Search
Search
About
Log in
Join
Experiences with
Chorionic villus sampling (CVS)
Posts
Communities
6,477 public posts
Filter results
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
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
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
9 months ago
Want to take advantage of all our features? Just log in!
Log in
or
Join
is HCG 735 at 18 days post ovulation normal?
is HCG 735 at 18 days post ovulation normal?
is HCG 735 at 18 days post ovulation normal?
Leyla1989
in
Fertility Network UK
10 months ago
Never have I ever … and neither has anyone else 😳 *sensitive pic for some (( my pic got removed as was “offensive” to some ))
many of you know my last story and post on here. I last miscarried on the 22 nd July. I was 13 weeks. I gave birth to her on the floor in a cold hospital room as she just gushed out. I had a d&c after I fainted not that there was anything to come out .. or was there? I remember when I did hcg back
many of you know my last story and post on here. I last miscarried on the 22 nd July. I was 13 weeks. I gave birth to her on the floor in a cold hospital room as she just gushed out. I had a d&c after I fainted not that there was anything to come out .. or was there? I remember when I did hcg back
Corchi
in
Fertility Network UK
10 months ago
Pain in the spleen/splenomegaly
Hello, maybe someone has an idea. After 5 years w&w my spleen has now enlarged (splenomegaly). I've also been having pain on my left side for a few days now. Are there any natural or herbal ways I can support my spleen? Because I don't want to have a spleen removed. I don't take any other medicine,
Hello, maybe someone has an idea. After 5 years w&w my spleen has now enlarged (splenomegaly). I've also been having pain on my left side for a few days now. Are there any natural or herbal ways I can support my spleen? Because I don't want to have a spleen removed. I don't take any other medicine,
Omaschnabel
in
CLL Support
10 months ago
Mutation Levels
I have seen other discussions re bad mutations , on my regular letter to my doctor from my haematologist it states : Chronic Lymphocytic Leukemia associated with high risk variants including loss of the LEU and ATM genes. As per my normal blood results, do these have a high and low level and if so
I have seen other discussions re bad mutations , on my regular letter to my doctor from my haematologist it states : Chronic Lymphocytic Leukemia associated with high risk variants including loss of the LEU and ATM genes. As per my normal blood results, do these have a high and low level and if so
uide3095
in
CLL Support
10 months ago
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
10 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
10 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
8 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
10 months ago
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
11 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
11 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
11 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
10 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
10 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
10 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
10 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
11 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
10 months ago
1
...
18
19
20
...
100
Next page
10
20
30
40
50
60
70
80
90
100
Filter results
Clear filters
Posted in
All communities
Fertility Network UK
1590 results
CLL Support
1569 results
Lung Conditions Community Forum
383 results
View top 10 communities
Sort by
Most Relevant
Newest