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Lyme: My Story

Posted By: CrystalRiver
Date: Monday, 12-Feb-2018 20:41:32
www.rumormillnews.com

Dear RM Agents and Readers,

Sometimes it is so hard to stay the course. I've wondered why isn't this accepted. Was this done to kill a group or just bring them to their knees?

Keep on Keeping on, something must change soon!

Many Blessings,
CrystalRiver

Lyme
I was diagnosed with Lyme Disease in September of 2014 after several months of misinformation, misdiagnosis and near despair after being given the runaround by multiple medical organizations. “You need to realize you are now officially on an island,” a fellow Lyme patient said. “Nobody wants to deal with you.” At the time I found this difficult to believe, but after more than two years of dealing with the condition I have come to fully understand the minefield that is Lyme Disease. For many of you with Lyme you will know precisely what I’m referring to, and for those of you without Lyme, just know that this disease is an unpopular disease, denied by insurance companies, governments and several of the major medical organizations. If you think medical “strangeness” doesn’t happen in first-world, wealthy countries then you simply don’t know what’s happening with Lyme. This section of my site will share my story, but also the treatments and lifestyle changes I’ve found most effective in dealing with Chronic Lyme. For those of you suffering, stay the course. At some point the world must take notice. The numbers of cases is exploding, including several high profile people, but at some point in the near future it will be impossible to ignore. I am not a medical professional, only a patient. What works for me may or may not work for you, but I think the more information we can share the better off we are. If we don’t do it, who will?

From this link: http://shifter.media/category/lyme/





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