I always worry about our comfort zone. How comfortable it gets. I’m not sure I like the idea of being comfortable at all. I want
I have started an app on a basic concept. Socialization to combat isolation from chronic illness and disability. I took your basic dating platform so
I was excellent a catastrophizing. It was a skill. A very bad skill but I also have Major Depressive Disorder so it was a skill
I wrote an article about gratitude and actually put it in the menu on my page. It was one of the things my psychologist has
I am an introvert. And because I am an introvert when I am in pain I react a certain way. I retreat more and more.
Tell us about a missed special occasion or strategy you’ve discovered to avoid missing out. You know it is hard to say I use a
How has Migraine or Headache affected your family? The pain may be mine to feel but it has a radius and touches all those around
I celebrated my 40th birthday on the 28th. That is now 20 years of migraines to date. But it went extremely well. Migraines have
With pain comes isolation. With winter comes hibernation. I see a psychologist for pain management who is rather insistent I socialize more. Good for mood.
This is the case of someone’s medical claim that was denied because of social media. We all know social media is a reflection of life
A friend calls you up to go to a concert, or to a dinner party or to go drinking? A family member invites you out
New year’s resolutions are essentially a moot point to the chronically ill. Sorry, I already am loaded up on short-term and long-term goals right now.
I managed to go out to my spouses work Christmas party. I think that these sort of social gatherings are vital to boosting the mood
I went to a concert today, which is always a tricky venture if you have fibromyalgia and migraines. For FM it is the sitting. A