One in Thousands my life as a rarity
- JANE DOE
About - my life as a rarity

One in Thousands:
my life as a rarity
During lockdown I found an EDS-site on Facebook. About a million things made sense for the first time. The same things were still a problem for thousands of others: Despair, shame, confusion, and above all lack of information and support. From family members, partners, bosses and many self-important and downright stupid doctors.
Somebody needed to tell everybody about living a life in unnecessary pain. And maybe causing others unnecessary pain.
So I wrote “One in Thousands – my life as a rarity”.
An autobiography with a twist.
Buy here, from Amazon, or order in your bookshop
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WHAT THEY SAY ABOUT MY BOOK:
I am still reading it… and it is marvellous I must say! … I really would like to recommend it to EVERYBODY! And certainly to doctors, nurses, government personnel, etc… It is so honestly written, with nice pieces of humor. At the same time as a reader I can almost ‘feel’ the sufferings. Everybody should know what EDS is and what it means to live with it. (Woman in Belgium)
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I am so happy, my dear friend, so absorbed in the exquisite sense of mere tranquil existence, that I neglect my talents.
Emilia Clarke
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Something that happened in your body before you were even born can never be your fault.