MS is #NotContagious! You cannot "catch" MS from another person. The cause is unknown. However, #MSawareness is contagious. Spread some today! 🧡 #MSWarrior #MSBrave #CureMultipleSclerosis

Vote! Vote! Vote! Vote! Vote! Vote! Vote! Vote! Vote! Vote! Vote! Vote! Vote! Vote! Vote! Vote! Vote! Vote! Vote! Vote!

@Inspireu2Action You are right, you need to first write the vision down, any vision that is not written down is lost to thoughts. You are showing your seriousness about any vision when it is properly documented

Join me and #BeAVoter in the US election. Get started to find your polling place and see who is on your ballot. gettothepolls.com/?utm_source=tw… Remember that many groups had to fight to get this right and many others bled and died.

We are trying our best to live the fullest life but roadblocks of pain often derail us.

This is so very true. The letter of the law has to be rewritten. As a juror, I want to do the right thing. The applicable laws often change your mind right before deliberation.

“The complete loss of #selfworth. People always say that being a productive member of society is the most important thing, so what happens when you can no longer be ‘productive?'” 31 Difficult Side Effects of #ChronicIllness buff.ly/2MaCi0b #ChronicPain #Spoonies

MS can make people feel very #Alone #MSers need a great #supportsystem! It's hard enough to hear "You have Multiple Sclerosis." For many the next thought is "Who can I turn to for support? Who will be there for me?" Be there for them! Sometimes all you have to do is #listen. 🧡

There is power in the positive and negative. The abyss of the negative is lonely and should never be battled alone.

“No matter how long we’ve been suffering for, it still hurts. Having pain for an extended period of time does not give us superpowers to feel it less. However, most people with #ChronicPain have learned overtime to exhibit less pain.” buff.ly/2PJ1DRv #invisibleillness

You are not Multiple Sclerosis. You HAVE Multiple Sclerosis. Don't get the two confused. Let me tell you what you are. You are beautiful, amazing, strong, wonderful, incredible, unique, downright spectacular, and filled with lots and lots of greatness. And don't you forget it.

“A huge burden for patients with #chronicpain and #fatigue is not being believed.” Social Media is a Lifeline for Patients buff.ly/2DnRnLT #chronicillness #raredisease #NERVEmber #spoonies

“While you may have never heard of my disease, do not doubt its magnitude. The truth is anyone living with a disease is facing adversity, and we should all be recognized for our raging courage and #strength…even if we don’t always feel strong.” buff.ly/2SP0wSe #NERVEmber

I don't often ask anything of you, but please, will you do just one thing for me today, please put a smile on your face and be happy :-) #PSMyWords

After being stuck inside for most of the summer, fall allows those with MS to get some much-needed time outside in the cool fresh air: multiplesclerosis.net/?p=36239 #MS #multiplesclerosis

You have power in your words. Please choose them carefully as they will impact many.

I am down but not out. It is real work when you deal with #chronicillness or #MS to survive. Day by day, I pray I will make it.