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Juvenile idiopathic arthritis
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Arthritis
I have arthritis all over and now in my back. My dr. Wants me to see a Reumatologist to check for Rheumatoid Arthritis. How different would treat be if it is RA? I have Hughes syndrome and hypothyroidism also. Thanks My sister has RA is that hereditary?
I have arthritis all over and now in my back. My dr. Wants me to see a Reumatologist to check for Rheumatoid Arthritis. How different would treat be if it is RA? I have Hughes syndrome and hypothyroidism also. Thanks My sister has RA is that hereditary?
Nanny23
in
Pain Concern
3 years ago
Undifferentiated Inflammatory arthritis here to stay and methotrexate looming..very unsure...anybody have any experience?
Hello. I hope it‘s ok to post here. I feel a bit homeless with my diagnosis of persistent undifferentiated inflammatory arthritis for now. Initially the rheumatologist said he thought it would likely remit, now he says he thinks it is here to stay but sadly not enough evidence to give a firm diagnosis
Hello. I hope it‘s ok to post here. I feel a bit homeless with my diagnosis of persistent undifferentiated inflammatory arthritis for now. Initially the rheumatologist said he thought it would likely remit, now he says he thinks it is here to stay but sadly not enough evidence to give a firm diagnosis
Hidden
in
NRAS
3 years ago
Rheumatoid arthritis
Hi I'm new here I was with my rheumatologist today who will be putting me on methotrexate injection Question is I got a steroid injection for RA today I'm looking to know if anyone would know if its advisable to get the covid vaccine 6 days after this jab my rheumatology told me to get the vaccine
Hi I'm new here I was with my rheumatologist today who will be putting me on methotrexate injection Question is I got a steroid injection for RA today I'm looking to know if anyone would know if its advisable to get the covid vaccine 6 days after this jab my rheumatology told me to get the vaccine
Eva9
in
NRAS
3 years ago
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Butterfingers! Feeling frustrated and poor.
I am dyspraxic, which means that I have always been extremely clumsy and have terrible executive functioning. With advancing age, my dyspraxia has also meant that I have also experienced increasing aphasia - I can often see/hear the word in my brain, it just doesn't make it to my mouth. Since being on
I am dyspraxic, which means that I have always been extremely clumsy and have terrible executive functioning. With advancing age, my dyspraxia has also meant that I have also experienced increasing aphasia - I can often see/hear the word in my brain, it just doesn't make it to my mouth. Since being on
Hidden
in
PMRGCAuk
3 years ago
Newly diagnosed /First Post
I have been suffering from Rheumatoid arthritis for 15 years and was recently told that I also have Polymalgia overlap. Last week I was told that in addition to that I have Fibromyalgia. In truth I have never felt so unwell. Obviously I have had chronic muscle and joint pain for a long time which I have
I have been suffering from Rheumatoid arthritis for 15 years and was recently told that I also have Polymalgia overlap. Last week I was told that in addition to that I have Fibromyalgia. In truth I have never felt so unwell. Obviously I have had chronic muscle and joint pain for a long time which I have
Painful2021
in
Fibromyalgia Action UK
3 years ago
What is a “Flare”
Hi everyone. This may appear a very silly or odd question but can anyone explain what a “flare” is? I was diagnosed in August with Rheumatoid Arthritis. I’m on Methotrexate and Folic Acid. They have been working extremely well until about two weeks ago when I had to miss a week of my Methotrexate
Hi everyone. This may appear a very silly or odd question but can anyone explain what a “flare” is? I was diagnosed in August with Rheumatoid Arthritis. I’m on Methotrexate and Folic Acid. They have been working extremely well until about two weeks ago when I had to miss a week of my Methotrexate
Moonjean
in
NRAS
3 years ago
Does anyone wear a medical alert bracelet?
I am thinking I should have a medical alert bracelet in that I am immunosuppressed now. Does anyone else wear one??? I was diagnosed with some sort of inflammatory arthritis. Sometimes the doctor calls it RA, but then she says that it could be psoriatic without the rash.. I guess it is hard to diagnose
I am thinking I should have a medical alert bracelet in that I am immunosuppressed now. Does anyone else wear one??? I was diagnosed with some sort of inflammatory arthritis. Sometimes the doctor calls it RA, but then she says that it could be psoriatic without the rash.. I guess it is hard to diagnose
smilelines
in
NRAS
3 years ago
Gastric stasis and nausea
Has anyone any advice/experience of nausea and gastric stasis? I have been taking LDN since last May and it has been wonderful for osteoarthritis. Just 2 days on 0.5 gave me pain relief. So happy. I could never get higher than 1.75 without nausea so I stayed there. But noticed after 6 months that my
Has anyone any advice/experience of nausea and gastric stasis? I have been taking LDN since last May and it has been wonderful for osteoarthritis. Just 2 days on 0.5 gave me pain relief. So happy. I could never get higher than 1.75 without nausea so I stayed there. But noticed after 6 months that my
21litha
in
LDN Research Trust
3 years ago
I am positive for about 4 years now. Can this disease suddenly attack your whole body?
I now have arthritis had hip replacement in September. Have hypothyroidism my teeth are rotting have spinal stenosis Barrett’s Esophagus ulcers colon polyps. I feel like my body is breaking down. I am 71 and attribute a lot to age but it seems it’s one thing after the other. All of you in health unlocked
I now have arthritis had hip replacement in September. Have hypothyroidism my teeth are rotting have spinal stenosis Barrett’s Esophagus ulcers colon polyps. I feel like my body is breaking down. I am 71 and attribute a lot to age but it seems it’s one thing after the other. All of you in health unlocked
Nanny23
in
Hughes Syndrome APS Forum
3 years ago
Can any one advise pain killers for rheumatoid arthritis. Most ones I’ve tried don’t touch the pain
I’ve tried ibuprofen, paracetamol, naproxen, gabapentin, co codamol to many to mention
I’ve tried ibuprofen, paracetamol, naproxen, gabapentin, co codamol to many to mention
Catr12
in
Pain Concern
3 years ago
Rheumatology post - updates
Hi everyone - thank you all for your support yesterday. Today I took the drop from 40 to 20 mg and started on Co-codamol - I’m amazed at how much less pain I have, but I guess that’s because I’m addressing the real issue of Osteoarthritis rather than PMR so I’m almost certain the moment Rheumatologist
Hi everyone - thank you all for your support yesterday. Today I took the drop from 40 to 20 mg and started on Co-codamol - I’m amazed at how much less pain I have, but I guess that’s because I’m addressing the real issue of Osteoarthritis rather than PMR so I’m almost certain the moment Rheumatologist
Fiddlersmum
in
PMRGCAuk
3 years ago
Hello
Hello everyone had my Covid jab so it’s been 2 weeks this Friday since I had it so back to taking my arthritis injections now 😊😊
Hello everyone had my Covid jab so it’s been 2 weeks this Friday since I had it so back to taking my arthritis injections now 😊😊
Beth72
in
NRAS
3 years ago
Fought through the pain
Fought through Arthritis pain in my feet to start and finish Week 1 Run 2. I’ll be suffering in the morning but at the moment it feels worth it
Fought through Arthritis pain in my feet to start and finish Week 1 Run 2. I’ll be suffering in the morning but at the moment it feels worth it
BlackMon
in
Couch to 5K
3 years ago
Rheumatology appt
Thought I would update you lovely people . . . I had an urgent referral to rheumatology today after being put on 40 mgs of Pred ... going through my notes, experiences etc the doctor has come to the conclusion that I have Osteoarthritis of the spine rather than PMR - I think he's probably right given
Thought I would update you lovely people . . . I had an urgent referral to rheumatology today after being put on 40 mgs of Pred ... going through my notes, experiences etc the doctor has come to the conclusion that I have Osteoarthritis of the spine rather than PMR - I think he's probably right given
Fiddlersmum
in
PMRGCAuk
3 years ago
I have arthritis pain in my feet and find it difficult to run. Any tips on what can make it easier?
Arthritis in feet
Arthritis in feet
BlackMon
in
Couch to 5K
3 years ago
Covid injection side effects
Since having my Oxford jab,some 6 weeks ago now my various arthritis's are much worse and just won't settle back to normal, I just wondered if anyone else has experienced the same? My costoscondritis is much worse, dry eyes and rheumatoid arthritis too.
Since having my Oxford jab,some 6 weeks ago now my various arthritis's are much worse and just won't settle back to normal, I just wondered if anyone else has experienced the same? My costoscondritis is much worse, dry eyes and rheumatoid arthritis too.
Jacqui2017
in
NRAS
3 years ago
Query on shielding
Hi I’m looking for advice on shielding I have lupus arthritis asthma epilepsy tachycardia and osteoporosis in and out hospital with respiratory problems and infections can someone please help me with this thank you
Hi I’m looking for advice on shielding I have lupus arthritis asthma epilepsy tachycardia and osteoporosis in and out hospital with respiratory problems and infections can someone please help me with this thank you
Liz2468
in
LUPUS UK
3 years ago
Query on shielding
Hi Paul I hope you don’t mind me asking but should I be on the shielding list as I have lupus arthritis asthma epilepsy tachycardia and osteoporosis
Hi Paul I hope you don’t mind me asking but should I be on the shielding list as I have lupus arthritis asthma epilepsy tachycardia and osteoporosis
Liz2468
in
LUPUS UK
3 years ago
Where can I buy Tylenol or do I need a prescription?
Do I need a prescription for Tylenol for my arthritis
Do I need a prescription for Tylenol for my arthritis
Gooby1
in
Arthritis Action
3 years ago
Information for people in the UK on Tocilizumab (Ro-Actemra) injections
Hello, and apologies for not posting for such a long time. As one of the few (and greatly privileged) LVV-GCA sufferers in the UK lucky enough to have been prescribed subcutaneous Tocilizumab injections, I have a couple of items of news. First of all, along with my husband, I have been a participant
Hello, and apologies for not posting for such a long time. As one of the few (and greatly privileged) LVV-GCA sufferers in the UK lucky enough to have been prescribed subcutaneous Tocilizumab injections, I have a couple of items of news. First of all, along with my husband, I have been a participant
Suzita76
in
PMRGCAuk
3 years ago
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