Hi there the name’s Tom, and I was diagnosed with love. Ha, ha Lyme I’m back in early July.
My major symptoms are fatigued and neurological symptoms , like lime fog angry outbursts and difficulty concentrating.
I I am finding it increasingly difficult to deal with some of these symptoms and it appears it’s going to take some time before they get better.
I I am looking for ideas on ways to live with these symptoms. I am doing the things most Lyme patients do including anti biotics, supplements, Paleo diet, and attending a monthly meeting.
I know how important it is to work on attitude, and as a result I do meditation, 12 step groups, and exercise when I can force myself to do it.
The exercise is probably the most important piece that I fall down on. And I am trying to find other people to exercise with. But my fatigue seems to come up whenever I should be getting to the gym or a yoga mat.
Thanks for listening to my rant. I often feel this is the only place I can safely vent these feelings . However, I am hoping to connect with other people through this bulletin board and other services.
When I am up I can be quite positive and funny. Funny how sometimes this disease makes one so terribly serious. Here’s to a lot more laughter in the new year.
Blessings to all of you,
Tommy in Minnesota