Something to consider…In 2017, after being rushed to the ER and experiencing all kinds of random pain, swelling, etc., I had my last-straw experience and decided to try to find out what was wrong with me. The PCP at a clinic I was going to chalked it up to anxiety. Anxiety. 🤦🏾♀️ (That’s why I hate mentioning my history of anxiety and depression on forms because they tend to not go any further.)
Anyway, after testing positive for Sjogren’s through bloodwork ordered by a NP, a rheumatologist that I went to later didn’t trust the test results. She ran a different kind of test that made her determine that I didn’t have it. Hmph.So, after switching to a rheumatologist that’s 45 minutes away, she believed the results, called the other doctor “textbook” and started a treatment plan.I was glad that I found a doctor who would listen, but I kind of wondered if I actually had some sort of unspecified autoimmune issue and not Sjogren’s.
Then…Guess who just tested positive for Sjogren’s as well? My older sister.
BOOM! 💥
Now I no longer have doubts, and I get to help my sister out on her own journey.I am sooooo tempted to write both of the doctors who doubted me and tell them why I’m not losing it. 😂
The end.

Wow! I agree that some doctors treat and don’t listen. It’s good that you found someone who does. Your journey will allow you to bless your sister. I pray all works out and you and she stay blessed.
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Doctors can be lazy sometimes. You can go in for an earlobe ache and they chalk it up to you being fat. I’m glad you found a Doctor Who paid attention to you.
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This frustrates me so bad. Good for you for not listening to that other doctor!
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Thanks for sharing this! It’s super important to know and awesome to hear your POV!
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Wow. I learn something new from you about this disease I’ve never heard of. Thanks for sharing your story!
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GIRL, you better write those doctors!!! I’m so happy that you shared this story on your blog!!
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Girl, it’s likena diamond in a rough finding a doc that listens instead of just hearing you. I’m happy that you have answers. Never stop fighting for yourself!
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I really related to this post. I have Myasthenia Gravis and my doctor thought I was crazy when I said I couldn’t swallow food.
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It’s so scary when doctors don’t believe you about your own body!
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As Melanin women it is critical that we make our doctors hear us and listen to us. I will keep you and your sister uplifted in prayer.
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Listen, we know our bodies better than anyone else. We have lived in them. We know what’s normal and what’s not. Always advocate for yourself, sis.
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Thanks for sharing. Stay strong and fight for what you believe in.
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