Thanks to all of you, I moved from LA. to FL. to be treated by Dr. C. in Tampa. After 6 wks rocephin and tendamax pulse I am much better! I start another 6 wks of the same tommorow. He will address obvious co's later. Love him, love you. Both daughters on IV also. 1 in LA. and 1 in FL. Husband in LA. is set to start treatment soon. Elderly mom and dad appear to have advanced neurological involvement. Mom is quickly losing control of her legs and I fear swallowing is next. How can they be so stupid as to say ther is no lyme in LA? I vow to become an activist like this world has never seen before when I am physically and mentally able. Who's with me? I hope to call on other state leaders in the lyme fight for direction and guidance when that time comes.
Are there any other Louisiana residents on this forum?