Please Help My 17 Daughter with Neurological Lyme
$5 raised
0% of $70k goal
1 contributor
4 Years running
Hello, I was diganosed with Neurological Lyme 10 years ago. I saw a Lyme specialist who treatment me with long term antibiotics back when the insurance companies did not put restritions on paying for it.I am feeling much better but now my poor ...
Hello, I was diganosed with Neurological Lyme 10 years ago. I saw a Lyme specialist who treatment me with long term antibiotics back when the insurance companies did not put restritions on paying for it.I am feeling much better but now my poor daughter is bedridden and is in constant pain, neurological nerve pain, daily seizures, constant debilitating stomach and muscle pains, numbness, she can barely walk from the bed to the bathroom. She has recently been diagnosed with neurological lyme with strong positive Lyme titer from Labcorp. However the insurance will not pay for long term treatment or any IV treatments that has helped me as I had coinfections as well. I am currently on disability due to some residual effects of Lyme disease and can't afford the 6-8,000 a month it will cost for IV treatment for her a month for a minium of 7-12 months. I don't know what to do, My daughter can't take the pain anymore and I feel helpless. I am usually a very proud person but right now I am so desperate to get the help she needs. I don't have any family to help. Her biologicial father abused her when she was 7 and is no longer a part of her life so we have to be discrete on our location because he is unstable. I am begging if anyone sees this and can pass it on to help please help her. Thank you in advance for anything you can do.
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