Mosaic Turner's Syndrome.

[Shetlander]

Hi!

I'm brand-spanking new to this site.

I've been diagnosed with mosaic turner's syndrome, I found out last week I had turner's and was told not to try to get pregnant again,
and then today I got the energy to go and camp out at the RE's office til they gave me the actual karyotyping results.
Which show that I have 30% mosacisim of turner's.

I don't know a thing about this syndrome and had never ever heard of it before last week when I was told "you have a birth defect, no IFV, no babies".

I really just want as much info as is possible to help me make the decisions that will be upon me to make.

I'm 27 and have been married for about a year, my husband and I have had 2 miscarriages, which is what prompted my being pushy enough to not accept "bad luck" as a medical answer for anything.

I thought my hormone levels were off, because they were so very low in both pregnancies. But it turns out I just have Turner's.

Well that absolutely everything I know!

PS: I'm 5ft7, 27yrs, and show no other typical signs of Turner's, hence the not knowing til now and being shocked about it.


Ciao fa now!