I’m planning on retiring to Waco, Texas.Now I live in cold, snowy Chicago. I’m concerned about the Waco humidity. Is it huge problem that can’t be mitigated? I can’t escape the big increase in spasticity in Chicago’s cold by staying inside! Any experiences with high humidity areas would be greatly appreciated.
Hi Tim! Hoping that a community member can reach out with any personal experience, but I did want to share that many of our members are not affected by heat/humidity, but cold does! We’re sorry to hear that your spasticity is so bad in the coldness of Chicago. I actually visited Waco last year and it was a blast! We wish you a happy retirement, and hope the transition goes smoothly.
Best – Meagan, MultipleSclerosis.net Team Member
Heat and humidity adversely affect me. Temps above 72F is sufficient cause for retreat to cooler environs. Texas? Very hot, quite humid. Consider states north, south, and west of Colorado for the high and dry climate. Any thing east of the aforementioned states will be hot and humid. I’m biased, always lived in the west and Alaska.
As someone who has lived in Florida my entire life, over fifty years, I can tell you the only true escape from humidity is a good air conditioner. Of course, dressing in cool,cotton or other breathable fabrics. Heat is not my problem, well at least for whatever reason of late, if I get cold (Florida’s version say 40-50) degree plus if it’s rainy and overcast, I hurt I ache and I’m usually (used to be) the in my shorts and tank top,or t-shirt when others were freezing, now I’m the one freezing, very unlike me and hard for me to deal with, so I stay inside bundle up, curl up and hibernate until it gets warm again. Good luck.
Since my last reply I just completed IMRT radiation treatment
for recurrent prostate cancer. One obnoxious side effect are hot
flashes as hot as the surface of the sun. Regardless of inside or outside temps I’m about to self immolate to a crisp. Thank goodness this is occurring during the winter season when relief is just a matter of going outdoors for a while to cool off. Naturally, once I am cool I am cold and back indoors I retreat to the warmth of a cozy cave. Summers are warm and briefly hot. A/C to the rescue!
I am sorry you are dealing with hot flashes now, sevensix! I hope your treatment was successful, but I am sorry you are now stuck with this annoying side effect. I hope the winter keeps you cool and happy and that your A/C is ready for the summer heat! Best, Erin, MultipleSclerosis.net Team Member.
Heat does affect me. It seems that it will still affect me even if inside in a/c. I have to set thermostat lower than I like it seems, affected even if not low enough. I would prefer 74 or 75, but have to do 70 or lower. Does this make sense?
Hey there @cubbers1!
You aren’t alone – and yes, that makes sense! Many people with MS need it to be cooler to help alleviate their symptoms of MS. We are glad that lowering your AC temp helps!
Meagan, MultipleSclerosis.net Team Member
We moved to a slightly warmer climate from a slightly cooler environ into a house with AC. Being intolerant of temps above 72 our first summer was relatively hot so we set the thermostat at a chilly 69 degrees to match the average temp in our former 49th state. Now that we have been here several years acclimated to the wx the thermostat is set at 70 degrees. Cancer treatment was concluded last December although hot flashes persist, not as frequent nor as hot, AC keeps the body comfortable during these heated moments. I am happy to know someone else likes it cold!
Thank you so much for sharing with us! We are glad to hear that your cancer treatment is over and that the hot flashes have lessened! The cold has certainly proven to be many of our members favorite temperature!