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Diary of a Mad Lupus Patient: Shortness of Breath
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About Diary Of A Mad Lupus Patient: Shortness Of Breath
Little did she know, the very thing she was told would probably end her life-Systemic Lupus Erythematosus (SLE)–would become the very thing that saved her life. Diagnosed during her high school years, Hetlena began chronicling the journey of confusion, fear, and challenges of living with lupus. What once was a personal diary to record her pain, both physical and emotional, is now a testimony of how she’s taken control of her destiny and given lupus a run for its money.Diagnosed during her high school years, the author decided to keep a personal diary of her confusion, fear, and challenges of being diagnosed with Lupus. Lupus, also known as Systemic Lupus Erythematosus (SLE) is a disease that can affect many different body systems, including the joints, skin, kidneys, blood cells, heart, and lungs. Lupus is more common in women than in men. Research continues to be done on finding a cure for this life-threatening illness. This diary records thoughts and feelings for being diagnosed, to understanding and accepting the reality of living life with Lupus.Known as the “wolf disease”, lupus attacks almost every organ in the body, including the joints, skin, kidneys, blood cells, heart, and lungs. Today, Hetlena dedicates her time as a lupus awareness warrior ready to help the medical community, lupus patients and the world learn about this life-threatening illness. Diary of a Mad Lupus Patient reveals how one woman decided that her life would not be in vain. She knew that although wolves are formidable predators, her desire to live life abundantly was stronger than any prey a wolf could ever face.
