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Drs. Susan O'Brien and Catherine Wu Presented the Binet-Rai Medal at 20th International Workshop on Chronic Lymphocytic Leukemia
Two doctors who have spent many many hours helping the CLL community.
I FEEL SURE THAT WE ALL EXPRESS OUR MANY THANKS.
THIS IS AN AWARD THAT IS WELL DESERVED.
During this past weekend's 20th biennial International Workshop on Chronic Lymphocytic Leukemia (iwCLL), Susan M
Two doctors who have spent many many hours helping the CLL community.
I FEEL SURE THAT WE ALL EXPRESS OUR MANY THANKS.
THIS IS AN AWARD THAT IS WELL DESERVED.
During this past weekend's 20th biennial International Workshop on Chronic Lymphocytic Leukemia (iwCLL), Susan M
Kwenda
in
CLL Support
9 months ago
Glandular Fever virus and PMR?
Hello everyone, Does anyone know if the Glandular Fever virus could be linked with PMR? I contracted GF and Hepatitis B of the Liver in 2005, it took me 3 years to get over it and live my life normally, I took no drugs, it really was a case of rest and gentle exercise, the Drs warned me if I didn't
Hello everyone, Does anyone know if the Glandular Fever virus could be linked with PMR? I contracted GF and Hepatitis B of the Liver in 2005, it took me 3 years to get over it and live my life normally, I took no drugs, it really was a case of rest and gentle exercise, the Drs warned me if I didn't
MalloryMoss
in
PMRGCAuk
8 months ago
Shingles
I have CFS/ME, Fibromyalgia etcMy previous doctor from when I moved new what I had etc. I have had shingles maybe three times. But I can't understand why they have message my husband, who is younger then me and as diabetes for the first time for a shingles injections and he as never had shingles? Any
I have CFS/ME, Fibromyalgia etcMy previous doctor from when I moved new what I had etc. I have had shingles maybe three times. But I can't understand why they have message my husband, who is younger then me and as diabetes for the first time for a shingles injections and he as never had shingles? Any
sharron1
in
Fibromyalgia Action UK
8 months ago
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Spotlight on Chronic Lymphocytic Leukemia (CLL) May 24, 2023 Nicole Lamanna, MD- replay, slides and transcript
Spotlight on Chronic Lymphocytic Leukemia (CLL) May 24, 2023 Nicole Lamanna, MD https://www.lls.org/patient-education-webcasts/spotlight-chronic-lymphocytic-leukemia-cll https://youtu.be/6KziJk3zQ_I Topics Covered: Emerging therapies and clinical trials for CLL Managing side effects Strategies
Spotlight on Chronic Lymphocytic Leukemia (CLL) May 24, 2023 Nicole Lamanna, MD https://www.lls.org/patient-education-webcasts/spotlight-chronic-lymphocytic-leukemia-cll https://youtu.be/6KziJk3zQ_I Topics Covered: Emerging therapies and clinical trials for CLL Managing side effects Strategies
lankisterguy
Volunteer
in
CLL Support
9 months ago
LET'S TALK CLL- Patients & Doctors Discuss the Latest Live! SATURDAY, OCTOBER 14, 2023 Virtual program starts at 10am CDT 11am EDT
LIVE & IN-PERSON EVENT- LET'S TALK CLL Patients & Doctors Discuss the Latest Live! DATE: SATURDAY, OCTOBER 14, 2023 LOCATION: MD ANDERSON CANCER CENTER Virtual program begins at 10am (CT). Register here: https://us06web.zoom.us/webinar/register/5216926341361/WN_8BHNtMXZR9Gjf211Nh_lhA - We're
LIVE & IN-PERSON EVENT- LET'S TALK CLL Patients & Doctors Discuss the Latest Live! DATE: SATURDAY, OCTOBER 14, 2023 LOCATION: MD ANDERSON CANCER CENTER Virtual program begins at 10am (CT). Register here: https://us06web.zoom.us/webinar/register/5216926341361/WN_8BHNtMXZR9Gjf211Nh_lhA - We're
lankisterguy
Volunteer
in
CLL Support
9 months ago
Prolia
I have just received an email from my GP who has arranged for a F2F appointment to see me beginning January to discuss me starting to take Prolia. My last Dexascan in 2021 did show that I have osteoporosis, and I did take Alendronic Acid for the first two years of having Polymyalgia. Since then I have
I have just received an email from my GP who has arranged for a F2F appointment to see me beginning January to discuss me starting to take Prolia. My last Dexascan in 2021 did show that I have osteoporosis, and I did take Alendronic Acid for the first two years of having Polymyalgia. Since then I have
Purplegloss
in
PMRGCAuk
6 months ago
Shingrix availability on PBS in Australia from 1 November has been confirmed
[u][i]SEE THIS REPLY [/i][/u][u]for the latest update to this post[/u]: https://healthunlocked.com/cllsupport/posts/150056558/shingrix-availability-on-pbs-in-australia-from-1-november-has-been-confirmed?responses=150067213 Earlier this year, I posted about a possible change to the PBS to make Shingrix
[u][i]SEE THIS REPLY [/i][/u][u]for the latest update to this post[/u]: https://healthunlocked.com/cllsupport/posts/150056558/shingrix-availability-on-pbs-in-australia-from-1-november-has-been-confirmed?responses=150067213 Earlier this year, I posted about a possible change to the PBS to make Shingrix
CLLerinOz
Administrator
in
CLL Support
9 months ago
Pneumonia
HiJust wondering how long people have taken to recover from pneumonia. . Was in hospital for 6 days. Although I know I am on the mend I was wondering what other peoples experience were. I have asthma and bronchietasis. I am feeling very sorry for myself.. Appreciate any reply. Xx
HiJust wondering how long people have taken to recover from pneumonia. . Was in hospital for 6 days. Although I know I am on the mend I was wondering what other peoples experience were. I have asthma and bronchietasis. I am feeling very sorry for myself.. Appreciate any reply. Xx
teddyd
in
Lung Conditions Community Forum
8 months ago
Richters Transformation
I recently informed here that after nine therapy free years since 2014 (FCR) my CLL bounced back in 10/2022 with an DLBCL and a suspicion of Richters. Biopsy and Lab tests predicted that. Therefore I was immediately treated with R-CHOP 14 CI Therapy first in Hospital one week and then within the ambulance
I recently informed here that after nine therapy free years since 2014 (FCR) my CLL bounced back in 10/2022 with an DLBCL and a suspicion of Richters. Biopsy and Lab tests predicted that. Therefore I was immediately treated with R-CHOP 14 CI Therapy first in Hospital one week and then within the ambulance
seoul1949
in
CLL Support
9 months ago
Not positive but not negative?
I’ve just had a Day 5 FET and my hcg has come back at 17 on my first blood test. So it’s a wait and see! We have never gotten out the start gate before so I don’t know whether to be too hopeful or not. Has anyone had similar and had a good outcome? I’m 43 so I bit scared to get any kind of excited.
I’ve just had a Day 5 FET and my hcg has come back at 17 on my first blood test. So it’s a wait and see! We have never gotten out the start gate before so I don’t know whether to be too hopeful or not. Has anyone had similar and had a good outcome? I’m 43 so I bit scared to get any kind of excited.
winningreid
in
Fertility Network UK
9 months ago
Illness and taking T3 - something to consider?
just a thought I wanted to put out there and see what everyone else thinks… I am now prescribed T4 and T3 and it has been a bit of a life changer for me. Previous to the T3 being added, I was on mono T4 for years. To get out of bed and function, I had to have my T4 over range, whilst my T3 was scrapping
just a thought I wanted to put out there and see what everyone else thinks… I am now prescribed T4 and T3 and it has been a bit of a life changer for me. Previous to the T3 being added, I was on mono T4 for years. To get out of bed and function, I had to have my T4 over range, whilst my T3 was scrapping
Gilbo72
in
Thyroid UK
8 months ago
Slow rising HCG - bleeding and clots - ivf
Hi. I had a FET on 20/09. Tested positive on 02/10 with hcg blood reading of 592. Started spotting on 06/10 which has got progressively heavier - like a period and shedding lining. Went to EPAU today and nothing detected on scan but per transfer would be 5+3 and too early to detect anyway. My bloods
Hi. I had a FET on 20/09. Tested positive on 02/10 with hcg blood reading of 592. Started spotting on 06/10 which has got progressively heavier - like a period and shedding lining. Went to EPAU today and nothing detected on scan but per transfer would be 5+3 and too early to detect anyway. My bloods
Toffeepudding99
in
Fertility Network UK
9 months ago
IVF Positive - good HCG- bleeding 5 days later
I wonder if I am holding on to hope. Had FET and on testing date was positive- HCG level 592 at first blood test. 5 days later and I have started brown spotting - not enough to fill a liner but with a few streaky bits- like the start of a period perhaps….. is this an impending miscarriage? Did anyone
I wonder if I am holding on to hope. Had FET and on testing date was positive- HCG level 592 at first blood test. 5 days later and I have started brown spotting - not enough to fill a liner but with a few streaky bits- like the start of a period perhaps….. is this an impending miscarriage? Did anyone
Toffeepudding99
in
Fertility Network UK
9 months ago
shingles vaccination
hello. Has anyone had the shingles vaccination, I have PV and on Hydroxycarbamide. Wondering if to have it or not. take care x
hello. Has anyone had the shingles vaccination, I have PV and on Hydroxycarbamide. Wondering if to have it or not. take care x
Maisie10
in
MPN Voice
8 months ago
Feeling Cold
Does anyone feel really cold with AF? My partner says he feels cold all the time when he always used to be rather than me.
Does anyone feel really cold with AF? My partner says he feels cold all the time when he always used to be rather than me.
Natty_Knitter
in
AF Association
8 months ago
Round and round
had last O treatment end of June. I have been sick since 3 rounds of upper respiratory which has turned to pneumonia I can’t get out of this cycle. Supposed to see ms dr tomorrow to discuss pushing O back to 6 months I’ve been on 5 month. X-ray showed Mass on lungs which is either pneumonia or the big
had last O treatment end of June. I have been sick since 3 rounds of upper respiratory which has turned to pneumonia I can’t get out of this cycle. Supposed to see ms dr tomorrow to discuss pushing O back to 6 months I’ve been on 5 month. X-ray showed Mass on lungs which is either pneumonia or the big
NanaCC179
in
My MSAA Community
8 months ago
What does having a NEW KIDNEY feel like?
Hi All, I have been in the transplant list for a year now and still waiting to get called. I can’t just help to wonder what having a kidney transplant will feel like. Apart from the fact that it will be a gift of life and freedom from being tied down to dialysis. What does it feel like? Will you
Hi All, I have been in the transplant list for a year now and still waiting to get called. I can’t just help to wonder what having a kidney transplant will feel like. Apart from the fact that it will be a gift of life and freedom from being tied down to dialysis. What does it feel like? Will you
Imaanforever
in
Kidney Dialysis
7 months ago
Implantation Issues
Hi. I have been through 4 transfers with donor eggs. The first one was a miscarriage at 6 weeks. The other 3 were implantation failures. Following the 2nd and 3rd transfer, we went through KIR testing to check compatibility with donor and then had our three embryos PGTA tested. They all tested normal
Hi. I have been through 4 transfers with donor eggs. The first one was a miscarriage at 6 weeks. The other 3 were implantation failures. Following the 2nd and 3rd transfer, we went through KIR testing to check compatibility with donor and then had our three embryos PGTA tested. They all tested normal
75Toria
in
Fertility Network UK
9 months ago
flow cytometry is showing about 74% CLL involvement.
Is it likely that treatment might be needed in the near future? Husband is trisomy 12, TP53 negative. Mutated. He has splenomegaly, and enlarged nodes. Fish is in process. INTERPRETATION A phenotypically abnormal population with forward and right-angle scatter features of small lymphocytes constitutes
Is it likely that treatment might be needed in the near future? Husband is trisomy 12, TP53 negative. Mutated. He has splenomegaly, and enlarged nodes. Fish is in process. INTERPRETATION A phenotypically abnormal population with forward and right-angle scatter features of small lymphocytes constitutes
juniper1975
in
CLL Support
9 months ago
CLL and mRNA Vaccines
Just saw this abstract, which is one of the papers being presented at the Boston CLL conference: https://journals.plos.org/plosmedicine/article?id=10.1371/journal.pmed.1004157 I don't understand most of it, but this is one of the "Findings": [i]CLL patients and other immunocompromised populations
Just saw this abstract, which is one of the papers being presented at the Boston CLL conference: https://journals.plos.org/plosmedicine/article?id=10.1371/journal.pmed.1004157 I don't understand most of it, but this is one of the "Findings": [i]CLL patients and other immunocompromised populations
BWHR
in
CLL Support
9 months ago
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