Angela's Living Proof 2020 MS

Angela's Living Proof 2020 MS Welcome! ANGELA'S AVENGERS WALK MS 2017

This is my 9th year participating in Walk MS; however this is "Year 14" living with Multiple Sclerosis (MS). OR

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My name is Angela Nasraoui, I have had MS for 17 years and I have been off of DMD's (disease-modifying drugs) for almost 6 years now after taking Avonex 6 months, Copaxone 10 years, Ticfidera2 years I have been an MS Ambassador for the Pacific South Coast Chapter of the MS Society since 2010 to bring awareness about the disease. I walk so that I can contribute in doing something for myself, my fa

mily and to show the other people who have been newly diagnosed with this debilitating disease, that they are not alone. Today, there is no cure for multiple sclerosis, and with diagnosis occurring most frequently between the ages of 20 and 50, many individuals face a lifetime filled with unpredictability. I am so thankful for my family and friends & honestly even people I don't know that remind me; I am not alone! Can you join me in creating a world free of MS? TO JOIN MY TEAM
http://main.nationalmssociety.org/site/TR/Walk/CASWalkEvents?team_id=500166&pg=team&fr_id=28528

You can do this in 5 ways REGISTRATION IS FREE!!!!

1. Join my team "ANGELA'S SOULJAS" by clicking the link on the right of this screen on Saturday, April 29, 2017 at UC Irvine campus and walking 2 miles with me.

2. Make a donation by clicking the link on the right of this screen "DONATE TO ANGELA" for a minimum of $10 online or more. You can DO BOTH 1 & 2

4.SURPRISE ME and JOIN ME ON APRIL 29, 2017

5. Register as a "Virtual Walker" its free to you and you are not actually there with me but in spirit. Your support and love mean everything to me. Angela a.k.a. Truffle

A LIFE CHANGER FOR MS. I recommend this book to anyone seeking Everyday Health & Fitness even with Multiple Sclerosis  g...
01/20/2017

A LIFE CHANGER FOR MS. I recommend this book to anyone seeking Everyday Health & Fitness even with Multiple Sclerosis goes on sale February 1st wherever books are sold, and is available for pre-order at these retailers or at your favorite independent bookstore: Amazon, Barnes & Noble, Indiebound.org, Powells.com, and Indigo. Even though I received an advanced copy, my presale order should be here this week. Yayy!! https://www.quartoknows.com/books/9781592337415/Everyday-Health-and-Fitness-with-Multiple-Sclerosis.html?direct=1

Achieve Your Peak Physical Wellness While Working with Limited Mobility Achieve real gains and remove obstacles in your path to fitness with Everyday Health and Fitness with Multiple Sclerosis.David Lyons' program is designed to help you maintain a healthy lifestyle maintain a healthy lifestyle andโ€ฆ

As a child growing up I loved fall and winter, it was a time to watch the seasons change ๐Ÿ and to bundle up and snuggle....
12/21/2016

As a child growing up I loved fall and winter, it was a time to watch the seasons change ๐Ÿ and to bundle up and snuggle. A time to celebrate the holidays๐ŸŒฒ๐ŸŽ๐Ÿ•Ž However, as an adult with MS this cold weather is so hard on my body. Literally I'm like the tin man in the wizard of Oz, oil, oil. I will ease on down the road. Slow as I am, stiff as I feel, I say to myself, this too shall pass. Keep it moving, til you can't move anymore. Make it a great day peeps.

C'mon peeps assist me in creating a world free of MS in one of 3 ways. See my page link below.  The walk is 4/29/17. It'...
11/22/2016

C'mon peeps assist me in creating a world free of MS in one of 3 ways. See my page link below. The walk is 4/29/17. It's only 2 miles, if I can do it. You can too.

1. By joining my team (it's free)
2. By donating $10 (2 coffees at Starbucks)
3. Do the first 2 you can be a Virtual Walker. meaning not there but supporting me in spirit!

http://main.nationalmssociety.org/site/TR?px=5263153&pg=personal&fr_id=28528&s_src=boundlessfundraising&s_subsrc=:sub_source

Walk MS connects people living with MS and those who care about them.

We all have friends/family members who have MS. If you didn't know, you do now.  I don't say these things to sadden you,...
02/12/2013

We all have friends/family members who have MS. If you didn't know, you do now. I don't say these things to sadden you, I say them to encourage you to not take your friends/family for granted. Love them, laugh with them now. XOXO Ang

02/08/2013

Cold weather just doesn't bode we'll with me. I can only laugh at myself in the rain, stiff as a board. Loving Life

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Irvine, CA
92697

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