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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
Genetic Testing
Greetings, I'm concerned about my condition (chronic/acute pancreatitis) being a health risk to my children/grandkids. I am wondering if anyone has a good opinion of the many testing companies out there. It seems they all have good/bad points. Any comments and/or suggestions would be appreciated.
Greetings, I'm concerned about my condition (chronic/acute pancreatitis) being a health risk to my children/grandkids. I am wondering if anyone has a good opinion of the many testing companies out there. It seems they all have good/bad points. Any comments and/or suggestions would be appreciated.
IH8EPI
in
Chronic Pancreatitis Support
1 day ago
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Update and question about Olaparib
Its my 60th birthday today! Glad to still be here! CT scan was stable but CA15 continues to rise on Trodelvy. CA15 is an important indicator for me. This info plus a comprehensive new Gardian DNA blood genetic test showed us some new options based on my mutations/bio markers (I am an architect so firgive
Its my 60th birthday today! Glad to still be here! CT scan was stable but CA15 continues to rise on Trodelvy. CA15 is an important indicator for me. This info plus a comprehensive new Gardian DNA blood genetic test showed us some new options based on my mutations/bio markers (I am an architect so firgive
Iwasborntodothis
in
SHARE Metastatic Breast Cancer
1 day ago
Seeking any info: Our son was recently diagnosed with kidney disease
Hi, I'm a parent who is looking for possible answers or similar situations out there. Our 16-year-old son was diagnosed with kidney disease in March 2024. We've been trying to find medication and treatment to help with it. This all started in January 2024, when our son was complaining about back pain
Hi, I'm a parent who is looking for possible answers or similar situations out there. Our 16-year-old son was diagnosed with kidney disease in March 2024. We've been trying to find medication and treatment to help with it. This all started in January 2024, when our son was complaining about back pain
BlueGuitar123
in
Parents of Children with Kidney Disease
4 days ago
Advancing Prostate Cancer Care: Treatment Approaches to Precision Medicine, Biomarker Innovations, and Equitable Access -ASCO - May 23, 2024
While not a lot of specific focus on PCa (Like at the GU ASCO Meeting earlier this year), this full-access section from their Educational Book released at this week's ASCO Annual Meeting in Chicago may be of interest to those here who want to understand the oncology community's current view on precision
While not a lot of specific focus on PCa (Like at the GU ASCO Meeting earlier this year), this full-access section from their Educational Book released at this week's ASCO Annual Meeting in Chicago may be of interest to those here who want to understand the oncology community's current view on precision
cujoe
in
Fight Prostate Cancer
13 days ago
lost my brother to SADS
Hello, I recently lost my brother at Christmas, he was only 30 years old and was fit, active and health. Was studying at university to become a physiotherapist and had his whole life ahead of him. We recently got his cause of death which was due to SADS. I’m due to go for genetic testing and have
Hello, I recently lost my brother at Christmas, he was only 30 years old and was fit, active and health. Was studying at university to become a physiotherapist and had his whole life ahead of him. We recently got his cause of death which was due to SADS. I’m due to go for genetic testing and have
MeganR13
in
British Heart Foundation
13 days ago
PSA rockets up to 344
Hello - I received quite shocking news during my visit to the Mayo Clinic last week. My PSA has jumped to 344 from a low of 3.6 last November, when I completed chemo with cabazitaxel. PSA did start to rise quite soon, into double digits, but this is by far my highest PSA ever. Dr. Kwon recommended
Hello - I received quite shocking news during my visit to the Mayo Clinic last week. My PSA has jumped to 344 from a low of 3.6 last November, when I completed chemo with cabazitaxel. PSA did start to rise quite soon, into double digits, but this is by far my highest PSA ever. Dr. Kwon recommended
Arcticfox44
in
Advanced Prostate Cancer
13 days 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
15 days ago
New Post, community only please
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
20 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
22 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
26 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
27 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
29 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
1 month 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
1 month 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
2 months 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
2 months 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
2 months 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
2 months ago
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