Experiences with

Genetic test

My son has recently been diagnosed with DCM and I came across some info suggesting first degree relatives should be referred to a specialist clinic to be checked out. The BHF apparently will provide a letter to your GP to support this referral. How does this work. Will there be a fee for the letter?

My doctor decided to test me for this. I did a genetic test says I have the mutations for this and now she want to send me for this nose noxide test. I was wondering if if anyone else got tested for this before and wondering how accurate the genetic test is. I appreciate any responses

Since then, researchers have been developing a genetic test for the condition, which they plan to make available in the UK.

Since my C-peptide level is still quite high and I have no antibodies, a genetic test for MODY was done. It turns out I have MODY Type 10 (INS), which seems to be a very rare form of MODY. Is anyone else here with Type 10?

test 6 - Vitamin D for the bones (from dr Saad) and Bone Protective Agents are great also to prolong OS, especially with Radium 7 - Clinical trials are becoming more widespread and secure 8 - Thanks Prostate Cancer Foundation for helping research That's basically it (I intentionally did not pay

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 was originally told it was not genetic.

He told me that the hospital still had my tumor and he requested a genetic test on the sample. Sure enough, I tested positive for VHL. I am one of the lucky ones that accidentally for the kidney tumors during a CT scan for something unrelated.

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 me if I get this wrong) posting in case anyone needs info for themselves later: ESR1 suggest: Elacestrant (option) and Letrozole(already had)

Got a copy of my Tempest test. My MO says "No actionable results" meaning plan of action doesn't change (Triplet Therapy). He also stated I had nothing to pass on to my son as far as hereditary gene problems. I have no clue what any of it means. DNA mismatch expression (normal) Homologous recombination

I am concerned about the new genetic test AvertD just approved by the FDA https://www.washingtonpost.com/health/2024/03/25/dna-test-opioid-addiction/ It uses DNA to predict whether a person is likely to get addicted to opioids.

test t o see what kind of medications i can take, which im not keen on because i started lexapro when i was younger and couldnt metabolize it and it made my anxiety 10x worse. and the genetic test revealed that i have the anxiety and depression gene, like the genetic that is connected to anxiety. it

I am adding some nutritional supplements - and want the genetic test to let me know about the MTHFR gene as well. I feel so overwhelmed trying to navigate all of this. Those of you who have found a good combination of meds and are seeing progress for your kids have given me hope to keep trying.

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

You can get a free, saliva germline genetic test of 30 genes from Color, Inc. as part of the PROMISE registry.

I found out as hubby bought me a Family history genetic test as a present and it included health DNA results.

In November 2023 my iron labs were increased. Ferritin 117 TSAT 58 my doctor said we would retest in six month and do genetic testing but wasn’t concerned. My results just came in and it showed homogenous for H63D. I haven’t been able to speak with him yet. I am extremely scared.

Hi everyone I did a thyroid genitic test through Blue Horizons Here are the results, any advice on them Thanks in advance Dawn

He also ordered another genetic test from a different company other than Gardiant 360 to see if any new mutations will show up. Then he suggested that I give LU-177 a try.. that's when I kinda lost it..!!

My brother tested positive so GP did genetic test. I don’t know what is ahead of me but I am glad I have a diagnosis

I was recently diagnosed with hemochromatosis based on slightly off bloodwork and genetic test. Neither of my parents had hemochromatosis but both were carriers and I inherited the gene from both.