View Full Version : Marilyn Edwards
Marilyn Edwards
June 23rd, 2008, 05:55 PM
Hi, I'm a new member. I am caregiver for my partner Ross who was diagnosed with PD in 2001
suzie Q
June 23rd, 2008, 06:03 PM
Hi Marilyn welcome to the forum .i am 53 and have had P.D. for 5 years this a great place for information about P.D. every body is so friendly hope to talk to you some more .
Sue
Marilyn Edwards
June 23rd, 2008, 06:06 PM
Thanks for your quick reply Suzie. Have only just heard about this website and it looks good. Through this have also found www.nwpf.org which looks interesting. Living with PD is challenging for sufferer and caregiver but fortunately we now have good healthcare support systems in place
I imagine I will be chatting with you again.
suzie Q
June 23rd, 2008, 06:11 PM
Marilyn
am at work and just looked to see what was going on looks like we on together .I live in Tasmania Australia .and i better get and do some work talk soon
ltd-addition
June 24th, 2008, 09:34 AM
Hi Marilyn
A big welcome from me to you.
Im a young spring gazelle from the UK.
45 yrs young 6 years diagnosed, still working full time, married with a 6 yr old son and I've got a size 6 shoe. (Just thought I'd share that info haa ha . Apologies in advance but I haven't been certified yet! )
Drew Saunders
June 24th, 2008, 10:45 AM
Hi Marilyn,
Welcome to the family. I'm 62 yo diagnosed 8 years ago. Married to Elaine 3 1/2 years and size 9 shoes (you started it Ltd). We are here to help in any way we can and hopefully make you smile, laugh even. There is a vast amount of information available on the site but if there is a particular problem which you need help with then do please ask. Enjoy the experience,
God Bless
Drew
mwright305@comcast.net
June 24th, 2008, 10:59 AM
Hi Marilyn,
I am a caregiver for my husband who was diagnosed with PD appx 2 years ago, like every one else, he probably had it several years before diagnosis. We have two children 15 year old boy and 12 year old girl. My shoe size is 9.5 (just joining the group).
Welcome, this is a great forum for real information. Everyone on here seems so positive, which is so important in this disease.
Talk to you soon.
Mary
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