My aim is to share some info with the people who know my family. I'd like them to get it what we're going through (yeah we all do right?), and I hope I'd find someone who could help me get the money for treatment... or something.
So videos, blogs, articles, studies...? Something not too complicated and not too long (Under Our Skin is too long and slow for non-native-speakers). Something that doesn't feature only wheelchair patients and others whose illness you can clearly see... because I'm not one of them. My symptoms are annoying, weird, constant... like head pressure, light sensitivity, strange nerve sensations, intoxicated feeling etc. etc. etc. My Lyme reactivated after seven years by antibiotics and stress. Or this is what it seems.
Something that explains the SEVERITY of this disease. If they have come across some newspaper articles only, they have no idea, they might think it's only sore knees and fever... sigh. I'd like them to understand at least to some extent that this global mystery epidemic is not just an illness that you know you have, but it is something that you can feel _under your skin_ all the time and not only that: it also affects every part of you and your life, it's a whole new world, it's about
Please make this a bit easier, I can't review all of them now. xx
Post Edited (Eaglet) : 2/20/2018 3:26:01 PM (GMT-7)