Dear Lupus and Fibromyalgia, I will never forgive you for being such a burden in my life and I will always hate you and I will continue to defeat your ass as much as I can!! However, you have allowed me to see the world and people in a different aspect and My heart is just to big too allow you to control me so, Thank you for that! I am not Bitter, but my anger towards you is insane! As Horrible as you are, I am always finding ways to prove too you that I am a Survivor! I will
#WriteaboutLupus, #SingaboutLupus, #DanceaboutLupus, and #SpeakaboutLupus, and #Fibromyalgia too allow others too know that they,too, are not alone! We must Fight the Fight! #ChronicPainSucks, but the Willingness too Survive is worth the Battle, based on my opinion and my experiences! I have too be strong, Mentally, because every second of this pain is not a joke! Talk about it and Be About it! Have a Productive week everyone! Thanks for the support and Prayers! Butterfly Hugs and kisses to each of you!! Since the age of THREE, I remember dealing with so much joint pain! My Legs, Feet, Knees, and my Hands would hurt constantly! However, I was blessed with an Amazing Grandmother and Mother who paid attention to my Voice and I was never ignored about it! In Addition to that, my Family and Friends have never treated me any different because of my Battle with Lupus! I AM GRATEFUL FOR THE SUPPORT I HAVE RECEIVED OVER THE YEARS FROM MY FAMILY! However, Life with Lupus has always been about me because Lupus is the Reason I am a Fighter, I am Kind, and I am Appreciative about Life and the Blessings I have! I find it so Funny when PEOPLE, think that Everything is surrounding solely on me because I am Sick! If you do not have Lupus, or any type of CHRONIC Conditions to understand the Pain I go through, than I suggest that the hole in your mouth stay quiet! I love speaking about Lupus and Fibromyalgia because its my burden and I think its important for me to stay motivated no matter how impossible my days may seem! I go to bed afraid that I may not wake up but I am thankful to have seen the day and I am thankful when I get up and see the next day! How can someone question me as a person, when they are the biggest hypocrites themselves! In my Family, IT HAS ALWAYS BEEN about Wilda because Wilda is Admiration just as much as Wilda is Motivated because of her Atmosphere! I am a Mother first and Foremost and being a Mother with Chronic Conditions has only added Fuel to the Fire that burns within me because I will not stop until Heaven is Ready for me! My health was taken away from me at such a young age, but I will not allow it to Define me as a Person! However, I have noticed that some people are not as accepting to any illness because Life just isn't fair! I am not bitter and I have dealt with people who have said stupid things because I do not look like I am Sick or in Pain! To you I say, Kiss my SICK ASS AND STAY SWALLOWED IN YOUR BITTERNESS! WILDA WILL CONTINUE, WILDA WILL STRIVE, WILDA IS ALL ABOUT WILDA, AND THAT IS THE REASON I HAVE SURVIVED! I love who I am as a person and I will continue being That I am! I HAVEN'T LOVED ME FOR SO LONG AND I REFUSE TOO ALLOW ANYONES STUPID REMARKS TO KNOCK ME DOWN! NO MATTER YOUR SITUATION, SMILE AT BITTER, NOT SO FRIENDLY PEOPLE, BECAUSE EVERYONE NEEDS A HUG SOMETIMES!! ESPECIALLY STUPIDITY!! HYPROCRITES NEED LOVE AS WELL BUT RESPECT IS SOLEY UP TOO YOU!!
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AuthorMy name is Wilda Riggs and I am so proud to have published a book about my Life and basically, my Journey, both good and bad with Lupus! I enjoy being a mother to my beautiful blessings and I love Writing,Singing, and Dancing as much as I am able too!! Stay Smiling People! Life is a Beautiful Thing!!!! Archives
October 2017
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