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Misleading the desperate
It's disgusting that there are people who offer instant relief from the debilitating conditions such as arthritis,.We are desperate for relief from the pain we go through each and every day.To try to make money from our suffering is beyond dishonest,belief and wrong.
It's disgusting that there are people who offer instant relief from the debilitating conditions such as arthritis,.We are desperate for relief from the pain we go through each and every day.To try to make money from our suffering is beyond dishonest,belief and wrong.
50schick
in
NRAS
4 years ago
Back pain
New to this so don’t know if it’s me or anything to do with the arthritis but I’m getting a lot of pain at the bottom of my back and help would be welcome
New to this so don’t know if it’s me or anything to do with the arthritis but I’m getting a lot of pain at the bottom of my back and help would be welcome
Jonnie1leg
in
NRAS
4 years ago
Pain all over body
Hello everyone. I was diagnosed with RA back in 2014. Rheumatoid factor 94. Anticccp 120. It effected my left lung mainly (bronchiectasis). A few months ago I started feeling pain at the soles of my feet when waking up. Now my wrists, feet and right elbow hurt. My right hands pinky finger was swollen
Hello everyone. I was diagnosed with RA back in 2014. Rheumatoid factor 94. Anticccp 120. It effected my left lung mainly (bronchiectasis). A few months ago I started feeling pain at the soles of my feet when waking up. Now my wrists, feet and right elbow hurt. My right hands pinky finger was swollen
ks1966
in
NRAS
3 years ago
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Self diagnosis of possible aphasia. I’m new to this community.
Just recovering from two migraines today, the secon one had similar symptoms to aphasia which I have had before. I have read that this could be linked to Fybromyalgia. My GP had previously given me a provisional diagnosis of Polymyalgia and then possibly Fybromyalgia, but I saw the Rheumatologist two
Just recovering from two migraines today, the secon one had similar symptoms to aphasia which I have had before. I have read that this could be linked to Fybromyalgia. My GP had previously given me a provisional diagnosis of Polymyalgia and then possibly Fybromyalgia, but I saw the Rheumatologist two
Rachmaninov2
in
Fibromyalgia Action UK
4 years ago
World Arthritis Day
To commemorate World Arthritis Day today 12th October, Arthritis Action has released findings of a survey looking at the impact of covid-19 for people with arthritis in the UK. We found that more than 4 in 5 people with arthritis reported having experienced loneliness. You can read the full survey report
To commemorate World Arthritis Day today 12th October, Arthritis Action has released findings of a survey looking at the impact of covid-19 for people with arthritis in the UK. We found that more than 4 in 5 people with arthritis reported having experienced loneliness. You can read the full survey report
arthritis_action
Partner
in
Arthritis Action
4 years ago
World Arthritis Day 2020
Today on #WorldArthritisDay and we want everyone to recognise that there is still more to do to make RA a priority; RA is not done. Watch Claire King share her story and talk about why RA needs to be a priority bit.ly/34P26vP #werapriority https://youtu.be/lTaXK89Gg9A
Today on #WorldArthritisDay and we want everyone to recognise that there is still more to do to make RA a priority; RA is not done. Watch Claire King share her story and talk about why RA needs to be a priority bit.ly/34P26vP #werapriority https://youtu.be/lTaXK89Gg9A
Anita-NRAS
Partner
in
NRAS
4 years ago
Very interesting article
Explains such a lot answers a lot of the questions some of us have been asking. https://www.nras.org.uk/keep-taking-the-pills-the-critical-importance-of-adherence-in-the-management-of-rheumatoid-arthritis
Explains such a lot answers a lot of the questions some of us have been asking. https://www.nras.org.uk/keep-taking-the-pills-the-critical-importance-of-adherence-in-the-management-of-rheumatoid-arthritis
Brychni
in
NRAS
4 years ago
Arthritis and hypothyroid
Anyone heard of flare of osteoarthritis from mild hypothyroidism? Thx for comments/experience.
Anyone heard of flare of osteoarthritis from mild hypothyroidism? Thx for comments/experience.
bmrj
in
Thyroid UK
4 years ago
Arthritis
Hi everyone, I’m new to this site or forum. I’m a 51 year old female, I’ve had JRA (juvenile rheumatoid arthritis) since I was 8 yrs old. I thought when I was younger that it was the dark meat from the turkey at thanksgiving that caused it. Lol I had rheumatic fever at the start of mine with swollen
Hi everyone, I’m new to this site or forum. I’m a 51 year old female, I’ve had JRA (juvenile rheumatoid arthritis) since I was 8 yrs old. I thought when I was younger that it was the dark meat from the turkey at thanksgiving that caused it. Lol I had rheumatic fever at the start of mine with swollen
DaisyNancy
in
Arthritis Action
4 years ago
Shingles and vaccinations
Gilden D (2015) Prevalence and distribution of VZV in temporal arteries of patients with Giant Cell
Arteritis
. Neurology 84: 1918-1919) Like most people in the UK, I was offered the Zostavax vaccination just after I reached 70.
Gilden D (2015) Prevalence and distribution of VZV in temporal arteries of patients with Giant Cell
Arteritis
. Neurology 84: 1918-1919) Like most people in the UK, I was offered the Zostavax vaccination just after I reached 70.
Suzita76
in
PMRGCAuk
3 years ago
Confused
Hi. My doctor has ordered lupus anticoagulant and antiphospholipid antibody blood tests. I have been diagnosed with rheumatoid arthritis. When I asked why I was being tested she said it was to rule out APS. I am really confused as to why she thinks I could have this syndrome. I am in my early 20s, never
Hi. My doctor has ordered lupus anticoagulant and antiphospholipid antibody blood tests. I have been diagnosed with rheumatoid arthritis. When I asked why I was being tested she said it was to rule out APS. I am really confused as to why she thinks I could have this syndrome. I am in my early 20s, never
MapsavvyTraveller
in
Hughes Syndrome APS Forum
4 years ago
SSC with lungs fibrosis
Hello everyone, Hope all doing well. 8yrs ago I was diagnosed with SLE and Rheumatoid arthritis and have been on med for the same but 2 weeks ago my new Rheumatologist said I have Systemic sclerosis with lungs fibrosis at initial stage and not SLE. Has anyone been in such situation I unable to understand
Hello everyone, Hope all doing well. 8yrs ago I was diagnosed with SLE and Rheumatoid arthritis and have been on med for the same but 2 weeks ago my new Rheumatologist said I have Systemic sclerosis with lungs fibrosis at initial stage and not SLE. Has anyone been in such situation I unable to understand
Jkan
in
LUPUS UK
4 years ago
Does anyone know about Inflammatory PolyArthritis
Inflammatory PolyArthritis, I have been diagnosed and wonder if anyone knows how this differs from Rheumatoid Arthritis and Polymyalgia Rhumatica. Thank you.
Inflammatory PolyArthritis, I have been diagnosed and wonder if anyone knows how this differs from Rheumatoid Arthritis and Polymyalgia Rhumatica. Thank you.
Rachmaninov2
in
NRAS
4 years ago
2nd session of week 1
Just finished my 2nd session .... was tough but got on with it .... not sure if I'm 'cheating' by doing it on my treadmill at home .... but have osteoarthritis in my knees & find the treadmill is lessening the pain ! I guess the fact I'm attempting this challenge is enough .... I'm feeling proud of myself
Just finished my 2nd session .... was tough but got on with it .... not sure if I'm 'cheating' by doing it on my treadmill at home .... but have osteoarthritis in my knees & find the treadmill is lessening the pain ! I guess the fact I'm attempting this challenge is enough .... I'm feeling proud of myself
Flipflopbabe
in
Couch to 5K
4 years ago
Isn’t Rheumatoid like long Covid?
So the government has set up a £10million investment for one stop physical and mental services for Covid. Reading about the symptoms it seems to reflect what many who have Rheumatoid also suffer. It’s time we had as much support and and interest in our well being. Our Long Rheumatoid needs exactly
So the government has set up a £10million investment for one stop physical and mental services for Covid. Reading about the symptoms it seems to reflect what many who have Rheumatoid also suffer. It’s time we had as much support and and interest in our well being. Our Long Rheumatoid needs exactly
Cal48
in
NRAS
4 years ago
HRT and arthritis
Hello! I’m a post menopausal woman who has been dealing with all the effects of menopause and also a new psoriatic arthritis diagnosis. I recently started HRT for the menopause symptoms but have been noticing that my joints feel really good since I started HRT. I think it has reduced my inflammation.
Hello! I’m a post menopausal woman who has been dealing with all the effects of menopause and also a new psoriatic arthritis diagnosis. I recently started HRT for the menopause symptoms but have been noticing that my joints feel really good since I started HRT. I think it has reduced my inflammation.
tthiele
in
Arthritis Action
4 years ago
Psoriatic arthritis
Hi all... is there anyone one here that has been diagnosed with psoriatic arthritis? I had a telephone appointment yesterday with a rheumatologist phycho and he wants to see me face to face as an urgent appointment!! He is suggesting I have psoriatic arthritis. I would love to hear anyone’s experiences
Hi all... is there anyone one here that has been diagnosed with psoriatic arthritis? I had a telephone appointment yesterday with a rheumatologist phycho and he wants to see me face to face as an urgent appointment!! He is suggesting I have psoriatic arthritis. I would love to hear anyone’s experiences
Dazakella2010
in
Arthritis Action
4 years ago
What Next?
Should I have had a consultation regarding my Diagnosis of PMR, i went to the doctor with pain and said I was fed up of being fobbed off with the usual diagnosis Old age arthritis and being obese. I have never hear of this before I thought I may have rumathoid arthritis as places have been swollen,
Should I have had a consultation regarding my Diagnosis of PMR, i went to the doctor with pain and said I was fed up of being fobbed off with the usual diagnosis Old age arthritis and being obese. I have never hear of this before I thought I may have rumathoid arthritis as places have been swollen,
Cats64
in
PMRGCAuk
4 years ago
Chronic joint weakness, easily brake bones???
I do suffer with fibromyalgia all over my body & the Fog plus arthritis But i have noticed a drastic weakness to my joints. I've never broken a bone until now. Ive broke my left wrist & thumb joint, I am left handed too. The hosp consultant after attending A&E said i should of been potted but given a
I do suffer with fibromyalgia all over my body & the Fog plus arthritis But i have noticed a drastic weakness to my joints. I've never broken a bone until now. Ive broke my left wrist & thumb joint, I am left handed too. The hosp consultant after attending A&E said i should of been potted but given a
sssglsjhs
in
Fibromyalgia Action UK
4 years ago
is it norming to have pain while on a biologic
I was diagnosed with zero negative Rheumatoid Arthritis and have been on a biologic for 3 months and take sulfasalazine. My blood test has shown my inflammation markers are at 1 which is very good however I am in constant pain with hands, wrist and shoulder pain is this common trait with RA.
I was diagnosed with zero negative Rheumatoid Arthritis and have been on a biologic for 3 months and take sulfasalazine. My blood test has shown my inflammation markers are at 1 which is very good however I am in constant pain with hands, wrist and shoulder pain is this common trait with RA.
pau1
in
NRAS
4 years ago
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