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Seeking understanding
I was diagnosed with seronegative rheumatoid arthritis 8 weeks ago. I am 40 years old. I used to work in a factory 40+ hours a week, have 3 teenage sons, and used to enjoy crafting and fishing. I have a hard time just getting out of bed these days. My rheumatologist started me on 15 mg meloxicam and
I was diagnosed with seronegative rheumatoid arthritis 8 weeks ago. I am 40 years old. I used to work in a factory 40+ hours a week, have 3 teenage sons, and used to enjoy crafting and fishing. I have a hard time just getting out of bed these days. My rheumatologist started me on 15 mg meloxicam and
kgk92
in
NRAS
10 years ago
Always exhausted
I was diagnosed with Fibromyalgia ten years ago after two years of constant pain and tiredness, sore throats, hoarse voice etc etc. Until the summer of last year, I survived - but with a much-changed lifestyle - taking the pain killer Meloxicam, Omeprazole to counter its effects, Duloxetine for depression
I was diagnosed with Fibromyalgia ten years ago after two years of constant pain and tiredness, sore throats, hoarse voice etc etc. Until the summer of last year, I survived - but with a much-changed lifestyle - taking the pain killer Meloxicam, Omeprazole to counter its effects, Duloxetine for depression
stiltzski
in
Thyroid UK
10 years ago
Gideons Cysts?
I just noticed a squishy lump under the ball of my left big toe (metatarsal joint) and I think it may be a Gideons cyst after a quick search online. This comes after three different fingers showing small cysts on dip joints (Wikipedia had a picture of what looked to be the same thing also under the entry
I just noticed a squishy lump under the ball of my left big toe (metatarsal joint) and I think it may be a Gideons cyst after a quick search online. This comes after three different fingers showing small cysts on dip joints (Wikipedia had a picture of what looked to be the same thing also under the entry
Karen77
in
NRAS
10 years ago
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I have been to my general practician, full blood work up, rheumatologist, ob/gyn, and no one knows why I cannot tolerate heat.
My blood feels on fire, I sweat profusely from the scalp to my toes. My husband says my skin is very hot even in the shade. My clothes get soaked & I want to pass out. They tested me with autoimmune but say I tested negative for lupus. I have suffered 4 yrs now. They gave me meloxicam for my joint pain
My blood feels on fire, I sweat profusely from the scalp to my toes. My husband says my skin is very hot even in the shade. My clothes get soaked & I want to pass out. They tested me with autoimmune but say I tested negative for lupus. I have suffered 4 yrs now. They gave me meloxicam for my joint pain
Hidden
in
LUPUS UK
10 years ago
Diagnosed with RA today. My RA doctor put me on Meloxicam 15 MG and Doxycycline Hyclate 100MG and Curcumin. Has anyone else taken this
kind of regiment and if so could you share your experience? Thanks….
kind of regiment and if so could you share your experience? Thanks….
Hidden
in
NRAS
10 years ago
Elevated blood pressure....
Has anyone had problems with elevated blood pressure since being on RA medication? I've always had some problems with my blood pressure having been on medication for about 8 years now, however in the last few months my BP has gone up needing more medication. It's a genetic problem rather than weight
Has anyone had problems with elevated blood pressure since being on RA medication? I've always had some problems with my blood pressure having been on medication for about 8 years now, however in the last few months my BP has gone up needing more medication. It's a genetic problem rather than weight
Hidden
in
NRAS
10 years ago
Has anyone tried using diet to put their RA into remission? Any success?
I was diagnosed with RA January 2012 and was put immediately on 15 mg Meloxicam (NSAID). I started MTX at the end of that month (10 mg). My condition steadily worsened even as my MTX was increased up to 25mg by June 2012. Over that summer I started taking high doses of fish oil and Vitamin D. In late
I was diagnosed with RA January 2012 and was put immediately on 15 mg Meloxicam (NSAID). I started MTX at the end of that month (10 mg). My condition steadily worsened even as my MTX was increased up to 25mg by June 2012. Over that summer I started taking high doses of fish oil and Vitamin D. In late
Karen77
in
NRAS
11 years ago
Work, mind and body
Ive still not been diagnosed as yet,I'm now in the possibly fibromyalgia/connective tissue disorder? Dont really know category . Im up and down, and am on 150mg levothyroxine, B12 injections, hydroxychloroquin, meloxicam and tramadol. I have good days and bad. Every day I ache. Roof of mouth sore. Ulsers
Ive still not been diagnosed as yet,I'm now in the possibly fibromyalgia/connective tissue disorder? Dont really know category . Im up and down, and am on 150mg levothyroxine, B12 injections, hydroxychloroquin, meloxicam and tramadol. I have good days and bad. Every day I ache. Roof of mouth sore. Ulsers
tmh66
in
LUPUS UK
11 years ago
Croaky old voice anyone ....?
Hey everyone, over the last 48 hours I seem to have developed the worst croaky voice, in fact I've nearly lost my voice. I have no sore throat or cold symptoms. It's a little hard to tell if I'm going down with something cos I always feel like I'm going down with something at the minute!! Also, I'm not
Hey everyone, over the last 48 hours I seem to have developed the worst croaky voice, in fact I've nearly lost my voice. I have no sore throat or cold symptoms. It's a little hard to tell if I'm going down with something cos I always feel like I'm going down with something at the minute!! Also, I'm not
Rosie_rabbit
in
NRAS
11 years ago
What were your first symptoms of fibro?/Initial reasoning you saw doc? 99% sure I may have it.
For years and years, I have seen my Dr with the same symptoms over and over. BUT I'm thinking that maybe he didn't put two and two together BC a lot of the visits were separate for each symptom. I would go and complain about the aches all over my body, or how my face is numb on one side, about the numbing
For years and years, I have seen my Dr with the same symptoms over and over. BUT I'm thinking that maybe he didn't put two and two together BC a lot of the visits were separate for each symptom. I would go and complain about the aches all over my body, or how my face is numb on one side, about the numbing
SultryEyes71281
in
Fibromyalgia Action UK
11 years ago
Blood results help please! I FEEL underactive, but as per usual, am told ...NORMAL!
RAI treatment 2010 - so no working thyroid of my own. (no ref range written for Free T4 and most of the others are missing - but verbally over phone Doc said - range is 6 - 22 (?) so perfectly acceptable within range! I feel LOW!) Serum Free T4 - 9pmol/L Serum TSH - 0.06 (LOW result - 0.30-5.00)
RAI treatment 2010 - so no working thyroid of my own. (no ref range written for Free T4 and most of the others are missing - but verbally over phone Doc said - range is 6 - 22 (?) so perfectly acceptable within range! I feel LOW!) Serum Free T4 - 9pmol/L Serum TSH - 0.06 (LOW result - 0.30-5.00)
jimjim
in
Thyroid UK
11 years ago
Bad day - coccyx and thighs - and now a headache!
I'm trying to get essential things done, but my headache is really getting to me - as is my coccyx. Not looking forward to the journey tomorrow, although it's shorter than most and Mark is an excellent driver - and I don't think we use the Dartford crossing this time! The floor and sofa are still very
I'm trying to get essential things done, but my headache is really getting to me - as is my coccyx. Not looking forward to the journey tomorrow, although it's shorter than most and Mark is an excellent driver - and I don't think we use the Dartford crossing this time! The floor and sofa are still very
missrat
in
Pain Concern
11 years ago
Does anyone have any experience with Pregabalina (Lyrica)?
I was on Amytriptyline for some time for neuropathetic pain even though I was on 50mgs it wasn't really working. I tried a Bustrans patch to which I reacted so the GP suggested Pregabalina, I've been on it for a month or so however it makes me feel rather whoozy & I'm nor sure it's helping with pain
I was on Amytriptyline for some time for neuropathetic pain even though I was on 50mgs it wasn't really working. I tried a Bustrans patch to which I reacted so the GP suggested Pregabalina, I've been on it for a month or so however it makes me feel rather whoozy & I'm nor sure it's helping with pain
Hidden
in
NRAS
11 years ago
Is anyone on any of these: azathioprine, Arcoxia (etorocoxib), lidocaine plasters?
I have atypical PMR (i.e. with normal blood results) and also degenerative changes in my spine. I saw my rheumatologist yesterday. Because I have diabetes and hypertension, and because steroids worsen my depression, she feels it is best to give a steroid-sparing medication and slowly reduce my prednisolone
I have atypical PMR (i.e. with normal blood results) and also degenerative changes in my spine. I saw my rheumatologist yesterday. Because I have diabetes and hypertension, and because steroids worsen my depression, she feels it is best to give a steroid-sparing medication and slowly reduce my prednisolone
missrat
in
Pain Concern
11 years ago
Is anyone on azathioprine? Arcoxia (etarocoxib)? Versatis (lidocaine) plasters?
I have atypical PMR (i.e. with normal blood results) and also degenerative changes in my spine. I saw my rheumatologist yesterday. Because I have diabetes and hypertension, and because steroids worsen my depression, she feels it is best to give a steroid-sparing medication and slowly reduce my prednisolone
I have atypical PMR (i.e. with normal blood results) and also degenerative changes in my spine. I saw my rheumatologist yesterday. Because I have diabetes and hypertension, and because steroids worsen my depression, she feels it is best to give a steroid-sparing medication and slowly reduce my prednisolone
missrat
in
Foggy's "Invisible Illness" Support
11 years ago
Is anyone else on azathioprine? Also Arcoxia (etorocoxib)?
I have atypical PMR (i.e. with normal blood results) and also degenerative changes in my spine. I saw my rheumatologist yesterday. Because I have diabetes and hypertension, and because steroids worsen my depression, she feels it is best to give a steroid-sparing medication and slowly reduce my prednisolone
I have atypical PMR (i.e. with normal blood results) and also degenerative changes in my spine. I saw my rheumatologist yesterday. Because I have diabetes and hypertension, and because steroids worsen my depression, she feels it is best to give a steroid-sparing medication and slowly reduce my prednisolone
missrat
in
PMRGCAuk
11 years ago
Active Duty US Marine With AMN
My story began when my 7-year-old nephew was diagnosed with ALD due to the symptoms he had and through all the tests that he had done the summer of 2007. Once my nephew’s mother, Audrey, was informed this disease was hereditary, my immediate family (siblings and mother) received the same testing to conclude
My story began when my 7-year-old nephew was diagnosed with ALD due to the symptoms he had and through all the tests that he had done the summer of 2007. Once my nephew’s mother, Audrey, was informed this disease was hereditary, my immediate family (siblings and mother) received the same testing to conclude
Chacho308
in
Leukodystrophy Support
11 years ago
Newbie!
Hullo, I am new here after finally getting a diagnosis yesterday. Fourteen years of getting ignored / dismissed by doctors and a few misdiagnoses later, and yesterday was finally told that I am "a bit loopy" - I have individual, verifiable symptoms yet it doesn't show in my blood. I am now on
Hullo, I am new here after finally getting a diagnosis yesterday. Fourteen years of getting ignored / dismissed by doctors and a few misdiagnoses later, and yesterday was finally told that I am "a bit loopy" - I have individual, verifiable symptoms yet it doesn't show in my blood. I am now on
chrissiij
in
LUPUS UK
12 years ago
What do you do when everything happens at once?
Hi guys, So for some reason I seem to be having a really rough go. I've never had THIS many health issues at the same time before. And since I have a newish job on top of it, it's been kind of scary. Anyways, I've taken 4 days off of work this month, which is actually the most I've ever taken. I wasn't
Hi guys, So for some reason I seem to be having a really rough go. I've never had THIS many health issues at the same time before. And since I have a newish job on top of it, it's been kind of scary. Anyways, I've taken 4 days off of work this month, which is actually the most I've ever taken. I wasn't
Hidden
in
Asthma Community Forum
12 years ago
At last the day has come :)
As you are all aware, i had my GP appointment today to start my Treatment,.... Great news my ALT has gone down to 49, So that is great compared to 100 2 weeks ago :) What i didn't know or forgot lol, was that i had a liver function test done in July before taking the Meloxicam, and it was only 26, My
As you are all aware, i had my GP appointment today to start my Treatment,.... Great news my ALT has gone down to 49, So that is great compared to 100 2 weeks ago :) What i didn't know or forgot lol, was that i had a liver function test done in July before taking the Meloxicam, and it was only 26, My
shirlthegirl
in
NRAS
12 years ago
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