I am new to this forum and extremely relieving to know there are so many nice sharing thoughts in here for a better outcome for all.
I am opening this thread to discuss the [B]prenatal genetic tests[/B] usually performed for IUI and IVF cycles for couples.
Me - 31 normal
DH - 34 morphology
Married for 7 years and TTC for 2 years.
Two failed IUIs in Oct-2012 and Dec-2012
Planning to go for IVF with ICSI in Feb or March once my cycle starts.
We are planning to go thru IVF for the first time and below are the prenatal genetic tests performed for us.
- Cystic Fibrosis for us
- Fragile X for me
- Spinal Muscular Atrophy for me
- Heamoglibin for us
- Karyotype for us
All the above tests done came back negative and is told by my doctor that everything is clear.
- Will there be anyother prenatal tests to be performed, that can help us have a healthy pregnancy with healthy babies?
- Has anybody went through Counsyl Test or Inheritest, which is a genetic test that helps to identify if the parents are carriers of any genetic issues.