RogueWolf
@RogueWolf2001
Southern woman whose not Red or Blue living in a deep Red VERY conservative state. Living w/EDS, dysautonomia, Chronic migraines, chronic pain, etc 1 day@time.
PSA: If you have a fever, “laryngitis,” hoarseness, “the stomach bug,” or are otherwise ill in the middle of summer, you probably have Covid. A large new wave is underway. Everyone has forgotten summers used to bring much-needed disease reprieves, but those days are over now.
Disability is not a moral failing. Disability isn’t actually a failure at all. Disability is as natural as breathing. We all experience disability if we’re lucky enough to age, including animals. Disability is not a tragedy, it’s a human condition.
“I fight so much to just exist… I’m never pain-free… Why must I fight bad doctors, bad pharmacies and now the government? I am so tired—and it is not the just the #fibromyalgia and #CFSME. I just want to get the help I need.” buff.ly/oCRGdNU #chronicpain #opioidhysteria
This woman OWNS 37 acres of land. The government STILL told her she can’t put a tiny home on it. “I said, I own the land. It's massive. What's the problem?” Even when you own the land, the government still tries to tell you what you're allowed to do with it.
What’s going on with the @FDA_Drug_Info @MartyMakary and the OxyContin label? Now on our Patreon page We are closely monitoring the situation patreon.com/posts/whats-fd…
Let me tell you the story of someone here who caught Covid while attending hospital for cancer treatment and died.
Just heard that Bridget died on July 14th, the day after this post. She was 47 years old. I hope it is a terrible mistake, that Bridget is still with us, but the source is a credible one. THIS is the isolation/abuse so many of us face with chronic illness, especially #MECFS
I called my mom. I told her I'm afraid I'm going to die. Her response? She hung up. 😫#MECFS
Living in pain will shorten our lives. Pain isn’t benign. Some doctors seem to think it is. Long term pain leaves the body in fight or flight constantly.
When the Night Is Heavy and the Fan Still Roars. by Michael Whelan Its 4:21 AM. I barely slept a wink. Rebecca didn’t either. The night unraveled in whispers and weight... her body refusing to cooperate, her eyes pleading for help she never wanted to need. She’s 120 pounds,…
Now Bridget is gone. This is why you need to take people seriously when they’re struggling. Heartbreaking
I called my mom. I told her I'm afraid I'm going to die. Her response? She hung up. 😫#MECFS
Do you ever feel like chronic illness has put a wall between you and everyone else? Not because you pushed them away but because they didn’t know how to stay close.
Too many people swallow the myth that “people on benefits are scroungers” - a narrative the media pushes to justify slashing disability benefits. We face rising hate and hostility. There is a growing contempt for disabled people. Being disabled in this country means living on a…
“If you can use the internet you can work!” Is such a privileged ableist take. It goes to show how little the average person understands chronic illness. How little thought they give to the unique challenges we face or the multiple barriers to holding down a job 🧵