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Venous ulcer compression system
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ulcers and boils ???
Hi Can anyone inform me please , do you get mouth ulcers , sores & boils up nose & a runny nose , as if you’ve got a constant cold with PmR ? I go through boxes and boxes of tissues !
Hi Can anyone inform me please , do you get mouth ulcers , sores & boils up nose & a runny nose , as if you’ve got a constant cold with PmR ? I go through boxes and boxes of tissues !
TedTheMaineCoon
in
PMRGCAuk
10 months ago
horrible taste in mouth, nothing tastes good
After looking in my mouth, my GP said, I think you have thrush. A dentist had said an X-ray showed no tooth infection was causing the bad taste. GP prescribed nystatin. After taking it the bad taste is worse than ever, especially in the morning, and the area behind my top and bottom teeth feels
After looking in my mouth, my GP said, I think you have thrush. A dentist had said an X-ray showed no tooth infection was causing the bad taste. GP prescribed nystatin. After taking it the bad taste is worse than ever, especially in the morning, and the area behind my top and bottom teeth feels
Mstiles
in
PMRGCAuk
11 months ago
What is your experience with oral thrush and nystatin?
I’m experiencing a bad taste in my mouth that’s affecting my taste of food and sometimes feeling like there’s a lump in my throat when swallowing. . My GP looked in my mouth and said “you may have thrush”. She prescribed Nystatin. I don’t have the white plaques that bleed, etc., just
I’m experiencing a bad taste in my mouth that’s affecting my taste of food and sometimes feeling like there’s a lump in my throat when swallowing. . My GP looked in my mouth and said “you may have thrush”. She prescribed Nystatin. I don’t have the white plaques that bleed, etc., just
Mstiles
in
PMRGCAuk
11 months ago
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mouth ulcers
anyone have mouth ulcers on tongue whilst taking hydroxycarbamide ? I have ET jak 2 Painful mouth ulcers on my tongue. Any suggestions how to treat ? Thanks Hazel
anyone have mouth ulcers on tongue whilst taking hydroxycarbamide ? I have ET jak 2 Painful mouth ulcers on my tongue. Any suggestions how to treat ? Thanks Hazel
HazeBlue
in
MPN Voice
11 months ago
Mouth ulcers
Hello does anyone else or us there any link between hashimotos and mouth ulcers and cold sores. I suffer terribly from both. Particularly if I've drank too much alcohol or run down or have pmt. My mouth ulcers can be terrible and struggle to eat/drink. It normally happens after damaging my mouth
Hello does anyone else or us there any link between hashimotos and mouth ulcers and cold sores. I suffer terribly from both. Particularly if I've drank too much alcohol or run down or have pmt. My mouth ulcers can be terrible and struggle to eat/drink. It normally happens after damaging my mouth
Billy2023
in
Thyroid UK
1 year ago
Carbimazole & Antithyroid arthritis
Hello, I’m a 33 year old woman, I was diagnosed with an overactive thyroid around 2months ago, was put on 15mg carbimazole a day. Started with a painful mouth ulcer so stopped medication & waited to see my consultant for advice as I didn’t know how bad the mouth ulcer had to be, he advised me to go back
Hello, I’m a 33 year old woman, I was diagnosed with an overactive thyroid around 2months ago, was put on 15mg carbimazole a day. Started with a painful mouth ulcer so stopped medication & waited to see my consultant for advice as I didn’t know how bad the mouth ulcer had to be, he advised me to go back
Abimilne
in
Thyroid UK
1 year ago
carbimazole & antithyroid arthritis
Hello, I’m a 33 year old woman, I was diagnosed with an overactive thyroid around 2months ago, was put on 15mg carbimazole a day. Started with a painful mouth ulcer so stopped medication & waited to see my consultant for advice as I didn’t know how bad the mouth ulcer had to be, he advised me to go back
Hello, I’m a 33 year old woman, I was diagnosed with an overactive thyroid around 2months ago, was put on 15mg carbimazole a day. Started with a painful mouth ulcer so stopped medication & waited to see my consultant for advice as I didn’t know how bad the mouth ulcer had to be, he advised me to go back
Abimilne
in
NRAS
1 year ago
behcets, mouth ulcers and gum disease
has anyone here with behcets experienced poor oral health? i found it was never an issue for me until recently, i went to the dentist and she said that i had gingivitis. ive yet to go back as it was a bit traumatic, but has anyone had experience with "poor oral health" being linked to behcets i.e your
has anyone here with behcets experienced poor oral health? i found it was never an issue for me until recently, i went to the dentist and she said that i had gingivitis. ive yet to go back as it was a bit traumatic, but has anyone had experience with "poor oral health" being linked to behcets i.e your
jaquarius
in
Behçet's UK
1 year ago
On another subject …
Inspired bya post on another site I’d like to ask if anyone has high risk mutations and has NOT had a stem cell transplant and has NOT progressed to leukaemia? On the other site there were a few who had had MF for quite few years but with treatment were doing ok, and weren’t having transplants, for
Inspired bya post on another site I’d like to ask if anyone has high risk mutations and has NOT had a stem cell transplant and has NOT progressed to leukaemia? On the other site there were a few who had had MF for quite few years but with treatment were doing ok, and weren’t having transplants, for
lizzziep
in
MPN Voice
1 day ago
The Bone-Marrow-Transplant Revolution
https://www.theatlantic.com/health/archive/2024/04/bone-marrow-transplant-mismatched-donor/678100/
https://www.theatlantic.com/health/archive/2024/04/bone-marrow-transplant-mismatched-donor/678100/
EastBayDad
in
CLL Support
13 days ago
Stem cell transplant
I haven’t posted for a while as things have gotten very complicated for me recently my partner was diagnosed with stomach cancer and around the same time I ran out of options and stem is my last shot I have held off as long as I can so my partner could have surgery and get back on his feet but my dates
I haven’t posted for a while as things have gotten very complicated for me recently my partner was diagnosed with stomach cancer and around the same time I ran out of options and stem is my last shot I have held off as long as I can so my partner could have surgery and get back on his feet but my dates
Leighcox85
in
MPN Voice
17 days ago
Platelets dropped after obinituzumab and won't rise even after transfusion 🚨
Dear all, First of all, thank you very much for all the help and care I have always found on HealthUnlocked. I had my first infusion of obinituzumab and in my case, mainly due to my nephrotic syndrome kidney problem, I had a few problems. High fevers, which are common Attacks of hiccups that last
Dear all, First of all, thank you very much for all the help and care I have always found on HealthUnlocked. I had my first infusion of obinituzumab and in my case, mainly due to my nephrotic syndrome kidney problem, I had a few problems. High fevers, which are common Attacks of hiccups that last
BMFCDRW
in
CLL Support
18 days ago
Human stem cell transplantation for Parkinson’s disease: A systematic review
Interestinghttps://www.researchgate.net/publication/379454508_Human_stem_cell_transplantation_for_Parkinson's_disease_A_systematic_review_of_in_situ_survival_and_maturation_of_progenitors_derived_from_human_embryonic_or_induced_stem_cells_in_Parkinsonian_models
Interestinghttps://www.researchgate.net/publication/379454508_Human_stem_cell_transplantation_for_Parkinson's_disease_A_systematic_review_of_in_situ_survival_and_maturation_of_progenitors_derived_from_human_embryonic_or_induced_stem_cells_in_Parkinsonian_models
Farooqji
in
Cure Parkinson's
26 days ago
Momelotinib for Myelofibrosis
Hi, I have been suffering from primary MF for 9 years and have been on Ruxolitinib. However recently I was advised that Ruxolitinib is no longer effectively managing my MF. My platelets and Hb are low and my spleen has enlarged again. My consultant is trying to get me approved for Momelotinib. She
Hi, I have been suffering from primary MF for 9 years and have been on Ruxolitinib. However recently I was advised that Ruxolitinib is no longer effectively managing my MF. My platelets and Hb are low and my spleen has enlarged again. My consultant is trying to get me approved for Momelotinib. She
Cazbolac
in
MPN Voice
28 days ago
Travel and Ibrance
I was diagnosed with MBC in June, 2023. I am on Ibrance and letrozole. My medical history is complicated by having had a donor stem cell transplant in 2018 for T cell lymphoma. My immune system was compromised from that but now with Ibrance I'm not sure what to expect in terms of traveling and
I was diagnosed with MBC in June, 2023. I am on Ibrance and letrozole. My medical history is complicated by having had a donor stem cell transplant in 2018 for T cell lymphoma. My immune system was compromised from that but now with Ibrance I'm not sure what to expect in terms of traveling and
Artesa
in
SHARE Metastatic Breast Cancer
1 month ago
stem cell for et?
Would stem cell transplant be an option for ET? I cannot take the Hydrea or Anagralide. Thanks for your feed back
Would stem cell transplant be an option for ET? I cannot take the Hydrea or Anagralide. Thanks for your feed back
Preacherswife
in
MPN Voice
1 month ago
AXSL1 gene mutation
Hello Everyone, I have pmf-MF with JAK2 mutation and have been taking Rux since the end of 2018. Currently, Rux is took in combination with interferon. From the biopsy and blood routine, I have now reversed to PV (Hemoglobin has significantly improved, and the size of spleen has also shrunk a lot, although
Hello Everyone, I have pmf-MF with JAK2 mutation and have been taking Rux since the end of 2018. Currently, Rux is took in combination with interferon. From the biopsy and blood routine, I have now reversed to PV (Hemoglobin has significantly improved, and the size of spleen has also shrunk a lot, although
merlisa
in
MPN Voice
1 month ago
SCT journey update No.2
Hi all, following on from my last post, have just heard from my clinical nurse that they have found three very good donor matches on the registers!! Have been somewhat impatient waiting but as this situation is so new and different for everyone, has been difficult to gauge what is right or wrong. Anyway
Hi all, following on from my last post, have just heard from my clinical nurse that they have found three very good donor matches on the registers!! Have been somewhat impatient waiting but as this situation is so new and different for everyone, has been difficult to gauge what is right or wrong. Anyway
LFCLove
in
MPN Voice
1 month ago
Still on hold for stem cell transplant
David has now completed 3 cycles of Vidaza. He had a bone marrow biopsy several weeks ago. At first we thought the results were good, that his cancer cells had been reduced sufficiently to proceed with transplant. After our local oncologist spoke to the transplant specialist at Mayo, we received word
David has now completed 3 cycles of Vidaza. He had a bone marrow biopsy several weeks ago. At first we thought the results were good, that his cancer cells had been reduced sufficiently to proceed with transplant. After our local oncologist spoke to the transplant specialist at Mayo, we received word
dwolden
in
CLL Support
2 months ago
HSCT early in MS
This is an interesting story about two women who went to Mexico and got Hematopoietic Stem Cell Transplantation early in their disease. One, who was diagnosed with PPMS, received her transplant in the third year after diagnosis. The other, who was diagnosed with RRMS, got her transplant just twelve
This is an interesting story about two women who went to Mexico and got Hematopoietic Stem Cell Transplantation early in their disease. One, who was diagnosed with PPMS, received her transplant in the third year after diagnosis. The other, who was diagnosed with RRMS, got her transplant just twelve
BettysMom
in
My MSAA Community
2 months ago
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