I'm suffering from an active fatigue that is very rheumatic, typically gritty and hot within core areas - chest, kidneys, muscles, neck and head. Typically increasing to a high point, from torso to neuralgic with 'flu like' symptoms and headaches/eye aches, when experiencing severe flare ups. Light sensitivity and brain fog. An inability to function or process anything, when in the clutches of a severe bout. Typically caused by 'post exertion' with a delay of hours or days. It feels fiery and causes a stretchiness in the gut, an 'uh' feeling tied holistically to all areas - brain, nervous system, immune system, gut fauna, and what I would deem areas of possible viral persistence - chest and kidneys. I have had 'Long Covid' as a result of being hit by the first wave, early in 2020. It has shifted into an M. E format. I would argue that Long Covid primes the body, via the spike protein pathology, for rheumatic disease such as Sjogren's and Lupus, within an M. E format. I am also displaying Sjogren symptoms. So several conditions can precipitate from Long Covid, including a higher tendency towards developing Lymphoma (5%), if you develop Sjogren's disease. The autoimmune system and the Mitochondria is very much tied to the conditions known feably as CFS M. E. It is anything but feable as an experience, more like a virulent rheumatic fever that sucks away at your overall stamina and inflames your muscles and organs. What really annoys me is the lack of empathy or support from the almost 'fascist' centred health care system, that trundles along like some ignorant beast, ticking boxes and demonising people. Jesus would have deemed them 'modern day' Pharisees! Yet the elephant (of Long Covid and M.E CFS) is still in the room, and isn't going anywhere soon. However, a big thankyou to the real doctors and nurses who put their heart and soul into their profession, despite the lack of research into the above mentioned conditions.
What US locations and/or climates are better for people with CFS? Is hot dry better? Are places with cold winters better? Thanks! Like would it be better to live in Nevada or Pennsylvania?
I'm suffering from an active fatigue that is very rheumatic, typically gritty and hot within core areas - chest, kidneys, muscles, neck and head. Typically increasing to a high point, from torso to neuralgic with 'flu like' symptoms and headaches/eye aches, when experiencing severe flare ups. Light sensitivity and brain fog. An inability to function or process anything, when in the clutches of a severe bout. Typically caused by 'post exertion' with a delay of hours or days. It feels fiery and causes a stretchiness in the gut, an 'uh' feeling tied holistically to all areas - brain, nervous system, immune system, gut fauna, and what I would deem areas of possible viral persistence - chest and kidneys. I have had 'Long Covid' as a result of being hit by the first wave, early in 2020. It has shifted into an M. E format. I would argue that Long Covid primes the body, via the spike protein pathology, for rheumatic disease such as Sjogren's and Lupus, within an M. E format. I am also displaying Sjogren symptoms. So several conditions can precipitate from Long Covid, including a higher tendency towards developing Lymphoma (5%), if you develop Sjogren's disease. The autoimmune system and the Mitochondria is very much tied to the conditions known feably as CFS M. E. It is anything but feable as an experience, more like a virulent rheumatic fever that sucks away at your overall stamina and inflames your muscles and organs. What really annoys me is the lack of empathy or support from the almost 'fascist' centred health care system, that trundles along like some ignorant beast, ticking boxes and demonising people. Jesus would have deemed them 'modern day' Pharisees! Yet the elephant (of Long Covid and M.E CFS) is still in the room, and isn't going anywhere soon. However, a big thankyou to the real doctors and nurses who put their heart and soul into their profession, despite the lack of research into the above mentioned conditions.
Fatigue is ruining my life. I allways have to lay down
What US locations and/or climates are better for people with CFS? Is hot dry better? Are places with cold winters better? Thanks! Like would it be better to live in Nevada or Pennsylvania?
He said it's certainly a mouthful I'm sure he like that one
There is no living with this.
You can live. You need a good kind friend and good counselling.