Fibromyalgia or MCAS?

Sylvie has been ill since she was 9 years old and doctors are not very sure why. One doctor has said fibromyalgia, and another has said Mast Cell Activation Syndrome (MCAS). She said on her application form “I think that this has impacted my life in a large way. This issue has caused me to not be able to partake in everyday activities, do little to no exercise on a weekly basis and it has prevented me from hanging out with friends as much as most people would.” Sylvie made a very fast recovery using The Switch. Here is an update from her one year later.

I just thought I would share a little something that I did last week.
I was participating my in a charity event called “Run for Starship” in honour of a past student at my school. Essentially the event was to run/walk as many laps as you can from 1pm-3pm.
I ran most of it and walked whenever I needed a break, and managed to do 14km (running on flat path, up stairs and hills too)! I think it is the most I have run which is such a big moment I am very proud of.
Thank you so much for giving me the resources to be able to do this, as I don’t think I could’ve if I hadn’t done the course.
I just thought I’d let you know as I owe a lot of thanks to you for helping me be able to take part in a lot of this sort of thing again!
Thank you,
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