I have been undergoing biologic treatment since the onset of my consultations with a rheumatologist, preceding even the confirmation of a formal diagnosis. Commencing with weekly injections of Humira, I transitioned to monthly doses of Cimzia following an inadequacy of response. Recently, I have developed Palmoplantar Pustulosis Psoriasis (PPP) on the palms of my hands and the soles of my feet. It is noteworthy that PPP can arise as a result of biologic treatment, which is remarkable considering their common prescription for psoriasis. Furthermore, the manifestation of psoriasis as a symptom of Ankylosing Spondylitis (AS) exacerbates the situation. I am currently awaiting an appointment with a dermatologist to effectively manage this condition, as it has significantly impeded the use of my hands and walking due to the accompanying pain. There may be intermittent gaps in my future posts as I navigate this newfound illness. Despite the deviation in tone from my usual posts, I am deeply passionate about this blog. My primary intention is to utilize my narrative and experiences to assist others. I understand that this particular post differs in tone, but I aim to provide a candid portrayal for those who choose to engage with it. My ultimate objective is to genuinely reassure anyone feeling isolated that they are not alone and potentially offer guidance to those grappling for a diagnosis, as medical marginalization is regrettably prevalent in cases of chronic ailments.
If you are currently reading this and have encountered Palmoplantar Pustulosis Psoriasis, I kindly request that you share your personal experiences and any remedies that have provided relief. I am currently enduring significant challenges with this condition.
Wishing you the very best and looking forward to providing you with an update soon.