(((((((((((((((Linda))))))))))))))))))))))))
(((((((((((((((John)))))))))))))))))))))))))
No, you are not alone. There are too many of us out here! Make sure you do
what you can to build off-line support too -- friends, family, a caregivers
support group. Their hugs don't look like parentheses. <G>
I'm glad the doc is taking your concerns seriously and making sure to screen
out anything else that could be causing the cognitive loss. However, there
is Early Onset Alzheimers as well.
I'm glad he has accepted not driving. That's a tough one for men in
particular, but the risk of hurting someone (himself or an innocent party)
is just too high.
Hang in there and keep us posted. We care.
Songbird
> thanks
> being able to read and learn from all of you is a help to me. Makes me
[quoted text clipped - 4 lines]
>> direction. There's not much I can say, but I wanted to let you know
>> that I feel for you, and I wish you courage.
LindaJean - 01 Oct 2005 16:32 GMT
it is unfortunate that John has no family at all and the only friends he has
are thru work. My family has very young children and live 3 hours away so I
am going to have to find help in some other way. I went to my first consult
at the AD office and our GP told me very firmly to make sure I find a group
to keep attending. The Neuro may have to be changed but our GP is very
supportive and helpful. We all figure it is EOAD but the GP told me it is
better to rule out any chance it is something fixable before we face AD and
I guess he is right. The Neuro just kept stalling things so I went and sat
down with the GP and he pushed the other doctor. Thank God for that help
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> (((((((((((((((Linda))))))))))))))))))))))))
> (((((((((((((((John)))))))))))))))))))))))))
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>
> Songbird
> thanks
> being able to read and learn from all of you is a help to me. Makes me
> feel less alone
Hi LindaJean,
When my mother in law started showing signs of impairment, it was very scary
for me. We never were really close, and she lived two hours away from us,
and was very independent. There was no other person to help her, it was us
or nobody.
And how does one help someone who doesn't want help, or understand that they
even needed help? It was little by little and a slow process. This
newsgroup kept me sane and got me through an awful lot right up until she
died last April. It was 5 years ago or so that I found this group and it
was a lifesaver for me.
LindaJean, if I found the courage to work with the situation, as unwilling
as I was originally, you are going to be just fine. Plus because it is
your husband, that fact will make it a more natural situation for you to be
there for him and you may get more cooperation than some of us who weren't
so close to our loved ones. There is a trust factor with a spouse that is
often not there with other relationships.
It is true that 56 just seems so young to have this awful illness, but the
scary truth is that we have heard of younger ones in rare cases. Keep
your courage up and stay in touch.

Signature
Best Regards,
Evelyn
(to reply to me personally, remove 'sox')
LindaJean - 01 Oct 2005 16:35 GMT
It is hard to deal with this as we have only just celebrated our first
wedding anniversary the day they did the EEG last week. Since we have no
info on John's relative's it makes it more possible for AD they say. I feel
like Alice down the rabbit hole hahaha I know I can do this I just have to
learn fast :-)
LindaJean
> Hi LindaJean,
>
[quoted text clipped - 19 lines]
> scary truth is that we have heard of younger ones in rare cases. Keep
> your courage up and stay in touch.
Dennis P. Harris - 02 Oct 2005 07:47 GMT
> It is true that 56 just seems so young to have this awful illness, but the
> scary truth is that we have heard of younger ones in rare cases. Keep
> your courage up and stay in touch.
An old school friend was caregiver for a fellow that was a year
younger than us. He was diagnosed at 46 and died at 50.
From the cases that I've seen, it appears that the decline with
EOAD is more rapid, at least in the early stages.
LJ - 02 Oct 2005 15:06 GMT
that is what I have been reading. Most web info states average of 4.2 years
for males. Right now trying to switch our lives around is more than I can
deal with. We will have to let go of the apt near his work and move full
time to our retire to house. I am torn between I want the 20 years that can
be possible with AD and then again I hate watching what my husband is
already going thru and don't want him to suffer any more than he needs to. I
guess God will decide and I will follow <s>
Linda
> > It is true that 56 just seems so young to have this awful illness, but the
> > scary truth is that we have heard of younger ones in rare cases. Keep
[quoted text clipped - 5 lines]
> From the cases that I've seen, it appears that the decline with
> EOAD is more rapid, at least in the early stages.