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Tenoxicam
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Missymoo !
Hi all havnt been on for while due to ongoing pains n more symtoms everyday new symtom is waking at night n threwing up all over good job i got bathroom in bedroom i wasnt really woried untill last night the was blood in sick so rang Docs this morning n she ordered ultra sound for me so she thinks it
Hi all havnt been on for while due to ongoing pains n more symtoms everyday new symtom is waking at night n threwing up all over good job i got bathroom in bedroom i wasnt really woried untill last night the was blood in sick so rang Docs this morning n she ordered ultra sound for me so she thinks it
Hidden
in
Fibromyalgia Action UK
8 years ago
Medication for fibromyalgia
Hello has anyone tried Meloxicam was given with Omeprazole to protect my stomach
Hello has anyone tried Meloxicam was given with Omeprazole to protect my stomach
Muddle
in
My Fibro Community
8 years ago
Feeling discouraged
Hello! So my Rheumy increased my Plaquenil 200mg to twice daily along with Meloxicam 15mg and hydrocodone for pain. I think I'm feeling better since I'm not in constant pain. The problem is when I go out with my family it it requires a lot of walking and/or pushing our double stroller ( for our 7mo
Hello! So my Rheumy increased my Plaquenil 200mg to twice daily along with Meloxicam 15mg and hydrocodone for pain. I think I'm feeling better since I'm not in constant pain. The problem is when I go out with my family it it requires a lot of walking and/or pushing our double stroller ( for our 7mo
Twinks80
in
NRAS
8 years ago
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Onward, but with your love.
Thank hou my dear ones on the Other Side of The Pond. Interstitial lung disease, AND shrinking lung disease, are causing me great pain. Even hallow breathing hurts, and i still feel winded. I am demoralized, then alternatively, in high spirits knowing that i CAN heal this inspite of Western Allopathic
Thank hou my dear ones on the Other Side of The Pond. Interstitial lung disease, AND shrinking lung disease, are causing me great pain. Even hallow breathing hurts, and i still feel winded. I am demoralized, then alternatively, in high spirits knowing that i CAN heal this inspite of Western Allopathic
Casimir
in
LUPUS UK
8 years ago
Anything I can do at home to lessen severity of possible lupus?
Hi! I've been experiencing a lot of symptoms that lead me to believe I have lupus, though am unable to get a diagnosis until January at earliest. Sorry this is very long TL;DR- I have lots of lupus like symptoms, no diagnosis and would like home remedies for stomach + lung pain and fatigue I'm 22 female
Hi! I've been experiencing a lot of symptoms that lead me to believe I have lupus, though am unable to get a diagnosis until January at earliest. Sorry this is very long TL;DR- I have lots of lupus like symptoms, no diagnosis and would like home remedies for stomach + lung pain and fatigue I'm 22 female
Kyla65
in
LUPUS UK
8 years ago
Sulfasalazine medication for RA and lupus
I have lupus and RA. I was on Methotrexate and Meloxicam but due to side effects and high blood pressure, my rheumatologist took me off these meds and I'm starting sulfasalazine. Does anyone have any experiences with this drug? My doctor stated that this drug stays in your body for years even after
I have lupus and RA. I was on Methotrexate and Meloxicam but due to side effects and high blood pressure, my rheumatologist took me off these meds and I'm starting sulfasalazine. Does anyone have any experiences with this drug? My doctor stated that this drug stays in your body for years even after
Cindymc
in
LUPUS UK
8 years ago
When will it ever get better?
I've been in so much pain and having horrible fatigue for months, it just seems to not get any better. I'm still on the never ending rounds of steroids, which I hate how they make me feel. This is really depressing...how long will this last until I will have some relief? 🙁 I'm also on week 2 of the
I've been in so much pain and having horrible fatigue for months, it just seems to not get any better. I'm still on the never ending rounds of steroids, which I hate how they make me feel. This is really depressing...how long will this last until I will have some relief? 🙁 I'm also on week 2 of the
Twinks80
in
NRAS
8 years ago
MEDS REVIEW
Just a reminder to all who are on meds. Please ensure that you ask for a regular review to ensure that you protect your internal organs from permanent damage. I found out to my cost that not having this discussion removes options and now due to Meloxicam I have irreversible kidney damage. I now am off
Just a reminder to all who are on meds. Please ensure that you ask for a regular review to ensure that you protect your internal organs from permanent damage. I found out to my cost that not having this discussion removes options and now due to Meloxicam I have irreversible kidney damage. I now am off
Alexandria
in
Fibromyalgia Action UK
8 years ago
MEDS REVIEWS
Just a reminder to all who are on meds. Please ensure that you ask for a regular review to ensure that you protect your internal organs from permanent damage. I found out to my cost that not having this discussion removes options and now due to Meloxicam I have irreversible kidney damage. I now am off
Just a reminder to all who are on meds. Please ensure that you ask for a regular review to ensure that you protect your internal organs from permanent damage. I found out to my cost that not having this discussion removes options and now due to Meloxicam I have irreversible kidney damage. I now am off
Alexandria
in
LUPUS UK
8 years ago
New here!
Hello, I'm new to the group! I've recently been diagnosed with RA by my pcp, I also have a pending upcoming rheumatologist appt. My symptoms of RA started shortly after I delivered my twins earlier this year on 1/1/2016. Before we were discharged from the hospital, I had to get an MMR booster because
Hello, I'm new to the group! I've recently been diagnosed with RA by my pcp, I also have a pending upcoming rheumatologist appt. My symptoms of RA started shortly after I delivered my twins earlier this year on 1/1/2016. Before we were discharged from the hospital, I had to get an MMR booster because
Twinks80
in
NRAS
8 years ago
New here!
Hello, I'm new to the group! I've recently been diagnosed with RA by my pcp, I also have a pending upcoming rheumatologist appt. My symptoms of RA started shortly after I delivered my twins earlier this year on 1/1/2016. Before we were discharged from the hospital, I had to get an MMR booster because
Hello, I'm new to the group! I've recently been diagnosed with RA by my pcp, I also have a pending upcoming rheumatologist appt. My symptoms of RA started shortly after I delivered my twins earlier this year on 1/1/2016. Before we were discharged from the hospital, I had to get an MMR booster because
Twinks80
in
Cure Arthritis Community
8 years ago
Warfarin and pain medicmedications
I suffered terrible back pain for many years but successfully kept it under control using NSAIDS, namely meloxicam intermittently plus Omneprazole daily to protect against ulcers. But when I developed AF I was put on Warfarin and told not to take any more and told to take up to 2000mg .. acetaminophen
I suffered terrible back pain for many years but successfully kept it under control using NSAIDS, namely meloxicam intermittently plus Omneprazole daily to protect against ulcers. But when I developed AF I was put on Warfarin and told not to take any more and told to take up to 2000mg .. acetaminophen
tony85
in
AF Association
8 years ago
Black eyes
Hello :) hope everyone is as ok as possible. Just wondering if anyone has experienced puffy and bruised coloured eyes (under the eyes, where bags are!) with Ra? As I keep getting this and I'm not sure why. I recently stopped taking meloxicam as my consultant said it can cause water retention which she
Hello :) hope everyone is as ok as possible. Just wondering if anyone has experienced puffy and bruised coloured eyes (under the eyes, where bags are!) with Ra? As I keep getting this and I'm not sure why. I recently stopped taking meloxicam as my consultant said it can cause water retention which she
Simone_Holly
in
NRAS
8 years ago
White eyebrow!
I started Hydroxychloroquine in September as at that time thought to be MCTD - now undifferentiated inflammatory arthritis, ? Psoriatic arthritis, but posting here as some of you have experience of Hydroxychloroquine. I realise its a small thing compared to not being able to change a pillowcase or walk
I started Hydroxychloroquine in September as at that time thought to be MCTD - now undifferentiated inflammatory arthritis, ? Psoriatic arthritis, but posting here as some of you have experience of Hydroxychloroquine. I realise its a small thing compared to not being able to change a pillowcase or walk
mirren
in
NRAS
8 years ago
White eyebrow!
I started Hydroxychloroquine in September as at that time thought to be MCTD - now undifferentiated inflammatory arthritis, ? Psoriatic arthritis, but posting here as you have experience of Hydroxychloroquine. My left eyebrow is turning white. And my hair at hairline. Has anyone else had this? (Also
I started Hydroxychloroquine in September as at that time thought to be MCTD - now undifferentiated inflammatory arthritis, ? Psoriatic arthritis, but posting here as you have experience of Hydroxychloroquine. My left eyebrow is turning white. And my hair at hairline. Has anyone else had this? (Also
mirren
in
LUPUS UK
8 years ago
Anti-inflammatory diet....
Hi all, Happy New Year, I wonder if any of you can off me any advice and experience.... I'm under pressure to stop my Meloxicam which I managed quite well over the Autumn then struggled towards xmas and am back on 15mg a day. I think I need to look at my diet and wondered what experience people have
Hi all, Happy New Year, I wonder if any of you can off me any advice and experience.... I'm under pressure to stop my Meloxicam which I managed quite well over the Autumn then struggled towards xmas and am back on 15mg a day. I think I need to look at my diet and wondered what experience people have
Valent48
in
Fibromyalgia Action UK
8 years ago
Midiagnosed - update
Hi guys , just an update on my misdiagnosis. Had an appointment with my rheumatologist who agrees with the consultant radiologist that I do in fact have Dercums disease and not Lupus. I completely understand where and why it was over looked so I have stopped being angry. In fact I think I feel more
Hi guys , just an update on my misdiagnosis. Had an appointment with my rheumatologist who agrees with the consultant radiologist that I do in fact have Dercums disease and not Lupus. I completely understand where and why it was over looked so I have stopped being angry. In fact I think I feel more
chandlermandy
in
LUPUS UK
9 years ago
Misdiagnosed ?
Hi. I apologise for how long this is but worth reading and has been pretty cathartic for me to write . Last week I had a scan for kidney stones. Nothing there. I was however lucky enough to be scanned by a consultant radiologist who was teaching a student doctor. During the ultrasound they pressed
Hi. I apologise for how long this is but worth reading and has been pretty cathartic for me to write . Last week I had a scan for kidney stones. Nothing there. I was however lucky enough to be scanned by a consultant radiologist who was teaching a student doctor. During the ultrasound they pressed
chandlermandy
in
LUPUS UK
9 years ago
Any connections?
I have had Ra for approx 8yrs, had a few surgical procedures on left foot and ankle, been on MTX for the past 5yrs also sulfasalazine, meloxicam and all that comes with it. Have been plodding along, some times the pain is worse than others. In April I noticed a small lump in the corner of my right eye
I have had Ra for approx 8yrs, had a few surgical procedures on left foot and ankle, been on MTX for the past 5yrs also sulfasalazine, meloxicam and all that comes with it. Have been plodding along, some times the pain is worse than others. In April I noticed a small lump in the corner of my right eye
madambutterfly
in
NRAS
9 years ago
Thyroid Test Results....comments please.
I've had new test results and could do with some advice please. I've had hypothyroidism for eighteen years, I'm sixty eight now. My results at the moment are..... Plasma free T4 level 15.8 pmol/L (7.5 - 21.1 ) Plasma TSH level 0.37 mu/L (0.34 - 5.6 ) I've been
I've had new test results and could do with some advice please. I've had hypothyroidism for eighteen years, I'm sixty eight now. My results at the moment are..... Plasma free T4 level 15.8 pmol/L (7.5 - 21.1 ) Plasma TSH level 0.37 mu/L (0.34 - 5.6 ) I've been
Clover
in
Thyroid UK
9 years ago
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