Bryce's Biopsy
I wanted to share some great news with everyone. But first, the backstory...a not-so-great email we received on the 2nd from my mom's first cousin (we're a very close family).
Hi everyone,
Facebook seems fairly inappropriate for this, but calling everyone seems more difficult. We had some very sad news today concerning our 26 year old son, Bryce.
About three weeks ago, Bryce had a seizure in the middle of the night. No one saw it and Bryce couldn't remember it, but he was bruised and extremely sore the next day. Bryce lives with our oldest son, Scott and our two grandchildren, Hannah and Gabrielle, in Bentonville, AR. Scott is a physician and so had some tests ordered. Those tests came back normal and after consulting with other docs, decided not to pursue more invasive and expensive procedures. This past Sunday night, Bryce had another seizure similar to the first. So an appointment was made with a neurologist for next week. Then, last night Scott witnessed bizarre behavior from Bryce that led him to believe that we needed to move faster with a diagnosis.
Bryce had a C-scan early this morning. We were all shocked to learn that he has a brain tumor. An MRI was immediately scheduled for a couple of hours later. Scott was able to get Bryce an appointment with a neurological surgeon in Tulsa at 2 pm this afternoon. Roger, Ross and I met Scott and Bryce in Tulsa for the appointment.
So, if there is good news when you have a brain tumor........
He has an oligodendroglioma high in the right frontal lobe of his brain. Scott says if you have to have a brain tumor this is the kind you want. There is a 75% survival rate at 5 years for this type of tumor. This doesn't sound great until you realize that those numbers include all ages, people who are not very young, people who have other health risks, etc. Bryce has his youth, his excellent health, the relative good placement of the tumor, all in his favor. Also, it does not appear that this tumor is malignant. This is an extremely slow growing tumor.
The not so good news...... The tumor is quite large. 8 x 6 centimeters. The doctors were actually surprised that we had not noticed any behavioral changes in Bryce. Operating on this type of tumor is not recommended. There is the chance of doing harm to his brain. The main symptoms of this type of tumor is seizure. He will be on seizure medications for the rest of his life, barring some wonderful new medical treatment. Frequent MRIs will also be ordered to be sure the tumor doesn't change.
The treatment.... Bryce has been placed on seizure medication with the hopes of getting control of these seizures. He is taking steroids to hopefully reduce the edema (swelling) in his brain. Next Wednesday, the 29th, Bryce will have a biopsy done. This is an invasive procedure, drilling a small hole into his skull. There will be an active MRI going on during the surgery so the physician can see where he is placing the needle. Several areas of the tumor will be sampled. We will have the results in 3-5 days. He will be in the ICU following the procedure, then on to the surgical floor for about one day. They are keeping him so they can watch for bleeding in the brain which is a side effect of the biopsy.
Bryce is in very good spirits and as Scott said he is taking this news better than the rest of us. My sons started in on the 'tumor jokes' right away. What does your tumor think about that? Just think, if either of you two ever get a tumor, mine is the biggest. Oh, you go first, tumor boy. Man, I bet you feel bad about the way you treated me when we were kids, knowing I have this tumor and all. It got worse and I'm sure it will only continue.
And because we can't have just one family emergency, my dad is having open heart surgery, probably this Thursday. He needs a mitral valve repair or replacement. His surgery will take place in Oklahoma City. We were on our way to see his surgeon when Scott called with the news about Bryce. It has been a difficult day.
We need your prayers. I am home tomorrow so if you want, you may call. Bryce is also probably home tomorrow. Also on the good news side, Bryce, Scott and friends had a trip planned to Las Vegas for this weekend. The doctor said he can go! He, of course, is not allowed any alcohol -- his mother has no problem with that -- and he's just thrilled he still gets to go. No calls on Thursday, please, as Dad will most likely be in surgery.
I will update you on Dad and Bryce when we know more. Thanks to all of you for your good wishes and prayers.
Deb
xoxo
Followed by an update sent out today:
Yesterday, we got our report from Dr. Wilson on Bryce's biopsy. We have a change in diagnosis. Bryce's tumor is a low grade oligoastrocytoma (WHO grade II).
First the World Health Organization grade II -- There is a standard rating of tumors, grades I - IV. Dr. Wilson says a grade I is "is this even a tumor". He has never seen a grade I. So, this is good news. It says that this tumor is "about as benign as they get". Obviously great news.
An oligoastrocytoma is a mixed glioma. There are four classes of gliomas: oligodendrogliomas, astrocystomas, anaplastic astrocystomas, and glioblastoma multiforme. These are in order, least malignant and lethal to more malignant and lethal. So, we have a mix of an oligo and an astrocytoma.
This tumor can do one of three things: it can continue to grow so slowly that with seizure medication it might not be a problem for Bryce for a number of years; it can begin growing more rapidly and become a larger problem very soon; it can de-compensate and become aggressive and malignant.
Dr. Wilson has released Bryce as a patient and is sending us to MD Anderson. We already had an appointment there, but nice to know that this was Dr. Wilson's recommendation as well. Dr. Wilson is positive that there may be new treatments available for the treatment of his tumor. We are also seeing a neurosurgeon in Dallas on Friday to get his opinion.
Bryce is off steroids as of yesterday and is feeling much more like himself. Nasty stuff, those steroids. He is tired and ready to move forward in this fight.
The entire family is very positive about Bryce's complete recovery. We need your prayers. Yes, please put Bryce on the prayer chains you are a part of -- we know the power of prayer in our home.
You may feel free to contact Bryce via email. brycemusick@hotmail.com
He is staying here at our home at this time. 1214 HIckory, Weatherford, OK 73096
He isn't able to work because of the medications but hopes to return to work soon.
Friends of Bryce who have his phone number, call him. He would love to talk to you.
Thanks for all your good wishes and prayers.
Debi, Roger, Scott, Hannah, Gabrielle, Ross, Kendra, Jordan, Casey, Cierra, Fitz, and Bryce
xoxo
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Bryce's Mom here -- We went back to the Brain Suite at 5:30. Bryce has on a cute gown and really sexy white stockings. We have met his prep nurse -- from OU, but we like her anyway. I just came out to let Roger go back for a few minutes. They usually only allow one person back with a patient, but are allowing Scott to stay as he is a physician -- nice perk! We are on the 5th floor surgical waiting area, in the Geranium section. Nice chairs, lots of puzzles, and helpful staff.
From Scott -- The surgery could take anywhere from 5-8 hours. The large time difference is based on the BrainSuite complexity. They will MRI Bryce's brain prior to surgery and then 1-3 more times during surgery. Each MRI takes 30-45 minutes, because the table rotates and slides across a huge room into the MRI machine. Bad scene to have metal scalpels and retractors flying at surgeons and nurses! His nursing staff and anesthesiologist are amazing and efficient. He will have a total of 2 IV's and an arterial line in his left wrist that monitors blood pressure and pulse with every beat of his heart. The anesthesiologist is the head neuro-anesthesiologist at MD Andersen.
Bryce is very relaxed as is mom, surprisingly. I think that is mostly related to the confidence exuded by every nurse, tech and doctor we have met today. His surgery should begin about 7:30 or so. After he is done he will go to the Post Anesthesia Care Unit for about 2 hours and then to the post-neuro-surgery non-ICU, ICU. It's unbelievable how specialized their areas, nurses, and techs are. We should receive a update about 2-3 hours into surgery and will update everyone then. Keep up the prayers and thoughts for Bryce! Love the Musicks.
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