![]() The combination of all these things has me currently living without most of my chronic symptoms. It’s a wearable device that communicates with the body’s cells through LED light for wellness management. I also sleep with a wellness device called the WAVE 1 by Fremedica. I make sure to get enough sleep, eat organic food as much as possible, I practice yoga, and I meditate every day. My life is far from perfect, but I try to keep things in balance. We should learn not to judge how somebody feels by the way they look on the outside. It’s so important we learn to listen to people, as many of us are suffering in silence. If it weren’t for my children, I don’t think I would be here today. Many nights I wished to die, and prayed I would just be free of the pain. For some time, it didn’t even feel like living at all. I can’t begin to describe the darkness, the pain, and the hell I lived through every day. You were once quoted as saying you had reached a point where you couldn’t contemplate living another day. Looking back, all those difficult times in my life were blessings in disguise. I’m grateful for every moment I get to spend on this planet with family and friends. I’ve also learned to love my authentic self with all my imperfections. My “new normal” is much slower and more in tune with who I am. My decade-long journey was an absolute nightmare, but my diagnosis taught me a lot about life, about how much patience and dedication are needed in order to survive. How have your, Bella, and Anwar’s diagnoses impacted the way in which you approach your work, your relationships, and your lives in general? As the saying goes: You don’t truly get it until you get it. Most people still don’t seem to believe that chronic Lyme disease even exists. It’s much easier for us to have compassion for somebody with visible external symptoms. Like with many chronic diseases and mental health issues, the unfortunate truth is that you appear to be healthy on the outside, which is difficult for people to reconcile. You’ve referred to Lyme disease as an “invisible disability,” and there does appear to be a tendency for sufferers to not always be taken entirely seriously. I was eventually diagnosed by a doctor in Belgium. I fought tooth and nail to keep things together in front of my family and friends, but as things got progressively worse, there was no hiding from the truth any more. My body sent me early warning signs, but my type-A personality didn’t leave me much room to be vulnerable with myself. My symptoms included severe fatigue, brain fog, memory loss, difficulty with word retrieval, anxiety, insomnia, migraines, joint pain, muscle weakness, intolerance to bright light, flu-like symptoms, swollen lymph nodes, and slight Bell’s palsy in my face-all of which left me feeling depressed. I used to be a multitasking, single mother of three and social butterfly who, slowly, started to lose her magical powers. ![]() ![]() We never noticed any ticks or bull’s-eye rashes on us, but we’ll never know for sure.Ĭould you tell us a bit about your diagnosis and symptoms? ![]() My children grew up on a farm in Santa Barbara, California, riding horses and spending a lot of time in nature. Do you have any idea where the three of you might have contracted it? In addition to Bella and yourself, there’s a third person in your family suffering from Lyme disease: Anwar. By sharing the uncomfortable parts of our lives, we have the power to raise awareness.” “We have to turn our mess into a message. Much like daughter Bella Hadid, who recently went public about her battle against Lyme disease on her Instagram Stories, Yolanda, 57, is now hoping to take the lid off what she calls an “invisible disease.” In conversation with Vogue, the former Real Housewives of Beverly Hills star opened up about her personal struggles, sharing glimpses of her darkest hour and offering hope for a brighter future. It’s all the more surprising, then, that there is still no agreed-upon treatment to speak of. It has even led some to contemplate suicide. Symptoms, which include fatigue, muscle pain, and serious memory impairment, can become chronic, significantly impacting a patient’s quality of life. Yet, 46 years later, there is still stunningly little reconcilable information on the tick-borne illness to be found. With celebrities such as Avril Lavigne, Alec Baldwin, and, more recently, Yolanda and Bella Hadid opening up about their struggles with Lyme disease, you might be surprised to learn that the first recorded case of Lyme disease dates back to 1975.
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