World Scleroderma Day!! What do you know about this disease?
Many of our readers deal with Systemic Scleroderma on their skin, in patches around their legs, hips, and joints. Many of your hands are inflamed, sore, and taught. Many of you just wish for some relief, minus the piles of pills, heating pads, and ice packs. Minus the breathing machines, chemo meds, and insomnia.
On World Scleroderma Day, it’s everyone’s chance to help spread the word on this autoimmune disease. One of the worst in the list of diseases, this hardens your body often from the inside out, or vice versa- from the outside in. Normally there is no rhyme or reason. Something triggers inside your body, and your body begins attacking its own organs. Over and over. Relentlessly. The only way to stop the attacks are to take massive amounts of steroids, chemo, or other immune suppressants to control the flares. Sometimes those meds cause a whole other list of issues that sometimes, don’t feel necessary to go through.
This blog post is from our friend, Author Skye Falcon. She deals with Scleroderma, and often writes about the tribulations and trials that life throws in her way. She asks for people to help spread the word about this, “excuse the humor…..very HARD disease.” Check out her post.
Please take a moment to like this blog, or share it, if you know someone who has, or is going through, a fight with an autoimmune disease. Comment with the disease that’s stealing days away from your friends or loved ones. Let’s spread the word on all the diseases, and get more accessible endocrine and genetic testing! Consider using this icon on your social media pages to show your support!!