Pre MS, I enjoyed long, hot showers.

Seam and fog everywhere.

Fogged mirrors daily.

Then MS hit.  Intolerance to heat made the shower get progressively colder.

CCSVI changed that.  Hot showers were back.

But after the shower, it was hard to get dressed.  Right leg problems got worse.  Difficult t dress.  But I did it.

Next physical therapy noticed something.  I like early, first in the morning showers. On days I showered very early (before PT), I was really a poor performer.  However, on days I showered later,  I had more energy.

The PT noticed this issue as well.

So tell me, does anyone else see this post shower problem?

Cold showers are better?

Any other suggestions?

Thanks ya'll.

Keep fighting and keep moving forward.