Chronic Fatigue Syndrome / Myalgic Encephalomyelitis

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The original was posted on /r/cfs by /u/Flashy_Shake_29 on 2025-01-18 17:40:45+00:00.

After a year, I think I finally reached my breaking point and my mental health is tanking. I’m ready to talk to my doctor about a SSRI. Are there any that are known to be more or less helpful for MECFS symptom management as well? My biggest pain point is cognitive PEM and not being able to talk to my family. I could continue being bedridden if I could just regain my communication.

I’m already taking LDN Valtrex, Celebrex, Zyrtec, and oxaloacetate. Currently trailing LDA. Even with all these meds, I’m close to being very severe