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Does anyone have someone with Fronto Tempral Lobe Dimentia. It's really hard to get info on this form of dimentia other than refer to Altzimers. My Mother has progressed at a rapid rate and I still dont feel I know what is happening to her brain.
Hi Dexter, welcome to the forum. All I've found so far is this - although it's a site aimed at disabled children, the information is quite useful, and there is a contact link.
I'm sure it must be difficult to deal with when its progessing quickier than you can learn whats happening. I have found the following links that I hope can guide you.