It does work the same way...I found out this breakthrough as soon as I got married. It is a new technology. Talk to his geneticist. They will refer you to someone that will give you more information. They will help you have the baby.
Good Luck
----- Original Message ----
From: teresaisgroovy79 <teresaisgroovy79@...>
To: huntingtonsdiseasesupportclub@yahoogroups.com
Sent: Monday, May 5, 2008 11:08:27 AM
Subject: [Huntingtons Disease Support Club] Re: Having children
Thank you Heather! That is really amazing news to hear:) Do you know
if it works the same way if the its the male who carries the HD gene?
Well, I can't wait to talk to my boyfriend about it! We are both
teachers so I don't know what to say about the expense, but we can
start a fund. We are both 28 so we have a few years to save.:) Thats
amazing, and thanks again!!
Teresa
--- In huntingtonsdiseasesupportclub@yahoogroups.com, Heather Dugdale
<i_am_miss_world@...> wrote:
>
> Hey... I am married and have HD. My husband and I have looked into
it. They can do prenatal scanning. They give you fertilizer. They
scan to see if they have HD. If they do then they will get rid of the
egg. If they don't then they will keep it. It costs tons of money
though. In Canada here it would cost 10,000 dollars. You are
guaranteed to have one that way...
>
> Heather Dugdale
>
>
>
>
> ----- Original Message ----
> From: teresaisgroovy79 <teresaisgroovy79@...>
> To: huntingtonsdiseasesupportclub@yahoogroups.com
> Sent: Sunday, May 4, 2008 2:41:30 PM
> Subject: [Huntingtons Disease Support Club] Having children
>
> My boyfriend has HD and I have been learning about the disease and
its
> symptoms. He had the genetic testing and supposedly he wont begin to
> show symptoms until his early 60s. Many people in his family have
it,
> and they have all had similar results.
>
> We both want to have children together very much, but we are
> especially concerned about juvenile HD if we have a child. It was
> passed to him through his mother, and with him being a male, we have
> heard the chances of having a child with juvenile HD is much higher
> for us. He has had a vasectomy to prevent an uninformed pregnancy,
but
> if we can find out more about the disease and medical breakthroughs
in
> treatment, he might have it reversed.
>
> We both have agreed that if it comes down to it we can go the
adoption
> or artificial insemination route. Any information would be greatly
> appreciated.:) Thanks for the help!!
>
>
> ------------------------------------
>
> Yahoo! Groups Links
>
>
>
>
>
______________________________________________________________________
______________
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> know-it-all with Yahoo! Mobile. Try it now.
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>
------------------------------------
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From: teresaisgroovy79 <teresaisgroovy79@...>
To: huntingtonsdiseasesupportclub@yahoogroups.com
Sent: Monday, May 5, 2008 11:08:27 AM
Subject: [Huntingtons Disease Support Club] Re: Having children
Thank you Heather! That is really amazing news to hear:) Do you know
if it works the same way if the its the male who carries the HD gene?
Well, I can't wait to talk to my boyfriend about it! We are both
teachers so I don't know what to say about the expense, but we can
start a fund. We are both 28 so we have a few years to save.:) Thats
amazing, and thanks again!!
Teresa
--- In huntingtonsdiseasesupportclub@yahoogroups.com, Heather Dugdale
<i_am_miss_world@...> wrote:
>
> Hey... I am married and have HD. My husband and I have looked into
it. They can do prenatal scanning. They give you fertilizer. They
scan to see if they have HD. If they do then they will get rid of the
egg. If they don't then they will keep it. It costs tons of money
though. In Canada here it would cost 10,000 dollars. You are
guaranteed to have one that way...
>
> Heather Dugdale
>
>
>
>
> ----- Original Message ----
> From: teresaisgroovy79 <teresaisgroovy79@...>
> To: huntingtonsdiseasesupportclub@yahoogroups.com
> Sent: Sunday, May 4, 2008 2:41:30 PM
> Subject: [Huntingtons Disease Support Club] Having children
>
> My boyfriend has HD and I have been learning about the disease and
its
> symptoms. He had the genetic testing and supposedly he wont begin to
> show symptoms until his early 60s. Many people in his family have
it,
> and they have all had similar results.
>
> We both want to have children together very much, but we are
> especially concerned about juvenile HD if we have a child. It was
> passed to him through his mother, and with him being a male, we have
> heard the chances of having a child with juvenile HD is much higher
> for us. He has had a vasectomy to prevent an uninformed pregnancy,
but
> if we can find out more about the disease and medical breakthroughs
in
> treatment, he might have it reversed.
>
> We both have agreed that if it comes down to it we can go the
adoption
> or artificial insemination route. Any information would be greatly
> appreciated.:) Thanks for the help!!
>
>
> ------------------------------------
>
> Yahoo! Groups Links
>
>
>
>
>
______________________________________________________________________
______________
> Be a better friend, newshound, and
> know-it-all with Yahoo! Mobile. Try it now.
http://mobile.yahoo.com/;_ylt=Ahu06i62sR8HDtDypao8Wcj9tAcJ
>
------------------------------------
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<*> To visit your group on the web, go to:
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<*> Your email settings:
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<*> To change settings online go to:
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(Yahoo! ID required)
<*> To change settings via email:
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Be a better friend, newshound, and know-it-all with Yahoo! Mobile. Try it now.