Deborah, I love that you decided not to “call it mine” anymore regarding psoriasis! I know many people over the years who call whatever they have “my diabetes”, “my cancer”, etc. Those statements are owning the disease, and it’s always been disconcerting to hear that. I don’t call LC or any related issues “mine”. I had the virus in early September.. not a mild case but not in my chest. I had extremely low energy, but was able to do exercises I had been doing for years, I just did a few sets of ten or less at various times throughout the day every day except two. I believe that saved me from the LC fatigue, but digestive issues and rash were debilitating. So I lost weight and muscle fast, and the two lingering issues continued into December. When they subsided I started having neurological issues affecting my vision, along with brain fog and all that it entails. It’s been extremely frustrating because I’m very aware of these temporary deficits. I cannot accept these things as fate or destiny. I search for answers and help, and have several protocols I’m about to begin. Meanwhile, I can do 60 squats with arm movements a couple times a day, and walk or hike for an hour when weather permits. I’m thankful you are sharing your story, as it’s validated an inspiring..! 🙏🏽🌺💪🏽🥳
Thank you for this video. Very inspiring.
Thanks for sharing this❤.
Deborah, I love that you decided not to “call it mine” anymore regarding psoriasis! I know many people over the years who call whatever they have “my diabetes”, “my cancer”, etc. Those statements are owning the disease, and it’s always been disconcerting to hear that. I don’t call LC or any related issues “mine”. I had the virus in early September.. not a mild case but not in my chest. I had extremely low energy, but was able to do exercises I had been doing for years, I just did a few sets of ten or less at various times throughout the day every day except two. I believe that saved me from the LC fatigue, but digestive issues and rash were debilitating. So I lost weight and muscle fast, and the two lingering issues continued into December. When they subsided I started having neurological issues affecting my vision, along with brain fog and all that it entails. It’s been extremely frustrating because I’m very aware of these temporary deficits. I cannot accept these things as fate or destiny. I search for answers and help, and have several protocols I’m about to begin. Meanwhile, I can do 60 squats with arm movements a couple times a day, and walk or hike for an hour when weather permits. I’m thankful you are sharing your story, as it’s validated an inspiring..! 🙏🏽🌺💪🏽🥳
its damage from the jab you took
I had long covid long before there was a jab to take, but when I did get one , it made me feel better for a few weeks.