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The "ABCDE minus L" diet for fighting CLL
Fewer lipids: https://ashpublications.org/blood/article/132/Supplement%201/3117/263679/Chronic-Lymphocytic-
Leukaemia
-Relies-on-Lipid I'm at the watch and worry stage with my CLL. I'll let you know after my next blood test If it appears to be working for me.
Fewer lipids: https://ashpublications.org/blood/article/132/Supplement%201/3117/263679/Chronic-Lymphocytic-
Leukaemia
-Relies-on-Lipid I'm at the watch and worry stage with my CLL. I'll let you know after my next blood test If it appears to be working for me.
HowardR
in
CLL Support
4 years ago
Surgery vs. CyberKnife
Had another PET 9/1 and the tumor grew from 1/8-2.2cm in three months. The needle biopsy I had in June was 'inconclusive'. The thoracic surgeon I went to for a second opinion wants to take the top lobe of my right lung. I looked into CyberKnife and had a consult with a radiology oncologist. She said
Had another PET 9/1 and the tumor grew from 1/8-2.2cm in three months. The needle biopsy I had in June was 'inconclusive'. The thoracic surgeon I went to for a second opinion wants to take the top lobe of my right lung. I looked into CyberKnife and had a consult with a radiology oncologist. She said
dunnellon
in
Lung Conditions Community Forum
4 years ago
CLL Australian Webinar 21 October 2020. Keynote speaker Prof Peter Hillmen, Leeds UK. Interview of Sharon Winton CEO Lymphoma Australia, Q&A
Join MC
Julie McCrossin
and keynote speaker - the world renowned clinician and researcher -
Prof. Peter Hillmen
from St James’s University Hospital Leeds, for a webinar that
promises
to be energetic and full of new information. People from all countries are welcome to join the webinar
Join MC
Julie McCrossin
and keynote speaker - the world renowned clinician and researcher -
Prof. Peter Hillmen
from St James’s University Hospital Leeds, for a webinar that
promises
to be energetic and full of new information. People from all countries are welcome to join the webinar
AussieNeil
Partner
in
CLL Support
4 years ago
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Wildfire smoke more dangerous than other air pollutants for asthma patients.
For people who suffer from asthma, wildfire smoke is more hazardous than other types of air pollution, according to a new study from the Desert Research Institute (DRI), the Renown Institute for Health Innovation (Renown IHI) and the Washoe County Health District (WCHD). The study, which published last
For people who suffer from asthma, wildfire smoke is more hazardous than other types of air pollution, according to a new study from the Desert Research Institute (DRI), the Renown Institute for Health Innovation (Renown IHI) and the Washoe County Health District (WCHD). The study, which published last
2greys
in
Lung Conditions Community Forum
4 years ago
MF for 30 years
Hello I was first diagnosed with MF in my late 30s when I had two young children. It had a massive effect on my life, as although I didn't have any symptoms at that stage, I was told that I might become seriously ill and potentially die within 10 years. This meant that I gave up worrying about my (non-existent
Hello I was first diagnosed with MF in my late 30s when I had two young children. It had a massive effect on my life, as although I didn't have any symptoms at that stage, I was told that I might become seriously ill and potentially die within 10 years. This meant that I gave up worrying about my (non-existent
Bullace
in
MPN Voice
4 years ago
Please join us and become involved in our Spot Leukaemia campaign during September
We may be living in uncertain times, but there is one thing we are certain of: awareness of
needs to be dramatically improved Read about the campaign here:
How can you get involved?
1.
We may be living in uncertain times, but there is one thing we are certain of: awareness of
needs to be dramatically improved Read about the campaign here:
How can you get involved?
1.
HAIRBEAR_UK
in
Leukaemia Support
4 years ago
Night Sweats
Hello CLL Community Friends. I hope you are all doing well, remaining healthy and safe, especially during these unprecedented crazy times. I was diagnosed with CLL in May of 2018. I've been on wait and watch. Just had a visit with my hematology oncologist last week. My numbers look good and my appointment
Hello CLL Community Friends. I hope you are all doing well, remaining healthy and safe, especially during these unprecedented crazy times. I was diagnosed with CLL in May of 2018. I've been on wait and watch. Just had a visit with my hematology oncologist last week. My numbers look good and my appointment
CouldBworse
in
CLL Support
4 years ago
On bone marrow biopsy (BMB)?
Hello everyone, People with PV/ET regularly (e.g., per month) test their blood to keep track of cell counts and other things. How about bone marrow biopsy (BMB)? Are there repeats of BMB test to check changes after the first one that was performed to detect any mutation like JK2 ? If yes, how the results
Hello everyone, People with PV/ET regularly (e.g., per month) test their blood to keep track of cell counts and other things. How about bone marrow biopsy (BMB)? Are there repeats of BMB test to check changes after the first one that was performed to detect any mutation like JK2 ? If yes, how the results
samiris
in
MPN Voice
4 years ago
VenR in Relapsed CLL: 4-Year Results and Evaluation of Impact of Genomic Complexity and Gene Mutations from MURANO 3 study
This is an important evaluation and insight into how your CLL profile affects your response to VR in relapsed and refractory CLL. Sadly it looks like bad genetics is still relatively bad news in terms of PFS even on VenR. "[i]In previous analyses of the MURANO study, fixed-duration venetoclax plus rituximab
This is an important evaluation and insight into how your CLL profile affects your response to VR in relapsed and refractory CLL. Sadly it looks like bad genetics is still relatively bad news in terms of PFS even on VenR. "[i]In previous analyses of the MURANO study, fixed-duration venetoclax plus rituximab
Jm954
Administrator
in
CLL Support
4 years ago
Joint pain/Bone pain with MF
Recently diagnosed with post ET MF, I have started to get aching in my knees and wrists/hands. I will be able to ask my consultant about it next week but I wondered if this is common with MF or possibly to do with Ruxolitinib. I'm not clear on what bone pain would feel like. It seems to happen more
Recently diagnosed with post ET MF, I have started to get aching in my knees and wrists/hands. I will be able to ask my consultant about it next week but I wondered if this is common with MF or possibly to do with Ruxolitinib. I'm not clear on what bone pain would feel like. It seems to happen more
Otterfield
in
MPN Voice
4 years ago
MPN-u unclassified
Hi I’ve only just been diagnosed with MPN-u unclassified so still trying to get my head around things .Am I right I’m thinking it’s a slow growth blood cancer ? I have no mutations but slightly raised platelets ( for 21years & I’m 51) but slight scarring on bone marrow which is a little fibrous .Really
Hi I’ve only just been diagnosed with MPN-u unclassified so still trying to get my head around things .Am I right I’m thinking it’s a slow growth blood cancer ? I have no mutations but slightly raised platelets ( for 21years & I’m 51) but slight scarring on bone marrow which is a little fibrous .Really
Lizzy19
in
MPN Voice
4 years ago
Some good news and hope
A very special day today. My wife Jan was diagnosed with an incurable blood cancer CLL this day 9 years ago age 39. We are in Ireland. After 3 very sick years we were fortunate that she was able to access a clinical trial in the UK and in 2014 started a drug Ibrutinib which targets the cancer. Her
A very special day today. My wife Jan was diagnosed with an incurable blood cancer CLL this day 9 years ago age 39. We are in Ireland. After 3 very sick years we were fortunate that she was able to access a clinical trial in the UK and in 2014 started a drug Ibrutinib which targets the cancer. Her
Irishcll
in
CLL Support
4 years ago
Newly diagnosed and hoping for a bit of advice
I always assumed it was something autoimmune that would everntually show itself and didn't really consider a lymphoma/
leukaemia
type disease. Before Christmas a few lymph nodes popped up in my neck. Not big but enough for me to notice them.
I always assumed it was something autoimmune that would everntually show itself and didn't really consider a lymphoma/
leukaemia
type disease. Before Christmas a few lymph nodes popped up in my neck. Not big but enough for me to notice them.
Pdaquinas
in
CLL Support
4 years ago
Are immature cells bad and why do I need another bone marrow biopsy?
Have been MF for 15 months and being treated with Ruxolitinib. Not showing any symptoms and feel well, other than an enlarged spleen. Blood counts are good, except for a slightly lower Haemaglobin concentrate, and slightly increased white cells. My last blood test showed some immature velds, so they
Have been MF for 15 months and being treated with Ruxolitinib. Not showing any symptoms and feel well, other than an enlarged spleen. Blood counts are good, except for a slightly lower Haemaglobin concentrate, and slightly increased white cells. My last blood test showed some immature velds, so they
billybrock
in
MPN Voice
4 years ago
Starting hydroxycarbamide and scared!
Hi everyone. It's been a while since I posted but I have been reading a lot on here and find it so reassuring and comforting. I an 60, have PRV Jak2+ diagnosed 4 years ago and thought I was going to start Peginterferon in a couple of weeks (I had delayed starting last year as had holiday booked in
Hi everyone. It's been a while since I posted but I have been reading a lot on here and find it so reassuring and comforting. I an 60, have PRV Jak2+ diagnosed 4 years ago and thought I was going to start Peginterferon in a couple of weeks (I had delayed starting last year as had holiday booked in
Tmg59
in
MPN Voice
4 years ago
Who s tried to get a blue badge with an advanced MPN
My wife is pushing me to apply to get a blue badge. My last pre transfusion Hb was 47 and I really thought that I was at risk of a severe superior mesenteric artey failure . Pre transfusion I did not eat for 4 days as anything in my stomach caused ischaemic symtoms which were only relieved by lying on
My wife is pushing me to apply to get a blue badge. My last pre transfusion Hb was 47 and I really thought that I was at risk of a severe superior mesenteric artey failure . Pre transfusion I did not eat for 4 days as anything in my stomach caused ischaemic symtoms which were only relieved by lying on
skodaguy
in
MPN Voice
4 years ago
Night Sweats
I was diagnosed with CLL May of 2018. Still on wait & watch. I am 61. Over the last 40 years I would get periodic night sweats, very randomly. Once a year, then over the last 20 years, I would have a few night sweats year. Over the last 5 years, I get them a few days in a row, then nothing for months
I was diagnosed with CLL May of 2018. Still on wait & watch. I am 61. Over the last 40 years I would get periodic night sweats, very randomly. Once a year, then over the last 20 years, I would have a few night sweats year. Over the last 5 years, I get them a few days in a row, then nothing for months
CouldBworse
in
CLL Support
4 years ago
Myelofibrosis - thank you for the support
A few days ago I posted about my new diagnosis of post ET Myelofibrosis and I just want to say thank you for all the responses and support I received. Without this forum I would feel quite lost. I'm feeling absolutely exhausted today, as if having my morning shower was enough exertion for one day. However
A few days ago I posted about my new diagnosis of post ET Myelofibrosis and I just want to say thank you for all the responses and support I received. Without this forum I would feel quite lost. I'm feeling absolutely exhausted today, as if having my morning shower was enough exertion for one day. However
Otterfield
in
MPN Voice
4 years ago
CLL Expert Access 2nd Opinion from CLL Society from your home at no cost -unfortunately for USA Residents only
A CLL EXPERT PHYSICIAN CAN GIVE YOU A 2nd OPINION ONLINE AT NO COST TO YOU! APPLY NOW! • Easy to qualify • Easy to apply online • No need to leave your house https://cllsociety.org/cll-society-expert-access/ CLL Society Expert Access™ Program application: https://cllsociety.org/2019-expert-access-start
A CLL EXPERT PHYSICIAN CAN GIVE YOU A 2nd OPINION ONLINE AT NO COST TO YOU! APPLY NOW! • Easy to qualify • Easy to apply online • No need to leave your house https://cllsociety.org/cll-society-expert-access/ CLL Society Expert Access™ Program application: https://cllsociety.org/2019-expert-access-start
lankisterguy
Volunteer
in
CLL Support
4 years ago
Aussies, please consider enrolling in this study into the personal impact of CLL and help our world wide CLL/SLL community
Australians diagnosed with chronic lymphocytic
leukaemia
/small lymphocytic lymphoma (CLL/SLL), whether in watch and wait or in treatment:- [i]- Are you ready to have your say on the support, care & information patients need? - Are you ready for your experience to help others in the future?
Australians diagnosed with chronic lymphocytic
leukaemia
/small lymphocytic lymphoma (CLL/SLL), whether in watch and wait or in treatment:- [i]- Are you ready to have your say on the support, care & information patients need? - Are you ready for your experience to help others in the future?
AussieNeil
Partner
in
CLL Support
4 years ago
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