Experiences with

Genetic test

After we finished chemo we did another genetic test that looks like Keytruda is and option especially since my overall tumor burden was 34%. Any input would be helpful.

Please can someone explain to me in a very simple way what the BRCA genetic test is. My result on this test was NEGATIVE. I have 3 kids. 2 males and 1 female. What impact does this result have on my children ??? Thank you

Upon my doctor's advice I had a Decipher Genetic Test done to help decide on treatment for my prostrate cancer. I received a $1,500 bill (USA, obviously), but also an application for the Decipher Assist program. Does anyone have experience with this?

I had the genetic test done at 18 weeks and everything came back normal. Can I ask what test did you have done for your baby?

My MO went back and looked at the Foundation One Genetic Testing done in July of 2019. Apparently, they are doing some work at Jefferson on targeting P300/CBP right now. The link below is dated May 2021. This mutation was listed 2 years ago but they said there were no known targeted therapies. The picture

Oh, and I had the genetic test thing done last month which showed I am CDK12 positive and my MO didn't even tell me !!!! Anyone possibly seen this before and can help me understand what's going on here? Thanks

I just received the results of a genetic test ordered by my oncologist. It shows that I have a genetic variant in the FANCA gene. I have an appointment with my oncologist in a few weeks and he is going to to set up a meeting with a genetic counselor to go over the results.

He have had two dosis of carboplatin chemo when they realized It was not lung cancer but a neuroendocrine diferenciation from the prostate( after the genetic test I have been requesting since I started in this forum 3 years ago)After this two rounds two of the tumors "dissapear" and the doctor has decided

He will have to have a genetic test beforehand. Has anyone here been on this trial? He is on xtandi but it is failing unfortunately. Appreciate any responses x

And Dr has also just sent some samples of the tissue to do some genetic test. From there he will decide on the next path forward. Any suggestion from anyone will be very much appreciated.

What worries me is that he kept talking about mutiple system atrophy (MSA) and I have been diagnosed to be sca3 in genetic test 4 years ago. Has anyone of you had the same experience? l am worried that once I have been in hospital, things may be detiorated faster.

I was on the ropes and out of options when a genetic test said I was MSI-h and qualify for immunotherapy Keytruda ; it was a Hail Mary. It was a good year. Now over a year later I’m seeing a PSA bump. I’ve got a lot of genetic diversity in my PC.

Genetic test: negative My case was reviewed by three MOs and it was concluded that although I have a high Gleason score, based on CHAARTED and LATTITUDE I have low -volume low-risk disease (no visceral involvement, 1 site of bony disease). So it was recommended to follow the STAMPEDE trial.

I requested the genetic test on the NHS, but according to my family history, I do not need an appointment in the Genetics Clinic. However, with endometriosis, it should be apparent that there is oestrogen dominance?

I recently had a genetic test and found out I have a gene mutation that can mimic bipolar disorder among other things. It is called the MTHFR gene and it is responsible for breaking down b vitamins or something like that.

• Diagnosis of RTH is usually based on the clinical finding of discrepant thyroid function tests and confirmed by a genetic test.

Hi ladies, Just wondering, has anyone had a private week 10+ prenatal genetic blood test for under £350 anywhere in or near London? I threw the kitchen sink at the IVF and keen to save.. Thanks xo

Genetic counselling post DIO 2 test. Thinking that because my daughter seemed to have a sensible GP we could save £80 daylight robbery by asking for her results to be sent to him, we did that. He says he doesn’t understand them, so cancelled the request. Regenerus won’t release the results to her.

Zhang ( Duke OC ) had a genetic test run and the report to be brief stated tumor volume was too low to get a good read. Related to either early stage disease (not the case) or successful treatment, or stable disease...Pretty good stuff .

He had a genetic test for osteogenesis imperfecta and came back with 2 variants of uncertain significance in LRP5 gene and P4HB gene. His dad and I were both tested for those genes and we carry one each. His dad has the LRP5 gene which is a bone affecting gene.