One of the biggest obstacles for people with POTS is actually getting an official diagnosis. I was nineteen when I got my diagnosis even though I have dealt with symptoms my entire life. It took me at least ten different doctors and specialists and around three years after the day Read more…
Since there is no official cure for POTS, the biggest thing for someone who has been diagnosed with POTS is finding the best way to manage symptoms. With the help of my doctors, my mother, and some creators on the internet, I have found some really amazing products that help Read more…
Understanding your rights and resources is a huge thing for potsies. If you are anything like me, advocating for yourself can be extremely hard. With POTS being an invisible disability, quite often people can think that you are faking your issues just to get special treatment and accommodations but that Read more…
My journey to get diagnosed started back in high school, around my sophomore or junior year, even though it wasn’t until I was in my sophomore year of college that I finally received the answer I was desperately searching for. My search for an answer started when I began having Read more…
Hi! My name is Kat and this is my blog! Being diagnosed with a disability can leave someone feeling extremely isolated and alone, as if they are somehow different from everyone around them. Having an invisible disability can make that feeling even more amplified, as the struggles are not immediately Read more…