Cumulative effects of over doing it?
Posted , 8 users are following.
Hello all
I'm interested to know how others perceive the triggers of a bad relapse? Do you find relapses come on suddenly without a particular trigger or can you always identify a trigger? Or do they happen after a prolonged better spell during which time you do much which then seems to have an accumulative effect in bringing on a relapse?
I've been trying to figure out my trigger factors for years and can't seem to suss it.
After being bed bound for a year then house bound for another year I finally got into a position where I could work part time and enjoy the odd social event and holiday albeit with a constant reminder of symptoms and fatigue. I was immensely grateful though for this period of relative respite. This carried on for nearly four years with the odd couple of bed bound weeks here and there. Now I'm in the midst of a long bed bound relapse again and wish I knew why.... Was I cumulatively over doing it all this time or was it the shingles I had? If I hadn't had shingles would I be ok now? I guess I'll never know but I'm very interested to hear how others manage their activities during prolonged good spells and whether they think a good spell always precipitates a bad one? This is the second time in the 10 years I've had ME that I've had this roller coaster big up and big down.
Thanks everyone I'm really finding this forum helpful, it was lonely before I found folk who I could relate to :-)
1 like, 8 replies
Jk1952 Sleepysheepy
Posted
jackie00198 Sleepysheepy
Posted
Bunnyhugger Sleepysheepy
Posted
Bunnyhugger Sleepysheepy
Posted
Izzie_Lizzie Sleepysheepy
Posted
I have had M.E. for a very long time. Early on I was much more aware of how a relapse was triggered but they were, with hindsight, very short ones.
During the past 10 years I have no idea what has caused some really dire turns for the worst. Somethimes just a non-descrip bug caused the worst relapses...a bug I should have gotten over easily even with M.E. started it...
Maybe it's different for most.
But you describe some real extremes but it offers hope for me as you describe being bed bound to being able to work part time - awesome!
If you were able to be at this level before I don't see why it won't happen again. I am hoping to get back to a time when I could do much more... though not sure how this is going to happen!
will be interesting to see other's answers!
Hope you're having a better like day
dawn94288 Sleepysheepy
Posted
Gized Sleepysheepy
Posted
For me I know if I'm on the phone talking for about 5 minutes, my glands feel swollen. That's it for me. Also too much loud noise, is a trigger for me.
2 tasks or appointments in one day, triggers for me.
I do hope you feel better. Soon.
Gized
dillemma Sleepysheepy
Posted
Combine that with ME/CFS and you have a relapse.
My ME/CFS is triggered daily by sensitivities to foods (easy to control) and airbourne particles or smells (not so easy) but I do know for the most part what is triggering me...
But if I get a virus; It all gets much, much worse; I become very ME/CFS like... i.e. all the classic symtoms and much, much more sensitive to things around me, even things that I had previously been OK with. And that's with a common cold or flu virus, let alone shingles.
Take care of yourself and good luck on your journey with this very difficult illness.