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I do know most of my family is from western Europe and I am the
gggggggggggggg Granddaughter of King Henry II of England and his last and nuttiest son John was also a grandfather of mine.
How cool!! I'm sure there's plenty of nutters in my family as well, but not sure about any famous ones!
Jen
RRMS 2005, Copaxone since 2007
"I hope to be the person my dog thinks I am."
My parents immigrated here in 1956, I have four sisters. My father died when I was 8, we were ostracized by his family afterwards. My mother was a suicide when I was 19, I have never met anyone from her side of the family and she refused to talk about them. I have little family history to share with medical professionals. I am the only one with MS that I know, but I only have my sisters as comparisons.
Having sisters is actually huge. DNA-wise, they will be more like you than anyone...more so than your parents, your kids, even your brothers.
When my brother requred a bone marrow transplant, the doctor was only interested in testing us siblings for maximum combatability. I was the match. Sadly, it didn't take, but part of the problem was there is a difference between male and female marrow. Had our other brother been a blood match, I might still have the both of them. Sigh...
Tawanda
___________________________________________ Diagnosed with Multiple Sclerosis 2004; First sign of trouble: 1994
My sister did 23 and me and it came up for her with an elevated risk of auto-immune diseases but also a better than average response to interferon.
I actually scored way higher for Crohn's Disease than MS, but there was nothing for RA like my brother has, and a lowered risk for Lupus. I am now interested in following M.S. "Conversations" as opposed to general autoimmune disease conversations. Methinks all AI are not treated equally, so I will stick to what I know best if I am to offer any useful dialogue.
Tawanda
___________________________________________ Diagnosed with Multiple Sclerosis 2004; First sign of trouble: 1994
Can still get your ancestry, just not the health data. I had 2 markers for MS and wanted to know if my DD had any. Not a guarantee she would or would not have MS, but I wanted to see. I guess that won't be happening. November was the end of the "pioneers" as the company refers to us "oldies"!
Tawanda
___________________________________________ Diagnosed with Multiple Sclerosis 2004; First sign of trouble: 1994
I luckily ordered mine before the cut off date! I still need to send it in though...
People who recently applied can get a full refund, and anyone strictly interested in the ancestry, still pretty cool, can still get the kit. That part doesn't compromise the FDA. Let us know how it goes with your kit, my fellow pioneer!
Tawanda
___________________________________________ Diagnosed with Multiple Sclerosis 2004; First sign of trouble: 1994
They still process your DNA just like they always did but now they can't give you their interpretation of the health data. You still get the Raw Data which you can put into a 3rd party program that will interpret it for you.
I got this from their blot comments (I didn't write it):
to download Promethease for free. It will take 4 hours to analyse your raw data and give you all the health and trait information 23andme used to give you, and more. Or if you are impatient, you can use the website to analyse it faster and give you a nicer GUI, but that costs $5 so I just use the free version.
In your Promethease report, Click on "Topics" then click on 23andMe/SNPs to find the same information 23andMe used to give you (but not explained as clearly). The other parts of the report are also interesting.
This is just an FYI. I'm not promoting or suggesting anything, please do your research but I did want everyone to know that the option is there to still get your raw data.
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