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Genetic counseling & testing
Meanwhile, my oncologist at MN Oncology has recommended that I do
genetic
counseling
and further
genetic
and tumor testing. I am 43% Ashkenazi Jew (source: 23 & Me), which makes sense since my Mom's parents were both Jewish, from Hungary and Czech Republic.
Meanwhile, my oncologist at MN Oncology has recommended that I do
genetic
counseling
and further
genetic
and tumor testing. I am 43% Ashkenazi Jew (source: 23 & Me), which makes sense since my Mom's parents were both Jewish, from Hungary and Czech Republic.
Skifanatic
in
Advanced Prostate Cancer
1 year ago
Webinar: Research into inherited retinal disease and the benefits of genetic counselling
Research optometrist Shelley Black and genetic counsellor Claire Kirk join us from the Northern Ireland Clinical Research Network (NICRN) this month for our second My Macular and Me webinar. Shelley will be sharing information on the latest macular and inherited retinal disease research, while Claire
Research optometrist Shelley Black and genetic counsellor Claire Kirk join us from the Northern Ireland Clinical Research Network (NICRN) this month for our second My Macular and Me webinar. Shelley will be sharing information on the latest macular and inherited retinal disease research, while Claire
Carol_MacularSociety
Partner
in
Macular Society
8 months ago
SC5NA Gene mutation
hey, I’ve just been diagnosed with an SC5NA gene mutation after having genetic testing done which has identified the cause of my Brugada, I’ve now been advised I’m at risk of cardiomyopathy. Has anyone else experienced this diagnosis and can offer any advice?
hey, I’ve just been diagnosed with an SC5NA gene mutation after having genetic testing done which has identified the cause of my Brugada, I’ve now been advised I’m at risk of cardiomyopathy. Has anyone else experienced this diagnosis and can offer any advice?
Lilbandit88
in
British Heart Foundation
16 hours ago
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HiI found out I had APS during my 8th pregnancy in 2006. I had PEs. Fast forward to 2024. One of my adult daughters had PEs in pregnancy, horrific treatment from hospital, which was minutes from losing both my daughter and her baby (at 39 weeks) I'm now waiting to have a genetic test for APs as I
HiI found out I had APS during my 8th pregnancy in 2006. I had PEs. Fast forward to 2024. One of my adult daughters had PEs in pregnancy, horrific treatment from hospital, which was minutes from losing both my daughter and her baby (at 39 weeks) I'm now waiting to have a genetic test for APs as I
Dawnm10
in
Hughes Syndrome APS Forum
6 days ago
First PSA post surgery
Hello, Just had my first 3 month PSA test post surgery. <0.01. Good news but need to monitor every 3 years due to intraductal component. I just want to thank everyone that has been so supportive and has given me positive feedback on this forum. I am also getting genetic testing done this week as well
Hello, Just had my first 3 month PSA test post surgery. <0.01. Good news but need to monitor every 3 years due to intraductal component. I just want to thank everyone that has been so supportive and has given me positive feedback on this forum. I am also getting genetic testing done this week as well
Granolaberry
in
Prostate Cancer Network
7 days ago
Arcticfox44
Hello - I'm about to return to the Mayo for the first review since my previous visit last November. As I've reported here, my last major treatment was chemo with cabazitaxel at the Oncology Center in Nicosia, Cyprus, where I live. This was successful: PSA fell from 83 at the start of chemo to about 3
Hello - I'm about to return to the Mayo for the first review since my previous visit last November. As I've reported here, my last major treatment was chemo with cabazitaxel at the Oncology Center in Nicosia, Cyprus, where I live. This was successful: PSA fell from 83 at the start of chemo to about 3
Arcticfox44
in
Advanced Prostate Cancer
12 days ago
Prostate biopsy from rib ?
My dad , 83 , diagnosed with pc with mets to bones as per mri and psma. Not done biopsy yet as nervous to put dad through it and one oncologist said it’s not needed as the treatment would be ADT but then 3 other oncologists say it’s good to get it done as we would know what exactly we dealing with
My dad , 83 , diagnosed with pc with mets to bones as per mri and psma. Not done biopsy yet as nervous to put dad through it and one oncologist said it’s not needed as the treatment would be ADT but then 3 other oncologists say it’s good to get it done as we would know what exactly we dealing with
Tinkudi
in
Advanced Prostate Cancer
13 days ago
List of good Genetic Tests in Homologous Recombination Deficiency in PCa and the Mechanisms of Resistance to PARP Inhibitors
I was searching RAD50 and PARPinhibitors and since i am going for a high risk genetic consult i came across this good explanation of different genetic testing. Title of article:
Homologous Recombination Deficiency in Ovarian, Breast, Colorectal, Pancreatic, Non-Small Cell Lung and Prostate Cancers
I was searching RAD50 and PARPinhibitors and since i am going for a high risk genetic consult i came across this good explanation of different genetic testing. Title of article:
Homologous Recombination Deficiency in Ovarian, Breast, Colorectal, Pancreatic, Non-Small Cell Lung and Prostate Cancers
KocoPr
in
Advanced Prostate Cancer
15 days ago
Stage 4 A Prostate cancer
My partner was diagnosed with stage 4 A prostate cancer with spread to pelvic lymph nodes. Oncologist has recommended surgery followed by radiation and hormone therapy for a good prognosis. He is 65 healthy and no symptoms. PSA was 11. Has a history of prostrate cancer. Was wondering if we should get
My partner was diagnosed with stage 4 A prostate cancer with spread to pelvic lymph nodes. Oncologist has recommended surgery followed by radiation and hormone therapy for a good prognosis. He is 65 healthy and no symptoms. PSA was 11. Has a history of prostrate cancer. Was wondering if we should get
SherryKahn
in
Advanced Prostate Cancer
22 days ago
Genetic diagnosis
Hi all, sorry I haven't posted anything for ages but sometimes life is like that. I have finally got some sort of diagnosis. I had more genetic testing a couple of years ago and they have found that I have two anomalies on gene SPG7. This means that my disability is more spastic based than ataxia.
Hi all, sorry I haven't posted anything for ages but sometimes life is like that. I have finally got some sort of diagnosis. I had more genetic testing a couple of years ago and they have found that I have two anomalies on gene SPG7. This means that my disability is more spastic based than ataxia.
ww-wibblywobbly
in
Ataxia UK
30 days ago
So my sister has just found that she has haemochromatosis...
I've nagged her to follow up on her high ferritin results for the last year or so, though GP seemed disinterested with it above 700 so I sent her to give blood which bought it down to 400. Since then we have successfully got her GP to acknowledge her Hypothyroidism and prescribe T4 and I got her to
I've nagged her to follow up on her high ferritin results for the last year or so, though GP seemed disinterested with it above 700 so I sent her to give blood which bought it down to 400. Since then we have successfully got her GP to acknowledge her Hypothyroidism and prescribe T4 and I got her to
TiggerMe
in
Thyroid UK
1 month ago
5 failed ET from first cycle. recurrent implantation failure.
I had 5 embryos as part of my first cycle, transferred 1 fresh and 2 single transfers and the last one a double transfer. All failed. My doctor has me on manufactured cycle for the last 3 and on steroid,antibiotics and low dose aspirin and did hcg fusion on the last 2. I am going to do another cycle
I had 5 embryos as part of my first cycle, transferred 1 fresh and 2 single transfers and the last one a double transfer. All failed. My doctor has me on manufactured cycle for the last 3 and on steroid,antibiotics and low dose aspirin and did hcg fusion on the last 2. I am going to do another cycle
Harvey123456
in
Fertility Network UK
1 month ago
anyone else had genetic testing?
Hi well I’m back after a long break after previously having 2 BFN when we tried donor eggs with icsi. We’ve saved up again and decided to give it one last shot and this time the consultant recommended we try genetic screening before having any embryos implanted. Just wondered if there is anyone else
Hi well I’m back after a long break after previously having 2 BFN when we tried donor eggs with icsi. We’ve saved up again and decided to give it one last shot and this time the consultant recommended we try genetic screening before having any embryos implanted. Just wondered if there is anyone else
Miaow1975
in
Fertility Network UK
1 month ago
After Four Cycles of Ra-223
After four cycles of Ra-223 sadly it seems not to be doing as well as we would of liked. I have numinous new uptakes (to numinous to mention) as well as an increase in size of some of the older sites while a few have decreased in size or disappeared the new activity is outweighing the overall success
After four cycles of Ra-223 sadly it seems not to be doing as well as we would of liked. I have numinous new uptakes (to numinous to mention) as well as an increase in size of some of the older sites while a few have decreased in size or disappeared the new activity is outweighing the overall success
TheWizardofWesley
in
Advanced Prostate Cancer
1 month ago
Does Immunotherapy cause Vasculitis?
Hi, my Mum had vasculitis in 2013 following a bad infection, she continues to take 5mg prednisone to this day.Sadly she has been diagnosed with a stage 2 tumor of the cecum which because of her age and frailty at 81 years old is suggested to be inoperable. Genetic testing reveals its a type of cancer
Hi, my Mum had vasculitis in 2013 following a bad infection, she continues to take 5mg prednisone to this day.Sadly she has been diagnosed with a stage 2 tumor of the cecum which because of her age and frailty at 81 years old is suggested to be inoperable. Genetic testing reveals its a type of cancer
luggsey
in
Vasculitis UK
1 month ago
BRCA genetic testing providers
I have signed up to take part in the NHS Jewish-BRCA screening programme https://nhsjewishbrcaprogramme.org.uk/ but I will not get the test or the results before the first round of my IVF starts next month. I only have 1 Jewish grandparent so my risks are low but not as low as non-Jewish person. My grandparent
I have signed up to take part in the NHS Jewish-BRCA screening programme https://nhsjewishbrcaprogramme.org.uk/ but I will not get the test or the results before the first round of my IVF starts next month. I only have 1 Jewish grandparent so my risks are low but not as low as non-Jewish person. My grandparent
Rachiebabe
in
Fertility Network UK
1 month ago
Blue Horizon Thyroid Genetic Test results
Afternoon, My Blue Horizon Thyroid Genetic Panel results have arrived after a long wait and I’d appreciate some help understanding them. I undertook the test to check my DIO1 and DIO2 status, both of which appear ‘normal’ (no inherited defects). However, three variants are flagged up in either red
Afternoon, My Blue Horizon Thyroid Genetic Panel results have arrived after a long wait and I’d appreciate some help understanding them. I undertook the test to check my DIO1 and DIO2 status, both of which appear ‘normal’ (no inherited defects). However, three variants are flagged up in either red
J972
in
Thyroid UK
1 month ago
PGTA testing embryos made from donor eggs
Hello I appreciate there will be differing views and experiences with this. Has anyone PGTA tested their egg donation embryos? I have had 2 miscarriages and TFMR at 15 weeks (all own eggs) due to chromosomal issue that we didn't know about until we went for our NHS scan at 12 weeks. I will never forget
Hello I appreciate there will be differing views and experiences with this. Has anyone PGTA tested their egg donation embryos? I have had 2 miscarriages and TFMR at 15 weeks (all own eggs) due to chromosomal issue that we didn't know about until we went for our NHS scan at 12 weeks. I will never forget
Skittles11
in
Fertility Network UK
1 month ago
Please join the INHERIT study -
Join the
INHERIT Study
to help us better understand the genetic (or inherited) risk for lung cancer,
and what can be done for prevention and treatment of lung cancer.
Our goals are to learn more about:
-Inherited or genetic risk for developing lung cancer in certain people or families
Join the
INHERIT Study
to help us better understand the genetic (or inherited) risk for lung cancer,
and what can be done for prevention and treatment of lung cancer.
Our goals are to learn more about:
-Inherited or genetic risk for developing lung cancer in certain people or families
AmyKamp
Partner
in
Small Cell Lung Cancer Support
1 month ago
Please join INHERIT Study
Join the INHERIT Study to help us better understand the genetic risk for lung cancer, and what can be done for prevention and treatment. Our goals are to learn more about: -Inherited or genetic risk for developing lung cancer in certain people or families -Changes in lung cancer tumors in people with
Join the INHERIT Study to help us better understand the genetic risk for lung cancer, and what can be done for prevention and treatment. Our goals are to learn more about: -Inherited or genetic risk for developing lung cancer in certain people or families -Changes in lung cancer tumors in people with
Miranda_GO2
Partner
in
Lung Cancer Support
1 month ago
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