Monday, October 8, 2012

This is the most difficult thing that I have ever had to write. Therefore, I am going to stick to the facts. As we learn more, I will post the information.

On Monday, October 1st I brought Mom to the emergency room at Froedert. Her oncologist, Dr. Riche, was concerned about her growing inability to walk. The ER doctor was fairly certain that the problem was neuropathy. But, Dr. Riche ordered an extensive MRI of her brain and spinal cord.

After 8 hours of tests and waiting, the ER doctor confirmed our worst fears. Mom’s cancer has spread to her brain and is pretty extensive. It can best be described as “salt and peppering” the back and top areas of her brain.

She was immediately admitted to the hospital. They put her on a steroid to reduce the swelling caused by the lesions and reduce the symptoms that she has been experiencing.

The hospital doctors met with us the following day. They said that the cancer was no longer curable. They believed that the plan was going to be to administer radiation to prolong her life, which may give her 6 months to a year before her body would succumb to the disease.

On Wednesday, October 3rd, Mom was released at 12:00. At 12:30 we met with Dr. Gore, her radiologist. Dr. Gore was not in total agreement with the prognosis the hospital doctors had given us. She said that although the cancer is considered incurable at this point, many people live with uncurable disease. She said that she will continue to fight the disease, taking it step-by-step. The first step is ten days of radiation. The second step will be determined by how the cancer responds to the radiation.

All things considered, Mom is doing amazing. The resilience of her spirit is her backbone. Her love for her family and friends is her fuel. She meets every day accepting this challenge and amazes us with her determination. Stay strong, Mom. We are with you.

If anyone has specific questions, please call me. I will do my best to return your calls and answer your questions. 262-945-4872

No comments:

Post a Comment