Search
Search
About
Log in
Join
Experiences with
Tenoxicam
Posts
Communities
198 public posts
Filter results
Hi I am a newbie
I am 52yrs old woman who is having to come to terms with the fact that I can no longer do the job I love due to my prolapsed disc and facet joint problem🙁 I have had injections for the last 4 years then in march I had radio frequency nerve block but nothing has helped and now I don't know what else
I am 52yrs old woman who is having to come to terms with the fact that I can no longer do the job I love due to my prolapsed disc and facet joint problem🙁 I have had injections for the last 4 years then in march I had radio frequency nerve block but nothing has helped and now I don't know what else
hctrom
in
Pain Concern
7 years ago
Meloxicam
Hi,I just read that you shouldn't take meloxicam and methotrexate together. I was prescribed the meloxicam before my RA diagnosis. I take 25mg methotrexate and 15mg meloxicam. I presumed since the hospital had a list of my medications this was right. Has anyone else been prescribed both?
Hi,I just read that you shouldn't take meloxicam and methotrexate together. I was prescribed the meloxicam before my RA diagnosis. I take 25mg methotrexate and 15mg meloxicam. I presumed since the hospital had a list of my medications this was right. Has anyone else been prescribed both?
Tiggerlkr
in
NRAS
7 years ago
Medication combination
Is it advisable to take meloxicam along with Plaquenil and methotrexate?
Is it advisable to take meloxicam along with Plaquenil and methotrexate?
determined4321
in
NRAS
7 years ago
Want to take advantage of all our features? Just log in!
Log in
or
Join
Constant infections ...
So I'm feeling pretty fed up right with what seem like never ending infections. I've been trying to find the right biological for a while now and I've been on abatacept for just over 6 months. I also take mtx 20mg injections, 8mg preds daily plus meloxicam and a few other bits n bobs!! I usually stay
So I'm feeling pretty fed up right with what seem like never ending infections. I've been trying to find the right biological for a while now and I've been on abatacept for just over 6 months. I also take mtx 20mg injections, 8mg preds daily plus meloxicam and a few other bits n bobs!! I usually stay
Rosie_rabbit
in
NRAS
7 years ago
Letter to GP from Connective Tissue Clinic
I spoke on the phone to my GP about whether he had a report following my 30 March appt. I'll see him to get a copy of the letter but this is what he's told me as "good news". ANA down "a little". Diagnosis is query mild lupus/scleroderma, with definite secondary Raynaud's, plus OA lower spine, hips,
I spoke on the phone to my GP about whether he had a report following my 30 March appt. I'll see him to get a copy of the letter but this is what he's told me as "good news". ANA down "a little". Diagnosis is query mild lupus/scleroderma, with definite secondary Raynaud's, plus OA lower spine, hips,
Lupiknits
in
LUPUS UK
7 years ago
treatment help
Hey guys, My names Kristy, I'm 21year old and i was diagnosed with JIA at age 6 in my knees and hips, been in and out of remission since then. Usually my episodes only last 6 months or so, and I have no pain at all just noticeable swelling.. but this time has been very different, it's now affecting my
Hey guys, My names Kristy, I'm 21year old and i was diagnosed with JIA at age 6 in my knees and hips, been in and out of remission since then. Usually my episodes only last 6 months or so, and I have no pain at all just noticeable swelling.. but this time has been very different, it's now affecting my
kkristynikoo
in
NRAS
7 years ago
JIA treatment help
Hey guys, My names Kristy, I'm 21year old and i was diagnosed with JIA at age 6 in my knees and hips, been in and out of remission since then. Usually my episodes only last 6 months or so, and I have no pain at all just noticeable swelling.. but this time has been very different, it's now affecting
Hey guys, My names Kristy, I'm 21year old and i was diagnosed with JIA at age 6 in my knees and hips, been in and out of remission since then. Usually my episodes only last 6 months or so, and I have no pain at all just noticeable swelling.. but this time has been very different, it's now affecting
kkristynikoo
in
JIA-at-NRAS
7 years ago
Biologics?
I am new here and I have the opportunity to go on these biologic drugs by injection. It is just like the diabetic injection you do your self so no big deal. Methorexate was working for my RA for years but I was having operations for nodules on my arms and hands which kept re-ocurring! So last July they
I am new here and I have the opportunity to go on these biologic drugs by injection. It is just like the diabetic injection you do your self so no big deal. Methorexate was working for my RA for years but I was having operations for nodules on my arms and hands which kept re-ocurring! So last July they
Brede
in
NRAS
7 years ago
No rush....
I have had pain from my sij on and off for many years. Posture through sight loss and being a gardener have taken their toll. Couple of years ago my hip decided to join in and an Xray showed bad wear in left hip together with left sij. Physio was too painful, acupuncture worked well so...resigned I
I have had pain from my sij on and off for many years. Posture through sight loss and being a gardener have taken their toll. Couple of years ago my hip decided to join in and an Xray showed bad wear in left hip together with left sij. Physio was too painful, acupuncture worked well so...resigned I
Bananas5
in
Pain Concern
7 years ago
Are there any benefits available.
My husband has been diagnosed with fybromyalgia. He works 30 hours weekly over 6 days . Some days its really hard to get out of bed. Hes in agony. Hes at doctors this week for medication. He also has arthritis for which he takes omeprazole, meloxicam and co codamol daily. Is there any benefits he could
My husband has been diagnosed with fybromyalgia. He works 30 hours weekly over 6 days . Some days its really hard to get out of bed. Hes in agony. Hes at doctors this week for medication. He also has arthritis for which he takes omeprazole, meloxicam and co codamol daily. Is there any benefits he could
Amospower123
in
Fibromyalgia Action UK
7 years ago
Hydroxychloroquine and Meloxicam
I feel I'm one of the lucky ones compared with others writing in this forum, though it still feels RA has had a big impact on my life over the last year. My Rheumy put me on HXQ four months ago and following my last appointment in Feb told me I was in remission. (No swollen joints, anti CFPP very low
I feel I'm one of the lucky ones compared with others writing in this forum, though it still feels RA has had a big impact on my life over the last year. My Rheumy put me on HXQ four months ago and following my last appointment in Feb told me I was in remission. (No swollen joints, anti CFPP very low
Bubblemania
in
NRAS
7 years ago
Disgusted with meds
Hello I am using the name Brazant. I was diagnosed with RA 2 years ago. My family doctor started treating with Diclofenac and Meloxicam for inflammation before I saw a Rheumatologis. My symptoms were not that bad until I started the medications. the first doctor I went to see due to my family doctor
Hello I am using the name Brazant. I was diagnosed with RA 2 years ago. My family doctor started treating with Diclofenac and Meloxicam for inflammation before I saw a Rheumatologis. My symptoms were not that bad until I started the medications. the first doctor I went to see due to my family doctor
brazant
in
Cure Arthritis Community
7 years ago
Help anyone?
I was diagnosed with seronegative RA last summer. I am currently on Methotrexate 25mg, prednisolone and Meloxicam for pain management. I will probably be having sulfasalazine added in a few weeks. The last few weeks, I've been really suffering with pain managemen and have been prescribed something to
I was diagnosed with seronegative RA last summer. I am currently on Methotrexate 25mg, prednisolone and Meloxicam for pain management. I will probably be having sulfasalazine added in a few weeks. The last few weeks, I've been really suffering with pain managemen and have been prescribed something to
JaydeeM
in
NRAS
7 years ago
Pain advice
I was diagnosed last summer with RA. Taking Methotrexate and Prednisolone(for 2 months now). Pain relief is Meloxicam 15mg a day. I work part time. The last few weeks my pain and inflammation has ramped up. And, I'm not sure what to do next? My Rheumatologist has suggested adding in Sulfazaline. I'm
I was diagnosed last summer with RA. Taking Methotrexate and Prednisolone(for 2 months now). Pain relief is Meloxicam 15mg a day. I work part time. The last few weeks my pain and inflammation has ramped up. And, I'm not sure what to do next? My Rheumatologist has suggested adding in Sulfazaline. I'm
JaydeeM
in
NRAS
7 years ago
Dealing with fibromyalgia pain
I have been taking tramadol for years.I used to take it with meloxicam until I developed CHF so now I have to take 2 every 6 hours, wow.
I have been taking tramadol for years.I used to take it with meloxicam until I developed CHF so now I have to take 2 every 6 hours, wow.
Connie60
in
Fibromyalgia Action UK
7 years ago
Newly diagnosed need help from experienced people
I'm newly diagnosed with Sjorgens having symptoms like dry eyes, dry mouth, a lot of joint pain and swelling especially in my hands and inner elbows, legs and feet, and fatigue like Ive never felt before. My Dr prescribed Meloxicam daily when pain was bad which worked well, but then I started to have
I'm newly diagnosed with Sjorgens having symptoms like dry eyes, dry mouth, a lot of joint pain and swelling especially in my hands and inner elbows, legs and feet, and fatigue like Ive never felt before. My Dr prescribed Meloxicam daily when pain was bad which worked well, but then I started to have
Janslade
in
The Australian Sjögren's Syndrome Association
7 years ago
Meloxicam
Has anyone taken meloxicam for pain? If so how did it work for you? I just started it on Monday and other than being a little woozy, it seems to be working.
Has anyone taken meloxicam for pain? If so how did it work for you? I just started it on Monday and other than being a little woozy, it seems to be working.
Fee09
in
My MSAA Community
7 years ago
Could which of these supplements interact with Levothyroxine?
I take a huge number supplements due to a condition of mine, and was wondering which ones of them could interact with Levothyroxine. I thought I won´t be a bad idea to ask here. Alpha-lipoic acid Vitamin C Vitamin D and Calcium Niacin Coenzyme Q-10 Selenium L-carnitine Vitamin B complex Magnesium Vitamin
I take a huge number supplements due to a condition of mine, and was wondering which ones of them could interact with Levothyroxine. I thought I won´t be a bad idea to ask here. Alpha-lipoic acid Vitamin C Vitamin D and Calcium Niacin Coenzyme Q-10 Selenium L-carnitine Vitamin B complex Magnesium Vitamin
Joshua2016
in
Thyroid UK
8 years ago
Fibromyalgia related ?
The Doctor has me on amnitriptyline 25 mgs. at bedtime. gabapantin 300mg 3x a day and Meloxicam 15mgs. a day. I'm putting on a lot of water weight and wonder witch pill is doing this. Do you have any idea?
The Doctor has me on amnitriptyline 25 mgs. at bedtime. gabapantin 300mg 3x a day and Meloxicam 15mgs. a day. I'm putting on a lot of water weight and wonder witch pill is doing this. Do you have any idea?
Linzyandsamsmom46
in
Fibromyalgia Action UK
8 years ago
Unexplained pelvic, hip & leg pain
Hello! In 2006, I was 18 years old when I fractured my right hip and the back of my pelvis in a car accident. I'm now almost 29 and ever since I've been having a sharp, shooting, sometimes radiating pain that starts in my hips or pelvis and shoots down my legs to my feet. I've been seeing a doctor and
Hello! In 2006, I was 18 years old when I fractured my right hip and the back of my pelvis in a car accident. I'm now almost 29 and ever since I've been having a sharp, shooting, sometimes radiating pain that starts in my hips or pelvis and shoots down my legs to my feet. I've been seeing a doctor and
Mbarkerphoto
in
Pelvic Pain Support Network
8 years ago
1
...
5
6
7
...
10
Next page
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