Losing hope

Hi guys,

I started supplementing for B12 2 Weeks ago after a very long standing deficiency (>5 years).

At first I thought I'd be fine as I didn't notice most of the symptoms but now I unfortunately have realised it doesn't look good and the damage looks permanent. I have * Tingling in hands, arms, feet, legs, and face every day when I wake up. I'm not sure if this is permanent as it's intermittent but it's around for a while so I don't think it looks good. * PoTS with my heart rate going from 75 to 110 when I stand up. This also is present the whole day so I think it pretty much indicates permanence. * Dry eyes and dry mouth. Also, long standing autonomic issues that probably won't go away.

The good news is that at least my brain and spine MRI didn't show any damages somehow.

I am so annoyed with myself and my doctors for letting this happen. I'm 27 years old and it feels so unfair to have serious chronic conditions like PoTS and peripheral neuropathy so early on in my life.

😢