Showering with Sjogren’s
I wonder if anyone had input on how often to shower with Sjogren’s. I know that dry skin often leads some to shower less, and I have found I itch more when I shower every day. So, how does one deal with that?
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This is very interesting. So, from what I’m reading, I would be one of the only Sjogrens patients whose only symptom is dry eye.
I cannot cry, either and I have very dry eyes. My mouth gets dry, too, but have not been diagnosed with Sjogren’s Syndrome. My neurologist believes I have Myasthenia Gravis. I am in the process of getting an appointment with the Maya Clinic.
Lots and lots of moisturizer!❤️
I use a natural soap from India and shower twice a week. After I don't towel dry, I directly apply baby lotion to my whole body. Less itching and skin does not look or feel dry. Hope this helps. But I do think the environment, and what you do for work would influence this. I am retired and home.
Before Nizoral did you notice your scalp being super dry and tiny white flakes (dead dry skin) everywhere ? I was diagnose but haven't been able to find a decent shampoo that doesn't dry me out even more