posted
I'm a 39 year old mother of 4 under the age of 8. I am doing my best to keep my spirits up through all this. I began treatment for Lyme on 11/19 after the onset of some frightening neuro-symptoms. Thankfully for now, I am feeling better...But it looks like a long road. In the last week my husband has begun experience some of the same numbness and tingling in his hands and feet as well.
It was recommended by a friend that I go see Dr. M up in WI for a second opinion on treatment. I did that and have another appointment in 2 weeks. My husband has one on Monday.
After reading so much on this board and elsewhere about the controversy surrounding this disease and it's treatment, I totally understand that folks would want to protect the names of these doctors. I am hopeful to get a sound recommendation for an LLMD or get some reassurance that the one I found is the one to trust. I can't help but want to have a back up in mind, in case something doesn't "fit" with Dr. M in WI.
I am hopeful to connect with others in IL/WI to share our experiences and such. I tried joining an online Yahoo, members only WI/IL group but noone has gotten back to me yet. I haven't had any luck yet finding a support group around here...
If you have any advice or direction you feel you would like to share, please do. In the meantime, I'll get around to posting more as time permits. With 4 children, that's no easy task! Right now the youngest is still napping;) I still find myself in a "read and absorb as much as I can" mode. I'm very, very grateful to have found this forum.
Best wishes for a healthier 2008 for you or your family member(s) who are fighting this fight.
Brandie
-------------------- "You play the hand you're dealt. I think the game's worthwhile."
C. S. Lewis Posts: 36 | From Illinois | Registered: Jan 2008
| IP: Logged |
just don
Frequent Contributor (1K+ posts)
Member # 1129
posted
Welcome aboard,,,,
AND for what its worth,,,I think you are doing the absolute BEST thing possible for YOU and your family!! Keep on,,,keeping on!!!! ib--just don--
-------------------- just don Posts: 4548 | From Middle of midwest | Registered: May 2001
| IP: Logged |
The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:
The
Lyme Disease Network of New Jersey 907 Pebble Creek Court,
Pennington,
NJ08534USA http://www.lymenet.org/