← Return to Does anyone have any info on MGUS treatment or risk of progression?

Discussion
Comment receiving replies
@mguspixi25

No worries at all @nick86, it was no trouble at all 🙂
I hope things go well with the immunologist, and they dig a little deeper for you.
It’s very interesting regarding daily ice baths, as cryotherapy is used in other immune disorders to control symptoms and address immune function. I’m very glad it’s helping you.
Before I started losing feeling in my lower arms and legs, I was an avid motorcyclist, and would ride rain, hail, snow or shine, and I did notice a marked improvement in immune function during winter when body temp would drop due to very low ambient temp combined with wind chill at speed (ice would form on the bike and on my leathers at motorway speeds, riding at night). I used to have cold water showers to imitate the same response, however I had to stop because the change in body temp was affecting brain function (I have chronic brain inflammation on MRI and significant temperature changes cause me to sometimes faint if they’re too hot or cold).
I hope cryotherapy continues to work well for you into the future 🌺
And best of luck with the research.
I hope you get to enjoy the week ahead!

Jump to this post


Replies to "No worries at all @nick86, it was no trouble at all 🙂 I hope things go..."

I'm so sorry to hear of your troubles. It must be really difficult to not be able to do some of the things you used to enjoy. The cold baths have been so helpful. I'm very grateful that I started, no matter how uncomfortable they are at times. I will continue my research and raise this with the haemotologist that I'll be seeing in December. Finger's crossed that everything stays stable until then. Best wishes and have a great week.