If You Are Diagnosed with Chronic Lyme Disease, You Are on Your Own. Part II.

Just came across this on Facebook. It’s written by an RN, and pretty much sums up what I was trying to say in my previous post:

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It’s so important that the Lyme community unite & stand up for Lyme patients globally! So many of us have lost so much to this horrific disease & tick borne infections.

1. Some have infected our children in utero, & they will grow to suffer horribly just like us!
2. We have permanent damage to our immune systems, and with no cure in sight!
3. We have lost EVERYTHING we have worked so hard for…careers, savings, family & friends, quality of life, and at times our sanity.

We have been forgotten & ignored by the medical system, the CDC, & our government. Its time we come together like AIDS patients did & fight for the help we desperately deserve! We are all sick & because of greed and lies we are all left with NOTHING! NO CURE, NO TREATMENTS, NO RESEARCH, NO DISABiLITY, NO QUALITY OF LIFE.

We can not sit quietly and expect others to fight this fight for us! Please share this post & invite family, friends, & Lyme warriors to stand with us May 4th, 2018 at the CDC in Atlanta, Ga. Its time our voices are heard!!!πŸ’šπŸ‘ŠπŸ’šπŸ‘ŠπŸ’šπŸ‘Š

https://www.facebook.com/lymearmy/

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