Search
Search
About
Log in
Join
Experiences with
Tenoxicam
Posts
Communities
199 public posts
Filter results
Irritability and fatigue
I despair of myself. I have such a short fuse due to everything taking much more of an effort than before I got RA. I am 53 and a single parent with a 10 year old son. I never get 'time off' as his dad chooses not to see him. By the end of the day I am stuffed, and if I have overdone things (like
I despair of myself. I have such a short fuse due to everything taking much more of an effort than before I got RA. I am 53 and a single parent with a 10 year old son. I never get 'time off' as his dad chooses not to see him. By the end of the day I am stuffed, and if I have overdone things (like
lizcoll2312
in
NRAS
12 years ago
Morning.......
Hi Everyone hope you are having a pain free morning......... As you know i haven't been felling very unwell since Tuesay, after coming of Meloxicam, I had not notice this much at all before i stop taking them, I so much appreciate your advice and experience you all have,................ I've been having
Hi Everyone hope you are having a pain free morning......... As you know i haven't been felling very unwell since Tuesay, after coming of Meloxicam, I had not notice this much at all before i stop taking them, I so much appreciate your advice and experience you all have,................ I've been having
shirlthegirl
in
NRAS
12 years ago
GP rang.....Never Got any real answers
Hiya, Got a call from a GP today, But it was a waste of time, The GP that i spoke to on Monday, that told me to come of meloxicam was not in, and my GP was on holiday, I ask for another GP to call me. When i explained to him about my results from the rheumy, And the telephone call i had on Monday, He
Hiya, Got a call from a GP today, But it was a waste of time, The GP that i spoke to on Monday, that told me to come of meloxicam was not in, and my GP was on holiday, I ask for another GP to call me. When i explained to him about my results from the rheumy, And the telephone call i had on Monday, He
shirlthegirl
in
NRAS
12 years ago
Want to take advantage of all our features? Just log in!
Log in
or
Join
Is the steroid injection wearing off
Morning... Not a good one for me, As you know i had to stop taking Meloxicam (Nsaid drug) yesterday,I shouldn't think it has anything to do with that,..... But who knows,........... Last night i was getting a lot of pain in the top part of my arms, I thought shit my shoulder pain is coming back,( Had
Morning... Not a good one for me, As you know i had to stop taking Meloxicam (Nsaid drug) yesterday,I shouldn't think it has anything to do with that,..... But who knows,........... Last night i was getting a lot of pain in the top part of my arms, I thought shit my shoulder pain is coming back,( Had
shirlthegirl
in
NRAS
12 years ago
A call from my doctors today....
I received a call from one of the GP at my surgery today, My GP is on holiday, She said they have received my results, She has arranged for my next steroid injection on the 10th December, But unfortunately because my ALT was high i will need another blood test which i new about, But i have to stop
I received a call from one of the GP at my surgery today, My GP is on holiday, She said they have received my results, She has arranged for my next steroid injection on the 10th December, But unfortunately because my ALT was high i will need another blood test which i new about, But i have to stop
shirlthegirl
in
NRAS
12 years ago
Update on what's been going on.
I've been reading posts but haven't posted for a while. I've got both OA & inflammatory arthritis & am on Plaquenil & sufasaalsine plus amytriptiline, Meloxicam, & solpadol. I had to stop the sulph as it was thought that it was giving me bad taste/smell problems. Stopping it didn't improve the taste
I've been reading posts but haven't posted for a while. I've got both OA & inflammatory arthritis & am on Plaquenil & sufasaalsine plus amytriptiline, Meloxicam, & solpadol. I had to stop the sulph as it was thought that it was giving me bad taste/smell problems. Stopping it didn't improve the taste
Hidden
in
NRAS
12 years ago
What to try next? Advice needed please!!!!!
I have a much awaited appointment with my gp tomorrow as i am in so much pain im going dolally! I have fibro, 2 bulging dics in my spine and since a severe car crash in \december last year i have severe pain in my right hip which is all being looked at by the other drivers insurance and going to see
I have a much awaited appointment with my gp tomorrow as i am in so much pain im going dolally! I have fibro, 2 bulging dics in my spine and since a severe car crash in \december last year i have severe pain in my right hip which is all being looked at by the other drivers insurance and going to see
charlii
in
Fibromyalgia Action UK
12 years ago
Change of pain relief, fingers crossed it works.
After using BuTrans patches for over 12 months and having really good results in the beginning, I have had to change them. The patches were literally burning my skin and now my arms are very badly scarred but I put up with it for the pain relief. As this allergy started I was getting more joint pain
After using BuTrans patches for over 12 months and having really good results in the beginning, I have had to change them. The patches were literally burning my skin and now my arms are very badly scarred but I put up with it for the pain relief. As this allergy started I was getting more joint pain
sue59
in
Fibromyalgia Action UK
12 years ago
OK....what has horrible mr fibro caused this time!
Hi to you all, i have a problem and i need to know if anyone else has experienced this. I have got the most horrific pain right in my elbow joints but mainly my right arm is affected. I couldnt even lift the kettle yesterday and as for housework....forget it! It hurts if i even try to straighten my arms
Hi to you all, i have a problem and i need to know if anyone else has experienced this. I have got the most horrific pain right in my elbow joints but mainly my right arm is affected. I couldnt even lift the kettle yesterday and as for housework....forget it! It hurts if i even try to straighten my arms
charlii
in
Fibromyalgia Action UK
12 years ago
I just remembered i have a question,
How foggy is that! i went to another doctor in our practice and he has given me some Meloxicam 7.5 tablets, they are to try for a month , he says he wants to be sure i have fibro, but the doctor i usually see said i did have it and that i didnt need to see a specialist to diagnose it, has anyone
How foggy is that! i went to another doctor in our practice and he has given me some Meloxicam 7.5 tablets, they are to try for a month , he says he wants to be sure i have fibro, but the doctor i usually see said i did have it and that i didnt need to see a specialist to diagnose it, has anyone
susie59
in
Fibromyalgia Action UK
12 years ago
Combination of drugs? What do people take?
I have a combination of inflammatory artthritis & OA. For the last year I have been taking Hydroxychloroquine with Sulfasalazine added in 6 months ago. I also take amytriptyline 35mgs, Meloxicam 7.5mgs; paracetamol 1gm/60 mgs codeine at least 3 times a day. I still don't feel that I am on top of
I have a combination of inflammatory artthritis & OA. For the last year I have been taking Hydroxychloroquine with Sulfasalazine added in 6 months ago. I also take amytriptyline 35mgs, Meloxicam 7.5mgs; paracetamol 1gm/60 mgs codeine at least 3 times a day. I still don't feel that I am on top of
Hidden
in
NRAS
13 years ago
Sulphsalazine - not sure I want to continue taking it!
I've been on sulphsalazine for a few months now along with Hydroxycloroquine, plus amytriptiline & meloxicam as well as co codamol. For the last 4-5 weeks I have had a revolting taste in my mouth along with heightened sense of smell. I haven't got a sinus infection, my teeth are fine, I haven;t got
I've been on sulphsalazine for a few months now along with Hydroxycloroquine, plus amytriptiline & meloxicam as well as co codamol. For the last 4-5 weeks I have had a revolting taste in my mouth along with heightened sense of smell. I haven't got a sinus infection, my teeth are fine, I haven;t got
Hidden
in
NRAS
13 years ago
Hi I'm newish on here
I'm not still not sure if I should be on here or not! My blood markers for the RA factor are always negative although I do have OA. However my consultant says that I have a combination of both OA & inflammatory arthritis. I had to see him privately as the original appt with the rheummy clinic 3 yrs
I'm not still not sure if I should be on here or not! My blood markers for the RA factor are always negative although I do have OA. However my consultant says that I have a combination of both OA & inflammatory arthritis. I had to see him privately as the original appt with the rheummy clinic 3 yrs
Hidden
in
NRAS
13 years ago
Is it just me or is all this completely frustrating!?
Sooo, this is my first blog...I suppose spurred on by feeling a bit sorry for myself. I'm 23 years old and had just started my first 'proper' job in Sep after graduating from my masters when in October I started getting all the symptoms of RA...I'm sure I don't need to list them to anyone reading this
Sooo, this is my first blog...I suppose spurred on by feeling a bit sorry for myself. I'm 23 years old and had just started my first 'proper' job in Sep after graduating from my masters when in October I started getting all the symptoms of RA...I'm sure I don't need to list them to anyone reading this
Hidden
in
NRAS
12 years ago
First Post!
Hi everyone. I am new to this and this is the first thing I have written on here. I started with RA symptoms 2 years ago and was treated with Plaquenil and Meloxicam. Been going to see Consultant every 3 months but in February he decided that I had "crossed the line" and should come back in a month -
Hi everyone. I am new to this and this is the first thing I have written on here. I started with RA symptoms 2 years ago and was treated with Plaquenil and Meloxicam. Been going to see Consultant every 3 months but in February he decided that I had "crossed the line" and should come back in a month -
Loulou
in
NRAS
13 years ago
GP appointment tomorrow - any idea what they might suggest?
I am having a terrible flare for the first time in 10 years since going on 20mg MTX, folic acid and Meloxicam which I've managed on really well - till now - so frustrating. I'm seeing GP tomorrow and I wonder what they might suggest? Any ideas of what I can expect? Thanks for any thoughts.
I am having a terrible flare for the first time in 10 years since going on 20mg MTX, folic acid and Meloxicam which I've managed on really well - till now - so frustrating. I'm seeing GP tomorrow and I wonder what they might suggest? Any ideas of what I can expect? Thanks for any thoughts.
kezza
in
NRAS
13 years ago
Is there anything else that can help RA other than drugs?
I'm on Humira, MTX, Sulfasalazine and Meloxicam. I've just had my check up and my specialist is reducing my mtx as he was concerned that I'm on a very high dose. I appreciate that the drugs are doing the job and that I am so much better than was. However, I still get stiffness and joint pain most
I'm on Humira, MTX, Sulfasalazine and Meloxicam. I've just had my check up and my specialist is reducing my mtx as he was concerned that I'm on a very high dose. I appreciate that the drugs are doing the job and that I am so much better than was. However, I still get stiffness and joint pain most
CatherineL
in
NRAS
13 years ago
Fed up and in pain AGAIN!
I have just had six weeks holiday (education) during which time I had a minor flare. I have been on Methotrexate since April along with Folic Acid, Ramipril for high blood pressure and Paroxetine for depression. My next appt with the rheumatologist is not until mid-Nov. Only 4 days into the new term
I have just had six weeks holiday (education) during which time I had a minor flare. I have been on Methotrexate since April along with Folic Acid, Ramipril for high blood pressure and Paroxetine for depression. My next appt with the rheumatologist is not until mid-Nov. Only 4 days into the new term
Lillibet
in
NRAS
13 years ago
have i got this all wrong??????
I have been looking with great interest at peoples problems with sciatica and facial sciatica. I have been suffering with the most excruciating pain down the right side of my face and body which has been going on for a couple of months now. It used to come and go but now seems to be a permanent fixture
I have been looking with great interest at peoples problems with sciatica and facial sciatica. I have been suffering with the most excruciating pain down the right side of my face and body which has been going on for a couple of months now. It used to come and go but now seems to be a permanent fixture
charlii
in
Fibromyalgia Action UK
12 years ago
1
...
9
10
10
Filter results
Clear filters
Posted in
All communities
NRAS
73 results
LUPUS UK
28 results
Fibromyalgia Action UK
19 results
View top 10 communities
Sort by
Most Relevant
Newest