LymeNet Flash: SCR0004 New Hampshire legislation

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Posted by treepatrol (Member # 4117) on :

SCR0004

This is what lymenet had posted there link didnt work so thats why I posted it I emailed them about the link not working. The one I gave works.

New Hampshire Legislative News
On January 6, 2005, the New Hampshire Senate introduced Senate Concurrent Resolution 4 (SCR4) which is now in the Senate Human Services Committee. SCR4 supports federal funding for Lyme disease research.

The resolution was sponsored by NH Senator Joseph D. Kenney, who requested input from LDA prior to development. NH resident Pam Dugas held an awareness event in NH last year where several prominent Lyme doctors spoke. Go to http://www.state.nh.us/ for the text of the resolution.
posted

[This message has been edited by treepatrol (edited 28 February 2005).]

Posted by swissmoeka (Member # 1577) on :

Sorry double posted. see next post.

[This message has been edited by swissmoeka (edited 27 February 2005).]

Posted by swissmoeka (Member # 1577) on :

Don't want to sound stupid but I have some ?'s

Has this already been passed and if not when will it be presented?

and if not how can we help pass it though?

Thanks,
Swiss

Posted by treepatrol (Member # 4117) on :

up for swissmoeka

Posted by swissmoeka (Member # 1577) on :

Thank you for all the info. treepatrol.

I looked at the website and still have no clue as to what this means, hopefully someone will come along and know the answer my questions.

I feel like I'm working with 1/2 a brain when it comes to this stuff.

Posted by swissmoeka (Member # 1577) on :

Thank you for all the info. treepatrol.

I looked at the website and still have no clue as to what this means, hopefully someone will come along and know the answer to my questions.

I feel like I'm working with 1/2 a brain when it comes to this stuff.

Posted by lymebrat (Member # 3208) on :

"NH resident Pam Dugas held an awareness event in NH last year where several prominent Lyme doctors spoke."

I went to this seminar and hope to go to it again this summer. It was a great seminar and I was able to speak to a couple of great LLMD's who knew both my LLMD and Dr.Jones.

There was also a spokesperson from Igenex there who went into great detail about what type of testing they do and why it is important for people with lyme to be tested correctly...

Pam Dugas is a remarkable lady..her story is like so many here... she was sick and went through hell trying to find out what was wrong with her...

she now know she has Lyme and has become a great advocate for educating people ( and doctors) about Lyme.

The next seminar is going to be this summer, though I don't have the date yet...but I plan to go and hope others here will go as well.

~LymeBrat

Posted by Starphoenix (Member # 2402) on :

This is encouraging.

I plan to relocate to NH in about five years.

Lymebrat, if you don't mind answering: what region are you in? I'm looking at the Dartmouth/Lake Sunapee Region.

Steph