MNA Speaks: From Lent to Easter

"MNA: The Voices of Dysautonomia" Newsletter Is Now Available

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A TinyLetter Email Newsletter

Dysautonomia Book... "No More Tears" Reading I: Author Note & Author's Thanksgiving (book by @DysautonomiaMD)

A book written for fellow dysautonomics, by a doctor living with dysautonomia.

MissNikkiAnn Reacts to @POTsieChik's "Visit with Doctard Shirley Inowzit...

Visit with Doctard Shirley Inowzit-Yudont

My Invisible Disability

My mom who has ME and around people with lots of energy. Like me Carrie ...

Dysautonomia Awareness

I Am.

That I Am is not sick.

My mind.

My mind and body.

My mind and body, that they are, are sick.

~MissNikkiAnn, Fellow Dysautonomic

MissNikkiAnn Is Very Sick (cc: @OccupyHartford)

And though my mind and heart want me to be physically active with Occupy Hartford at the Turning Point Park occupation site, my Dysautonomia (a progressive and chronic illness) prevents me from doing so at this time.

I am with my fellows in spirit, and will continue to do what I can to support and further the work we are doing.  Occupy Hartford is an amazing and talented group of diverse people.  And regardless of the false image that Mass Media (not true journalists) wants to project, those within the cause know the truth.  And as the numbers grow, more and more we will begin to ignore the vanity of the media, and seek not their approval, but the approval of those wanting to delve deeper into the myriad of issues that are darkening the spirits of humankind.

Compassion and solidarity are the true answer, and if anyone tries to convince you otherwise, I'd take a closer look into that person's personal motive.

MissNikkiAnn, from her sick bed


*Unedited, so don't belittle my effort by looking for mistakes.

Occupy Wall Street Haters? - Spreecast

View my first live broadcasting of MissNikkiAnn's House! >>> Occupy Wall Street Haters? - Spreecast:

'via Blog this'

New Time, New Adventure

I'm on a new adventure. And when using the word "adventure," there is always the sense of the unknown lingering about. I try not to feel one way or the other, just centered in each moment that I am given, knowing that my moments won't last forever. And with things being the way the are with my body, I am forced to move at a snail's pace, the difference is that I've made peace with it and am learning not to be consumed by what others may (or may not) be thinking about the way I must live my life. Overall, I doubt it's an existence that would satisfy the average First-Worlders' need for extravagance and privies, but in the chronic illness and disability world, my life ain't so bad.

"Be good.
Be patient.
Be in the moment."

~MissNikkiAnn

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