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How Long Does Ivig Last For Myasthenia Gravis
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IVIG Day 4 and… here we go. 😣 The steroids are winding down, and the symptoms are kicking in—hard. I honestly think the only reason I made it through the first few days “better” than usual is because we hammered everything with antihistamines, steroids, benzos, and the 20 meds and supplements I take just to keep my body calm. MCAS is no joke!😳 But now? The reality: rash everywhere. Intense itching. Night sweats. Body aches. Chills. Flu-like misery. Plus the massive migraine, face pressure, and
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Unfortunately my body hasn’t been responding to its current treatment plan… So, going forth I will now be having both Rituximab & IVIG on alternative fortnights. Looks like the day infusion centre is goibg to become my second home!! #chronicillness #invisibleillness #autoimmunedisease #foryou #fyp #rituximab #IVIG #hospital #immunotherapy
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