Ha! It took Maya about 20 minutes to get all the saliva needed for the 23andme test.
Zachary (age 3) well, we are still attempting it!
We are waiting for the infant test kit for Marnie, there are no updates yet as to when they will ever arrive.
I received notification that my sample has reached the lab, sending Maya's today, then Zac's .....that is whenever he has decided that he wants to spit in the tube ;)
I just need to get mum and dad and the sister to partake, this is so interesting!
Off to buy some ingredients for a raw style ganache - and then Valentine crafts.
Thursday, February 14, 2013
Tuesday, February 12, 2013
Great link
Found this on my travels
http://www.mindmeister.com/12694596/mthfr-related-health-problems
It is a mind map of MTHFR related problems by Dr Stephen Smith MD at Agapenutrition.com
Monday, February 11, 2013
So apparently the A1298C mutation is nothing.
We have an appointment for the geneticist..in May.
In speaking with the genetic counselor, being homozygous A1298C is nada, nothing, zilch.
They do want to check her homocysteine levels, but apart from that, they say just having this mutation means nothing.
We do need to push for more research, as there is scant research on these mutations.
Still not going ahead with another revision, I just cannot do it to her. We are getting her checked for EDS as there are some warning signs in the family history that could point to this being a reason as to why she is such a slow healer.
Sent off my 23andme test, now have to get the kidlets to spit in their tubes and send those off, that will be interesting!
Found a great study - Craniofacial expression of human and murineTBX22 correlates with the cleft palate and ankyloglossia phenotype observed in CPX patients
http://hmg.oxfordjournals.org/content/11/22/2793.full
This will be my homework tonight, as I have three kidlets running around and thinking is nigh to impossible right now.
In speaking with the genetic counselor, being homozygous A1298C is nada, nothing, zilch.
They do want to check her homocysteine levels, but apart from that, they say just having this mutation means nothing.
We do need to push for more research, as there is scant research on these mutations.
Still not going ahead with another revision, I just cannot do it to her. We are getting her checked for EDS as there are some warning signs in the family history that could point to this being a reason as to why she is such a slow healer.
Sent off my 23andme test, now have to get the kidlets to spit in their tubes and send those off, that will be interesting!
Found a great study - Craniofacial expression of human and murineTBX22 correlates with the cleft palate and ankyloglossia phenotype observed in CPX patients
http://hmg.oxfordjournals.org/content/11/22/2793.full
This will be my homework tonight, as I have three kidlets running around and thinking is nigh to impossible right now.
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