Thought for the Day:

Hope is the thing with feathers
That perches in the soul.
And sings the tune
Without the words,
and never stops at all.

- Emily Dickinson

Monday, December 10, 2018

My M.E. Exercise Experiment

For 7 weeks now I've been engaging in an experiment. I've been swimming at the local pool (it's two blocks away, I drive).  Almost every week, once a week, I've gone and done some laps in the late morning (my best/highest energy) time of day.

There are many reasons why this is a bad idea.

First, while most Dr.s and the general public are ignorant about the detrimental effects of exertion and exercise on people with M.E., the research is starting to show that what patients and specialists have been claiming for years and years is true: M.E. is a disease that effects metabolism on a cellular level.  Also, there is a quantity of research now which demonstrates that activity, exertion, or "pushing" makes M.E. folks sicker (there is both an immune and inflammatory response).

Anecdotally, I know a couple folks with M.E. who had a better period, tried to engage in life/work/exercise again, and ended up permanently relapsed and worse than they were when they originally got ill.  Finally, since I crash from just standing too long (e.g. doing dishes standing), taking my dad on an outing, driving, being exposed to too much noise and/or florescent lighting, visiting on the phone too long, why would I add more exertion to my life?

All these are logical arguments against me doing this experiment.

Then why did I do it anyways?


  • Since I've started a low dose Beta Blocker for POTS, I've gained some weight and often feel disgusted by my own body. I can't see eating much less, which leaves few options for losing a little.
  • For someone who used to love being outdoors and athletic, and who now understands this disease is never going away, lately I've felt trapped in my own body. I just want to push and sweat. I miss being active so much I could scream.
  • I've been reading about POTS and how sometimes exercise can really make a difference, it's not a cure, but it can help.
  • While exertion makes M.E. symptoms worse, I know that de-conditioning over 16+ years now is also not good for me and could eventually lead to other health problems.
  • I love to swim - I swam competitively as a child and teen.
  • Ultimately I was curious to see what would happen. I know I don't have a mild case of M.E., but I've only been severe here and there. I'm one of those moderate cases. That said, moderate M.E. means I'm mostly home bound and have less energy and resilience than most people with a whole host of other illnesses.


So what have I discovered thus far?:

First, I've done the same amount of swimming each time.  I decided if I felt a slight improvement over time I would add a little. It sure hasn't happened yet.

Interestingly, my best swim, the one where I felt the strongest and most capable, was the first!  The next best swim was the 2nd week.

By the 3rd swim/week my arms and legs fatigued more easily, like there was a complete inability on a muscular cellular level to produce any energy/strength. Why didn't I quit there? I thought, "What if this is the point where I just need to push through?" Or, "Perhaps this is a bad one due to monthly fluctuations?"

One week I went 2x (early and late in the week) and the next week I was in bed much more and felt just terrible - then I had to skip a week.  Last week I was so weak, sore, and burning during the swim it was all I could do not to cry during.  I had to take more breaks and after the swim my body felt particularly poorly (achy, weak, shaky). I was horribly crashed for 2 days, there was one day I could barely stand at all. I decided I should quit.

I went back this week and thankfully I wasn't quite as poorly, still, I was far far worse/less capable than week one. (I also don't know how badly I will crash). Problematically, I had horrid air hunger during the swim like I wasn't getting enough air/oxygen and my chest hurt.  I'm curious how high my heart rate was and whether this breathlessness was a heart-related symptom?

Will I continue with the experiment? I haven't yet decided.  Is the M.E. overall worse? It's hard to say,  October was a bad month and November a little better overall.  Following each session, though, I'm definitely worse and this worsening lasts a day or two and clearly impacts my immune system with worsened sore throat (worse than I've had in ages) and flu-like fatigue and weakness. Overall my ability to exercise/exert is much worse.

Do I have more muscle? I must have, I won't believe I don't, even though I'm not swimming much, I've been doing this almost every week for 2 months!  Do I have better aerobic capacity?  No! I would guess that my aerobic capacity has actually diminished or gotten progressively worse.


3 comments:

  1. I enjoyed this post, Gail as I am at a similar spot in my ME journey.

    I SOOO want to push and sweat. I really miss the wonderful after feelings of exercise,but ME seems to have different ideas.

    I have also recently came to the same conclusion about POTS ie exercise is good for it/can help. I had been walking between 2 - 3 km per day (most days, but not every day. It all depended on how my body was feeling each day and I paid very close attention to it. I did not push myself if I wasn't feeling up to it and I went at my own pace). I do feel it helped with my POTS issues (as you said, it didn't cure it, but helped)

    Then I started going to a chiropractor for issues with my back (which he has helped). He is very big on exercises, doesn't understand what ME is and what it isn't. He really pushed me to exercise, even though I gave him a lot of documents about ME. Long story short, I attempted beginner Tai-Chi and had a significant crash/set back.

    I haven't been able to do my walking now since I crashed (just starting to try again but not up to my 2-3 kms).



    ReplyDelete
  2. Yes, I know what you mean. It's ridiculous that we are better off ignoring or avoiding the advice of Dr.s if we want to stay as well as possible. I hope you can get back up to where you were. Happy Holidays - Upnorth

    ReplyDelete
  3. Yes, agreed, thanks for your comments. - Upnorth

    ReplyDelete