I was diagnosed with Lyme disease in 2012, after getting sick nine months earlier and trying to see what was wrong with me. The road to diagnose was slippery, but I got treated with antibiotics right away after being diagnosed. However, the symptoms prevailed and I went for years feeling the symptoms with no doctor willing to retest or retreat me for lyme. After being sent to various doctors so see if I have something else causing the symptoms, I ended up in the hospital in 2020 only to find out I have neuroborreliosis. Why is diagnosing and treating lyme disease so difficult and why are people not getting the help they need? I am sharing my personal experience and views on this very complicated disease in hopes to help others who are struggling with the same problems. I am not a doctor and this video is not intended to give any medical advice, but rather to share my story and bring awareness of the lyme disease.
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