Bartonella Babe

Hi everyone! My name is Jake Picker and I make "edutainment" videos about bartonellosis, mast cell activation syndrome (MCAS), SIBO, and other related conditions. Unfortunately, I have been suffering with bartonellosis symptoms for over ten years but became debilitated by those symptoms in August of 2018.

Almost every single minute that I feel well enough, I spend researching, writing, filming, and editing my videos for Bartonella Babe. The best way to support me is to shop my Bartonella Babe merch at www.teespring.com/stores/bartonella-babe. I have chosen to donate 25% of all proceeds to the Bartonella Project at the North Carolina State University College of Veterinary Medicine. 

If you are looking for support, please join our Facebook support group called Breaking Down Bartonella. To stay updated with my life, make sure to subscribe and hit the notification bell. Also, follow me on Instagram @bartonella_babe and on Facebook (Bartonella Babe). Thanks Bartonella buddies!