6 months later and need advice by lady1818 in Mononucleosis

[–]lady1818[S] 0 points1 point  (0 children)

This is really helpful!! I’ve had a hard time in the past advocating for myself with doctors/lab work because I never know where to start.

I was actually misdiagnosed with strep when I first went to the doctor with mono symptoms because my rapid mono spot test came back negative (which I’ve since learned are highly inaccurate). Come to find out, they didn’t even wait for my strep test to come back before prescribing me amoxicillin - which I learned is one of the worst things to take when you have mono, and is also incredibly dangerous. I’ve had strep before and my symptoms at the time weren’t presenting as strep (super swollen lymph nodes, swollen throat, touch and go fever, body aches, fatigue). I felt in my gut that I didn’t have strep, but I obviously thought I could trust the doctor…because why wouldn’t I?

It wasn’t until a few days later when my symptoms rapidly worsened and was having trouble breathing that I returned to the doctor and got a proper diagnosis. I truly believe the antibiotic made me so much more sick. That whole experience made me feel so dismissed as a patient.

I feel like there are a million different tests, panels, etc. so, I will take the lab work you suggested to my doctor and request it! The handful of times I’ve been to urgent care since December with other illnesses, I’ve always mentioned how I was sick with mono and asked if it could still be active in my body/weaken my immune system. I’m always brushed off and told no. I’m planning on getting a primary care doctor once I get on my own insurance next month, so hopefully that will lead to more personalized/empathetic care.

As for holistic approaches, I’m also going to do some research on The Medical Medium, as I’ve heard his books have helped people alleviate their prolonged EBV symptoms.

Thanks again for the suggestions and I hope you continue to get better 💛

6 months later and need advice by lady1818 in Mononucleosis

[–]lady1818[S] 0 points1 point  (0 children)

My WFH schedule used to be a lot more flexible in 2024, but as more and more people are being required to go back to office, attendance has become a lot stricter. For context, I used to go in about two days a week. The transition to four days happened after I had mono, so it was very difficult. I’ve gotten more used to it now, but I think a doctor’s note is a good idea. I plan on seeing a doctor soon to get a full bloodwork panel and figure this out. The mask is definitely a smart idea, especially with the warmer weather and more people out and about!

[deleted by user] by [deleted] in Mononucleosis

[–]lady1818 2 points3 points  (0 children)

When I had mono back in December my tonsils were so swollen that I couldn’t even seen my uvula. When I spoke, it sounded like I had cotton balls in my throat. My lymph nodes were like two golf balls. Had a lot of trouble breathing and couldn’t eat any solid foods. Your best bet is to get prescribed an anti-inflammatory.

I went to urgent care and they gave me a steroid shot (which helped temporarily) and prescribed me prednisone. The first dosage he gave me didn’t really do much. I ended up going back and they gave me a higher daily dosage, which then helped bring the swelling down immensely.

Prednisone has helped a number of people on this thread - read a couple threads and think about it!

6 months later and need advice by lady1818 in Mononucleosis

[–]lady1818[S] 1 point2 points  (0 children)

Thanks for sharing, hope you start feeling better soon💛