For anyone in Michigan who can attend with friends, family, and doctors, please mark your calendar for an evening viewing of "Under Our Skin" -this event is being planned by Mary Patterson and will be attended by L Brooks too.
Linda from Michigan Lyme will be there as well.
Please try to get the word out to people who can help Michigan get better at treating and diagnosing Lyme.
Also, please tell everyone you know who would benefit by attending. Thanks so much! =)
Hope to see you and your family/friends there! Let's unite in the battle against Lyme in our own state.
Jenny
[ 03-20-2009, 05:58 PM: Message edited by: Jenny in MI ]
Posted by Jenny in MI (Member # 17225) on :
We are also looking for sponsors!! Any ideas?!! If you have a suggestion, please add to this board so I can contact them. Funds over and above the costs we have could go to the MLDA! Thanks sooo much for helping, everyone's ideas matter and are important.
Posted by bettyg (Member # 6147) on :
jenny, please break up your post for mich. neuro patients can read/compehend this better. GOOD FOR MICHIGAN!!
just click on pencil, 3rd box to right of your name to edit ok. thx Posted by seekhelp (Member # 15067) on :
YES, great news Jenny!! I got your PM. I wish my PCP who said you don't get Lyme w/o remembering a tick bite would show up. Perhaps he can expalin my eight positive IgG bands and active infection on my WB! Geeez...
I'm very familiar with the site it's being shown at. Posted by Jenny in MI (Member # 17225) on :
Who will be there? Can anyone help distribute flyers? If you can, please email me an address! Thanks!
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