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Multiple Sclerosis Awareness Month

We call Multiple Sclerosis a snowflake disease because the symptoms constantly change.  It has no cure, and no one can explain the why of the disease.  

I remember the day like it was yesterday.  On January 11, 2017, Dr. Gaw, after many tests, told me I had Multiple Sclerosis.  If I sound like a broken record, many people are just now getting diagnosed today, and I want them to know that they are not alone.  

You might have someone in your life sitting in a quiet doctor's office waiting on test results.  They are going to need you now more than ever.  Navigating a disease that is so unpredictable can take its toll on a person.  They need all the love and support that you can muster.  

Much Love,

Tina Louise

Comments

  1. Jose Anthony JrAugust 20, 2021 at 10:59 AM

    I was diagnosed with multiple sclerosis in 2015, and I was a woman of 50. They put me on Rebif which I took until 2017 and was switched to Copaxone. I had two relapses on Rebif, none so far on Copaxone. I do notice my balance was getting worse, and my memory, as well as erectile dysfunction and spasms’ had no choice to sick for other solution and I was introduce to multivitamincare .org which I purchase the MS herbal formula from the foundation, the herbal supplement has effectively get rid of my multiple sclerosis and reversed all symptoms. 

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