Cue the Neuro symptoms..

Okay, I've been taking a lot of multivitamins, minerals and health stuffs. I feel a lot better than I did a few weeks ago, yet my health is still getting worse. I've had some more tests done, waiting for the results.

I'm starting to get alot of joint and nerve pain now, my joints are clicking a lot and I'm hurting all over. I also have a weird tummy ache.

I've noticed that taking Magnesium gets rid of my twitching for about 6 hours, and then it comes back. I'm presuming that once I take the Magnesium, it takes about 30mins - 1hour to enter the bloodstream. I then become less deficient, stopping most of my neurological symptoms. Then the Bartonella hoards it, making me deficient in it again. Just like a circle. 

I don't currently have a headache or eye twitching, they've seemed to of stopped for now. But I know that they'll come back again though.

Is this nerve pain, nerve damage?

Post Edited (CaspianS) : 7/24/2015 2:52:39 PM (GMT-6)

I'm trying to detox as much as I can. Fruits, vegetables, chlorella, spirulina, yucca root, grapeseed extract, 10+ Manuka Honey, Epsom bath salts.

My doctor in the end agreed to put me on 1 month of Doxy 300mg per day, but that was last week. I only found out, that you can just buy it from the Pharmacy without a prescription, that's if you say you're going abroad to Africa and need some Anti-Malaria drugs lol.

I've been having the nerve pain for a few days now, sometimes it feels like my nerve's are being twisted.

My mum is starting to realise that it's not just anxiety anymore. I think she's starting to get concerned now, seeing how much pain I'm going through. Although I don't think she's convinced just yet, considering she wasn't sure whether she wanted to give me her supply of mineral tablets lol.

Mum: These tablets are for women and they're not healthy for people your age. (Reads: Osteocare tablets for Men and Women of all ages) Slowly hands me the box.. with a sigh.

I'm thinking of making a formal complaint to the NHS when/if my health gets worse. My mum is very good at making a fuss and shouting down the phone, so long as someone gets the blame. I'm hoping that a scientist somewhere can raise awareness of Bart, Babs and Lyme, but it seems to me like they're trying to cover up.

Do most doctors in the U.S know about Bart and Babs? I wish I could move to the US.

The only thing that's good about the NHS, is they pay for your operations. I'm getting Major chest surgery next year, in the US I think it would cost around $40,000, but here it doesn't cost anything. And I'm debating whether that's a good or bad thing.