{"id":702,"date":"2016-05-19T13:49:26","date_gmt":"2016-05-19T18:49:26","guid":{"rendered":"http:\/\/unclefunkysdaughter.com\/blog\/?p=702"},"modified":"2016-05-20T12:30:55","modified_gmt":"2016-05-20T17:30:55","slug":"im-not-my-diagnosis","status":"publish","type":"post","link":"https:\/\/unclefunkysdaughter.com\/chatbox\/2016\/05\/19\/im-not-my-diagnosis\/","title":{"rendered":"I\u2019m Not My Diagnosis"},"content":{"rendered":"<p><span style=\"font-weight: 400;\">2011 was supposed to be the year I showed up and showed <a href=\"http:\/\/unclefunkysdaughter.com\/blog\/wp-content\/uploads\/2016\/05\/May_2016_Altonia.jpg\" rel=\"attachment wp-att-706\"><img loading=\"lazy\" decoding=\"async\" class=\"alignright wp-image-706\" src=\"http:\/\/unclefunkysdaughter.com\/blog\/wp-content\/uploads\/2016\/05\/May_2016_Altonia-595x650.jpg\" alt=\"May_2016_Altonia\" width=\"380\" height=\"339\" \/><\/a>out on life! I was preparing for my 40<\/span><span style=\"font-weight: 400;\">th<\/span><span style=\"font-weight: 400;\"> birthday bash when I first began to feel ill. \u00a0During\u00a0that time I was self-diagnosing; I was working 50+ hours per\u00a0week as the Executive Director of Majestic Divas, Inc (a social &amp; charitable organization based in Laurel, MD), all while juggling roles as a mentor, philanthropist, wife, mother, and grandmother. I chalked my condition up to exhaustion \u2013 I figured I simply needed a vacation, and to sleep and eat better. But in Spring 2011, I began to experience shortness of breath, hot flashes, extreme sweating, headaches, fatigue, anemia, gastrointestinal problems, weight gain, and insomnia.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">As the symptoms began to progress, I found I could not get out of bed. My feet and ankles were swollen and always hurting (I wore 5-6 inch stilettos heels every day). And most importantly (at that time, anyway), my physical appearance began to deteriorate at a frightening pace \u2013 skin rashes and black marks were forming on my forehead and spreading, dreadful dark circles enveloped around my eyes, and the skin on my nose would peel until there wasn\u2019t any left. I felt awful, and my confidence was nonexistent. I\u2019d visited several dermatologists who\u2019d diagnosed me with things like anemia, hyper pigmentation and adult acne.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">I was trying different remedies. Some worked for a while, and some never worked at all. Growing more and more frustrated and embarrassed by my appearance, I decided to seek the help of a specialist. Looking back, it\u2019s almost funny how I was way more concerned with my skin than I was with the fatigue and swollen ankles. <\/span><\/p>\n<p><span style=\"font-weight: 400;\">At my first visit at Callender Dermatology, I was seen by the physician assistant. She took pictures of my face, prescribed me a hydrocortisone cream and sent me on my way. I thought to myself, \u201cThat was easy! A $25 co-pay and hydrocortisone, I will be picture perfect in a few weeks, just in time for my birthday photo shoot.\u201d \u00a0<\/span><\/p>\n<p><span style=\"font-weight: 400;\">Like I\u2019d begin any normal day, I went to CVS hoping to come out with a tube of some magical cream that would clear up my so-called adult acne. The pharmacist informed me that my prescription required authorization. When he called to get authorization, the doctor instructed him not to fill it, and to have me come to the office. \u201cEven better!\u201d I said to myself. \u201cShe is going to give me the good stuff to clear this up.\u201d I made an appointment to see the doctor the next day, never bothering to mention it to my husband or friends. I didn\u2019t think it was anything to be at all concerned about.<\/span><\/p>\n<p style=\"text-align: left;\"><span style=\"font-weight: 400;\">But as the appointment began, and much to my surprise, Dr. Callender immediately made the suggestion that I get tested for Lupus. She wasn\u2019t clear as to why none of the physicians I\u2019d previously seen ever had tested me. She also believed that I was currently having a flare-up, which was causing the rash and dark circles. I was certainly taken aback by what she said, but I agreed to be tested. I had honestly never heard of Lupus and didn\u2019t have the slightest idea what it was. Dr. Callender handed me a few pamphlets and began to explain things in further detail. I had no idea at the time that I would be in for the fight of my life.<a href=\"http:\/\/unclefunkysdaughter.com\/blog\/wp-content\/uploads\/2016\/05\/Altonia_ChatBoxQuote-1.jpg\" rel=\"attachment wp-att-724\"><img loading=\"lazy\" decoding=\"async\" class=\"alignright wp-image-724 \" src=\"http:\/\/unclefunkysdaughter.com\/blog\/wp-content\/uploads\/2016\/05\/Altonia_ChatBoxQuote-1.jpg\" alt=\"\" width=\"1246\" height=\"172\" \/><\/a> <\/span><\/p>\n<p><span style=\"font-weight: 400;\">I was officially diagnosed with Systemic Lupus on July 9, 2011.<\/span> <span style=\"font-weight: 400;\">Lupus is a chronic autoimmune disease that can affect virtually any organ of the body. In Lupus, the body&#8217;s immune system, which normally functions to protect against foreign invaders, becomes hyperactive, forming antibodies that attack normal tissues and organs, including the skin, joints, kidneys, brain, heart, lungs, and blood. Lupus is characterized by periods of illness, called flares, and periods of wellness, or remission. <\/span><\/p>\n<p><span style=\"font-weight: 400;\">Symptoms vary from person to person, and may come and go. I typically experience: <\/span><\/p>\n<ul>\n<li style=\"font-weight: 400;\"><span style=\"font-weight: 400;\">Chest pain <\/span><\/li>\n<li style=\"font-weight: 400;\"><span style=\"font-weight: 400;\">Joint pain<\/span><\/li>\n<li style=\"font-weight: 400;\"><span style=\"font-weight: 400;\">Fatigue<\/span><\/li>\n<li style=\"font-weight: 400;\"><span style=\"font-weight: 400;\">Fever <\/span><\/li>\n<li style=\"font-weight: 400;\"><span style=\"font-weight: 400;\">Nauseous<\/span><\/li>\n<li style=\"font-weight: 400;\"><span style=\"font-weight: 400;\">Hair loss<\/span><\/li>\n<li style=\"font-weight: 400;\"><span style=\"font-weight: 400;\">Sensitivity to sunlight<\/span><\/li>\n<li style=\"font-weight: 400;\"><span style=\"font-weight: 400;\">Skin rash aka the \u201cbutterfly\u201d rash. The rash is most often seen over the cheeks and bridge of the nose, but can be widespread. It gets worse in sunlight.<\/span><\/li>\n<\/ul>\n<p><span style=\"font-weight: 400;\">Currently I\u2019m under the care of a neurologist, rheumatologist, endocrinologist, and dermatologist. I have a cocktail of meds that I take daily, in addition to B12 injections &amp; iron infusions. So far, I\u2019ve been lucky enough to not have any \u201cmajor\u201d procedures. But I\u2019ve been hospitalized six times due to complications of Lupus. I\u2019ve suffered a mild seizure, and complete hair loss from the chemotherapy treatments. I\u2019m in pain every day (similar to the body aches you feel when you have the flu), and I suffer with migraines, insomnia, and short-term memory loss. I do my best to hide my pain because I don\u2019t want to worry my family and, maybe most importantly, I don\u2019t want people to walk around feeling sorry for me.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">When I was first diagnosed, I was very angry that I had Lupus. I felt like my body had betrayed me and that God had betrayed me. I questioned why \u2013 why <\/span><i><span style=\"font-weight: 400;\">me? <\/span><\/i><span style=\"font-weight: 400;\">I live a good life, I give back, I support my community, my friends and my family. <\/span><i><span style=\"font-weight: 400;\">WHY ME??<\/span><\/i><\/p>\n<p><span style=\"font-weight: 400;\">I felt alone and shunned. My friends could not understand how I could feel fine one moment, and five minutes later felt like death warmed over. Some thought I was faking or making excuses and began to question whether they could truly depend on me. They didn\u2019t consider that most of the time, I don\u2019t look the way I feel. I\u2019ve heard a thousand times \u201cyou don\u2019t look sick,\u201d \u201cyou just need to work out,\u201d \u201cyou need to eat this\u2026.don\u2019t eat that.\u201d It takes a lot of work, effort, and energy to not look sick. <\/span><\/p>\n<p><span style=\"font-weight: 400;\"><a href=\"http:\/\/unclefunkysdaughter.com\/blog\/wp-content\/uploads\/2016\/05\/Screen-Shot-2016-05-19-at-12.38.25-PM.png\" rel=\"attachment wp-att-705\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-705 alignleft\" src=\"http:\/\/unclefunkysdaughter.com\/blog\/wp-content\/uploads\/2016\/05\/Screen-Shot-2016-05-19-at-12.38.25-PM-595x597.png\" alt=\"Screen Shot 2016-05-19 at 12.38.25 PM\" width=\"309\" height=\"318\" \/><\/a>I remember having a pity party and crying my eyes out. My oldest brother said to me, \u201cGod didn\u2019t send you this challenge to defeat you \u2013 He gave you this challenge to increase you. You are your mother\u2019s daughter. You may bend, BUT you won\u2019t break!\u201d My mother had bravely battled breast cancer and Alzheimer\u2019s disease (mom passed away September 23, 2013). I reflected, and remembered the strength in her fight and that I come from that \u2013 I knew it was in me to not only fight, but win! That day, I decided to live in peace with Lupus, instead of in pieces. <\/span><span style=\"font-weight: 400;\">I took steps to regain my health and wellness, and I formed <\/span><b><a href=\"http:\/\/www.lupiechick.com\" target=\"_blank\">The Lupie Chick Project<\/a><\/b><span style=\"font-weight: 400;\">, <\/span><span style=\"font-weight: 400;\">a charitable organization dedicated to raising awareness of lupus through advocacy, education<\/span><span style=\"font-weight: 400;\">, and FUNraising events<\/span><i><span style=\"font-weight: 400;\">.<\/span><\/i><span style=\"font-weight: 400;\"> I started <\/span><b>Selfies for Lupus<\/b><span style=\"font-weight: 400;\"> in May 2014, which is a social media awareness campaign to bring awareness via selfies. I also shared my journey, my pain, my fears, and my tears by utilizing social media outlets such as Instagram, Facebook, Snapchat, Facebook Live, and Periscope by putting a face to a little-known disease and have dedicated myself to keeping it \u201creal, raw,\u00a0&amp; relevant.\u201d\u00a0<\/span><\/p>\n<p><span style=\"font-weight: 400;\">I have learned that my ability is stronger than my disability. I have made many adjustments in my daily routine, in my relationships, in my life, and I\u2019M ABLE! I\u2019m stronger than Lupus and I make one hell of a cheerleader. Cheering for myself, maintaining a positive attitude, documenting my holistic lifestyle, clean-eating diet and fitness journey; continuing to advocate and educate my community, pray, and using my voice and platform to be the face of lupus are some of the courageous<\/span><span style=\"font-weight: 400;\"> steps I take to reach my goal of living well, despite the challenges of lupus.<\/span><\/p>\n<p>&nbsp;<\/p>\n<p><span style=\"font-weight: 400;\">Altonia Fowler-Dugar aka Naturally Lupie <\/span><\/p>\n<p><span style=\"font-weight: 400;\">The Lupie Chick<\/span><\/p>\n<p>&nbsp;<\/p>\n<p><span style=\"font-weight: 400;\">SOCIAL MEDIA<\/span><\/p>\n<p><b>WEBSITE:<\/b> <a href=\"http:\/\/www.lupiechick.com\/\"><span style=\"font-weight: 400;\">www.lupiechick.com<\/span><\/a><\/p>\n<p><b>INSTAGRAM:<\/b><span style=\"font-weight: 400;\"> Naturally_Lupie<\/span><\/p>\n<p><b>TWITTER:<\/b> <b>@NaturallyLupie <\/b><\/p>\n<p><b>SNAPCHAT<\/b><span style=\"font-weight: 400;\">: @NaturallyLupie <\/span><\/p>\n<p><b>FACEBOOK:<\/b><span style=\"font-weight: 400;\"> https:\/\/www.facebook.com\/TheLupieChickProject<\/span><\/p>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>2011 was supposed to be the year I showed up and showed out on life! I was preparing for my 40th birthday bash when I first began to feel ill.&hellip;<\/p>\n","protected":false},"author":11,"featured_media":737,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[1],"tags":[218,217,216,215,211,207,219],"powerkit_post_featured":[],"class_list":{"0":"post-702","1":"post","2":"type-post","3":"status-publish","4":"format-standard","5":"has-post-thumbnail","7":"category-hair-tips","8":"tag-health","9":"tag-lupie-chick","10":"tag-lupus","11":"tag-lupus-awareness","12":"tag-moms","13":"tag-mothers","14":"tag-wellness"},"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v24.8.1 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>I\u2019m Not My Diagnosis - Chat Box<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/unclefunkysdaughter.com\/chatbox\/2016\/05\/19\/im-not-my-diagnosis\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"I\u2019m Not My Diagnosis - Chat Box\" \/>\n<meta property=\"og:description\" content=\"2011 was supposed to be the year I showed up and showed out on life! 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