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Venous ulcer compression system
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Mouth Sores and HU
Hi Everyone, I've read most of the posts regarding mouth sores. I'm suffering right now and seems worse instead of better even with salt water baking soda rinse. I'm wondering if this is considered an allergic reaction to HU or a food perhaps, an immune system problem or is it viral like a cold sore
Hi Everyone, I've read most of the posts regarding mouth sores. I'm suffering right now and seems worse instead of better even with salt water baking soda rinse. I'm wondering if this is considered an allergic reaction to HU or a food perhaps, an immune system problem or is it viral like a cold sore
DH65
in
MPN Voice
8 years ago
Ulcers in mouth
Ladies, please help me with ulcers in my mouth. One I have is on my tongue, I haven't been eaten over a week now. I can't chew, swallow and talk (my husband is happy with me sitting quiet 😉), but I can't cope anymore. I've tried everything, lots of mouth washes, BMX, nystatin, salty water, coconut oil
Ladies, please help me with ulcers in my mouth. One I have is on my tongue, I haven't been eaten over a week now. I can't chew, swallow and talk (my husband is happy with me sitting quiet 😉), but I can't cope anymore. I've tried everything, lots of mouth washes, BMX, nystatin, salty water, coconut oil
Hairlessbeauty
in
My Ovacome
8 years ago
Stem cell transplant for AML 8 yrs on
Hi all as you can see from title I have been in remission for 8yrs following a HSCT from my brother. I would like to ask a question. I knew I would get lots of infections early post transplant which is to be expected. Now 8 yrs along I am still getting more than my fair share of colds, so much so I am
Hi all as you can see from title I have been in remission for 8yrs following a HSCT from my brother. I would like to ask a question. I knew I would get lots of infections early post transplant which is to be expected. Now 8 yrs along I am still getting more than my fair share of colds, so much so I am
Shazzzey
in
Leukaemia Support
8 years ago
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Need a little clarity..T cell histiocyte rich B cell lymphoma
I feel like a bit out of place as I'm not a lymphoma suffer. I have a younger brother in his 30s who was diagnosed with: T cell histiocyte rich B cell lymphoma in Sept 2013 He had 6 cycles of RCHOP completed by Jan 2014. Excellent response and PET scan clear. Relapsed in October 2014 Had 4 cycles
I feel like a bit out of place as I'm not a lymphoma suffer. I have a younger brother in his 30s who was diagnosed with: T cell histiocyte rich B cell lymphoma in Sept 2013 He had 6 cycles of RCHOP completed by Jan 2014. Excellent response and PET scan clear. Relapsed in October 2014 Had 4 cycles
1Anj1
in
Non Hodgkin's Lymphoma Friends
8 years ago
Act of Love
Hi I am new to this site and looking for people based in the Uk who have scleroderma. My sister who is also my best friend was diagnosed a year to date with diffuse systematic scleroderma. She is listed as Cole57 and we are both here to read about people's experiences, share what knowledge she has from
Hi I am new to this site and looking for people based in the Uk who have scleroderma. My sister who is also my best friend was diagnosed a year to date with diffuse systematic scleroderma. She is listed as Cole57 and we are both here to read about people's experiences, share what knowledge she has from
Shelley53a
in
Scleroderma & Raynaud's UK (SRUK)
8 years ago
Mouth sores
Have been on Hydroxy for 2 years now without suffering the dreaded mouth sores but all of a sudden I have had 2 cold sores and now have two very painful mouth ulcers. What is the best thing to treat these please. Even a cup of tea is so sore on my inner mouth. Cheers guys xx
Have been on Hydroxy for 2 years now without suffering the dreaded mouth sores but all of a sudden I have had 2 cold sores and now have two very painful mouth ulcers. What is the best thing to treat these please. Even a cup of tea is so sore on my inner mouth. Cheers guys xx
jillydabrat
in
MPN Voice
8 years ago
How do you deal with Methotrexate side effects
I had to come off subcut methotrexate after four weeks because of the nausea, stomach issues and oral thrush. It was decided to rechallenge it and I took my second dose on Saturday. After my first injection last week I was very sick. This week still tummy cramps etc and now I have the oral thrush back
I had to come off subcut methotrexate after four weeks because of the nausea, stomach issues and oral thrush. It was decided to rechallenge it and I took my second dose on Saturday. After my first injection last week I was very sick. This week still tummy cramps etc and now I have the oral thrush back
Frankiefarr
in
NRAS
8 years ago
1st week on venetoclax - WOW, not what we expected...
After reviewing jtaeross's post from 3 months ago I wanted to share our experience on venetoclax. My husband just stared venetoclax 20mg we are on day 6 after failing on Ibrutinib after 18months and he is 17p, 52 years old - diagnosed at 45 It has been a hell of a week with threats of TML - he had to
After reviewing jtaeross's post from 3 months ago I wanted to share our experience on venetoclax. My husband just stared venetoclax 20mg we are on day 6 after failing on Ibrutinib after 18months and he is 17p, 52 years old - diagnosed at 45 It has been a hell of a week with threats of TML - he had to
NMMP
in
CLL Support
8 years ago
Autologous stem cell transplantation
Going to do autologous stem cell transplant.for relapsed follicular lymphoma. And new dbcl. After 2 weeks. Any body has been through that? Let me know please. Thanks. And God bless you all.
Going to do autologous stem cell transplant.for relapsed follicular lymphoma. And new dbcl. After 2 weeks. Any body has been through that? Let me know please. Thanks. And God bless you all.
Bhlool
in
LSN
8 years ago
mouth ulcers
hello, I am dealing with ulcers in my mouth. about 2 or 3 from what i can see. They are in really crappy spots one on the side of my tongue so its constantly rubbing on my teeth and another on the back of my mouth like on the left side of the throat opening (kinda hard to explain) I also fee pain down
hello, I am dealing with ulcers in my mouth. about 2 or 3 from what i can see. They are in really crappy spots one on the side of my tongue so its constantly rubbing on my teeth and another on the back of my mouth like on the left side of the throat opening (kinda hard to explain) I also fee pain down
Jenniferlynn43
in
Behçet's UK
8 years ago
What to ask to be tested for
Hi guys, I haven't yet been diagnosed but have suffered all the same bad symptoms for many years but at 36 I am at my worst point. I am male very fit and active, I have been on dyoxicycline for well over a year which I feel had helped with mouth ulcers but I'm not sure what's going on with my skin, I
Hi guys, I haven't yet been diagnosed but have suffered all the same bad symptoms for many years but at 36 I am at my worst point. I am male very fit and active, I have been on dyoxicycline for well over a year which I feel had helped with mouth ulcers but I'm not sure what's going on with my skin, I
Hampo81
in
Behçet's UK
8 years ago
Autologous Stem Cell Transplantation for MS
Autologous Stem Cell Transplantation for MS: Progression-Free Survival Seen in Nearly Half of Patients By Amy Orciari Herman Edited by David G. Fairchild, MD, MPH, and Jaye Elizabeth Hefner, MD Autologous stem cell transplantation for multiple sclerosis might help slow neurologic progression in nearly
Autologous Stem Cell Transplantation for MS: Progression-Free Survival Seen in Nearly Half of Patients By Amy Orciari Herman Edited by David G. Fairchild, MD, MPH, and Jaye Elizabeth Hefner, MD Autologous stem cell transplantation for multiple sclerosis might help slow neurologic progression in nearly
erash
in
My MSAA Community
8 years ago
Post transplant feedback
Hello again. I am three months post stem cell transplant for NHL that crossed the blood brain barrier into my CNS. There are many restrictions for me and I wondered who else was in the same boat? Thank you.
Hello again. I am three months post stem cell transplant for NHL that crossed the blood brain barrier into my CNS. There are many restrictions for me and I wondered who else was in the same boat? Thank you.
Jennchap1
in
Non Hodgkin's Lymphoma Friends
8 years ago
Huge sore on roof of mouth
I have Lupus and other things too. Every 6 weeks or so I relapse and this involves having some mouth ulcers and needing to be in bed for a few days. I am on Methotrexate. I now have a huge mouth ulcer on the roof of my mouth, swollen mouth and glands up. Do others experience this?
I have Lupus and other things too. Every 6 weeks or so I relapse and this involves having some mouth ulcers and needing to be in bed for a few days. I am on Methotrexate. I now have a huge mouth ulcer on the roof of my mouth, swollen mouth and glands up. Do others experience this?
Iona467
in
NRAS
8 years ago
Sores in the mouth
Hi everybody. I have just taken my second table of Hydroxycarbamide. So far, so good. I am writing a 'just in case' post as I know that a lot people on this drug have mouth sores. A few weeks ago,on this sight, there was a very helpful post about a mouth rinse for mouth problems.I took down the details
Hi everybody. I have just taken my second table of Hydroxycarbamide. So far, so good. I am writing a 'just in case' post as I know that a lot people on this drug have mouth sores. A few weeks ago,on this sight, there was a very helpful post about a mouth rinse for mouth problems.I took down the details
Splb3317
in
MPN Voice
8 years ago
New here...
Diagnosed in July 2014- RCHOP treated in Pittsburgh at the Mario Lemieux Center for Blood Cancers. Relapsed in November of 2015, received RICE then BEAM before April 2016 auto stem cell transplant.
Diagnosed in July 2014- RCHOP treated in Pittsburgh at the Mario Lemieux Center for Blood Cancers. Relapsed in November of 2015, received RICE then BEAM before April 2016 auto stem cell transplant.
Mrjackwagon
in
Non Hodgkin's Lymphoma Friends
8 years ago
I'm new to this, please be gentle
So starting at the beginning I was diagnosed with Leukemia in 2014 at 23, then I had a stem cell transplant which is where it all went wrong; Being on all sorts of medication including steroids made me gain weight, then loose it, then gain it again; this wasn't helped by the fact I wasn't able to do
So starting at the beginning I was diagnosed with Leukemia in 2014 at 23, then I had a stem cell transplant which is where it all went wrong; Being on all sorts of medication including steroids made me gain weight, then loose it, then gain it again; this wasn't helped by the fact I wasn't able to do
lynn_dee_lou
in
Weight Loss Support
8 years ago
Disappointment.........needed a tooth axtraction ....
Will soon be participating in the flair trial so wanted to get this troublesome tooth out , to be honest should have had it out years ago but just carried on I have an irrational fear of dentists my achillies heel from childhood .......dentist said teeth were not in bad shape but the particular tooth
Will soon be participating in the flair trial so wanted to get this troublesome tooth out , to be honest should have had it out years ago but just carried on I have an irrational fear of dentists my achillies heel from childhood .......dentist said teeth were not in bad shape but the particular tooth
stewie
in
CLL Support
8 years ago
HCST
Has anyone looked into doing stem cell transplant? My neurologist told me that they wouldn't accept me because of my age 48 and because I have had MS for 9 years, think I want to try, this disease is so frustrating.
Has anyone looked into doing stem cell transplant? My neurologist told me that they wouldn't accept me because of my age 48 and because I have had MS for 9 years, think I want to try, this disease is so frustrating.
cnichols
in
My MSAA Community
8 years ago
Key questions to ask your consultant
Hi everyone, sorry if you thought from the title of this message that I am providing the answers - instead, I would like your views. If you want the main point of this post skip to end, but it might help give better answers if you read through] [
aside:
For anyone with the stamina, here is my
Hi everyone, sorry if you thought from the title of this message that I am providing the answers - instead, I would like your views. If you want the main point of this post skip to end, but it might help give better answers if you read through] [
aside:
For anyone with the stamina, here is my
Davdow
in
CLL Support
8 years ago
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