Does anyone know of a medicen to treat co-infections, besides the expensive malaron and mepron? Malarone works for me, i'v been on it for two months with good results for the first time in a year and a half of treatment. We are now tapped out and can't afford either med. Any idea would be a great help. Thanks, Shonna.
Posted by trueblue (Member # 7348) on :
Shonna, If you have no insurance and/or meet the income requirements, etc.. You might be able to get Mepron from Bridges to Access. It's worth giving a call to see if it's a possibility.
If you could qualify I believe Mepron is umlimited. I think they charge $10 per refill. Malarone they only allow, once a year, 16-30 tablets. It saved me some but not lots.
I hope it helps.
Posted by WildCondor (Member # 434) on :
Have you tried larium?
Also ask about free and needy meds programs for Mepron and malarone.
Posted by AmyJ (Member # 6192) on :
Can you share how much malarone you were on.... I was taking 100mg a day (not for my lyme)... but man I felt good while on it... trying to decide if that was the reason, and if so... if I should try to find a supply. Posted by got1bite (Member # 11955) on :
Thanks for the help. Yes i do have b/s HMO. Insurance won't cover Mepron or Malarone due to a negative lab test. I have one of the two dozen pick any one.... My LLD said i definnatley have a Babesia infection. I did receive several benefits from the malaron. The first month i took one pill a day...no changes but mild herxing. The second month i was taking three a day. Thats when night sweats and other side effects got better or even dissapeered. None of my other orals, rocefin and mepron did anything but made me herx/hurt more. I would choose to continue the malarone, but $ is the downfal, or lack of. Thanks for the info, anyother ideas? Shonna.
Posted by Lymetoo (Member # 743) on :