Parkinson's Disease Tulip


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Old 08-08-2007, 04:32 PM #11
adelle adelle is offline
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Thanks Carolyn. As the caregiver, I never stop looking for more and better info. We are working with Dr. Burton Scott at Duke. He is very considerate and returns phone calls in person within a few hours. I have not been able to transport husb. there for the past 15 months, but look forward to seeing him this fall. In the meantime, we see Dr. Francis Walker at Wake Forest Univ. Medical Center about every three months. Dr. W. has successfully used Botox on his feet to "stop" extreme drawing and spasticity.
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Old 08-08-2007, 06:48 PM #12
paula_w paula_w is offline
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Quoting (badly) Carolyn's post: "I will stay in my lovely circa-1900 row-house that my son-in-law was so kind to assist me in obtaining."

What a fine response Carolyn. I was there.

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"Time is not neutral for those who have pd or for those who will get it."

Last edited by paula_w; 08-08-2007 at 06:50 PM. Reason: clarity
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Old 08-08-2007, 09:01 PM #13
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Paula, for someone who has a healthy fear of the males of the world, my relationship with this son in law has been a challenge for me personally. Sharing too much personal information again...I am bad about doing so.

And, it is a lovely little place, just the right size for one, maybe two, people. I am enjoying it more than any place I have lived since my last marital home, and that was...yikes...22 years ago!!

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