Having an invisible illness means you cant see the symptoms I am experiencing. You cant see my racing heart, super low blood pressure, the dizzy spells, fatigue, muscle aches, pains, heat intolerance, nausea, and G.I. dysfunction. I worried about what others thought and if I was good enough. Sometimes I still do. But I know I am giving 110%. I am giving it my all and fighting as hard as I can everyday.
I push through and refuse to give up. It is not easy by any means. I have many days where I am feeling defeated and down. I sometimes want to give up. I feel its unfair I have all these added struggles. I am jealous of the people who can do whatever they please with no physical limitation. I am mad at the people who take the ability to do things for granted. I feel down on myself and think I am not good enough. I think this is a normal part of having an illness like this. Its ok to have bad days and feel sorry for yourself, as long as you don't stay there too long.
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| earlier this week after a bad episode |
I have decided that I want to workout like I used to before getting sick. I wanted to build back some muscle I lost from not being able to workout. I was feeling very self conscience and needed a change. I failed many attempts and threw in the towel more times than I care to admit. I started slow and learned to pace myself. I try to get some sort of workout in everyday. Maybe it will only be a 10 minute walk, but hey that is better than nothing at all. some days working out is out of the question. I am too symptomatic. Tomorrow is another day! Every workout is a challenge and I have to push through. I spend half of the workout laying on the floor recouping from 1 set of something. The point is I do it. The workout I do should take about 15 mins for someone without my struggles. It takes me about 45 mins. I am seeing results and noticing that some days it is easier. I sometimes flare after a workout and crash for the rest of the day. I like to workout close to end of the day so I can recoup at night.
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| heart rate after walking up stairs |
I focus on the fact that I am able to homeschool my daughter. Some days she brings her work to me in bed. When I am so symptomatic I cant get up. But I am doing it! I take care of my family, pets, and house. Plenty of days the house is messy, laundry not done, dishes in the sink, and we order pizza because I am too off to cook. But everyone is cared for and happy. I participate in turtle rescuing which is and has always been something I am passionate about. I attend co ops for my daughter's schooling. We have outings and play dates. Some days we have to cancel and that is OK. I am doing the best I can with the circumstances I was given. I have had to adapt to things and find a way to make them all work. Everyday I have to push and fight. It is not easy but it is worth it. You too cant fight! Focusing on what I can do and not what I cant do has helped me. It has made me thankful for everything I can do and made me fight that much harder. I hope this post has opened the eyes of some and inspired you to fight! P.O.T.S. does not define us!
Til next time xoxox






