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Chemical pregnancy but feeling more confused!?
Evening ladies, So Friday and Saturday faint positive tests. Sunday morning lighter, started to get cramps and bleeding and then clots today. Spoke to GP as clinic said can’t help as natural positive. GP said go A&E to be referred to EPU, they did pregnancy test and negative and then did bloods and
Evening ladies, So Friday and Saturday faint positive tests. Sunday morning lighter, started to get cramps and bleeding and then clots today. Spoke to GP as clinic said can’t help as natural positive. GP said go A&E to be referred to EPU, they did pregnancy test and negative and then did bloods and
BECIO
in
Fertility Network 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
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 CARE
3 years ago
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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
5 weeks post FET, good HCG but mega headache
Hi, I’m 5 weeks 2 days with good beta tests however have developed the most cracking headache. I normally get this kind of headache before my period so terrified that something is very wrong. No bleeding and too early for scan which is scheduled in 12 days time.
Hi, I’m 5 weeks 2 days with good beta tests however have developed the most cracking headache. I normally get this kind of headache before my period so terrified that something is very wrong. No bleeding and too early for scan which is scheduled in 12 days time.
Snurf
in
Fertility Network UK
3 years ago
Low beta hcg 100 d14p5dt and spotting - looking for similar stories where this is not ectopic!
I am 14 days post a fresh blastocyst transfer and my hcg is low but rising (36 day 11, 72 day 13, and today 102 😐). I have some very mild occasional cramps and spotting, with some stringy blood stained mucus discharge (hope not TMI!). I assumed when the bleeding started after the initial low beta it
I am 14 days post a fresh blastocyst transfer and my hcg is low but rising (36 day 11, 72 day 13, and today 102 😐). I have some very mild occasional cramps and spotting, with some stringy blood stained mucus discharge (hope not TMI!). I assumed when the bleeding started after the initial low beta it
singleswimmer
in
Fertility Network UK
3 years ago
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
Scientists discover novel oncogenic driver gene in human lung cancer
A research team led by Prof. WANG Yuexiang from the Shanghai Institute of Nutrition and Health (SINH) of the Chinese Academy of Sciences discovered a novel oncogenic driver gene in human lung cancer, the leading cause of cancer-related mortality worldwide. Their findings were published in Journal
A research team led by Prof. WANG Yuexiang from the Shanghai Institute of Nutrition and Health (SINH) of the Chinese Academy of Sciences discovered a novel oncogenic driver gene in human lung cancer, the leading cause of cancer-related mortality worldwide. Their findings were published in Journal
2greys
in
Lung Conditions Community Forum
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
Transplant at age 68 or not
I've had myelofibrosis for about 30 years and been on ruxolitinib successfully for about 8 years. We have just moved to Scotland and my new consultant has laid it on the line that rux doesn't go on working for ever and my only other option is transplant. This seems right to me but I am very nervous about
I've had myelofibrosis for about 30 years and been on ruxolitinib successfully for about 8 years. We have just moved to Scotland and my new consultant has laid it on the line that rux doesn't go on working for ever and my only other option is transplant. This seems right to me but I am very nervous about
Bullace
in
MPN Voice
3 years ago
Has anyone used cordyceps as an adjunctive treatment for kidney disease?
Cordyceps worm mold is widely used in China to treat kidney disease, and some scientific studies indicate that it may reduce creatinine values in patients with chronic kidney disease. I have never found found much personal benefit from it. Conclusions of recent Chinese study: "Current evidence shows
Cordyceps worm mold is widely used in China to treat kidney disease, and some scientific studies indicate that it may reduce creatinine values in patients with chronic kidney disease. I have never found found much personal benefit from it. Conclusions of recent Chinese study: "Current evidence shows
Falkenhayn
in
Kidney Transplant Patient Support
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
NICE Recommends Acalabrutinib for treating CLL for certain groups
NICE has approved Acalabrutinib as monotherapy and is recommended as an option for untreated
chronic
lymphocytic
leukaemia
(CLL) in adults, [u]BUT ONLY IF[/u]: * there is a 17p deletion or TP53 mutation, or * there is no 17p deletion or TP53 mutation, and fludarabine plus cyclophosphamide and rituximab
NICE has approved Acalabrutinib as monotherapy and is recommended as an option for untreated
chronic
lymphocytic
leukaemia
(CLL) in adults, [u]BUT ONLY IF[/u]: * there is a 17p deletion or TP53 mutation, or * there is no 17p deletion or TP53 mutation, and fludarabine plus cyclophosphamide and rituximab
Jm954
Administrator
in
CLL Support
3 years ago
Should FISH test be repeated?
Does anyone know if the FISH test is repeated for people with stage zero CLL? I had the test when I was first diagnosed in December 2017, and assume it hasn’t been repeated because my office exam with my hematologist this month didn’t reveal swollen lymph nodes or enlarged spleen.
Does anyone know if the FISH test is repeated for people with stage zero CLL? I had the test when I was first diagnosed in December 2017, and assume it hasn’t been repeated because my office exam with my hematologist this month didn’t reveal swollen lymph nodes or enlarged spleen.
Myfavoritecat
in
CLL Support
3 years ago
Greater Understanding of PV, ET Drives Potential New Treatment Options
“Continued high-impact research may soon foster the development of disease-modifying therapies for PV and ET and satisfy this need for the optimal management of patients with these MPNs,” they said. Researchers are also determining how to best optimize current treatment options, including JAK inhibitors
“Continued high-impact research may soon foster the development of disease-modifying therapies for PV and ET and satisfy this need for the optimal management of patients with these MPNs,” they said. Researchers are also determining how to best optimize current treatment options, including JAK inhibitors
Manouche
in
MPN Voice
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
Suggestions where to find CBC pre-made spreadsheets
I apologize up-front to ask the subject question as this topic previously had great responses. Then trying to find those references buried in posts was ... well a challenge I admit I failed at. So taking the easier route thought I’d ask question in a post. New in the CLL “adventure” and so I’m gonna
I apologize up-front to ask the subject question as this topic previously had great responses. Then trying to find those references buried in posts was ... well a challenge I admit I failed at. So taking the easier route thought I’d ask question in a post. New in the CLL “adventure” and so I’m gonna
Pin57
in
CLL Support
3 years ago
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