Posted 7/15/2017 8:56 PM (GMT -5)
Hi kw -
I completely understand not wanting to eat. I was like that my entire life, mostly. As a kid I hated food, never had an appetite - didn't change until I was in my 20s. But when I got really bad w/ Lyme & Co the appetite issues came back. And I was like you - no problem not eating, less to mess with and I didn't have to worry about all the food restrictions.
But starving yourself has its own impacts, and few of them are beneficial when you're also battling Lyme. 70% of your immune system lies w/in your digestive system so when it's not being fed or if what it's being fed is not optimal, it struggles and damage can occur. The last thing you want is to overwhelm your immune system.
I don't know about you, but now that I'm in intense treatment, when I don't eat my viral load takes over - even when I'm on a lot of antiviral meds. It can get scary.
I spent a few years eating nothing but soups and pureed foods, medical food powder. I HIGHLY recommend exploring foods like this, even baby food - just to get SOMETHING in your body.
Bone pain -
Bone pain is pretty common for bart so if that is not something you are treating you might want to explore it. I didn't have much noticeable bone pain MOST of the time until I started taking abx for Lyme... then it was very intense. It can take your breath away. I was never able to alleviate any bone pain except through more tx (once I started on abx for bart I definitely improved). The pain moments return still but very infrequently and they are just short spurts.
Hope that's helpful -
Please let us know how you're doing and if there is anything else we can help with.
-p