Advanced Lyme Disease

When I was 29, I was working outdoors in the Highlands.

That was four years ago.

I became progressively physically unable to undertake even simple tasks due to severe tremors and bodily weakness (I can’t walk now, or feed myself, or text).

My name is Noah and I have had Lyme Disease for three years, wrongly attributed to MS. I have been bed-bound and completely reliant on my parents, whose living room I am trapped inside.

I have discovered that intravenous antibiotics will cure me – at least to the point of standing, walking, losing the shakes and the eye problems.

This treatment is not offered on the NHS, unless they themselves diagnose Lyme’s.

The thing is, there are different tests for the disease: the NHS uses one type, private clinics generally use another.

Over the past six months, I have been in touch with one such clinic, who has confirmed I have Lyme Disease.

They are able to facilitate the treatment I need.

I desperately need my life back.

I am hoping to raise £40,000 for treatment and accommodation.

The course of intravenous antibiotics takes three to four weeks.

Absolutely any amount of money will be gratefully received: it will all add up to my rehabilitation, to being able to leave bed.