Sunday, February 10, 2008
Feb. 10th
This program was created to demonstrate, to the children, where their family members are going and to show them what & how medicine/treatments are being provided. They had an oncologist speak in general terms about good cells-bad cells and then toured the hospital. Of course the initial talk was a bit difficult for Bryce to comprehend and he verbally noted that he was bored. However, after we left the hospital and later in the day he asked very relevant and articulate questions about those 'cells.' We will continue to try and talk with the boys in an honest and appropriate manner. After the group meeting, Bryce got to go on a tour of the hospital with the other children. Each child was chaperoned by a staff member and we were given a pager to inform us if Bryce was upset or scared. He got to make 'fake' chemotherapy and a radiation pillow with his hand print in it. Apparently he got to work the pharmacy 'train' and did such a good job that he got an 'honorary pharmacist' sticker. After lunch, he made a pillow and shared it with the entire group of families and staff. He stood on the chair, held up his pillow, and was embarrassed to speak. Our social worker helped him through it and Robert and I couldn't have been prouder. He made a new friends that he is still talking about including; social worker, doctors, nurses, and peers.
In our meetings yesterday, the topic of cancer forcing 'lives' to become more public was addressed and the challenges that surround this new reality. For me being 'public' about our situation and emotions has been the easy part. We want as many people to know in the hopes that- the more people who know- the more people who will project positive thoughts and prayers. Our theory also extends in the opposite direction- we like to say- "don't tell anyone who doesn't like us, we don't want the negative energy." The challenging part has been finding ways to thank everyone for the amazing amounts of support that we have received and asking others to help in ways that we never needed before. We hope that through this blog we can continue to keep everyone informed and continue to articulate to you the gratitude that we have in our hearts.
My Condition - Glioblastoma Multiforme (or GBM)
I was diagnosed with Glioblastoma Multiforme (GBM). This condition has four different grades (I - IV). My tumor is a grade IV GBM. This is the most aggressive GBM tumor. I have included a little section of The Essential Guide to BRAIN TUMORS below to describe the condition more completely.
Astrocytoma
An astrocytoma develops from star-shaped glial cells (astrocytes) that support nerve cells. These tumors can be located anywhere in the brain, but the most common location is in the frontal lobe. Astrocytomas are the most common primary CNS tumor.
The physician, usually the neurosurgeon or neurooncologist, will discuss the type and location of an astrocytoma. The pathologist will assign it a grade. Astrocytomas are generally classified as low or high grade. Low-grade astrocytomas (grades I and II) are slow growing. High-grade astrocytomas (grades III and IV) grow more quickly. The main tumor type is listed for each grade. There are additional tumor types in each of these grades.
The WHO classification divides astrocytomas into four grades:
- Grade I Pilocytic Astrocytoma
- Grade II Low-Grade Astrocytoma
- Grade III Anaplastic Astrocytoma
- Grade IV Glioblastoma Multiforme (or GBM)
Characteristics
The characteristics of an astrocytoma vary depending on the tumor’s grade and location. Most people are functioning normally when diagnosed with a low-grade astrocytoma. Symptoms tend to be subtle and may take one to two years to diagnose. This is because the brain can often adapt to a slow-growing tumor for a period of time. Highgrade tumors may present with changes that are sudden and dramatic.
Symptoms
- Headaches
- Seizures or convulsions
- Difficulty thinking or speaking
- Behavioral or cognitive changes (related to thinking, reasoning, and memory)
- Weakness or paralysis in one part or one side of the body
- Loss of balance
- Vision changes
- Nausea or vomiting
1 comment:
Bryce...
That is soo super cool you got to be a real pharmacist for the day! You are such a hero man! We are soo proud of how super strong you are being for your family. Bryce...know that all the nurses and doctors are healing your daddy and getting him all better!
Tammy and Robert...
Thanks so much for the update. Yes indeed ....amazing many prayers and positive vibes of hope, healing, happiness and giggles and glory in your recovery! We are thrilled with your news of your final chemo for a while...relax and know we are all in your corner!! May God bless you and keep you. We are constantly sharing prayer requests for Robert and your entire family to carry you during this time. We love you so! Take care! Hoping for a great belly laugh today and many moments of giggly bliss with the kids!
XOXOXO Angie, Chuck, Gabbi, Maddi McLean
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