Hello all! My surgery was on 1/6/25 with Hackman. It is now 1/8/25 and I’m home and feeling pretty good. My styloid process was just over 2cm so not anything crazy. It was calcified with little bony spikes. Dr. Hackman was able to remove it through an incision around my ear, no neck incision was made.
Current Complication: the left side of my face is super slow to react. Blinking and smiling are noticeably weak but other than that, there’s truly no news.
As you’d expect, eating is hard but I’ve learned already that using a fork is easier than a spoon because I don’t have to open my mouth as wide. It’s the little things…
Discharge: I was given a Prednisone regiment that I will start today, along with drops for my left eye and pain meds. I’m allergic to codeine but Oxy doesn’t usually bother me but I woke up in hives and itching like crazy. I’ll be calling them for a replacement pain medication this morning.
My next goal is to get off of all of the meds I have been on for the last 2.5 years. Then I’ll be doing a liver and kidney detox and hoping I feel as good as new.
I will be happy to share any part of my journey if anyone has any questions or interest. My symptoms started in 2017, came to a head in 2022 and finally I got with the right doctors to take me seriously and help me figure out how to proceed. I truly believe surgery was my best option and I’m glad things moved quickly once we realized it was Eagle’s Syndrome. I am not sure if this is allowed but here’s a link to the TikTok I posted last night to explain my journey.
Wishing every one of you the absolute best. -Jenny