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Venous ulcer compression system
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mouth ulcer
I have a painful mouth ulcer under my tongue and am on mtx, sulfasalazine and have a systemic steroid injection approx. every 8 weeks, I know that mouth ulcers are a side effect, but should I contact the GP or just treat it? don't want to appear that I am overreacting to GP, I have ongoing issues with
I have a painful mouth ulcer under my tongue and am on mtx, sulfasalazine and have a systemic steroid injection approx. every 8 weeks, I know that mouth ulcers are a side effect, but should I contact the GP or just treat it? don't want to appear that I am overreacting to GP, I have ongoing issues with
Shelley04
in
NRAS
10 years ago
Please tell me this eventually sucks less? - Endometriosis.
I've had horrific periods since they first started. It was a blight all through secondary school. Midway through college I was put on the pill and then eventually the implant for the pain etc (I didn't want to use the pill as contraception as my memory is crap). They did tests and couldn't find any cysts
I've had horrific periods since they first started. It was a blight all through secondary school. Midway through college I was put on the pill and then eventually the implant for the pain etc (I didn't want to use the pill as contraception as my memory is crap). They did tests and couldn't find any cysts
Wishsprite
in
Endometriosis UK
10 years ago
Tried lots of oral drugs, where do i go now?
I was diagnosed three years ago with RA. Started on methetrexate, developed terrible mouth ulcers when i got to 8 pills a week. Started lefloridimide and lost hair. Then started a half dose (10 mg daily) of lefloridimide and 4 pills methetrexate weekly and that worked great on my RA symptoms without
I was diagnosed three years ago with RA. Started on methetrexate, developed terrible mouth ulcers when i got to 8 pills a week. Started lefloridimide and lost hair. Then started a half dose (10 mg daily) of lefloridimide and 4 pills methetrexate weekly and that worked great on my RA symptoms without
mainstreet
in
NRAS
10 years ago
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Cimzia/methotrexate/hydroxy = coldsores and mouth sores
I am quite used to my mouth shedding skin and having an occasional sore inside my mouth but since starting Cimzia a few months ago, am getting a recurring coldsore and more mouth sores than before (on the positive side, my joints feel much better, as do my energy levels). I am due to see rheumatology
I am quite used to my mouth shedding skin and having an occasional sore inside my mouth but since starting Cimzia a few months ago, am getting a recurring coldsore and more mouth sores than before (on the positive side, my joints feel much better, as do my energy levels). I am due to see rheumatology
Annielou
in
NRAS
10 years ago
Help with mouth ulcers! I have taken methetrexate for over 1 1/2 years without any mouth ulcers. Then a few started popping up. I upped my 1
Mg folic acid to 2 mg daily. I used magic mouth wash and a dental paste. I finally went off the mtx because they were awful. Been off for 5 weeks and they are worse then when i was on it. Has then happened to anyone? I'm still doing the mouth rinse and paste but they are awful. Any suggestions?
Mg folic acid to 2 mg daily. I used magic mouth wash and a dental paste. I finally went off the mtx because they were awful. Been off for 5 weeks and they are worse then when i was on it. Has then happened to anyone? I'm still doing the mouth rinse and paste but they are awful. Any suggestions?
mainstreet
in
NRAS
10 years ago
Rapid Generation of Virus-Specific T Cells Helps Fight Off Infection in Immunocompromised Patients
The lengthy, complex, and costly process required to produce target specific T-Cells to fight cancers and viruses is a huge barrier that needs to be overcome if this technique is ever going to be more than a laboratory curiosity that benefits only a select few patients. Despite this, researchers continue
The lengthy, complex, and costly process required to produce target specific T-Cells to fight cancers and viruses is a huge barrier that needs to be overcome if this technique is ever going to be more than a laboratory curiosity that benefits only a select few patients. Despite this, researchers continue
AussieNeil
Administrator
in
CLL Support
10 years ago
Bone marrow transplant with MF
I have been recently diagnosed with MF and am in the initial phase (being treated with PEGASYS). In your recent MF leaflet the article appears to indicated that a bone marrow transplant is a 'last resort' ('not commonly recommended'.... advanced disease). My hermatologist here in France appears to want
I have been recently diagnosed with MF and am in the initial phase (being treated with PEGASYS). In your recent MF leaflet the article appears to indicated that a bone marrow transplant is a 'last resort' ('not commonly recommended'.... advanced disease). My hermatologist here in France appears to want
crapaud
in
MPN Voice
10 years ago
Any suggestions for a painful mouth on Methotrexate?
After a recent increase in my Mtx, I have developed oral thrush and ulcers to my tongue. I am really struggling with the pain. Has anyone had any experience of this please?
After a recent increase in my Mtx, I have developed oral thrush and ulcers to my tongue. I am really struggling with the pain. Has anyone had any experience of this please?
Mazyanna
in
NRAS
10 years ago
GvHD of the lungs
Hi all I am new to this site. I am not posting about myself but about my 32 year old brother. 9 years ago he had a stem cell transplant to treat leukaemia (I was his donor), which has been in remission ever since. We have been lucky enough to have 9 good years during which time he has worked full time
Hi all I am new to this site. I am not posting about myself but about my 32 year old brother. 9 years ago he had a stem cell transplant to treat leukaemia (I was his donor), which has been in remission ever since. We have been lucky enough to have 9 good years during which time he has worked full time
elliemh
in
Lung Conditions Community Forum
10 years ago
newly diagnosed
hi i was diagnosed today with bechets its been queried for a while but now confirmed a bit daunting so any advice would be great from anyone that also has this disease. it all started really as a child with mouth ulcers after mouth ulcers and as i got older the ulcers got more and more persistant and
hi i was diagnosed today with bechets its been queried for a while but now confirmed a bit daunting so any advice would be great from anyone that also has this disease. it all started really as a child with mouth ulcers after mouth ulcers and as i got older the ulcers got more and more persistant and
shirley63_
in
Behçet's UK
10 years ago
Skin redness after removing compression stocking?
Hi everyone! I have a nagging doubt and as I don't know anyone with this condition, I'm reaching out to you to see if you can help. I'm relatively new to this condition and I'm still in the process of working my way to a proper diagnosis and will be having a lymphoscintigraphy next week. My left foot
Hi everyone! I have a nagging doubt and as I don't know anyone with this condition, I'm reaching out to you to see if you can help. I'm relatively new to this condition and I'm still in the process of working my way to a proper diagnosis and will be having a lymphoscintigraphy next week. My left foot
Chiquitita
in
LSN
10 years ago
Caelyx
Hi guys, if anyone out there has had caelyx, or is on it, experienced mouth ulcers? And the horrible taste that comes with it? I'm just getting over it but have another treatment this week. I have x 4 to go after this one. Any help would be great tks. Tess.
Hi guys, if anyone out there has had caelyx, or is on it, experienced mouth ulcers? And the horrible taste that comes with it? I'm just getting over it but have another treatment this week. I have x 4 to go after this one. Any help would be great tks. Tess.
cupakediva75
in
My Ovacome
10 years ago
German treatment of lymphoedema.
Do you know anything about german treatment? If you do, do you prefer still italian ( I belive it's english also) rather than german? All I know about it is that in Germany and Sweden, I guess, they prefer hard compression therapy, lymphatic drainage and at the end pneumatic massage. After this treatment
Do you know anything about german treatment? If you do, do you prefer still italian ( I belive it's english also) rather than german? All I know about it is that in Germany and Sweden, I guess, they prefer hard compression therapy, lymphatic drainage and at the end pneumatic massage. After this treatment
Aleksleg
in
LSN
10 years ago
Is anybody else troubled by sore mouth/tongue and loss of taste?
I have Raynauds and Scleroderma and just recently have been troubled by altered sensation in my mouth. It feels as if I have scalded my mouth (which I haven't) - tongue and mouth are sore and I haven't much sense of taste. I have been having reflux problems lately where my usual meds are not controlling
I have Raynauds and Scleroderma and just recently have been troubled by altered sensation in my mouth. It feels as if I have scalded my mouth (which I haven't) - tongue and mouth are sore and I haven't much sense of taste. I have been having reflux problems lately where my usual meds are not controlling
nannysue1950
in
Scleroderma & Raynaud's UK (SRUK)
10 years ago
Another Front Against Leukemia: Using Stem Cells to Make Bone Marrow Transplants Low-Risk
Another Israeli biotech firm (well, I guess that Karyopharm Therapeutics--the developer of KPT-330 being tested against Richter's--is only half-Israeli) is working on using stem cells to make bone marrow transplants extremely tolerable. It is an interesting technology. An article is here: http://israel21c.org
Another Israeli biotech firm (well, I guess that Karyopharm Therapeutics--the developer of KPT-330 being tested against Richter's--is only half-Israeli) is working on using stem cells to make bone marrow transplants extremely tolerable. It is an interesting technology. An article is here: http://israel21c.org
zevkalman
in
CLL Support
10 years ago
Has any one been told to prepare themselves for the possibility of a bone marrow transplant. I've had ET for 14years taking Hydrox in variou
Doses over the years. Told I had changed to MF only in November last year that was such a shock.Taken of Hydrox completely 4 weeks ago only take asprin at the moment. Due to anaemia sweats &fatigue & an enlarged spleen..its all happened so quickly. I feel they sew the seed to make you think talk to your
Doses over the years. Told I had changed to MF only in November last year that was such a shock.Taken of Hydrox completely 4 weeks ago only take asprin at the moment. Due to anaemia sweats &fatigue & an enlarged spleen..its all happened so quickly. I feel they sew the seed to make you think talk to your
softail
in
MPN Voice
10 years ago
sjogren's syndrome and sore swollen tongue???
I have sle and a handful of other auto immune disorders and have recently been diagnosed with sjogren's. My question is does anyone else suffer from a swollen sore tongue with sjogren's? My tongue is so swollen that it feels uncomfortable in my own mouth and even wakes me during the night. I'm currently
I have sle and a handful of other auto immune disorders and have recently been diagnosed with sjogren's. My question is does anyone else suffer from a swollen sore tongue with sjogren's? My tongue is so swollen that it feels uncomfortable in my own mouth and even wakes me during the night. I'm currently
sezzie
in
LUPUS UK
10 years ago
Misleading headlines - "Breakthrough cure" for MS
New results from stem cell transplantation research in mice have been published today, leading to misleading articles in a number of newspapers about what this could mean for people with MS. "Could stem cells help people paralysed by MS? Scientists reveal they are 'astonished' by landmark study" -
New results from stem cell transplantation research in mice have been published today, leading to misleading articles in a number of newspapers about what this could mean for people with MS. "Could stem cells help people paralysed by MS? Scientists reveal they are 'astonished' by landmark study" -
Sorrel_MS_Society
MS Society
in
Healthy Evidence
10 years ago
Bone marrow transplant
Hi. So I saw Dr Lachmann this week and he announces that my MRI shows a growing lesion on my brain, and that this means I may start getting ALD on top of my AMN. The only way to stop this is to do a bone marrow transplant, which is very very scary. Anyone has experience of this situation? And has anyone
Hi. So I saw Dr Lachmann this week and he announces that my MRI shows a growing lesion on my brain, and that this means I may start getting ALD on top of my AMN. The only way to stop this is to do a bone marrow transplant, which is very very scary. Anyone has experience of this situation? And has anyone
Nicolas
in
AMN EASIER
10 years ago
Hi. Anyone offer advice? I take steroid inhalers- recently diagnosed with oral thrush - not responding to Nystan and feeling like I have flu
Its been 6 days and everyday I am not feeling better - totally wiped out, no energy throat is sore although some of the white markings seem to have cleared up. Apart from my asthma i've generally been in good health and am 36 YO male. Is this a normal reaction to oral thrush? The fatigue/ill feeling
Its been 6 days and everyday I am not feeling better - totally wiped out, no energy throat is sore although some of the white markings seem to have cleared up. Apart from my asthma i've generally been in good health and am 36 YO male. Is this a normal reaction to oral thrush? The fatigue/ill feeling
mrrobinwu
in
Lung Conditions Community Forum
10 years ago
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