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Tenoxicam
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My doctors will drive me to... death due to conflicting medications.
Health insurers hate me. I am on about 15-10 medications. At age 53, I had a small heart attack. I was born with a defective heart valve that was replaced 7 years ago (Afib was the sign it needed replacement). I thought the afib was gone. Then, 2 months ago, that valve was again replaced along with
Health insurers hate me. I am on about 15-10 medications. At age 53, I had a small heart attack. I was born with a defective heart valve that was replaced 7 years ago (Afib was the sign it needed replacement). I thought the afib was gone. Then, 2 months ago, that valve was again replaced along with
Fish109
in
AF Association
6 years ago
Drug interactions
DRUG interactions: Can I take Gabapenten and meloxicam?
DRUG interactions: Can I take Gabapenten and meloxicam?
ADPSONNY
in
LUPUS UK
6 years ago
Meloxicam question....
Hi, I been taking meloxicam for over 4 months on a daily base. I am worry that I will have long term side affects. Does anyone out there take it for long term and if so how long? Please let me know . Thank you so much! Jen
Hi, I been taking meloxicam for over 4 months on a daily base. I am worry that I will have long term side affects. Does anyone out there take it for long term and if so how long? Please let me know . Thank you so much! Jen
Sunnyday1234
in
NRAS
6 years ago
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Nerve Pain?
Hi All, I have osteo-arthritis in both thumbs. I use Meloxicam for pain. Today I saw a hand specialist. He said it looks as if each thumb is becoming a trigger thumb. He suggested a steroid injection in the thumb joint. Since my right thumb is worse I went with the injection. I'm beginning to feel like
Hi All, I have osteo-arthritis in both thumbs. I use Meloxicam for pain. Today I saw a hand specialist. He said it looks as if each thumb is becoming a trigger thumb. He suggested a steroid injection in the thumb joint. Since my right thumb is worse I went with the injection. I'm beginning to feel like
krazy-girl
in
Arthritis Action
6 years ago
Multiple autoimmune conditions. Lupus too?
Where to start!I've been quite poorly with scleroderma, and I also have PBC, Sjogrens, and hypothyroidism. I have osteoarthritis and hyper flexibility joint syndrome. I am ACA pos, AMA pos, Igm pos, gastric parietal cell antibody positive, and I have just found out that I'm anti ro pos, and anti sm pos
Where to start!I've been quite poorly with scleroderma, and I also have PBC, Sjogrens, and hypothyroidism. I have osteoarthritis and hyper flexibility joint syndrome. I am ACA pos, AMA pos, Igm pos, gastric parietal cell antibody positive, and I have just found out that I'm anti ro pos, and anti sm pos
MissusTee
in
LUPUS UK
6 years ago
Eliquis and Meloxicam
I have just started on Eliquis 5mg twice a day because my episodes of AF have increased in frequency lately. I used to have 1-2 episodes per year, but I have had 7 or 8 since the end of November. I have taken Meloxicam (Mobic) for arthritis for a couple of years and it works great - once a day with
I have just started on Eliquis 5mg twice a day because my episodes of AF have increased in frequency lately. I used to have 1-2 episodes per year, but I have had 7 or 8 since the end of November. I have taken Meloxicam (Mobic) for arthritis for a couple of years and it works great - once a day with
suenygaard
in
AF Association
6 years ago
Can anyone help me with a question about PMR?
Hi there, i was just diagnosed with PMR after 6 months of of pain and fatigue. I have been on meloxicam 7.5g/anti inflammatory pill since Jan. 16th because i showed inflammation as my CRP levels were at 10 on my first blood work and then was 11.2 on my second blood work results.This was before i had
Hi there, i was just diagnosed with PMR after 6 months of of pain and fatigue. I have been on meloxicam 7.5g/anti inflammatory pill since Jan. 16th because i showed inflammation as my CRP levels were at 10 on my first blood work and then was 11.2 on my second blood work results.This was before i had
englandgirl
in
PMRGCAuk
6 years ago
CRP levels...
Hi guys I'm currently on Methotrexate 5mget steroids and meloxicam anti inflammatory. My fingers and wrists are still swollen as are my ankles toes and feet - using splints and braces- and I'm now 18 months onfrom RA diagnosis. Still waiting for scans re biologics. So....my CRP came back at 5 is that
Hi guys I'm currently on Methotrexate 5mget steroids and meloxicam anti inflammatory. My fingers and wrists are still swollen as are my ankles toes and feet - using splints and braces- and I'm now 18 months onfrom RA diagnosis. Still waiting for scans re biologics. So....my CRP came back at 5 is that
marie66
in
NRAS
7 years ago
Is this a normal feeling with Plaquenil ?
Hi, I'm new to this site and to treatments for RA and Lupus. I was diagnosised 35 yrs ago with RA and recent blood work put me on the path to see a Rhuematiod Specialist. Dr. put me on Meloxicam and Plaquenil a week ago. I also take Gabapentin for Fibromyalgia . I feel like I'm dying !! Since I started
Hi, I'm new to this site and to treatments for RA and Lupus. I was diagnosised 35 yrs ago with RA and recent blood work put me on the path to see a Rhuematiod Specialist. Dr. put me on Meloxicam and Plaquenil a week ago. I also take Gabapentin for Fibromyalgia . I feel like I'm dying !! Since I started
gmasheila
in
LUPUS UK
7 years ago
Dysphagia(difficulty in swallowing) with Sjogren's syndrome.
I am a long retired doctor who has had SS for about 30 years and besides the rheumatoid arthritis, dry eyes and mouth, also have a very intermittent (once every 2 to 4 weeks) complete inability to swallow food that does not reach the stomach and has to come back up and lasts some 6 to 12 hours. It is
I am a long retired doctor who has had SS for about 30 years and besides the rheumatoid arthritis, dry eyes and mouth, also have a very intermittent (once every 2 to 4 weeks) complete inability to swallow food that does not reach the stomach and has to come back up and lasts some 6 to 12 hours. It is
ROBERT_CARMICHAEL
in
The Australian Sjögren's Syndrome Association
7 years ago
on enbrel, now adding arava
Have been on enbrel for 20 weeks now and actually have experience more pain in wrist than before. Rheumatologist wants me to start arava along with enbrel. I am also taking 5mgs prednisone daily, meloxicam every now and then. I also have hashimotos (hypothyroidism) and take levothyroxine. For a person
Have been on enbrel for 20 weeks now and actually have experience more pain in wrist than before. Rheumatologist wants me to start arava along with enbrel. I am also taking 5mgs prednisone daily, meloxicam every now and then. I also have hashimotos (hypothyroidism) and take levothyroxine. For a person
jujubee43
in
NRAS
7 years ago
In praise of Hydroxychloroquine
Its coming up for a year since I was formally diagnosed with sero-negative RA by a consultant rheumatologist. Ive now been in remission for the last six months and its clear I have a lot to be thankful for. I was started off on 15mg daily Prednisolone followed a few weeks later by HXQ, then tapered
Its coming up for a year since I was formally diagnosed with sero-negative RA by a consultant rheumatologist. Ive now been in remission for the last six months and its clear I have a lot to be thankful for. I was started off on 15mg daily Prednisolone followed a few weeks later by HXQ, then tapered
tonyaffe
in
NRAS
7 years ago
Biologics Feedback, please:)
Hello! Due to side effects, I'm scaling back on Methotrexate and my rheumy doc is going to add Humira, Enbrel or Remicade. I have an appointment with him next week to discuss the options. Would love to hear your experiences with these drugs, both positive and negative. I also take plaquenil and meloxicam
Hello! Due to side effects, I'm scaling back on Methotrexate and my rheumy doc is going to add Humira, Enbrel or Remicade. I have an appointment with him next week to discuss the options. Would love to hear your experiences with these drugs, both positive and negative. I also take plaquenil and meloxicam
Maddi1208
in
NRAS
7 years ago
Hi Ive been researching.
Living in the UK Cannabis or related Cannabis products are strictly illegal. I have asked my GP if there is any type of Cannabis that he could prescribe. He rudely told me no way. Online I have seen a website called CBD Brothers the site has a lot of positive reviews about how the capsules/oil can
Living in the UK Cannabis or related Cannabis products are strictly illegal. I have asked my GP if there is any type of Cannabis that he could prescribe. He rudely told me no way. Online I have seen a website called CBD Brothers the site has a lot of positive reviews about how the capsules/oil can
Heltadelta
in
Fibromyalgia Action UK
7 years ago
Arthritis in foot and ankle
Hi this is my first post. Amongst other joints, I have arthritis in my right ankle and foot. I have a swelling on the side of the arch which is very painful even to touch. Although I take Zapain and Meloxicam for pain relief, I am still in considerable pain. I also have Lupus and fibromyalgia. Thank
Hi this is my first post. Amongst other joints, I have arthritis in my right ankle and foot. I have a swelling on the side of the arch which is very painful even to touch. Although I take Zapain and Meloxicam for pain relief, I am still in considerable pain. I also have Lupus and fibromyalgia. Thank
flossy1
in
Arthritis Action
7 years ago
Seronegative RA in remission
It's coming up to a year since I was diagnosed with seronegative RA. The good news is that I'm in remission. That doesn't mean I'm symptomless , I wake every morning with stiffness in both hands, my feet are often tingly and numb and I can get tired quite easily. But the pain is gone and compared to
It's coming up to a year since I was diagnosed with seronegative RA. The good news is that I'm in remission. That doesn't mean I'm symptomless , I wake every morning with stiffness in both hands, my feet are often tingly and numb and I can get tired quite easily. But the pain is gone and compared to
Staycalmandcarryon
in
NRAS
7 years ago
What do you do about pain?
I am counting the days until I can see my rheumatologist but it's not until Aug 23rd There just doesn't seem much they can do for me at my primary's office. They gave me one 6 day round of steroids that helped some but after a few days off everything came back. To be fair, it's the busiest weeks of
I am counting the days until I can see my rheumatologist but it's not until Aug 23rd There just doesn't seem much they can do for me at my primary's office. They gave me one 6 day round of steroids that helped some but after a few days off everything came back. To be fair, it's the busiest weeks of
cheshcat
in
NRAS
7 years ago
Should I be concerned?
I am 70 years old, female & Caucasian. I had labs done in May 2016 ( eGFR. 58). Labs again Nov 2016 (eGFR. 48). Labs again April 2017 (eGFR. 42). I'm taking Simvastatin, Meloxicam & Lisinopril. I try to eat healthy-no caffeine & have eliminated any forms of asprin. I excercise daily & drink water constantly
I am 70 years old, female & Caucasian. I had labs done in May 2016 ( eGFR. 58). Labs again Nov 2016 (eGFR. 48). Labs again April 2017 (eGFR. 42). I'm taking Simvastatin, Meloxicam & Lisinopril. I try to eat healthy-no caffeine & have eliminated any forms of asprin. I excercise daily & drink water constantly
MimiSyl
in
Early CKD Support
7 years ago
enbrel
Hi was diagnosed over a year ago with RA and have only taken prednisone and sometimes meloxicam. my left wrist has been hurting on and off for sometime now. my RA doc had me get an MRI and found that it was all from RA and has now advised me to start takin Embrel. I am nervous about taking this because
Hi was diagnosed over a year ago with RA and have only taken prednisone and sometimes meloxicam. my left wrist has been hurting on and off for sometime now. my RA doc had me get an MRI and found that it was all from RA and has now advised me to start takin Embrel. I am nervous about taking this because
jujubee43
in
NRAS
7 years ago
new diagnosis
i just got diagnosed like three weeks ago. i've been crying every day since. each day i wonder if it will be the day i accept it finally. i'm constantly on this rollercoaster of emotions. what's worse than being devastated is seeing my boyfriend and family in shock and denial. my boyfriend says i'm gonna
i just got diagnosed like three weeks ago. i've been crying every day since. each day i wonder if it will be the day i accept it finally. i'm constantly on this rollercoaster of emotions. what's worse than being devastated is seeing my boyfriend and family in shock and denial. my boyfriend says i'm gonna
kay814
in
LUPUS UK
7 years ago
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