Wednesday 29 April 2020

31 DAYS IN MAY 2020

Bonjour, 

May is M.E. awareness month leading up to M.E. awareness week from 11th to 17th May and Tuesday 12th May is ME/CFS and Fibromyalgia International Awareness Day. 

Even though I do some awareness raising all year round I like to do something special or different in May. 

You can see my contribution last year in this blog 

This year I will be posting and sharing a poem every day. 

It was a major undertaking last year and to great detriment to my health. Still I hope it was worth it. 

So this year I will not be sharing around so much and I will be hoping that others will share for me. 

Some of the poems I will be sharing are shortened or amended versions from my books. 

Some of the poems will be new. 

I know last year that I had a mixed reception towards my poems. Some people were upset by some of my poems. Some were pleased that I was prepared to be open and honest about the truth of living with M.E. 

So as last year I will post a warning with some of my more sensitive poems. 

I will continue to raise awareness and understanding. 

The way I can do this is through my poems and my blogs. 

So please help and support me. 

Every day you will be able to find my poems on my Facebook Page 





Thank you

 À bientôt

from the French Femme
xxx




Wednesday 1 April 2020

Pandemic v M.E.

Bonjour, 

At the moment I'm reading and hearing a lot about how 'normal' people are coping with this recent confinement because of the coronavirus. There are all these wonderful ideas and proposals to help with confinement and self isolation. Of course for them it's only temporary. 

BUT for those of of us with M.E. or any other long term chronic illnesses the situation is permanent. We live in a whole different form of isolation. 

My friend Shirls Chapman has written a great poem comparing the current pandemic versus M.E. 

Pandemic v M.E.

Welcome to my world
All you normal happy folk
Welcome to my life
No this really isn’t a joke
In the days of this pandemic
Self isolation and doubt
This is how I live my life
Day in and day out


You are raring to go
As you do your morning burn
Your creative brains on fire
As you paint then pose and gurn
You put it all on Instagram
Looking for applause
We get washed and that is it
We can’t even manage clothes


Yay, you made it to week three
Now you’re getting really bored
Your ideas have all dried up
Your workout has been floored
You can’t be bothered getting dressed
All your roots are showing through
Try doing this for twelve years
Can’t imagine it, can you?


Shirls Chapman

I have also written many poems about life with M.E. and in this blog I will share a couple of recent ones. 

As full recovery from M.E. is rare it's like we have been given a life sentence.  


Our confinement and self isolation is so completely different from what many healthy 'normal' people are experiencing right now. 

Healthy 'normal' people can not imagine what it's like to live with M.E. 
Only those who suffer the same can empathise. 
 

So we have no choice but to live with this illness and adapt. 

Please feel free to share my blog and poems - especially to healthy people!! 

À bientôt

from the French Femme

xxx