I had a moment earlier where I was thinking about my prospects for the rest of the year and beyond.
I also started thinking about the sacrifices I’ve made and what’s different in my life now compared to when I was 100% healthy.

Also, what would I be doing now if I wasn’t so damn fatigued all of the time. I came to an interesting conclusion …
Prospects
It really did dawn on my earlier that I could be in this for the long run. I’ve had a post viral ‘problem’ for a year and half now. I steer clear from saying to anyone that I have ME/CFS etc, etc. Largely because I’m probably in denial and still believe I will wake up tomorrow as right as rain. If 100% was me at my worse, I guess I’ve made a 20% recovery up to now, which though is great, living life at 80% of your capabilities is not fun. Ok, perhaps I’m underestimating my recovery figures due to being in the situation, but that’s where I believe I’m at.
As many will know, this is a long term illness - 10, 15, 20 years - a lifetime even people have this for. So where does that leave me? I guess the question is, if I felt like I did now in ten years, would that be ok? The answer to that is yes, because it has to be yes. What choice do I have in the matter? Giving up would be suicide, and I don’t know about you guys, but there’s so much beauty in the world and great experiences to be had that I wouldn’t give up for anything.
I’m ok if I have CFS for 10, 15, 20 years, or even for the rest of my life. I choose to accept that I have this illness.
Sacrifices
If I’m really honest about this, I’ve made no sacrifices at all, I just do less of what I used to do. I can’t think of one thing that I’ve given up since having this illness - I’ve been in a band that regularly gigs and rehearses, I still exercise, I still see friends, I still work (dropped a day a week), I still get immersed in music and my instruments on a daily basis, I still travel (our band went to the Alps for a tour back in February), I still see family, I still go shopping, I still eat a whole packet of biscuits when I really shouldn’t… The list goes on :)
All of the above are made that much harder for feeling tired and fluey (you know the symptoms by now), but I STILL do them.
I accept that I do less of what I did before, yet I’m still able to do the things I love.
Things that have helped me
In no particular order except for number 1 :)
1) REST!
- Supportive friends and family
- A compassionate and flexible employer
- My Doctor and local support teams
- A determination to get better
- Self-help work on thoughts, worries, guilt, anxiety etc *
- Supplements (no proof whether these work but who knows) **
* I believe that self-help work is one of the best things you can do, and one of the most rewarding journeys too. I had several episodes of anxiety, guilt etc, that I recognised weren’t helping me out.
I can thoroughly recommend this book to anyone.
The title sounds drastic - don’t be put off by that. It’s full of really good techniques to make you feel better about yourself from day to day.
** I tend to have quite high doses of Vitamin C and Zinc. I also take multivit and from time to time fish oils and magnesium.
If you have any similar stories, comments, questions, share them!