the fundraiser for my Lyme treatment launched yesterday
and we’ve been so overwhelmed by the generosity of others.
most, if not not all, of my treatment will have to be paid out of pocket…due to the vast misunderstanding of Lyme disease, insurances do not cover more than a small fraction (often 30 days) of treatment. sometimes nothing. my treatment will last about two years and the costs are much more than we can cover alone.
we humbly invite you to join us in whatever way you can:
both that we raise the funds we need and that I can sustain the long and painful treatment process. prayer also that the CDC will update their protocol for Lyme (they haven’t updated it in over 30 years) and that insurances change their policies to include proper treatment costs for patients with chronic Lyme disease.
through sharing our fundraiser + story
our reach can only go so far. if you are willing, please share the link to our fundraiser below or share this blog post. I also can send you an email version of our story with a link to the fundraiser – just send me a message with your email address.
no amount is too small. if you are able to give, it will bless us oh so much.
to visit our fundraiser click on the link below:
Help Kami Fight Lyme
thank you, thank you for your support!
it means so much to us.
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