Disclaimer: This page may contain affiliate links. We may earn a small commission for purchases made through links in this post, at no extra cost to you.

Living with Ms

by Sherry Day-Anderson
(Killeen, Texas )

I’m 45 years old and have Multiple Sclerosis. Back in 2005 I was diagnosis with Multiple Sclerosis. My signs were my foot would get freezing; I kept forgetting things, dizziness, and kept falling.

That same year I was told I have to stop working and apply for disability. At that time I thought I could still work, but it didn’t work for me because I couldn’t keep my balance. By this time I’m mad at the whole world, and thinking why this happen to me.

I was very depressed, angry, and upset, until I learned how to deal with living with Multiple Sclerosis. The first thing I did was to accept help from others, not let myself get to tired and get the proper sleep I needed.

In 2005 I wasn’t able to drive 'cause of the Multiple Sclerosis, now I’m taking an infusion called Tysabri every 28 days. I’m not able to walk or drive anymore. Now I have to have my son do everything for me. To the point of getting me up in the morning, change me, dress me, help me feed myself.

But you can’t let Multiple Sclerosis get you down; you have to fight to live. I have 3 beautiful who give me inspiration to go on.

Comments for Living with Ms

Average Rating starstarstarstarstar

Click here to add your own comments

May 01, 2016
Rating
starstarstarstarstar
More About Dignity Laws
by: Akrista

Thanks, Beth, for your comments.

I'm pretty sure I've heard about these laws, and have a vague idea of what they pertain to, however, do you thing you could give us a little summary of what they are? And what they mean for people with MS. Quality of life is so important to many. As a nurse, we would benefit from your knowledge and experience.

I hope that you are doing well since it has been 5 years from your initial diagnosis.

Take care,
Akrista

Apr 24, 2016
Rating
starstarstarstarstar
Dignity Laws
by: Beth

I am a nurse living with MS. I was able to work for 5 years after being diagnosed. I am a firm believer in quality of life. My wish is that all states pass the Dignity Laws.I will donate brain tissue for finding a cure for this horrific disease. Then donate my body to science. My family is 100% with me.

Mar 19, 2016
Rating
starstarstarstarstar
WORLD CCSVI AWARENESS MAY 3 - 10
by: Anonymous

So called Multiple Sclerosis (MS) is an UNPROVEN autoimmune THEORY based solely on SYMPTOMS !

Chronic Cerebrospinal Venous Insufficiency (CCSVI) is a treatable congenital recognized medical condition, science established significant role/part 43 Neurological afflictions and so called Multiple Sclerosis (MS)

Feb 11, 2016
Rating
starstarstarstarstar
The Right Attitude
by: Akrista

Sherry,
you have the right attitude. Thank you so much for sharing your story with us. We'd love to hear more if you don't mind. I'm not sure if you got cut off before you finished, however, you said you have 3 beautiful ______??? Children? If so, that is so great.

It's so important to have family members who support you and are there when you need them, no matter what.

Thanks again. We appreciate you for sharing,
Akrista & Cir

Click here to add your own comments

Join in and write your own page! It's easy to do. How? Simply click here to return to Share Your Life in Spite of MS Story .

Buy Me a Coffee at ko-fi.com

Dear Friends,

"Life in Spite of MS is a participant in the Amazon Services LLC Associates Program, an affiliate advertising program designed to provide a means for sites to earn advertising fees by advertising and linking to Amazon.com. We're also part of the Ebay Partner Network, another affiliate program."

We'd also like you to know it doesn't cost one cent more  when you click through the links here on our blog. Not one single penny. And we will make a little extra cash when you do click through. We'll be ever so appreciative. You also have our word that we'll only link to things that we would use ourselves, (or wish we could have or use).

Sincerely,

Cir & Akrista

You are reading original content written by Akrista or Cir L'Bert of Life in Spite of MS. If you enjoyed reading this blog, please consider following us on Facebook, Twitter, Pinterest, and Instagram. See you there!


Enjoy this page? Why not pay it forward? Here's how...

Would you prefer to share this page with others by linking to it?

  1. Click on the HTML link code below.
  2. Copy and paste it, adding a note of your own, into your blog, a Web page, forums, a blog comment, your Facebook account, or anywhere that someone would find this page valuable.

Privacy Policy ~ Advertising Policy ~ DisclaimerContact Us ~ About Us

SBI!