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Possible **sensitive** faint positive
Morning ladies, yesterday I posted after have a really faint positive after leaving the HPT for a while. Today did another test and was a slightly darker line but still faint with First response. I am so shocked and confused. I am 17 days past ovulation and when I wipe light brown on tissue sorry
Morning ladies, yesterday I posted after have a really faint positive after leaving the HPT for a while. Today did another test and was a slightly darker line but still faint with First response. I am so shocked and confused. I am 17 days past ovulation and when I wipe light brown on tissue sorry
BECIO
in
Fertility Network UK
3 years ago
CLL + Trisomy 8?
Was diagnosed with CLL in 2018 at 45yrs old, started treatment in 2019 and just finished my 19th month of Obinituzamab, Venetoclax, and Ibrutinib trial. Had BMB and showed remaining small population of B-cells - dang! Also showed Trisomy 8? Seems very rare for CLL patient to have Trisomy 8. Oncologist
Was diagnosed with CLL in 2018 at 45yrs old, started treatment in 2019 and just finished my 19th month of Obinituzamab, Venetoclax, and Ibrutinib trial. Had BMB and showed remaining small population of B-cells - dang! Also showed Trisomy 8? Seems very rare for CLL patient to have Trisomy 8. Oncologist
RyStock
in
CLL Support
3 years ago
Development of the world's first digital model of a cancer cell
The computer model, developed under the lead management of researchers at TU Graz, simulates the cyclical changes in the membrane potential of a cancer cell using the example of human lung adenocarcinoma and opens up completely new avenues in cancer research. Computer models have been standard tools
The computer model, developed under the lead management of researchers at TU Graz, simulates the cyclical changes in the membrane potential of a cancer cell using the example of human lung adenocarcinoma and opens up completely new avenues in cancer research. Computer models have been standard tools
2greys
in
Lung Conditions Community Forum
3 years ago
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Last Call - Places available for today's UK CLL treatments update webinar
Dr Munir’s main clinical and research special interests are in
chronic
lymphocytic
leukaemia
, particularly in the assessment of the mechanism of action of novel targeted therapies. • Lianne Palmer, CLL-specific CNS at Oxford University Hospitals.
Dr Munir’s main clinical and research special interests are in
chronic
lymphocytic
leukaemia
, particularly in the assessment of the mechanism of action of novel targeted therapies. • Lianne Palmer, CLL-specific CNS at Oxford University Hospitals.
HAIRBEAR_UK
Founder Admin
in
CLL Support
3 years ago
Kidney issues post liver transplant
Hi I'm 1 year post liver transplant, but my kidneys seem to be taking a hit. My GFR is reducing at each blood test. It is now 39 and drops by about 5 every time. They've not said if it's now CKD but I'm worried as the internet says 39 is stage 3B. They have reduced my tacrolimus to 1mg twice daily,
Hi I'm 1 year post liver transplant, but my kidneys seem to be taking a hit. My GFR is reducing at each blood test. It is now 39 and drops by about 5 every time. They've not said if it's now CKD but I'm worried as the internet says 39 is stage 3B. They have reduced my tacrolimus to 1mg twice daily,
TBSW
in
British Liver Trust
3 years ago
Scientists identify 160 new drugs that could be repurposed against COVID-19
Cambridge scientists have identified 200 approved drugs predicted to work against COVID-19—of which only 40 are currently being tested in COVID-19 clinical trials. In a study published today in Science Advances, a team led by researchers at the University of Cambridge’s Milner Therapeutics Institute
Cambridge scientists have identified 200 approved drugs predicted to work against COVID-19—of which only 40 are currently being tested in COVID-19 clinical trials. In a study published today in Science Advances, a team led by researchers at the University of Cambridge’s Milner Therapeutics Institute
2greys
in
Lung Conditions Community Forum
3 years ago
CLL Ireland and CLL Support First Joint Webinar
Our first joint webinar! 31 May 6.30 pm - 8.00 pm London (1.30 pm EST) We are very pleased to announce our first joint webinar with CLL Ireland. We are privileged to have as our keynote speakers Dr Brian Koffman, founder and principal of the CLL Society, and Professor Patrick Thornton, Consultant
Our first joint webinar! 31 May 6.30 pm - 8.00 pm London (1.30 pm EST) We are very pleased to announce our first joint webinar with CLL Ireland. We are privileged to have as our keynote speakers Dr Brian Koffman, founder and principal of the CLL Society, and Professor Patrick Thornton, Consultant
UK-Sparky
in
CLL Support
3 years ago
UPDATE: WARWICK's ASCT Journey...
Mon Jun 28, 2021 9:18 pm Hello MPNers Since my last post I left hospital but after 10 days 5 days at my parents house till my kids got over sniffles and 5 days at home my liver function deranged significantly again so I was readmitted to Westmead Public Hospital. Today is day 22 of my stay back at hospital
Mon Jun 28, 2021 9:18 pm Hello MPNers Since my last post I left hospital but after 10 days 5 days at my parents house till my kids got over sniffles and 5 days at home my liver function deranged significantly again so I was readmitted to Westmead Public Hospital. Today is day 22 of my stay back at hospital
socrates_8
in
MPN Voice
3 years ago
Has anyone had their first beta/OTD on d8p5dt?
I have had faint positives on FRER for 72h (since PM d5p5dt) that are getting slowly darker and pinker but remaining quite pencil like. Last night I had a faint positive on a clear blue for the first time. But today I’ve done a dumb thing and got my hcg tested, 3 days before OTD 🤦🏻♀️. It’s really
I have had faint positives on FRER for 72h (since PM d5p5dt) that are getting slowly darker and pinker but remaining quite pencil like. Last night I had a faint positive on a clear blue for the first time. But today I’ve done a dumb thing and got my hcg tested, 3 days before OTD 🤦🏻♀️. It’s really
singleswimmer
in
Fertility Network UK
3 years ago
Tww for scan
i got 2100+ HCG at 15dp6dt. today is 17dp6dt now booked for another two weeks wait for the scan. I am super nervous. my heartbeat is so fast. all negative thoughts are coming over my mind. I don't know what should I do? This wait becomes very hard for me.
i got 2100+ HCG at 15dp6dt. today is 17dp6dt now booked for another two weeks wait for the scan. I am super nervous. my heartbeat is so fast. all negative thoughts are coming over my mind. I don't know what should I do? This wait becomes very hard for me.
Hiramunir78
in
Fertility Network UK
3 years ago
6.3 weeks no symptoms!?!?
Hey lovley ladies xx So I'm 6. 3 weeks pregnant I had my beta HCG on the 23rd it came back as low at 66, did a repeat the nurse said congratulations your beta rose to 227 so a good increase and something to calm the worry for probably an hour before I realised I have the dreaded scan to look forward
Hey lovley ladies xx So I'm 6. 3 weeks pregnant I had my beta HCG on the 23rd it came back as low at 66, did a repeat the nurse said congratulations your beta rose to 227 so a good increase and something to calm the worry for probably an hour before I realised I have the dreaded scan to look forward
Helensafc
in
Fertility Network UK
3 years ago
Sensitive post... BFP finally❤️✌️Allhamdulillah
387.87 beta hcg value at day 12 of FET... Is it a good one? Having bloating and pressure in lower pelvis area.. Constipated🙄
387.87 beta hcg value at day 12 of FET... Is it a good one? Having bloating and pressure in lower pelvis area.. Constipated🙄
Rihab1
in
Fertility Network UK
3 years ago
HCG at 107 on d9p5dt
Is this good? 2nd blood test on Monday
Is this good? 2nd blood test on Monday
Snurf
in
Fertility Network UK
3 years ago
Jakavi
I started Jakavi treatment some months ago as I was progressing from PV to myelofibrosis. I had immediate relief from itching but it seems to have returned. Enlsrged spleen, haematocrit down, platelets low and white cells not well controlled. What now?
I started Jakavi treatment some months ago as I was progressing from PV to myelofibrosis. I had immediate relief from itching but it seems to have returned. Enlsrged spleen, haematocrit down, platelets low and white cells not well controlled. What now?
lucieboo
in
MPN Voice
3 years ago
Functional Consequences of Mutations in Myeloproliferative Neoplasms
« Of great interest, a set of epigenetic mutations can co-exist with the phenotypic driver mutations in 35%–40% of MPNs. These epigenetic mutations, such as TET2, EZH2, ASXL1, or DNMT3A mutations, promote clonal hematopoiesis and increased fitness of aged hematopoietic stem cells in both clonal hematopoiesis
« Of great interest, a set of epigenetic mutations can co-exist with the phenotypic driver mutations in 35%–40% of MPNs. These epigenetic mutations, such as TET2, EZH2, ASXL1, or DNMT3A mutations, promote clonal hematopoiesis and increased fitness of aged hematopoietic stem cells in both clonal hematopoiesis
Manouche
in
MPN Voice
3 years ago
Experience with Tacrolimus with or without Azathioprine
Hi all! My drs are suggesting to put me on tacrolimus alongside AZA to help with my joint pain. Has anyone been on tacrolimus? With or without AZA or another immunosuppressant? How is your experience? Anyone have any knowledge/experience of long-term tacrolimus? Also, I got told by the nurse
Hi all! My drs are suggesting to put me on tacrolimus alongside AZA to help with my joint pain. Has anyone been on tacrolimus? With or without AZA or another immunosuppressant? How is your experience? Anyone have any knowledge/experience of long-term tacrolimus? Also, I got told by the nurse
Sandy1212
in
LUPUS UK
3 years ago
Getting frustrated with the delay approval of ropeg In the US
Sometimes I can't help to think if enough is being done for MPN sufferers. According to multiple research ropeg has shown superiority over hydroxyurea with Ultimate possible significant molecular response in a selective number of MNP patients. So why there's a delay in getting access
Sometimes I can't help to think if enough is being done for MPN sufferers. According to multiple research ropeg has shown superiority over hydroxyurea with Ultimate possible significant molecular response in a selective number of MNP patients. So why there's a delay in getting access
markgenious1981
in
MPN Voice
3 years ago
Joint Committee on Vaccination and Immunisation (JCVI) advice on third primary dose vaccination
lymphoid
leukaemia
, myeloma, Waldenstrom’s macroglobulinemia and other plasma cell dyscrasias (note: this list is not exhaustive) immunosuppression due to HIV/AIDS with a current CD4 count of <200 cells/µl for adults or children primary or acquired cellular and combined immune deficiencies – those with
lymphoid
leukaemia
, myeloma, Waldenstrom’s macroglobulinemia and other plasma cell dyscrasias (note: this list is not exhaustive) immunosuppression due to HIV/AIDS with a current CD4 count of <200 cells/µl for adults or children primary or acquired cellular and combined immune deficiencies – those with
crashdoll
in
Lung Conditions Community Forum
3 years ago
Someone please answer this
My sister was diagnosed in October with cml after she said she needed some blood work done from feeling unwell. She has developed a mutation that is resistant to most treatments. She is going down hill. Someone please answer my question. 1 year prior to her Lukiema she randomly had both retinas detached
My sister was diagnosed in October with cml after she said she needed some blood work done from feeling unwell. She has developed a mutation that is resistant to most treatments. She is going down hill. Someone please answer my question. 1 year prior to her Lukiema she randomly had both retinas detached
Natweb76
in
Leukaemia Support
3 years ago
Introduction of myself, PMF, from China
Hi, I'm Qi, from China, I'm 34 years old this year. I confirmed PMF in 2017. At that time, the splenomegaly was high, but it was not very high, and it was not so high all the time. These symptoms began to happen to me one after another as early as 2013. JAK2V617F gene mutation, there is only one mutation
Hi, I'm Qi, from China, I'm 34 years old this year. I confirmed PMF in 2017. At that time, the splenomegaly was high, but it was not very high, and it was not so high all the time. These symptoms began to happen to me one after another as early as 2013. JAK2V617F gene mutation, there is only one mutation
merlisa
in
MPN Voice
3 years ago
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