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Celecoxib / Celebrex
Does anyone have experience with taking Celebrex longer term? I've found it seems to do a great job of controlling inflammation for me. I'm wondering how long I might be allowed to take it. A question for my doc of course, but my next appt is a month away so I thought I would turn to the seasoned
Does anyone have experience with taking Celebrex longer term? I've found it seems to do a great job of controlling inflammation for me. I'm wondering how long I might be allowed to take it. A question for my doc of course, but my next appt is a month away so I thought I would turn to the seasoned
CeeY
in
NRAS
2 years ago
Happy weekend....What are two things you have gained from pandemic with MS or and other illnesses that may exist. making a list.TY!
I am thankful to you all..i look as i can to see how everyone is doing and honestly to hang on. i barely make it thru each day but ido and that is the point.I dont know if you all know how special you are?! I pray fall brings joy and holidays or stay vacation , or if a real vacation! It has been so
I am thankful to you all..i look as i can to see how everyone is doing and honestly to hang on. i barely make it thru each day but ido and that is the point.I dont know if you all know how special you are?! I pray fall brings joy and holidays or stay vacation , or if a real vacation! It has been so
jackiesj
in
My MSAA Community
2 years ago
Stopped smoking, stopped having seizures
Hi. I just wanted to share my experience here in the hope that it might help others. Four years ago I crashed my car whilst having, what I later found out to be, an absence seizure (I crashed into a lorry, luckily no one was hurt). I went to the doctor, surrendered my driving license and booked an
Hi. I just wanted to share my experience here in the hope that it might help others. Four years ago I crashed my car whilst having, what I later found out to be, an absence seizure (I crashed into a lorry, luckily no one was hurt). I went to the doctor, surrendered my driving license and booked an
FlemClandango
in
Epilepsy Action
2 years ago
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Anxiety Sky High
Hi Everyone, the last 6 weeks have been an absolute nightmare. I was on a Trial and all appeared to be stable when I suddenly developed a pleural effusion. As this showed malignant cells I was taken off the Trial. I had 2 drains at the hospital and decided to opt for a semi-permanent drain so the
Hi Everyone, the last 6 weeks have been an absolute nightmare. I was on a Trial and all appeared to be stable when I suddenly developed a pleural effusion. As this showed malignant cells I was taken off the Trial. I had 2 drains at the hospital and decided to opt for a semi-permanent drain so the
doodoolatrice
in
My Ovacome
2 years ago
Slightly off topic...Methotrexate and hair...what would you do?
I've been on methotrexate for 3 years, and it's kept my RA nicely at bay. My hair has thinned and gone very straw like, which annoys me. However, hair in other places has also thinned out, and a big plus is not shaving my legs very often as a result. I'm thinking of trying biotin to improve my not
I've been on methotrexate for 3 years, and it's kept my RA nicely at bay. My hair has thinned and gone very straw like, which annoys me. However, hair in other places has also thinned out, and a big plus is not shaving my legs very often as a result. I'm thinking of trying biotin to improve my not
greynot
in
NRAS
2 years ago
worried about hair on neck
hi everyone ... I have been worried about the hair growth on my neck and chin for a while. it started off as a few hairs and I shaved them off and as you can imagine they've just grown back stronger and darker. its gotten to the point people have said to me it looks like you have a beard .. which obviously
hi everyone ... I have been worried about the hair growth on my neck and chin for a while. it started off as a few hairs and I shaved them off and as you can imagine they've just grown back stronger and darker. its gotten to the point people have said to me it looks like you have a beard .. which obviously
teachic2222
in
PCOS UK (Verity)
2 years ago
Hair loss
Hi I’ve been experiencing hair loss for quite some time now, unsure if it’s down to having an underactive thyroid (although controlled) or to having been on methotrexate for a number of years, was also taking folic acid but this didn’t seem to be doing anything to relieve the problem. I have also gone
Hi I’ve been experiencing hair loss for quite some time now, unsure if it’s down to having an underactive thyroid (although controlled) or to having been on methotrexate for a number of years, was also taking folic acid but this didn’t seem to be doing anything to relieve the problem. I have also gone
Ninsy
in
NRAS
2 years ago
Big pharma never rest. A sad tale of corporate greed run amok.
Johnson & Johnson and a New War on Consumer Protection The company has spent billions on cases about one of its most popular products. As its executives try a brazen new legal strategy to stop the litigation, corporate America takes note. "
But what few of those consumers grasped until a series of
Johnson & Johnson and a New War on Consumer Protection The company has spent billions on cases about one of its most popular products. As its executives try a brazen new legal strategy to stop the litigation, corporate America takes note. "
But what few of those consumers grasped until a series of
MBAnderson
in
Cure Parkinson's
2 years ago
Sudden hair loss - thyroidectomy 38 years ago
I have suddenly started losing my hair, I have a bald patch on the top of my head which I am quite alarmed about. The Gp is arranging some blood tests but thinks it could be due to my thyroid. I had a thyroidectomy 38 years ago, been on levothyroxine 100mcg for years and have been fine. So I am shocked
I have suddenly started losing my hair, I have a bald patch on the top of my head which I am quite alarmed about. The Gp is arranging some blood tests but thinks it could be due to my thyroid. I had a thyroidectomy 38 years ago, been on levothyroxine 100mcg for years and have been fine. So I am shocked
Queenie22
in
Thyroid UK
2 years ago
PBC/AIH1 Positive
Just as I was wrapping my head around my April PBC diagnosis and taking Urso (which does seem to me improving my liver enzyme levels) a liver biopsy also confirmed that I am also positive for autoimmune hepatitis type 1 (AIH1). I know PBC and other autoimmune conditions tend to run in packs. Does anyone
Just as I was wrapping my head around my April PBC diagnosis and taking Urso (which does seem to me improving my liver enzyme levels) a liver biopsy also confirmed that I am also positive for autoimmune hepatitis type 1 (AIH1). I know PBC and other autoimmune conditions tend to run in packs. Does anyone
lovesoccer
in
PBC Foundation
2 years ago
Anyone Used Pascoe B12 Depot (Hydroxy)
Hi Guys and thank you all for all your help in my previous posts.... Has any one used Pascoe B12 Depot and did they notice any difference to Panpharma (Rotexmedica) Depot Hydroxy? I know it is stronger and there is only one different ingredient to Panpharma being Sodium Chloride instead of Sodium
Hi Guys and thank you all for all your help in my previous posts.... Has any one used Pascoe B12 Depot and did they notice any difference to Panpharma (Rotexmedica) Depot Hydroxy? I know it is stronger and there is only one different ingredient to Panpharma being Sodium Chloride instead of Sodium
WorkingProgress
in
Pernicious Anaemia Society
2 years ago
help with drinking 2 to 3 litres of water a day.
post allogeneic stem cell transplant I have been told I need to drink at least 2litres of water a day. With the medication I'm on I cannot drink plain water and have to flavour it and have with plenty of ice. Butstill find it difficult. Any advice on managing to get my full amount of water would be
post allogeneic stem cell transplant I have been told I need to drink at least 2litres of water a day. With the medication I'm on I cannot drink plain water and have to flavour it and have with plenty of ice. Butstill find it difficult. Any advice on managing to get my full amount of water would be
Kraskie1915
in
CLL Support
2 years ago
My mother's good news!
Hello, ladies, I wanted to share some good news with you because this community has always given me and my family so much hope. Today we got my mother's PET results and they showed stable disease. Her CA125 is 13. We are beyond thankful for these results. ❤️ She was diagnosed with OC Stage 4A in Dec
Hello, ladies, I wanted to share some good news with you because this community has always given me and my family so much hope. Today we got my mother's PET results and they showed stable disease. Her CA125 is 13. We are beyond thankful for these results. ❤️ She was diagnosed with OC Stage 4A in Dec
Uniquem
in
My Ovacome
2 years ago
Can Blindness be caused by using Aldara (Imiquimod) with GCA?
My dermatologist is once again pushing Aldara (in the US, it's called Imiquimod) to help control my pre-cancerous skin "spots" (Actinic Keratosis) on my head. I have GCA, and I'm concerned because this med induces your immune system to go into overdrive against the spots, killing them, which leads to
My dermatologist is once again pushing Aldara (in the US, it's called Imiquimod) to help control my pre-cancerous skin "spots" (Actinic Keratosis) on my head. I have GCA, and I'm concerned because this med induces your immune system to go into overdrive against the spots, killing them, which leads to
LIVEORDIEHEREIAM
in
PMRGCAuk
2 years ago
imuran
I have been on Imuran 50mg for over 3 years and will be on it another 2 for autoimmune hepatitis. I also have PBC and take ursodiol for that. Imuran has lowered my liver levels and has kept them stable for me. It suppresses your immune system but it’s manageable. My dr is hoping that after being on it
I have been on Imuran 50mg for over 3 years and will be on it another 2 for autoimmune hepatitis. I also have PBC and take ursodiol for that. Imuran has lowered my liver levels and has kept them stable for me. It suppresses your immune system but it’s manageable. My dr is hoping that after being on it
JJBae
in
PBC Foundation
2 years ago
imuran /Azathioprine
i’ve been started on Imuran/Azathioprine, for arthritis. I will have to be monitored closely, with labs due to my PBC. I was wondering if anyone else had their liver enzymes(inflammation), Get better while on this medication? My hepatologist, and Rheumatologist . Both agree, that if monitored closely
i’ve been started on Imuran/Azathioprine, for arthritis. I will have to be monitored closely, with labs due to my PBC. I was wondering if anyone else had their liver enzymes(inflammation), Get better while on this medication? My hepatologist, and Rheumatologist . Both agree, that if monitored closely
LorraineLouise
in
PBC Foundation
2 years ago
Update(My Experience): Day 21 after Circumcision Fully Healed: Fast Healing: Removed my Stitches: Foreign Body
Please, don't do as I did, please visit your GP for advice. The reason I could tell there was something wrong with my cut is that all my wounds heal so so fast. Straight into it, I am doing so well actually. Amazingly well. But this is how I managed to accelerate my healing. What happened was that
Please, don't do as I did, please visit your GP for advice. The reason I could tell there was something wrong with my cut is that all my wounds heal so so fast. Straight into it, I am doing so well actually. Amazingly well. But this is how I managed to accelerate my healing. What happened was that
AnotherMan
in
Men's Health Forum (Penis Health)
2 years ago
Oestriol and Lupus
I am 71 and have had recurrent UTIs. My GP has prescribed me Oestriol cream and told to use it daily, on my genitals, to help with the post-menopausal atrophy of the general area but particularly around my urethral opening. With oestriol I do not need progesterone. The leaflet in the box
I am 71 and have had recurrent UTIs. My GP has prescribed me Oestriol cream and told to use it daily, on my genitals, to help with the post-menopausal atrophy of the general area but particularly around my urethral opening. With oestriol I do not need progesterone. The leaflet in the box
skylark15
in
LUPUS UK
2 years ago
Adalimumab and psoriasis side effect?
Hi I've been on adalimumab for about ten weeks and two days after my last injection I came out in a rash on my feet and calves. I've had it swabbed and it's negative for virus and bacteria and the consensus seems to be that it might be psoriasis,which I've never had before but which can apparently
Hi I've been on adalimumab for about ten weeks and two days after my last injection I came out in a rash on my feet and calves. I've had it swabbed and it's negative for virus and bacteria and the consensus seems to be that it might be psoriasis,which I've never had before but which can apparently
Julia31
in
NRAS
2 years ago
GREAT video on PMB! If you are thinking about buying any photobiomodulation red light therapy device... this is a MUST WATCH
Don't throw away your money on the cheap, junk 'red light toys' (about $300 or so) that promise a lot... but are totally worthless. Watch these two neuro scientists explain why: https://youtu.be/iZbP2IVekh0 Now watch this one and get the best info I've seen yet in one short video on the power of
Don't throw away your money on the cheap, junk 'red light toys' (about $300 or so) that promise a lot... but are totally worthless. Watch these two neuro scientists explain why: https://youtu.be/iZbP2IVekh0 Now watch this one and get the best info I've seen yet in one short video on the power of
PDWarrior1900
in
Cure Parkinson's
2 years ago
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