[quote=UCGal]We did it. For me – my family risk of cancer made me want to know. My husbands family leans torwards heart disease and stroke… As well as some family history of dementia. If we had the increased risks we wanted to know to address bucket list things sooner than later. For the most part we got good news… No increased risks.
For the biggies, you have to go through several locks to make sure you really wanted to know. Parkinson’s, Alzheimer’s, colon cancer, breast cancer.
As far as the family and genetic stuff… My husband has connected with several 3rd cousins in the old country…. (He chose to respond to the anonomyzed inquiries… And was able to trace back the common ancestor.). That’s been cool and we’ll probably meet them when we next go across the pond. Less luck on my side.
It was worth the $99 to us.[/quote]
Since this thread started we discovered something else from the 23andMe data that was impactful for our family. We found that we all (husband, me, kids) have variations of the MTHFR mutation. One son has a homozygous mutation of the C677T marker – which means his body produces a less effective version of the enzyme that breaks down folate. The rest of us have the heterozygous mutation – so we partially break down folate, but less effectively than folks with natural form of the gene. Folate needs to be broken down to cross the blood/brain barrier and is used to regulate neurotransmitters (seratonin, dopamine, melatonin, etc.). We now take OTC vitamins in the methylized form of the b vitamins.
Huge big deal to find an obscure but impactful problem.
