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hi amanda,

welcome to our group 

please tell us aobut your self and your siutatoin,

 

my name is sharon and my hubby donnie and i took care of my father who passed

away in 2005 with lbd, adn since then i to have ven givin the 99% probablitiy of

haivn g lbd myself,  at times my emails ma be diffiuclt to read as my lbd often

affercts my typing and speeling and grammar. i do the best i can adn if you have

to ask for me to repreat something plesase do an i wll attempt to try again  

so please undersnd that spellcheck etc doesnt work as my brain doesnt alway read

what i wrte which makes it more diffiult  ireas what i wanted to write instaed

of what i worte. so that might make it harder to gifure out what  i am trying

to say, i try to give you prrrespoecdtives from boht side as the cg *caregiver*

and the ptaient.  not easy at times, but i do my best,k  please undersnatndi

am not lookin g for symptather just freinds and understand.  i want to hlep you

undersand things why /how/ when we do things that arent clare to the normaml

mind. 

take care adn share your story with us please  hugs. sharon

I am the daughter of Leonard whom was diagnosed in May 2004 and  he died of

complicatons *blood pressure started dropping and wouldn't recover* on Sept 25,

2005. He had bad case of Dr Jekyl/Mr Hyde scenarios. He was showing

hallucinations and falling issues since prior to 1994. We moved in to take care

of him Jan 19, 2003 and still live in his house. And in feb 2009, i have been

diagonosed with 99% probability of lbd. Hoping that a cure or treatment will be

found before it's too late for me.

Subject: joining up

To: LBDcaregivers

Date: Monday, July 5, 2010, 11:14 PM

 

Please assist me in signing up.

Thanks,

amanda

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