've
Healthliving
in
PMRGCAuk
7 months ago
Baker's cysts update
I posted 10 days ago about knee pain and possibly baker's cysts. After blood test showed my crp level at 14 abd wbc at 16.4 I was concerned. My DR wasn't concerned. I've had scaly area on my foot soles and foot area for a few months so I emailed Dr photo's of this plus photo's of my swollen knees/lower
I posted 10 days ago about knee pain and possibly baker's cysts. After blood test showed my crp level at 14 abd wbc at 16.4 I was concerned. My DR wasn't concerned. I've had scaly area on my foot soles and foot area for a few months so I emailed Dr photo's of this plus photo's of my swollen knees/lower
Monkey321
in
PMRGCAuk
7 months ago
infliximab
Hi I’ve recently started on infliximab infushion for my rheumatoid arthritis I also have osteoarthritis and fibromyalgia. Since my first infusion three weeks ago I’ve had an upset stomach for a week which meant a gap of three weeks between infusions instead of two. A week ago from my left knee down to
Hi I’ve recently started on infliximab infushion for my rheumatoid arthritis I also have osteoarthritis and fibromyalgia. Since my first infusion three weeks ago I’ve had an upset stomach for a week which meant a gap of three weeks between infusions instead of two. A week ago from my left knee down to
Fortune7
in
Fibromyalgia Action UK
14 hours ago
infliximab
Hi I’ve recently started on infliximab infushion for my rheumatoid arthritis I also have osteoarthritis and fibromyalgia. Since my first infusion three weeks ago I’ve had an upset stomach for a week which meant a gap of three weeks between infusions instead of two. A week ago from my left knee down to
Hi I’ve recently started on infliximab infushion for my rheumatoid arthritis I also have osteoarthritis and fibromyalgia. Since my first infusion three weeks ago I’ve had an upset stomach for a week which meant a gap of three weeks between infusions instead of two. A week ago from my left knee down to
Fortune7
in
NRAS
14 hours ago
Rituximab
I’m due to have my first Rituximab infusion in a few weeks, I got diagnosed with anti CCP Rheumatoid Arthritis 3 years ago and have yet to find the right treatment. Does anyone have any experience of this drug and how it made you feel? I’m ever hopeful this will be the one.
I’m due to have my first Rituximab infusion in a few weeks, I got diagnosed with anti CCP Rheumatoid Arthritis 3 years ago and have yet to find the right treatment. Does anyone have any experience of this drug and how it made you feel? I’m ever hopeful this will be the one.
SG58
in
NRAS
7 days ago
Possibly not PMR
my husband was diagnosed with PMR in May after weeks of pain. GP diagnosed PMR and gave normal treatment of steriods which helped initially. He has been trying to cut them but has had many flare ups since then GP not been great and just wants him off steroids and have been getting mixed messages from
my husband was diagnosed with PMR in May after weeks of pain. GP diagnosed PMR and gave normal treatment of steriods which helped initially. He has been trying to cut them but has had many flare ups since then GP not been great and just wants him off steroids and have been getting mixed messages from
trafar
in
PMRGCAuk
9 days ago
Robstevens
I've been on prednisolone for 10 years. Can't get off it. Even with nucala injections every 4 weeks. I had churg Strauss syndrome. And still on 11 drugs to get by. Every day. Including heart drugs. But still can't get PIP. Even though I would probably die before someone with a bit of arthritis who
I've been on prednisolone for 10 years. Can't get off it. Even with nucala injections every 4 weeks. I had churg Strauss syndrome. And still on 11 drugs to get by. Every day. Including heart drugs. But still can't get PIP. Even though I would probably die before someone with a bit of arthritis who
Guccibee
in
Vasculitis UK
7 months ago
Carbimazole and weight!
I was diagnosed with Graves around 4yrs ago, I was put on Carbimazole and after about 18 months went into remission.. I was off the tablets for about 6months,and I relapsed .I have been on 10mg of Carb since,and recently had symptoms of being underactive. My lastTSH was 3.66 and T4 16.6. Carb reduced
I was diagnosed with Graves around 4yrs ago, I was put on Carbimazole and after about 18 months went into remission.. I was off the tablets for about 6months,and I relapsed .I have been on 10mg of Carb since,and recently had symptoms of being underactive. My lastTSH was 3.66 and T4 16.6. Carb reduced
debbiejayn
in
Thyroid UK
7 months ago
Osteo or rheumatoid arthritis in fingers
At the same time as being diagnosed with rheumatoid arthritis, I started getting sharp pain and swelling in the joints closest to finger tips. I was told this is osteoarthritis (while it is also acknowledged that RA can affect any joint). The pain is getting worse and I expect that if I do contact my
At the same time as being diagnosed with rheumatoid arthritis, I started getting sharp pain and swelling in the joints closest to finger tips. I was told this is osteoarthritis (while it is also acknowledged that RA can affect any joint). The pain is getting worse and I expect that if I do contact my
Gottarelax
in
NRAS
23 days ago
To Big Tow Arthritis
I have mild arthritis in my foot. I use Wiley's Wild Alaskan Fish oil 2300 MG, half a teaspoon daily and have no foot pain. If I forget it for a few days the pain returns. It's good for the heart and brain as high Omega 3. Apparently its stronger than other fish oils. Hope it helps.
I have mild arthritis in my foot. I use Wiley's Wild Alaskan Fish oil 2300 MG, half a teaspoon daily and have no foot pain. If I forget it for a few days the pain returns. It's good for the heart and brain as high Omega 3. Apparently its stronger than other fish oils. Hope it helps.
FyMyArt
in
Pain Concern
7 months ago
biologic medication and possible side effects
Wondering if anyone has had something similar happen. I’ve had severe p since 2020 and PA soon after and started the biologic adalimumab in January 2020 after systemic treatments failed/side effects became to bad. In June this month my adalimumab was swapped as it want working wellto ustekinumab which
Wondering if anyone has had something similar happen. I’ve had severe p since 2020 and PA soon after and started the biologic adalimumab in January 2020 after systemic treatments failed/side effects became to bad. In June this month my adalimumab was swapped as it want working wellto ustekinumab which
katienewland
in
NRAS
2 months ago
Biologics and possible side effects
Wondering if anyone has had something similar happen. I’ve had severe p since 2020 and started the bialogic adalimumab in January 2020 after systemic treatments failed/side effects became to bad. In June this month my adalimumab was swapped as it want working wellto ustekinumab which I had my first
Wondering if anyone has had something similar happen. I’ve had severe p since 2020 and started the bialogic adalimumab in January 2020 after systemic treatments failed/side effects became to bad. In June this month my adalimumab was swapped as it want working wellto ustekinumab which I had my first
katienewland
in
Beyond Psoriasis
2 months ago
Joint surgery and how to avoid it
I was diagnosed with RA in December and started methotrexate. I have been reading posts in this group and searching previous posts and finding them so helpful, thanks to everybody who shares their experiences. I have noticed quite a lot of people sharing about joint surgery and joint correction and
I was diagnosed with RA in December and started methotrexate. I have been reading posts in this group and searching previous posts and finding them so helpful, thanks to everybody who shares their experiences. I have noticed quite a lot of people sharing about joint surgery and joint correction and
purplecyclist
in
NRAS
2 months ago
Stills disease or other arthritis pain
Adult onset Stills disease diagnosed aged 17 in 1979 now 62 and not on RA drugs just pain relief and self management by living within the boundaries of what the condition allows. 2023 brought stress and may be the cause of worsening joint pain and new symptoms possible down to autoimmune thyroiditis
Adult onset Stills disease diagnosed aged 17 in 1979 now 62 and not on RA drugs just pain relief and self management by living within the boundaries of what the condition allows. 2023 brought stress and may be the cause of worsening joint pain and new symptoms possible down to autoimmune thyroiditis
Stills
in
NRAS
2 months ago
Armour Thyroid for over 20 years
I have been taking Armour thyroid since 2000... Have had my current Dr for at least 20. When I had COVID last time (about 2 years ago .. very mild case) I noticed my TSH was up (over 3...very high for me and on Armour). I mentioned it to my Dr and she suggested waiting, it could be temporary. In the
I have been taking Armour thyroid since 2000... Have had my current Dr for at least 20. When I had COVID last time (about 2 years ago .. very mild case) I noticed my TSH was up (over 3...very high for me and on Armour). I mentioned it to my Dr and she suggested waiting, it could be temporary. In the
NanaV54
in
Thyroid UK
7 months ago
Methotrexate and adalimumab
I have been using adalimumab for 3 years for my Ankylosing spondylitis and it has been great for my neck and lower back pain. I have now developed some finger pain, wear and tear in my knees and painful toes, as well as plantur fasciitis. My consultant has prescribed methotrexate Being someone that
I have been using adalimumab for 3 years for my Ankylosing spondylitis and it has been great for my neck and lower back pain. I have now developed some finger pain, wear and tear in my knees and painful toes, as well as plantur fasciitis. My consultant has prescribed methotrexate Being someone that
TraceyDevon
in
NRAS
2 months ago
Groin/hip pain
I’ve had really painful groin pain for 3 months now, finally spoke to my RA nurse today who tells me it’s not a rheumatoid problem because I’m zero positive rheumatoid. Just wondering if anyone has been told the same thing. I find the site helpful and hopefully will be again for this.
I’ve had really painful groin pain for 3 months now, finally spoke to my RA nurse today who tells me it’s not a rheumatoid problem because I’m zero positive rheumatoid. Just wondering if anyone has been told the same thing. I find the site helpful and hopefully will be again for this.
mmb50
in
NRAS
2 months ago
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