Search the web
Sign In
New User? Sign Up
huntingtonsdiseasesupportclub · Huntington's Disease Support Club
? Already a member? Sign in to Yahoo!

Yahoo! Groups Tips

Did you know...
Message search is now enhanced, find messages faster. Take it for a spin.

Best of Y! Groups

   Check them out and nominate your group.
Having problems with message search? Fill out this form to ensure your group is one of the first to be migrated to the new message search system.

Messages

  Messages Help
Advanced
Introduction.   Message List  
Reply | Forward Message #3455 of 10739 |
I just found your group today. I am 28 and from Finland. I am sorry to
say, I am not with my name, because my husband doesnt want me to talk
about HD to anyone. He is at risk and his mom and uncle and grandma
have died of HD. So, he is actually the oldest member on his family on
his moms side now. Creepy. I knew his mom for a few years, so I have
seen the disease myself.

We have a toddler, and are planning to have another child soon. That
is the main reason I am writing now. (Though I think I need to talk
about this to someone regardles of the babyproject.) We were
originally about to adopt. Not only because of HD, but for other
reasons. Like for there being so many people on the planet and also
many babies without parents. But in Finland there arent many kids
given for adoption. Then we thought about international adoption. But
it turned out too expensive at the moment, about one years salery for
me. Maybe later if we get our home repaired and save some money, but
not right now. So, we decided to take the risk and live through
possible consequinces. (sorry, dunno how that is spelled correctly =)
Our child is healthy, but obviously at risk like his father.

So, now we are with the same questions again. Should we have another
child, knowing he or she has about 50 percent chance of getting HD. I
am not asking you to decide for us, naturally, just want to hear other
points of views.

We are not religious. But I am not OK with the idea of first getting
pregnant and then doing the test for the baby inside me, and then
aborting if it has "bad" genes. So that is not an option for me.
Othervise I am open for anything. Hoping there will be a cure and
perhaps thinking life is worth living with or without HD. But I am not
in a good place to say that, as I am at almost zero risk myself. Just
watching people die around me.

Wife and a mother from Finland





Tue Jun 22, 2004 5:54 pm

wifeofhd
Offline Offline
Send Email Send Email

Forward
Message #3455 of 10739 |
Expand Messages Author Sort by Date

I just found your group today. I am 28 and from Finland. I am sorry to say, I am not with my name, because my husband doesnt want me to talk about HD to...
wifeofhd
Offline Send Email
Jun 23, 2004
8:08 pm

You could try invetro... then they test the fertilized eggs and implant the ones without hd... they don't have to tell you the results if they found any with...
Tara Bintliff
tara1644
Offline Send Email
Jun 23, 2004
8:21 pm

Thank you Tara, For your quick reply. :) I will talk to my husband about inverto. He is the one who suggested testing the fetus. (And yes, they do that in...
wifeofhd
Offline Send Email
Jun 29, 2004
3:20 am

My mom said that she wouldn't have had kids if she had known... Its hard for you to understand not being at risk.. what we have to go through every day.. but I...
Tara Bintliff
tara1644
Offline Send Email
Jun 29, 2004
3:49 am

I can understand your concerns about having another child knowing your husband has HD. I was tested for HD when I was 19 so I could decide if I was going to ...
nightshade
nightshade_cnd
Offline Send Email
Jun 29, 2004
3:20 am
Advanced

Copyright © 2009 Yahoo! Inc. All rights reserved.
Privacy Policy - Terms of Service - Guidelines - Help