P.S. I have no faith in dr.s I do most of my own research and glad I have decided to join the message boards. You all are a great help and give me hope...
It's better to have Lyme than MS because there is a cure even though it can be long and hard.
My pharmacist told me about a friend of hers who spent 20 years in a wheelchair with "MS" she learned about Lyme, saw an LLMD and is finally walking again. Such a waste.
And feel better, anxiety and depression can come as a side effect of Lyme or a co-infection.
You weren't stupid in pulling the ticks off of you ... the ticks were stupid to bother you! There are ticks everywhere, on pets, in city parks, you name it -- not just on farms. We are all exposed and just don't know it.
Don't be afraid of a Lyme diagnosis -- it's the first test to getting well, if it's what you have. I had Lyme and babesia, and it's a miserable combo. My doc treated the babesia first, and I felt a lot better already! Then Lyme treatment, and I was officially healthy again. I was tired and my body was worn out from the fight, but slowly and surely I regained my energy and strength.
Don't be afraid of treatment, either. Part of Lyme is that it messes with your moods and thought process, and makes it hard to think things through. Try the magnesium supplements and see how you feel -- it helped me a lot -- but it doesn't treat the infections, just lessens some of the side effects of the infections.
Be not afraid! We're pulling for you. Keep us posted, okay?
Neuropathy is common with Lyme, I am totally natural and take Multi B complex, Alpha Lipoic Acid and biotin for the neuropathy. Helps me immensely
How are you doing these day? I remember the good news when you said you'd reached remission! I am hoping you're still feeling good.
I have to tell you that your symptoms VERY MUCH sound exactly like mine when I first developed symptoms after my gallbladder surgery. I also had numbness in my face, feet and leg in addition to all you describe.\
I have lyme (dx by Igenex) and test positive time after time.
Sounds like lyme to me for sure!
I was screened for MS at UCSF and despite having 20+ lesions on my brain, they say this isn't MS. They say it's not lyme either though because my spinal tap did not show lyme but that is pretty typical I guess. I have made improvements with ABX but it's a long journey.