Hello and thank you for visiting!

This journey started when my symptoms got worse, i suppose. My vision. Speech, headaches, spinal pain and intermittent partial paralysis have all gone down hill in recent months.

while I have been studying Law at Hertfordshire University, I have been lucky enough to see the generosity and kindness people have in them first hand. I am now, unfortunatrly, praying that there is some kidness towards me, as withoutmit, we do nit know how much longer Iwill be able to be at University or as independent as I am.

At the moment, my symtpms are wide amd varies, incouding partial paralysis that comes and goes as it pleases, tingling in my feet, i fall unconcious when i look down or to the side and up, my neck dislocates comstantly, the headaches and nausea are constant, and my eye sight vanishes frequently. I also experience tachycardia each time i eat anything.

i sent my images off to the doctor expecting him to suggest my symptoms were due to my soine and that i could do with a fusion, instead he used words like advance, press upon the urgency to have surfery, and progressive. I will only get worse.

The truth is, I might die before i raise the money , but at least I will have tried.

Lexy x