Make Inanna House a Reality

This cause is truly so incredible that it sounds too good to believe. The wild thing is though, it’s not. Mara Williams (who guest posted here on Lyme Chick 6 months ago!) is the founder and CEO of this amazing vision, Inanna House. She is also a Nurse Practicioner and Energetic Healer who has worked as a healthcare provider for over 30 years. Oh yeah, and she wrote this stunning book, Nature’s Dirty Needle.

The always inspiring and awesome Sarah Lamando (of A Slice of Lyme) created this campaign in a tireless effort to fundraise for Inanna House; A supportive and safe place for Chronic Lyme patients to receive treatment, while integrating the best of all health modalities to achieve optimum results for each client, which includes a body, mind, and spirit connection and reintegration. Which she is fiercely fighting to see built.

Sarah and I collaborated to illustrate just how extraordinary The Inanna House has the potential to be, if we are successful in meeting our financial goal… That’s where this video came in to play. We both are keenly aware of how staggering and financially crippling the cost of this disease is. We also both would have given our right arm to have had access to a place such as the Inanna House at the start of our battles with this disease.

Put simply, ANY amount helps. If you are unable to contribute please watch and share the video. We can do this. This is within our reach. And we owe it to each other and ourselves to make this a reality.

Contribute: www.indiegogo.com/inannahouse

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About Lyme Chick

Lyme Disease advocate/warrior still learning about Lyme treatments/recovery and wishing to inform, support, and commiserate with others along the way.
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One Response to Make Inanna House a Reality

  1. I can’t contribute financially since I’m struggling for my own survival at the moment, but I can try to help raise awareness for this wonderful project! I would like to see hundreds of Inanna Houses be built across the country to help save the lives of our most severely ill Lymie friends, who often lose absolutely everything to this damned disease and its ugly co-infections.

    This is the first post I’ve seen from you in a while, LymeChick, I’ve missed you! How have you been? I’m still fighting, just had a meningitis scare the other day and got treated like crap at the ER as soon as they learned I was being treated for late stage Lyme. I wrote about it at my blog.

    My blog was mainly a political blog before I got so sick, kinda ironic that ‘d get a ‘political’ illness, huh? LOL I know my politic writing is a distraction for my Lymie friends though (and Lyme is a bipartisan/nonpartisan affliction anyway), so when I am up to it I have been putting together a new website & blog that will be just for Lyme & TBDs and separate from my political blogging. I had to shelve it while I have been dealing with a nasty flare up, but you can take a sneak peek if you want to by visiting LymeZilla.com.

    Thank you for all of the great work you do, LymeChick, you are a hero to me and many others.

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