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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. Website where you can buy my nature photos (digital& prints/ canvases, worldwide delivery): https://www.viivekairebane.com You can support my channel by "buying me a coffee" from here: https://www.buymeacoffee.com/viivekai... You can also follow me on social media: FACEBOOK / viivekairebane INSTAGRAM / viivekairebane #viivekairebane • Life with lyme disease- my neuroborre... #lyme #neuroborreliosis