Being Sick (Forever) taught me one of the most important things in life:**Your Health should never be taken advantage of**! Love, Appreciate, Laugh, Dance, Sing, Write,and Enjoy LIFE!! You are Unique and there is only one You!! Stop Bitching about Dumb Shit!!!! Thought I should share from my Heart, yes my heart is a bit Angry right now, because some of us, Dealing with Invisible Illnesses, will never know what being Healthy truly feels like!! My life is much more than Lupus, so I say too Everyone; Be Blessed with Little to Nothing because you are Alive and Having Life is such a Wonderful thing, regardless of the Obstacles that come along! Those Obstacles are meant to Build, Repair, and Rebuild a Brand new or a Better YOU!!! JUST MY PERSONAL OPINION!!
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Growing up with Lupus made my life extremely difficult at times because of my Chronic Fatigue, Sudden Loss of Memory, Joint Pain, Migraines,and the Depression that never left my Side! Each Day was always different but I could always rely on my Family and Friends for Support, Keeping me on my Feet, if possible, and with a Smile! I hated how I could not be outside in the heat sometimes, especially in Louisiana, because I could or would fall asleep within Thirty Minutes or even Five Minutes! Being Diagnosed at the age of Seven made me see things so much clearer in Life and I am not joking when I say that I am so Appreciative of my Life and the People that surround me because I would not be the Strong, Loving ,and Humble Woman I am today! Sometimes I felt like a Burden in my family because Lupus and its annoying Flare-ups , such as Chest Pains and Seizures! In addition to that,I felt like I was stopping everyone from having fun and enjoying Life!
Polly(Mother) and Herbert Sr.(Father) always told me that I should never feel ashamed or apologize for being sick because Lupus is and will never be my fault and if I can than I can and if I can not than, I can not! I get so frustrated when I can not get things done or attend events because of my Unexpected Pains from Lupus! However, I Thank God each and every day for seeing another day and looking at my Beautiful Children that have given me the Strength and Courage I need to make it through my roughest days! I am so Thankful for the Things I have and Blessed to say that I am Rich by having a Beautiful Heart, Mind, and Spirit! I always Speak from my Heart and I pray that my words Impact at least one of you! You are not alone in this battle and I want you too know that there is only one You and Know that you serve a Purpose, Believe that you can make a Difference,and Understand that Lupus may be a Burden but you are Blessed! My rules,and I do mean Mine alone, while surviving with Lupus and Fibromyalgia: Live, Laugh, Love, Pray, Dance, Eat, and Write!! God Bless you all my Fellow Supporters, Readers, and Followers! Thank you all for being Patient with Me!! |
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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