I'm hoping that there won't be any of you who are finding out about how the Sherman house was turned upside down last week for the first time via this blog entry. I've been trying my hardest to get in touch with all our family and
friends, but it's been pretty challenging because we're so blessed with such an amazing network of people who love us so much and are calling and emailing with questions and concerned thoughts. If this is the first time you're getting wind of this, I apologize. Please feel free to post your thoughts, comments, etc., to our blog and / or email either Jake or I whenever you'd like to reach out:
apriljsherman@gmail.com or
jacobqsherman@gmail.com. Our cell numbers: April - 414.248.1775, Jake - 414.248.1774. The good news is, although this is all very scary, serious and unexpected, my prognosis (as
unbelievable as it may sound) is good. I'm walking and talking, which is a true blessing. I'm told that once I'm through all that's coming in the next few weeks, I'll be on my way to a full recovery. Okay, now I'll get on with it...
On Tuesday of last week, I fainted while getting ready for work. Who knows why, but after regrouping, I continued on with my day and went to work (what? I needed to keep up the routine at least for Layla and get her off to daycare and jet out for my 9:00 meeting). ;) I did make an appointment with my doctor for that morning at 11:15, however. At the appointment, they ran some blood tests and did a C.T. scan. When my doctor called with the results, she said that my blood tests all came back looking good, but that the C.T. showed some swelling on the right, front of my brain. She immediately scheduled me to come back to the hospital for an MRI. A few hours later, the results of my MRI were in, and showed that I have an Atypical
Meningioma (most likely, a slow-growing, benign tumor). In fact, the radiologist that
reviewed my MRI results told my doctor that judging by its size and shape (1.5 inches and shaped like a small, chocolate
Easter egg... my description, not the doctor's), his recommendation was for me to continue on with life as usual and come back in 3 months for another MRI to see whether the tumor has grown. Of course, neither Jake or I are 100% comfortable with just "chilling" with a tumor in my brain (however "benign" it might be), and neither was my doctor, so we were scheduled to see a neurologist the next day at St. Luke's.
On Wednesday, we went to see the neurologist to get his
opinion on my MRI scans. The appointment took a long time, but when I finally did see a doctor, his instant opinion was that the tumor had caused a seizure (which caused me to lose
consiousness on Tuesday), and the seizure had caused brain swelling. He said the tumor needed to be removed, without a doubt (he also said that the radiologist who reviewed my MRI scans originally would be getting a call from him, uh oh). Then he told me that I would be admitted
into the hospital that day, meaning I wouldn't even get to go home. They wanted to get me in right away to do an EKG, EEG, and
angiogram. The EKG was fine (I think, because I never heard anything back on it), the EEG was mostly fine, but they did see some "activity" that assured them that a seizure had at least
occurred, and the
angio confirmed the suspicion that there are blood vessels connecting to the tumor that need to be blocked before surgery (to prevent stroke and / or excessive bleeding during surgery). So, on Tuesday of next week, I'll be admitted to have the procedure that will block the vessels and I'll stay in the hospital until Wed, when I'll have brain surgery. I'll be in the hospital anywhere from Tue-Fri or Sun. Not sure on that yet. I'm not allowed to drive for 3 months, which is
devastating because I think it feels like something has been taken away from me.
While at home (and thank God I get these few days to be at home to relax, sleep in my own bed, and snuggle all of the love out of my baby girl), I'm on a boat load of drugs that are keeping me safe while I'm not plugged into all of the high tech gadgets in the ICU (
steroids, anti-
seizure meds and
meds that are supposed to prevent ulcers or something).
Jake has been amazing. He is taking care of making all the phone calls that need to be made, setting up Layla care, drivers, etc. I am so thankful for that. He's also helping me focus on the now, rather than the future (meaning, focus on getting through next week instead of the "how will we do this?" and "what if that?").
Thank you to everyone for all of your phone calls, texts, emails, visits and good energy vibes and prayers. Thanks so much for all of the care packages and food too! I feel so amazingly blessed to have such a wonderful network of
family and friends in my life.
Lots of love and smiles,
April (aka: "Lumpy Brain")