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» LymeNet Flash » Questions and Discussion » General Support » Call from the dept of public health

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Author Topic: Call from the dept of public health
DJP
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Member # 5893

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Good news, I think. I got a call from the Dept of Public Health in our town because my daughter's Lyme was reported to them. I thought it good news because at least Lyme is getting reported.

At first I was a little paranoid to talk to them, but asked a lot of questions and got information from them as well.

It seems they have had a "handful" of cases reported in this town.

I told her my story, alot of the misconceptions that I've learned here, and offered to do anything to get the word out...do presentations at the school, talk to her daughter who is a nurse at another school, speak to other parents....whatever it takes.
She was going to give my name and number to someone else in town that she spoke with and
she invited me to the next town meeting to see what we can do to get the word out. They have a health fair and newsletter that maybe I could get involved in.
I'm go to send her some of the information that all of you have directed me to as she seems interested and wondered if she might have it.
Has anybody else worked with their dept of public health and have suggestions?


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bg2711
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Hi DJP,

Out of curiosity, what state do yo live in? When my family came down with Lyme about 12 years ago, our health dept. didn't want to know anything about it and were not very helpful. I live in Ohio, where of course, there is no Lyme.

I am glad your dept. was more helpful and is interested in it. Good luck and keep us posted. Barb


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DJP
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Sad to hear you live in one of those "no Lyme here" states! Could this disease be anymore frustrating?
I live in Massachusetts which at least is considered and endemic region.
I wonder if your board of health may be more interested since 12 years have passed.
I'm excited that lately I have bumped into people who are interested in what I have to say instead of them looking at me like I'm paranoid....

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BryteEyez24
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I also live in Mass. and I got a call when my hubby was first diagnosed. She sent us all kinds of info about lime and different support groups.

Joyce


Posts: 90 | From Haverhill,MA | Registered: Nov 2003  |  IP: Logged | Report this post to a Moderator
   

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