LOVE THOSE MACS!!!!
Nurse (MAC addict) Dee
Dee and Chemo Sabe,
HI ladies - Well Kim and I have some news to report. I feel a little awkward using the blog to report this as it represents making this type of change for the first time in over 20 years. Wendy and especially Karen, are not adapting to the news very well, so I will try to tread lightly. First a little background.
Cate and Amanda spent this past weekend in NYC. The Jersey girls, Kim, Wendy, Karen and I hooked up with them for a fun filled weekend. That was the plan anyway - nothing major just go with the flow and have fun.
That pretty much sums up how things were going. We had dinner on Friday talked about friends, life, family and the benefits and challenges with all of those topics. Very deep discussions peppered with a little bit of laughter.
Those conversations continued as we toured Ellis Island and the Statue of Liberty on Saturday. In fact, Amanda made some very compelling points about the pitfall of staying in the same place, doing the same thing whilst expecting different results. I think she said it was the definition of psychotic. She was such a facilitator of change that she immediately got us an appointment with an expert to help us work out the finer points of any transition being contemplated. After all there are a lot of things to think about since people, finances and home arrangements are all considerations .
The result, I really am not happy with the status quo and in fact less happy with what were supposed to be positive changes. I made the decision, I need to make a change and need to do it soon. Needless to say Saturday was a relatively sleepless night.
Our house guests, Cate and Amanda were very supportive of my decision. Who knew, when we called Kim and Wendy in the morning, they were having the same conversations and needed to make a change as well. We met for brunch to see Cate and Amanda off as they traveled back home and Kim and I were left to sort out how we would individually and collectively manage the transition.
This past weekend, KIM and I made a decisionNot sure what you all were thinking but the news I have to share is that we each (individually) purchased iMACS.;-)
The struggle for Karen and Wendy is the move from PC based Microsoft Windows to the MAC OS. That shift has Karen very worried. I understand Wendy has adapted a bit better. Perhaps it is the result of her "CEO job" (tee hee) being less demanding than Karen's nursing responsibilities. Or maybe Kim allows her time to use the MAC. Regardless, we have moved to the enlightened side and I am sure once we get through the differences we will all be fine. That's where the self help books are coming in handy.
My MAC buddy, Kim, keeps asking why she has not made this move before. I'm speechless. I thought Vista would be the solution MicroSoft promised, instead it turned out to be worse than any other piece of software I have ever purchased. An additional bonus is I have a lot more real estate on and under my home office desk in spite of the fact the monitor is MUCH larger than my PC based desk top. No tower and one cord, period; that is a beautiful thing and the one benefit that already has Karen thinking positively. She HATES clutter. Best of all, within one half hour of taking the computer home, it was up and running, with all my PC based files transferred - seamlessly!!! Amanda and Cate thank you for opening our eyes to a better way.
Kim, my MAC buddy, next lesson with Nurse Dee - "skyping" - are you ready???
Not too much news today but no kicks in the gut either (thank God for that). Yesterday was tough. Today was a little shopping excursion (Brenda picked out shoes for me to wear to my niece's wedding next month) followed by lunch out. Then we went to the medical center for a blood draw and an appointment with the radiation oncologist. There were no major plans made there because she needs to finish round three of chemo (that starts tomorrow for three days). After that she will most likely be scheduled for the neurosurgery in a few weeks (if the PET scan tomorrow is good). We got a lot of questions answered by the rad/onc nurse. The radiation won't start until she's healed from any surgery and that takes about four weeks. Surgery won't occur until a few weeks after round three of chemo. Then radiation will be five days a week for six to seven weeks. Head and neck radiation is tough because your throat gets so sore and it hurts to swallow. Staying hydrated and not losing weight are very important. We're looking at an all summer proposition here folks. Brenda is very strong but the enormity of it all is wearing on her. Keep your thoughts and prayers flowing. Keep the cards coming, she gets a big smile on her face when she gets them in the mail. Please post comments on the blog. It is very uplifting when she reads them.
Vicky
Brenda's lymph nodes are significantly smaller. Her white count is good and she won't need additional neupogen for this round. This morning she saw Dr. Hanna (an ENT surgeon who specializes in cranial base lesions). He did a fellowship at UPMC in Pittsburgh. His concern is a spot on the CT scan about the size of a penny. They cannot determine if it is up against the brain (the front part behind and slightly above the nose) or through the membrane that covers the brain (the dura). If it hasn't penetrated the dura it's less complicated.Dr. Hanna is proposing a neurosurgical procedure to remove that lesion. That would be done by a neurosurgeon. It would involve an incision behind the hairline from almost ear to ear. Then they fold down the skin and make a bone window to gain access to the lesion. They then repair the defect with her own tissue. It's on the surface of the brain so they don't have to cut through brain tissue to get to it (that's a good thing). It's also not in an area of the brain that controls speech or movement etc. They will be scheduling an appointment to see the neurosurgeon. If she has that surgery (because all of this is subject to change) she would be in the hospital for five days.
The blip in all this is a CT scan of the chest that showed a "prominent" diaphragmatic lymph node. It did not show any suspicious lesions in the chest, just a lymph node by the diaphram muscle that is prominent. We see reports like this all the time in medicine and usually they are nothing. They are going to do a PET scan to look at that. If it lights up it's suspicious. They are very thorough here and are leaving no stone unturned.
This afternoon she saw Dr. Gillenwater. She's the ENT doctor that saw Brenda when she first got here. She confirmed that the nodes are shrinking. She also said if they have to surgically remove any of the larger lymph nodes in her neck they would probably schedule both surgeries at the same time.
Tomorrow she sees the radiation oncologist and maybe the neurosurgeon if they can get her in. Then a big day on Thursday. She will have a PET scan at 9AM, an audiology appointment at 1:30PM and chemo for 7 hours beginning at 3:30PM. Then Friday another round of chemo in the afternoon.
Hope this helps,
Vicky (AKA: Ribby)
Ok,
Michele has attempted to divert the Pod from the truth about
Blue Bonnet by making a half-hearted parody of herself. Attached is
the true unmasking of BB.
Jeannie