Dear readers, I began this blog about a year ago after a fellow blogger Cathy Chester, who is a ferocious advocate for MS, suggested it during a twitter conversation.
Creating awareness should be our number one priority and also creating spaces where we can share what it is to live with MG with others who go through the same things on a daily basis.
Myasthenia isn’t called the snowflake disease for nothing, we all are different, but at the same time share common denominators. As so many other immune diseases.
We all aspire feeling well enough to complete tasks as simple as showering, walking, or eating. These simple day to day tasks are colossal for us sometimes and not only take away from our quality of life, but also from our very core.
We struggle each day with our feelings and emotions trying to find sense in our lives and figuring out how not to just give up.
It took me some time, but I think that finally I’ve found a glimpse on my way in this tumultuous road of wellness. Some of us tend to think that wellness is the same thing as health, and it’s not.
I ask myself, how can a person who is not healthy achieve a state of wellness that can overcome anything she or he has to endure?
To be honest, I don’t know. I’m trying to discover the answer to this question through my journal, jotting down how I feel along my journeys.
Each afternoon a flock of white birds fly above my yard and they are perfectly synchronized nevertheless, their perfection wasn’t achieved without at least falling down a couple of times and finding their exact place in the flock.
So my friends, I’m not going to find my purpose or be well without a bit of pain each time I fall. However, what brings me hope is believing that I will be able to fly at some point and find a perfect place for myself in this thing called life.
Thanks for stopping by and reading my blog and making me company in my journey through life.
See you around.