The Helena Alexander Lupus Awareness Foundation is hosting it’s 3rd Annual 3-Mile Walk

I’m honored to introduce my phenomenal, fascinating, inspiring, motivating, kind, glamorous omg I can go on with the adjectives to describe her to you, but let me add she’s a fighter, and her name is Helena Alexander.

You wouldn’t believe that we met on Facebook from a simple like and she has been an amazing support to me during the hardest time of my life.

Helena is a true sister friend.

As you all know I love fashion and traveling, but this Chic here is a true Diva, I’m not on her level lol. Every time I see her, she’s slaying the scene; she makes gym clothes look good! I keep telling myself I can fit her clothes and waiting for the day to raid her closets.

I remember one day we were chatting about taking a girls trip to the islands and I mentioned Jamaica, I have a few times and love it there. Helena said ”Oh, no I’m talking about Belize, Dubai, islands in the Dominican. If you loved Jamaica just wait until you see the waters where we are going! We’re going to travel!” She upgraded me and I been dreaming bigger and better ever since and not only in the realm of material things, but living and loving.

As I mentioned, we met via social media,and it feels just a genuine as my relationship with my friends I met in person. From post to events she supports and encourages me. And witnessing her life if only through my screen has helped pull me out of my depression. Helena lifts our spirits on days I’m certain she’s not feeling well herself. She ends written and verbal communication with the words I love you!

I’m so happy that our lives were destined to come together. I’m so busy tell y’all about our sistership that I forgot to tell you that Helena suffers from the autoimmune disease, Lupus.

Lupus is a complex autoimmune disease that causes inflammation and can damage any organ of the body with life-threatening consequences. I know the effects of this disease oh too well, I watched my Nanan, my Godmother Jeanne Robinson suffer mentally and physically from it. Once a New Orleans beauty queen, Lupus took her self esteem and physical appearance. She used to cry because she couldn’t recognize herself. Lupus took her body on a terrorizing and painful roller coaster ride to her grave. I never told Helena that she reminds me of my Godmother. But one would think they shared the same gene pool, from skin tone, eye color, personality, and fashion sense, Helena resembles my Godmother. She died when I was 18 years old…

I now have the opportunity to walk in honor of her because of Helena’s annual race, plus I get to support and fight for a cure alongside Helena.

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The following statements and photos are directly from Helena, and I’m confident you will feel moved by her words and how she’s determined to live with a smile on her face. She’s my inspiration and I hope that I can be like her when I grow up. 🥰💜

I’m a celebrity for Lupus! ( COME JOIN THE WALK ) I am on a mission to raise awareness for lupus a disease that has no cure for it. A disease that is invisible and take several tests to be diagnosed. Some people had lupus for several years before they been diagnosed with Lupus. ( I will educate my community in New Orleans Louisiana and around the world on Lupus. ) This’s My Mission and Dedication!!! For your family and friends with Lupus. We have to do this together!!! It is in my spirit to get it done!!! Helena Alexander Lupus Awareness Foundation ( Nonprofit ) My Smile is my Logo! Love y’all 💜

http://www.helenaalexanderlupusawarenessfoundation.org/

I’m a celebrity for Lupus! May 1 : Lupus is an unpredictable, and complex autoimmune disease that causes inflammation and can damage any organ in the body with life threatening consequences. I will be giving information regarding Lupus every day the month of May. This is my priority in my life to educate my Community and city here in New Orleans Louisiana on Lupus Awareness. My Smile is my Logo! Helena Alexander Lupus Awareness! Love Y’all 💜

http://www.helenaalexanderlupusawarenessfoundation.org/

I’m a celebrity for Lupus! May: 2 Ninety percent of the people who develop lupus are female. Males also can develop lupus and their disease can be more sever in some organs. Get educated on Lupus. Don’t forget to smile at someone today’s. Support Lupus Awareness!!!! Helena Alexander Lupus Awareness Foundation. My Smile is my Logo! Love Y’all 💜💜💜

http://www.helenaalexanderlupusawarenessfoundation.org/

I’m a celebrity for Lupus! Getting my liquid gold. This’s your Cup of Tea for Today’s!!! I’m Excited!!! Today is the beginning of Lupus Awareness Month. I will be educating y’all on Lupus Awareness everyday the month of May. Every 30 minutes around the world someone is diagnosed with lupus. I’ve been diagnosed with SLE Lupus for 34 years I have been through it all with lupus, and continuing to fight this disease that has no cure. ( “ There is no cure for Lupus “ ) this is my priority and dedication in my life to educate my community in New Orleans Louisiana and around the worlds on Lupus Awareness. ( I need your help to join me on this Mission!!! ) Support Lupus Awareness in join the Walk on May 18, 2019 Helena Alexander Lupus Awareness Walk in Audubon Park at 9 o’clock am New Orleans Louisiana. Hope to see y’all. Support your family’s and friends. No registration fee!!! everything is provided for you. Come an participate in the walk! Let us continuing to grow each years supporting the Lupus Awareness Walk in our Community in New Orleans Louisiana. We can do it!!! Helena Alexander Lupus Awareness Foundation. My Smile is my Logo ! Love y’all Thanks!!! 💜

helenaalexanderlupusawarenessfoundation.org

I’m a celebrity for Lupus!

helenaalexanderlupusawarenessfoundation.org

My Smile is my Logo! Love y’all 💜

Please visit The Helena Alexander Lupus Awareness Foundation to sign up for the walk and more information on the foundation.

http://www.helenaalexanderlupusawarenessfoundation.org/