LWAE is back…

LIVING WITH AUTOIMMUNE ENCEPHALITIS

Living With Autoimmune Encephalitis is mostly back online. Against advice of external assistance, I have made good will efforts to accomodate the allegations where possible and decide that others were not needed. As such, the majority of LWAE is back online.

It has been about 3 days since I replied to the complainant’s email I haven’t received any reply so either the concerns have been satisfied or as I fear, they are devising further actions and tactics.

In my email reply I wrote for requests for clarification on certain allegations to better rectify them, the changes I was implementing, and my gratitude for bringing their concerns to me and to reassure them that any similarities between us are purely coincidental. I also offered any assistance they wanted with rectifying similiar issues with their site as I found during the adjusting of LWAE.

I haven’t received any reply so, either the concerns have been satisfied or as I fear, they are devising further actions and tactics. In either case, Living With Autoimmune Encephalitis is going back to curating related information, articles, research, and writing our own content.

Apologies for the inconvenience experienced by those that were being helped by the site, but until I can sort this out, I am suggesting and redirecting anyone that has contacted me for help or that does contact me for help to either two great organizations which are the Autoimmune Encephalitis Alliance in the United States or The Encephalitis Society in the United Kingdom.