A young inspirational EM sufferer Lauren Fraser created this page.She says.......... "This is a place were I can share all my knowledge, experiences, misconceptions and understandings with other sufferers of the EM life. It's here to help others (especially just diagnosed) and save people from tough times (hopefully). I know from when I got this aged 12 how much of a dreadful impact this can be to you and on your life".


Lauren also has a FB page https://www.facebook.com/groups/Erythromelalgia/

Living with a rare disease letter

If you are living with a rare disease, feel free to print this letter and share it as is, or edit it to make it your own and share with those you wish to have improved understanding of your diagnosis.Written by Reta Honey Hiers (2015)

Find The EM Warriors Page On The Mighty.