I’m the mother of an 11-year-old dancer/cupcake baker/Survivor buff and wife to an amazing college baseball coach who contracted dermatomyositis in the months leading up to our wedding in 2010.
He was hospitalized in April 2011, where he finally was correctly diagnosed. Initially, his rheumatologist thought it was lupus. At the time, my once-athletic husband was a few months shy of 40.
This site is my attempt to understand, and hopefully shed light, on what seems to be an increasingly prevalent problem in people of all ages.
YAY!!!!
Im your first comment person!!!!
Cute picture!!
❤ Devin
Very nicely put. I look forward to reading your blog and learning more about autoimmune diseases, myositis diseases, in particular.
Nicole you are an inspiration! I look forward to reading your blog and learning about other people’s stories. Thank you! XOXO
WOW!!! You’ve been a busy bee!!! I certainly didn’t know that anyone could die from rheumatoid arthritis!! I’ve always known about arthritis, but hearing/learning about all these other ai diseases, is really a concern to me. It’s so alarming to see how many young people are affected
Isn’t it alarming? Since it impacts many young people, I can’t help but think there’s an environmental component. Our air? Our water? Our food?
Me, too. Have we suddenly just become more aware of these diseases? Surely ai diseases haven’t been hiding in the background all this time, except for arthritis, what is going on?!?!?!? Here’s a thought have previous generations abuse antibiotics too long and our immune systems are weaker because of it??????
Nicole ~ This is a great idea and I am here to support you anyway I can! Amazing when we learn more ourselves about a disease that effects us, we become more aware of it around us. I look forward to continuing to learn more about auto immune diseases. I would certainly love to be able to help my brother as well! Thank you for all you do!
Such a touching story about Taylor, so young and an athlete, too. Some of her symptoms and treatments seem similar to Pat’s. It really makes you wonder, do doctors actually know what their dealing with here?!?!?!?!?!
Still finding your blog so interesting and informative. Really liked the article about the frustration people have in finding a doctor that will listen to them!!!
Thank you! I’m going to post more info on that topic, and also on coping physically and emotionally with a chronic illness like an autoimmune disease. I posted an article on that subject this morning.
Nicole, after spending some time with your little family, i know you will do everything to reach your goal of good health for your husband. I look forward to your blog.
Thank you Joan. That means the world to me.
It is remarkable what Marissa Tucker has accomplished. Certainly has to be encouraging for Pat. It’s such a shame that most of her childhood has been spent dealing with this disease.
Great article about imagining your symptoms!!! Very, very interesting.
My 4 yr old daughter also has drematomyositis, I will keep you in my prayers
Four years old…my heart breaks for you. I’ll pray for your family as well. Next month, my husband and I are traveling to the Myositis Center at Johns Hopkins, in Baltimore (http://www.hopkinsmedicine.org/myositis). I plan to post what I learn about the treatments available there, and hopefully I’ll discover something that might help your daughter.
Hi there! Very interesting articles.