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ESR blood test
My previous
ESR
test
was only 4. Any help appreciated. Thank you
My previous
ESR
test
was only 4. Any help appreciated. Thank you
Thirtyone
in
Thyroid UK
2 months ago
ESR 39
Hi I’m wondering what you guys think about this
ESR
blood
test
result of 39 ? The rheumy says it’s normal . A gp at my surgery said it’s normal for my age - 63 ! King Regards Lesley
Hi I’m wondering what you guys think about this
ESR
blood
test
result of 39 ? The rheumy says it’s normal . A gp at my surgery said it’s normal for my age - 63 ! King Regards Lesley
TedTheMaineCoon
in
PMRGCAuk
5 months ago
Bowel inflammation - any link to PMR/GCA?
But I haven't had a CRP/
ESR
test
since July, and my levels were rising slowly but in July my CRP was down to 8 and ESR 25. Rheumy was happy not to see me again till February. He does the blood tests, not my GP who has nothing to do with my PMR/GCA. I'd appreciate your thoughts.
But I haven't had a CRP/
ESR
test
since July, and my levels were rising slowly but in July my CRP was down to 8 and ESR 25. Rheumy was happy not to see me again till February. He does the blood tests, not my GP who has nothing to do with my PMR/GCA. I'd appreciate your thoughts.
Broseley
in
PMRGCAuk
7 months ago
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Inflammatory Arthritis with Levothyroxine
18 years ago I had an
ESR
blood
test
at my G.P.'s surgery as I had severe pains on Levothyroxine, this proved I had Inflammatory Arthritis, so I bought Armour Thyroid from the US as the only alternative at that time.
18 years ago I had an
ESR
blood
test
at my G.P.'s surgery as I had severe pains on Levothyroxine, this proved I had Inflammatory Arthritis, so I bought Armour Thyroid from the US as the only alternative at that time.
Denise500
in
Thyroid UK
1 month ago
Update with some pleasant news! I think? and a question
. :0 I also had an
ESR
test
result of 7 down from 14. She hadn't done any other tests because with the CRP test, the labs in our town don't do the ones they need.
. :0 I also had an
ESR
test
result of 7 down from 14. She hadn't done any other tests because with the CRP test, the labs in our town don't do the ones they need.
catdance
in
PMRGCAuk
1 year ago
Recent blood test
On day 9 I had a blood
test
and the
esr
was 6. I have now dropped to 8mg and will see how it goes for a month, if all goes well I will follow the 5 week reduction plan. Should I go to 7 or 7.5?Thanks for all your help and advice.
On day 9 I had a blood
test
and the
esr
was 6. I have now dropped to 8mg and will see how it goes for a month, if all goes well I will follow the 5 week reduction plan. Should I go to 7 or 7.5?Thanks for all your help and advice.
camshall
in
PMRGCAuk
6 months ago
ESR & CRP
However, just had another blood
test
and my
ESR
is 125, last time about 7 weeks ago it was 115 and I was having a ‘flare up’. Currently I wouldn’t say I’m normal, my hip constantly hurts but I can manage fine.
However, just had another blood
test
and my
ESR
is 125, last time about 7 weeks ago it was 115 and I was having a ‘flare up’. Currently I wouldn’t say I’m normal, my hip constantly hurts but I can manage fine.
Whatnow1973
in
NRAS
4 months ago
Cortisol test result
All results are ok including PV,
ESR
, CRP. Also had a basal cortisol
test
(partially instigated by me as really struggle when reducing). The result is Serum cortisol level 164 nmol/l. So this is low I think? Thanks for any advice as always. 😊
All results are ok including PV,
ESR
, CRP. Also had a basal cortisol
test
(partially instigated by me as really struggle when reducing). The result is Serum cortisol level 164 nmol/l. So this is low I think? Thanks for any advice as always. 😊
Saffron23
in
PMRGCAuk
2 months ago
Newly diagnosed. Looking for advice
Stool calprotectin was in 150 with crp and
esr
raised. A positive fit
test
and I had a colonoscopy at the start of May. Where I saw the state of my colon the ulcerated parts and healthy parts the contrast was staggering. It was recorded as mayo score 2 which I read is moderate disease.
Stool calprotectin was in 150 with crp and
esr
raised. A positive fit
test
and I had a colonoscopy at the start of May. Where I saw the state of my colon the ulcerated parts and healthy parts the contrast was staggering. It was recorded as mayo score 2 which I read is moderate disease.
Raerae2781
in
Crohn's and Colitis Support
14 days ago
T3 only diagnosis
Hi, I had intolerance to T4 Levothyroxine 20 years ago, the results of my
ESR
blood
test
then was that I had Inflammatory Arthritis, I was in extreme pain and had put on 5 stone in weight with the help of another Thyroid Web site I went on Armour Thyroid and have been symptom free for 18 years, however
Hi, I had intolerance to T4 Levothyroxine 20 years ago, the results of my
ESR
blood
test
then was that I had Inflammatory Arthritis, I was in extreme pain and had put on 5 stone in weight with the help of another Thyroid Web site I went on Armour Thyroid and have been symptom free for 18 years, however
Denise500
in
Thyroid UK
2 months ago
Tinnitus and White Noise
Over the last 3 years my Tinnitus has deteriorated rapidly. It is constant and I have found one thing that makes me sleep at night is WhiteNoise on YouTube. Highly recommendable. I am getting hearing aids which the Audiologist hopes will reduce my Tinnitus. Meanwhile, it's really troublesome and affects
Over the last 3 years my Tinnitus has deteriorated rapidly. It is constant and I have found one thing that makes me sleep at night is WhiteNoise on YouTube. Highly recommendable. I am getting hearing aids which the Audiologist hopes will reduce my Tinnitus. Meanwhile, it's really troublesome and affects
Nana1944
in
Tinnitus UK
7 days ago
New to tinnitus and frightened
Hi everyone, I'm new to tinnitus, just 3 weeks in but have already been told my hearing is fine and there's no problems with my ears by an audiologist. I recently went through a stressful period at work followed by my mum being rushed into hospital and being told out of the blue that she only had days
Hi everyone, I'm new to tinnitus, just 3 weeks in but have already been told my hearing is fine and there's no problems with my ears by an audiologist. I recently went through a stressful period at work followed by my mum being rushed into hospital and being told out of the blue that she only had days
MiniRocket
in
Tinnitus UK
7 days ago
update on switching to digoxin from lopressor
Stopped digoxin this am and starting back on lopressor. bad heartburn and nausea just kept getting worse. Lots of hydrating and will explore ablation. Really felt sick on digoxin. Although don't feel generally great this was really not a good experience.
Stopped digoxin this am and starting back on lopressor. bad heartburn and nausea just kept getting worse. Lots of hydrating and will explore ablation. Really felt sick on digoxin. Although don't feel generally great this was really not a good experience.
farewelltoarms
in
Atrial Fibrillation Support
8 days ago
menieres
hi I’m new to group Diagnosed menieres about 8 yrs ago Suffer from severe hearing loss tinnitus Recently tinnitus just became very loud and leaving me unable to work and socially isolated Slowly loosing my confidence Anyone else feel similar as I feel alone X
hi I’m new to group Diagnosed menieres about 8 yrs ago Suffer from severe hearing loss tinnitus Recently tinnitus just became very loud and leaving me unable to work and socially isolated Slowly loosing my confidence Anyone else feel similar as I feel alone X
Bluerose57
in
Tinnitus UK
8 days ago
Hydroxychloroquine and tinnitus
I been on leflunomide and hydroxychloroquine for about ten months and have suddenly developed tinnitus, and feel as if I have a small electrical substation between my ears. From internet research I see that hydroxychloroquine can cause tinnitus and the rheumy team have suggested stopping it for just
I been on leflunomide and hydroxychloroquine for about ten months and have suddenly developed tinnitus, and feel as if I have a small electrical substation between my ears. From internet research I see that hydroxychloroquine can cause tinnitus and the rheumy team have suggested stopping it for just
spartacus101
in
NRAS
8 days ago
V + O for R/R CLL post FCR
I sent this to skyshark based on some info he posted but I was[u] hoping for the whole group to chime in.[/u] I had 3 rounds of FCR in 2018 stopped because of profound neutropenia. I relapsed exactly 2 years later and though I did not start Tx until the 5 year point in 2023, would have gladly started
I sent this to skyshark based on some info he posted but I was[u] hoping for the whole group to chime in.[/u] I had 3 rounds of FCR in 2018 stopped because of profound neutropenia. I relapsed exactly 2 years later and though I did not start Tx until the 5 year point in 2023, would have gladly started
skipro
in
CLL Support
11 days ago
An online Study….recruiting re Speech Disorders
A new study on speech disorders in ataxias is recruiting participants Do you have a diagnosis of ataxia, and experience speech disorders? If so, you could help researchers in a study investigating speech disorders across various ataxia types. This is an online study and does not require travel.
A new study on speech disorders in ataxias is recruiting participants Do you have a diagnosis of ataxia, and experience speech disorders? If so, you could help researchers in a study investigating speech disorders across various ataxia types. This is an online study and does not require travel.
wobblybee
in
Ataxia UK
14 days ago
supplements for a fibs???
Has anyone here used magnesium or L arginine for atrial fibrillations? If yes, and you had good results, what were the dosages and how often daily? Thank you.
Has anyone here used magnesium or L arginine for atrial fibrillations? If yes, and you had good results, what were the dosages and how often daily? Thank you.
peachtreepiggy
in
Atrial Fibrillation Support
14 days ago
Musical Ear Syndrome
Hi. I've been looking through to see if anyone has posted about hearing random music with tinnitus. It is very distracting and making me feel isolated and desperate. I developed sudden hearing loss and tinnitus in my left ear in winter 2022, then recently an ear infection in my right ear made the tinnitus
Hi. I've been looking through to see if anyone has posted about hearing random music with tinnitus. It is very distracting and making me feel isolated and desperate. I developed sudden hearing loss and tinnitus in my left ear in winter 2022, then recently an ear infection in my right ear made the tinnitus
SeashellSara
in
Tinnitus UK
18 days ago
Headsets
Hi there, I have had tinnitus most of my life but since developing Meniers disease last year it is unbearable at times. I have managed to adjust but I am finding work very difficult. My job is helping very vulnerable people over the phone, calls can last anything from 20 mins to 3 hours. I wear a headset
Hi there, I have had tinnitus most of my life but since developing Meniers disease last year it is unbearable at times. I have managed to adjust but I am finding work very difficult. My job is helping very vulnerable people over the phone, calls can last anything from 20 mins to 3 hours. I wear a headset
Loveclimbing
in
Tinnitus UK
19 days ago
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