Snizzles

60d

i recently got diagnosed with Sjogrens after many years of appointments and testing. i have my first appointment with a rheumatologist but it's not until mid January.. AFTER my intended follow up primary care appointment for that visit. I'm feeling frustrated. how do I manage until then? and has anyone had luck getting in sooner after scheduling? I just want the pain and fatigue to be treated for once

acute lethargy

Chronic Fatigue Syndrome (CFS)

Postural Orthostatic Tachycardia Syndrome (POTS)

Other Diseases of Sebaceous Glands

Sjogren's syndrome (SjS, SS)

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  • nubiansunflwr

    60d

    So I’ve had Sjorgens for about a year now & my pain went from mild to chronic bc of my lupus. For sjorgens i try to drink a lot of water, like always have bottles next to you bc the dryness can be unbearable sometimes. Eyedrops are good for dry & itchy eyes & for the pain i recently ordered a tens unit off of amazon & it works great! Definitely think it’s worth trying some of these things.

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