#ThisisME is
a blog chain event run by Louise Bibby of Get Up and Go Guru.
A link to her post about the initiative can be found on her site here:
This is M.E. – ME /CFS / Fibro Awareness Day 2014 – Blog Chain
She has requested that each participant answer a series of questions about their illness - either on their own blog, or by emailing the answers to Louise herself, for inclusion on her blog. My contribution follows:
A link to her post about the initiative can be found on her site here:
This is M.E. – ME /CFS / Fibro Awareness Day 2014 – Blog Chain
She has requested that each participant answer a series of questions about their illness - either on their own blog, or by emailing the answers to Louise herself, for inclusion on her blog. My contribution follows:
#ThisisME
What is your name & how long have you had ME / CFS / FM?
·
Dawn Derraven, I’ve had Fibro for a long time but
was only diagnosed just over a year ago.
Where do you live?
·
Wales, in the shadow of Twmbarlwm
Age?
·
47
5 things about you that the people in your life probably don’t know?
(non-illness related):
·
I may seem strong but I’m easily hurt.
·
I can’t stand bad feelings between anyone.
·
I have a very large, fluffy, purple onesie!
·
I really love my job.
·
I wish I’d never had my tattoo.
5 things about you that the people in your life
probably don’t know?
(illness related):
(illness related):
·
When I’m really tired I can’t talk, think, text or
even smile; breathing takes all my effort.
·
I’m not boring or up-tight, it’s just that laughing,
singing and dancing, use up too many spoons that I can’t afford to use.
·
I can’t function when I’m in pain as everything
hurts, even my teeth.
·
If I forget to do something or forget where I put
something, it’s not my fault, it’s my FM.
·
I get anxious if the route out of a room is blocked
by someone or something. Even if someone has their legs outstretched.
What one thing do you think most people wouldn’t know about living with ME / CFS / FM that you’d like them to know?
·
I’m never well; I just have various levels of
unwell. Some I can cope with, some I can’t.
What is the most frustrating aspect for you of
living with ME / CFS?
·
Having to cancel plans at the last minute as I feel
unwell, being unreliable.
Anything else you’d like to say before finishing?
·
Please take the time to learn about these invisible
illnesses, the more you understand the easier it will be for all of us.
****
Louise says:
·
Any other bloggers who want to join the blog chain,
please copy this and fill in your own answers.
·
Then email Louise@GetUpAndGoGuru.com so she can
link to your blog post in her original post.
I’d
Love You To Join In!!
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