Clearing out the Trash

Glad you enjoyed the article, Genevieve,

ICI (invisible chronic illness) seems to give many of us the chance to examine life a little more intimately. We have the time because we're not necessarily bogged down cramming things into already full lives, like healthy people.

Thanks for the book/author recommendation, I'll take note of his name.

Although I have to be honest, & say I have a pile of about 20 new non-fiction books laying unread next to my couch. i'm going through a stage of difficulty in reading - eyesight, memory, comprehension etc.

Takes me hours to write a post or Blog - I have to re-read it about 6 or 7 times to get it even half right.

Vicki

Vicki, I can certainly understand your reading difficulties. Mine are getting gradually better, but it goes in fits and starts.

I so agree about the gut instinct being very important in healing - no matter what varieties of healing we're using. One of the benefits of losing my brain is realizing how very good my intuition is.

By the way, for someone with neuro/verbal problems, you write a great blog post! And now you're semi-retired, maybe you can enjoy more nonverbal time as you described; beyond words is often where I get the most healing.

Hi Vicki, Just want you to know that I find your blog/posts extremely relatable to where I've been and am cuurently inhabiting.
Thanks for sharing your difficult moments and the upbeat. Your gardening images remind me of past herb and flower gardens that gave me pleasure during days too ill to tend but look out the window and feel content.. The first few years, I also copied every thing available, transferred to ME/cfs student. You have reinforced my beliefs that illness does not have to rob us of quality moments and efforts to thrive and fulfill our purpose. Afterall, we are alive and it is a gift no matter what our giftwrap appears to be. My posts are not often as it is cognitively difficult now to spell and type well (which make me grateful for your efforts). As one who excelled in English, your participation is valued.
I hope and pray that your current life/work transition has a smoother, less abrupt path than some. Sue C (Eastern coast US)

Hi Vicki, Just want you to know that I find your blog/posts extremely relatable to where I've been and am cuurently inhabiting.
Thanks for sharing your difficult moments and the upbeat. Your gardening images remind me of past herb and flower gardens that gave me pleasure during days too ill to tend but look out the window and feel content.. The first few years, I also copied every thing available, transferred to ME/cfs student. You have reinforced my beliefs that illness does not have to rob us of quality moments and efforts to thrive and fulfill our purpose. Afterall, we are alive and it is a gift no matter what our giftwrap appears to be. My posts are not often as it is cognitively difficult now to spell and type well (which make me grateful for your efforts). As one who excelled in English, your participation is valued.
I hope and pray that your current life/work transition has a smoother, less abrupt path than some. Sue C (Eastern coast US)

Thanks for the praise Sunday & Sue C,

I DO find it really hard to write a post or blog now. I read a phrase or book title on my shelf & suddenly I have an idea of what I want to write about. It's surprising how many books on mind/body I have.

I find it quite literally 99% impossible to write a post on any of the ME/CFS/FM threads. I cannot gather my thoughts or remember the details.

I cannot even write a post on the Buddhist thread (I have many books on Buddhism on my shelf & find great comfort in them) - I can't remember what was written in previous posts on that thread on the Forum, so can't enter a discussion.

My short term memory is far worse than you could imagine.

I'm not sure (at this early stage of my joblessness), that I could learn or do another job ever again. It hit me today when talking to my elderly parents (aged 83 & 86).

I can't imagine how I ever worked full-time 2 weeks ago. It's almost like my brain has suddenly released all the stress & information overload & "burst at the seams".

That is one of the reasons why I think I found the Social Services application forms & interview, and the Job Capacity Assessment interview, so stressful & exhausting.

I can copy a joke from my pile of jokes.

I can write about what happened today (the memory of today's events may be gone tomorrow).

My memory can recall certain episodes or information of my past, but fairly limited.

It's really quite scary.

If, in the future sometime, I did come down with alzheimers, you will all recall this moment in my life when I was confused & fearful of the reduced brain function & deteriorating memory.

If, these weeks are purely a settling in process of rest & recovery from severe stress, then no doubt you will see me recover. FM is the formal diagnosis for me (beside heart, spinal degenerative disease & other health issues), but I still wonder if CFS is also a possibility, after all they share some 85% of similar symptoms.

I don't have ME.

Genevieve,

Serendipity is one of my favourite words.

I have just visited my favourite UK Buddhist site called Wisdom Books (to see what's on sale).

And the second winter sale book on offer is, The Power of Now by Eckhat Tolle. What a coincidence. And the price was very reasonable - 55% off (even adding on intern'l freight), so I have added it to my small order & when it arrives in 10 days, i shall be able to share your "best friend's words".

Dear Victoria,

Much resonance with me. It is so true that seeing and appreciating what we have (and most of us at least have a home, clean water and food to eat) is better than focussing on what we've lost. Everyone gains and looses as the rollercoaster of life travels on, indifferent.

Who was it who said that 'If you do not appreciate what you have, then you don't deserve any more'
Being ill this year (only a year so far for me, how lucky am I!) has given me time to discover that I really enjoy writing. Over this year I spend maybe an hour a day on the phone to my youngest, in effect 'hanging out' with her by wire, being party to the upbringing of my two grandsons, at a distance. We could do with headsets, but then mine must not be wi-fi or bluetooth, as those seem to have a negative effect on my health.

Were you really working full-time until recently? That must have needed a steely determination to hold things together, while your body was really needing your full attention. No wonder you are at a stand cognitively, at the moment, after whipping your brain into coping mode for so long.

In England we have cabbage whites, we call them butterflies, and their larva make leaves into lace if you don't get efficient with the 'order of the boot' .

Serendipity, and penultimate. They are my two very most favoritist words. I believe in bin (trash can) power too. May your good days grow x

Thank you for your affirmative, practical blog.

Jace,

now that I'm improving beyond belief, at the start of my 4th week not working, I realise how devastating working full-time was on my health.

I have great will power & determination, but when I ran out of this, I knew deep down that it was time (to give up full-time work).

But it was always the financial aspect of NOT working that held me back.

So glad to hear you're feeling some relief, Vicki. I bet and pray (maybe it would be better to pray, then bet) that the rest will do you good. And that great will power and determination will still serve you, only in a different venue. Rest up!