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LBD caregivers is only the 2nd on-line group I have experience with.....both for less than a year.

I had no preconceived notions as to what this group should be, only hopes. My hope was that we would get to know each other, care about each other, give information, feed-back, and encouragement. If people wanted to talk about their flower garden, the music they loved, their children, pets....anything dear to them, I would love it. And, I also appreciate "warm fuzzies". In all likelihood, I would seldom 'tune in' if it were just an informational exchange.

Above all, perhaps, I need to feel safe from attack and unkindness. There is no place in my life for this, and I agree that it should not be allowed here.

LBD is an illness of misperceptions, and I believe this can cause volatility. I feel sad about , but I really feel we should be a group of caregivers only. I have learned to treat my husband with kid gloves....and whereas we should not be mean-spirited with each other, we also should not need to tread on eggshells here.

Mai-Liis

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