Over the next few weeks, I am going to have several blog posts that highlight specific topics for the Navigating POTS appointments π Since last week's Symptom of the Week was Heat Intolerance, and this week's Symptom of the Week is Sweating/Night Sweats, I decided to focus on Surviving Summer & the heat in this post βοΈπ₯΅πππ First, I am going to explain how heat affects POTS and then explain some of the specific challenges that come with these symptoms. Then I will give examples of how Navigating POTS appointments can help with these symptoms, I have included questions that I wanted to discuss as a patient, so I hope this is helpful for you π©΅
How does heat affect POTS patients? POTS patients often feel worse in the heat and can experience heat intolerance and either increased or decreased sweating βοΈπ₯΅ Heat intolerance can happen for a number of reasons, your autonomic nervous system controls temperature and sometimes has a difficult time regulating itself π‘οΈ This is especially true if you can't sweat π Also when you get hot your blood vessels dilate and your body increases blood flow to the skin which is why you can look "flushed" or red when it's hotπ©Έ These changes in blood flow and the sweating that occurs when you get hot often make POTS patients feel worse π₯΅
How does my heat intolerance affect me? Honestly, I kind of hate summer because I always feel so much worse πππ₯΅ I often joke that I "hibernate" during the summer and avoid going outside ποΈ βοΈπ₯΅ All of my symptoms are a lot worse, I sweat a lot, feel dizzy, nauseous, have headaches, get chest pain, presyncope and get really fatigued π I have a really hard time sitting in the sun, but I also sunburn pretty easily haha βοΈπ I need it cold in my house so I don't feel sick, but sometimes people can make insensitive comments about it π It can be really easy to feel isolated, discouraged and alone when I am dealing with these symptoms π
What are the social implications of heat intolerance? It can be really embarrassing to sweat a lotπ And it's hard to deal with heat intolerance because lot of people love summer, and most of our family trips happen during the summer because school is out π I live in Utah so it's not very humid, but it can get pretty hot, especially down in Southern Utah where all the National Parks areποΈ We also have family in North Carolina and Georgia and it is really hot and humid there π₯΅π¦ I have definitely had to miss some extended family trips because I knew I would feel too sick if I went and that can be really disappointing π There have been other times when I have gone, but I planned specific ways to deal with the heat while I was there π₯΅ And there have been other times when I have worked with my family members to plan a good time of year to go visit a particular place that might be hard for me during the summer ποΈ And aside from trips, there are a lot of outdoor activities during the summer like BBQ, hiking, picnics, etc. Honestly, trying to plan things in the summer is still one of the hardest things for me, but I have learned a lot!
So how can these Navigating POTS Appointments help with the physical, emotional and social affects of Summer & Heat symptoms in POTS patients?
-What are some specific ways I can manage heat intolerance during the summer?
*Just a reminder that your first appointment is 1/2 off, so $25 for a consultation and $50 for a coaching appointment! If you have any specific concerns about scheduling or prices please email navigatingpots@gmail.com
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