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Otitis externa
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Advice
Hi everyone hope you are all well. Haven't posted for a while but I am seeking some advice. Been to see the GP today after a request came from my consultant in the Heath to put me back on warfarin. Seems that my echo and CT scan came back fine and am now on waiting list for my third ablation(second pulmonary
Hi everyone hope you are all well. Haven't posted for a while but I am seeking some advice. Been to see the GP today after a request came from my consultant in the Heath to put me back on warfarin. Seems that my echo and CT scan came back fine and am now on waiting list for my third ablation(second pulmonary
Vissy
in
AF Association
9 years ago
Aspergillosis - Definitely from my old apartment...
I am having the city test the building, air and water... but wondering if anyone else has ever heard of a situation where multiple people developed aspergillosis (beginning as pulmonary or
otitis
externa
infections,,. the ear seemed most common denominator) from the water supply?
I am having the city test the building, air and water... but wondering if anyone else has ever heard of a situation where multiple people developed aspergillosis (beginning as pulmonary or
otitis
externa
infections,,. the ear seemed most common denominator) from the water supply?
petersonkc
in
Aspergillosis and Rare Fungal Infection Support
10 years ago
I read that feces matter can be used to fight/ cure C-DIFF
I wonder can this cure Colitis & Reflux. Both these problems surface after a colonoscopy. I am now on Lialda, with folic acid as well as Dexilant. Two of these medications have extremely high co-pays and there is nothing less costly to take. I supplement with probiotics. I still get bouts of the
I wonder can this cure Colitis & Reflux. Both these problems surface after a colonoscopy. I am now on Lialda, with folic acid as well as Dexilant. Two of these medications have extremely high co-pays and there is nothing less costly to take. I supplement with probiotics. I still get bouts of the
dwitt
in
Lung Conditions Community Forum
10 years ago
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Generic Drugs
There was some discussion recently about different batches of drugs causing different side effects so I thought I would talk to my mate at the pharmacy when I collected my December party bag (Have you got yours organised?) . It seems that in MOST cases the manufacturer (generic or specific) makes no
There was some discussion recently about different batches of drugs causing different side effects so I thought I would talk to my mate at the pharmacy when I collected my December party bag (Have you got yours organised?) . It seems that in MOST cases the manufacturer (generic or specific) makes no
BobD
Volunteer
in
AF Association
10 years ago
Changing from levonorgestrel to the mini pill?
Hi ladies! Just wondering if anyone on here is taking the mini pill to stop periods and how they're getting on with it? I used to take levonorgestrel back to back but after telling my doctor I was suffering with mirgraines for the past couple of weeks, she wouldn't prescribe me with any more due to the
Hi ladies! Just wondering if anyone on here is taking the mini pill to stop periods and how they're getting on with it? I used to take levonorgestrel back to back but after telling my doctor I was suffering with mirgraines for the past couple of weeks, she wouldn't prescribe me with any more due to the
Lucebyrne
in
Endometriosis UK
10 years ago
Problems, Problems.
For the last 12mths I have been having monthly injections of Simponi golimumab, and monthly blood tests, approx. 9 months ago I had a telephone call from the consultant at the hospital informing me that my "white blood count recorded 0.2" stop Simponi injections until further notice, within 2 weeks the
For the last 12mths I have been having monthly injections of Simponi golimumab, and monthly blood tests, approx. 9 months ago I had a telephone call from the consultant at the hospital informing me that my "white blood count recorded 0.2" stop Simponi injections until further notice, within 2 weeks the
Scorpius
in
NRAS
10 years ago
Simponi (golimumab)
I was injecting "Embrel" for 12 months for the control of my R/A after this time the medication ceased to work and caused suppression of my white blood cell count, I then changed to "Simponi" monthly injections and have been using this since Nov last year, over the last month the muscle pain has returned
I was injecting "Embrel" for 12 months for the control of my R/A after this time the medication ceased to work and caused suppression of my white blood cell count, I then changed to "Simponi" monthly injections and have been using this since Nov last year, over the last month the muscle pain has returned
Scorpius
in
NRAS
10 years ago
I may be trying for my RA , Simponi Aria! Has anyone tried or taking this?
After trying to get Enbrel , and not getting any funding to help pay for it right now. My doctor is now checking on a different drug called Simponi Aria . And wants to do IV infusions ! He's thinking the insurance may pay more if it's a IV infusion!! Any way just wondering if any one has any information
After trying to get Enbrel , and not getting any funding to help pay for it right now. My doctor is now checking on a different drug called Simponi Aria . And wants to do IV infusions ! He's thinking the insurance may pay more if it's a IV infusion!! Any way just wondering if any one has any information
gingeq
in
NRAS
10 years ago
I have Colitis & Reflux
I use Lialda for the colitis and it stays in check. For the reflux I use Dexilant and I thought this would also remain in check. Recently had surgery for PAD in my legs. Actually just the first leg and I came down with a server case of reflux where by bile would constantly come up. The hospital gave
I use Lialda for the colitis and it stays in check. For the reflux I use Dexilant and I thought this would also remain in check. Recently had surgery for PAD in my legs. Actually just the first leg and I came down with a server case of reflux where by bile would constantly come up. The hospital gave
dwitt
in
IBS Network
10 years ago
Susie
Diagnosis microscopic colitis 2010. Got two family member with Crohn 's and ulcerative colitis.
Diagnosis microscopic colitis 2010. Got two family member with Crohn 's and ulcerative colitis.
psychosue
in
Crohn's and Colitis Support
10 years ago
Help! Tongue and lip ulcer
Started Ibrutinib 12 days ago. Receiving 3rd of 4 weekly Rituximab infusions this week. Developed painful tongue ulcer about a week ago. Any ideas to reduce pain???
Started Ibrutinib 12 days ago. Receiving 3rd of 4 weekly Rituximab infusions this week. Developed painful tongue ulcer about a week ago. Any ideas to reduce pain???
Tovtovtov
in
CLL Support
10 years ago
Rituximab for RA
Hi, I'm new to this forum, but not new to RA. I'v been diagnosed 4 years ago and haven't discovered my cure yet. Tried Embrel, Simponi , RoActemra and now my rheumy wants to put me on Rituximab. My question is has it worked for anybody? I'm tired of using such strong medication myself without any
Hi, I'm new to this forum, but not new to RA. I'v been diagnosed 4 years ago and haven't discovered my cure yet. Tried Embrel, Simponi , RoActemra and now my rheumy wants to put me on Rituximab. My question is has it worked for anybody? I'm tired of using such strong medication myself without any
EleRA
in
NRAS
10 years ago
RA and colitis anybody??
Hi all. I've been taking 12.5 mg of Methotrexate for the last six years now for sera negative rheumatoid arthritis. However, for the last six months or so Iv been suffering with extreme bloating of my lower tummy area at the end of the day a few times a week. Very painful and lasts for hours. Long story
Hi all. I've been taking 12.5 mg of Methotrexate for the last six years now for sera negative rheumatoid arthritis. However, for the last six months or so Iv been suffering with extreme bloating of my lower tummy area at the end of the day a few times a week. Very painful and lasts for hours. Long story
Sweetie44
in
NRAS
10 years ago
Hi I am new to this site...I am about to move to injections. Can anyone share their experience
i have been asked if i want to take etanercept as a weekly jab, adalimumab as a fortnightly jab and golimumab as a monthly jab. mxt is doing nothing for me and my steroid injection lasted 8 weeks max. I have 2 permanently swollen fingers and another nodule growing on another finger. Can any any one
i have been asked if i want to take etanercept as a weekly jab, adalimumab as a fortnightly jab and golimumab as a monthly jab. mxt is doing nothing for me and my steroid injection lasted 8 weeks max. I have 2 permanently swollen fingers and another nodule growing on another finger. Can any any one
sarah1968
in
NRAS
10 years ago
Electronic Cigarettes
Hi Everyone, I have in front of me the latest document produced by the National Centre for Smoking Cessation and Training (NCSCT) that has been produced in partnership with Public Health England. I thought I would share it with you all :-) The National Centre for Smoking Cessation and Training (NCSCT
Hi Everyone, I have in front of me the latest document produced by the National Centre for Smoking Cessation and Training (NCSCT) that has been produced in partnership with Public Health England. I thought I would share it with you all :-) The National Centre for Smoking Cessation and Training (NCSCT
EmJay
Administrator
in
Quit Support
10 years ago
Has anyone developed a colitis post liver transplant?
And if so, do you know why? My local GI is a bit useless — he has contradicted himself at least three times in our last appointment and he recommended something that contradicted what another friend (not transplanted) was told by her GI doc about diet. I also checked online and my GI doc is totally,
And if so, do you know why? My local GI is a bit useless — he has contradicted himself at least three times in our last appointment and he recommended something that contradicted what another friend (not transplanted) was told by her GI doc about diet. I also checked online and my GI doc is totally,
SunnySideUpDawn
in
British Liver Trust
10 years ago
If I move out if the area will I still get my Simponi?
Hi, I have been on Simponi for almost 4 months, so have had 3 injections up to now and seeing good results . I was told I was only eligible for Simponi because I lived in an area that had full NHS funding. I may have to move as my husband has left me, but am worried if I go somewhere else I might not
Hi, I have been on Simponi for almost 4 months, so have had 3 injections up to now and seeing good results . I was told I was only eligible for Simponi because I lived in an area that had full NHS funding. I may have to move as my husband has left me, but am worried if I go somewhere else I might not
Deb16
in
NRAS
10 years ago
Beta 2 Microglobin - an exquisitely sensitive marker for disease activity in many hematologic disorders.
Increased serum beta2 microglobulin levels reflect increased activity of the disease process in question and can be an exquisitely sensitive marker for this purpose in many hematologic disorders. The reference range of beta2 microglobulin in urine samples is 0-0.3 µg/mL. In serum or plasma samples,
Increased serum beta2 microglobulin levels reflect increased activity of the disease process in question and can be an exquisitely sensitive marker for this purpose in many hematologic disorders. The reference range of beta2 microglobulin in urine samples is 0-0.3 µg/mL. In serum or plasma samples,
Mikey47
in
CLL Support
10 years ago
Coeliac & colitis flare up - is it possible that getting glutened could trigger a flare up of colitis
I have recently been diagnosed with colitis having been diagnosed with coeliac the previous year. I am just coming off prednisolone down to 2 a day & am starting to worry that if I accidentally get 'glutened' it may trigger off a flare up.
I have recently been diagnosed with colitis having been diagnosed with coeliac the previous year. I am just coming off prednisolone down to 2 a day & am starting to worry that if I accidentally get 'glutened' it may trigger off a flare up.
lessan
in
Gluten Free Guerrillas
10 years ago
my son has been diagnosed with RA, since he has been on salazopyrin his symptoms have improved dramatically .however he is still in agony
with his feet so much that he can hardly walk after his work .He has had steriod injections in his ankles and they have only helped a little . Any one with this experience
with his feet so much that he can hardly walk after his work .He has had steriod injections in his ankles and they have only helped a little . Any one with this experience
ronyrathie
in
NRAS
10 years ago
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