Managing MS in The Summer Heat

  • by  Mark O.
  •   August 14, 2017

Mark O. is a paid Advocate for Teva Neuroscience, Inc.

Summertime for millions of people is a time to take family vacations, bask in the sunshine, go to the beach, do yardwork and outdoor activities, work on home improvements, and more. However, for some living with multiple sclerosis (MS), even the word “summer” immediately brings to mind that dreaded word: HEAT. Personally, I’ve found that with some creativity, adaptation, planning, and time management, summer can be a very enjoyable time of year.

During the summer, water is my best friend because it calms my nerves and gives me a sense of relaxation. I carry a spray bottle with me everywhere I go so I can spray the back of my neck or mist my face when the heat really starts to affect me. On some very hot days, I may take two to three showers or a lukewarm bath just to let the water calm and cool me down. Sometimes I simply run my hands under the sink with cool water or choose to wear my cooling vest on hot summer days. There are even days I place ice packs against the back of my neck or on my wrists for short intervals to keep cool in the summer heat. They provide instant relief for me and make my summer days more enjoyable.

When it comes to being outside in the summer, I enjoy it, but I find I have to manage my time in the heat wisely. Remembering to wear lightweight moisture-wicking fabrics to keep my skin cooler, I may do light yardwork very early in the morning before the sun comes up or in the early evening right before it sets. Overall, it may take longer to do yardwork or other activities, but that’s alright because slow and steady wins the race.

Summertime can still be fun and I have learned to be as creative as possible to beat the summer heat.

Want to read more blog posts like this one? Sign up and we’ll send blog posts straight to your inbox!

Mark O.

RRMS Patient

COPAXONE® (glatiramer acetate injection) is a prescription medicine that is used to treat relapsing forms of multiple sclerosis (MS), to include clinically isolated syndrome, relapsing-remitting disease, and active secondary progressive disease, in adults.

Do not use COPAXONE® if you are allergic to glatiramer acetate or mannitol.

See Important Safety Information below and full Prescribing Information for Copaxone® (glatiramer acetate Injection).

COP-45259 June 2018
Leave a comment below

More posts you might like

Register today

Get the latest posts and resources from Teva's Lift MS®.

Thank you for your comment!
It is currently being reviewed to make sure it complies with our Rules of Engagement. If it does, it will be shared with the community shortly, so continue to check back. We appreciate you being a part of the Lift MS® community.
5 Comment(s)
  • Debi | August 14, 2017
    Another tip for summer gardening… Don't be afraid to hire someone to do your weeding!
    • Teva's Lift MS® Team | August 15, 2017
      Thank you for sharing this tip, Debi.
  • Tiffany | August 15, 2017
    Thank you for your great top advice. I have found humidity really drains me. Another challenge I am noticing where I live is the damp cold during the winters
    • Teva's Lift MS® Team | August 16, 2017
      Thank you, Tiffany. You should also check out this blog post titled 7 Tips for Managing Heat While Living With Multiple Sclerosis, which can be found here: Best wishes!
  • dee | August 16, 2017
    I also have had a hard time with the heat. I limit my time outdoors doing my yardwork in the evening and any grocery shopping that needs done. My friends are great at choosing things we can do inside during summer like antique shops, indoor tag sales etc. Love sitting on the deck in the morning with my paper and coffee. Just watch your energy levels. When fatigue starts to set in know your limit.
    • Teva's Lift MS® Team | August 16, 2017
      Thank you for sharing with the community, dee.
  • Myriam  | August 18, 2017
    For me I have no choice than stays 🏡 as soon as going out for a bit my body start melting as if were a candle, and trigger my other symptoms, so rather stay home during summer.😪😪😪
    • Teva's Lift MS® Team | August 21, 2017
      We appreciate your honesty, Myriam. Living with MS can have its difficulties, but we hope you continue to come here for support and a little lift.
  • Roberta | October 08, 2017
    How do you manage to motivate yourself to exercise three times a day when you cannot drive yourself to physical therapy and I'm stuck inside most of the day