| I am almost 55 years old and have had MCS/EI
since i was 19 and that was before it was recognized. I lost my husband
and when he died it made it really hard because he protected me from so
much. But I have been pioneering for well about 15 years. My partner
had pioneered for years but went off the list when she got this. Now we
team up. She is back on the list.
There are 32 of the friends that have it
in our hall so I understand.
This illness has helped me to be more loving
to people's illnesses, even when we don't understand. I'd have to write
a book to tell you all that happened to me but we are ahead of the rest.
Because the whole world is going to end up with this before it is
over, in one way or enother. We have so much more understanding.
Three pioneers have it in our hall. There
is a family that has it in Phoenix and never gets the meetings, except
on the phone and only does service on the phone.
Anonymous |