Hey girls, I'm not TTC but I couldn't think where to put this thread as it's related to OH and I for when we do TTC sometime in the future. Hope that's ok.

Has anyone had genetic testing done?

Niamh is a carrier of Cystic Fibrosis, which means either that OH and I are both carriers, or one of us is.

We were told we could have genetic testing done, and we are no where near ready to TTC but the not knowing is getting to me Like if we both have the faulty gene I don't want to risk getting pregnant again, and if we were to have an accident anytime before we're ready to TTC before we'd had tests, I would be beside myself with worry.

So what exactly is the process to get tested, and how long does it take? Is it worth doing sooner rather than later? Our GP seemed to think it was pointless until we were TTC but like I said, what about if an accident happens (We'd obviously take every precaution so maybe I'm being bit OTT with worrying) I've tried looking online, but it just seems to be information on the process for testing people with CF, not the process for testing for carriers.

Sam'sMum linked me to this awhile ago which I know is getting ahead of myself a bit, but curious if anyone knows anything about it, just in case. (Can never be too prepared I guess ) http://www.phgfoundation.org/news/817/

I dont know if it would be the same or its the same thing but I thought id let you know my situation!

Max has CF and so myself and OH are both carriers, to find out what gene we had it was simply a blood test. The results took about 2 weeks to get back to me.

With my next baby, I have to have CVS at about 10 weeks, with the results taking about 3 weeks to return. Im anxious about this and really worried. Its a horrible situation to be in.

Max lives a perfectly normal life and is a nice plump 27lbs at almost 10 months. He has had one cold since being born which didnt really affect him. I have a very positive outlook on CF and they are getting closer to a cure everyday..so CF doesnt have to be the horrific ordeal it once was.

Hope this helps xxx

I completely understand your concerns rafwife.

I have a very rare neurodegenerative disease called Friedriech's Ataxia (FA). Our child will definantly be a carrier; but my hubby had to get tested to make sure he wasn't carrying the bad gene. It took over a year , made me so angry.

Personaly I would get it done asap, but thats just my opinion.

I can also understand your concerns.. I'm currently waiting for chromosomal blood tests resuts as my dad and sister have a rare genetic disorder of the central nervous system. I've had recurrent m/c too. I had blood tests taken after my last m/c about 8 weeks ago, once I hear back (no idea how long this will take and can't seem to get a straight answer from anyone either!) then depending on the outcome of the results I will be referred for genetic counselling.

For me, like the above poster I want this done asap for my own piece of mind so I know what the next stage is, and depending on situation it can take some time.