I also had to take JR in for his anterior cruciate ligament repair yesterday morning before we left for Madison. Bill picked him up in the afternoon. He was pitiful last night -- still groggy from the anethesia, cone on his head that he hates, and very sore leg. This picture was taken a few minutes ago. He's still adjusting to the cone and he still looks pitiful! And the back leg that has been shaved is the one with the stitches. He has to go back next week for a check and in two weeks he'll get the stitches removed, so he's going to have to wear than cone for two weeks. Feeding him tonight should be interesting. He did take a "Beggin' Strip" from me this morning though! And so far, he drinks water if you hold the bowl up to him -- but he's going to have to learn how to negotiate the cone and water bowl soon. And it's really getting cold here, so he's going to have to learn to take care of his business a bit faster -- instead of checking out every last oak leaf that has fallen since the beginning of winter!

Things I love:
2. Antique crocks.
Gratitudes:
Finally having a plan and having Dr. Mehta explain a few things about this type of brain cancer. We all felt a bit more knowledgeable after his explanation.
Dr. Ian Robins (who prefers to be called Ian), the oncologist in charge of the chemo -- he explained what to expect. It's always nice to get a little insight on what to expect.
6 comments :
Isn't it nice to have a PLAN. It actually makes us feel like we are doing something. And you are! I'll continue to keep him in my prayers.
As for JR, I hope he heals up quickly. You should be able to take the cone off for meals. As long as you are watching him. Roogrr had the cone a little while ago. What a pain!!
We are still praying for your son and your whole family. I hope all goes well.
Your little dog looks so pitiful! I feel sorry for the little fellow. I'm sure he will pep up soon.
Kristie
Sounds like things will flow now that the plan is in place. You have my prayers!
Hello, Oscar Grimm here. I don't know any of Steve's story, but thought I'd mention that I was diagnosed with GBM about 11mo ago. I’m just getting back from 3.5 weeks traveling over the holidays and have about 300 emails to get back with, so I'll make this quick. I had an MRI on Dec 10 and it showed significant tumor shrinkage, after 7mo of no conventional (American) treatment.
I've studied and learned a lot in the last year, and am now (aside from some residual right-sided weakness from surgery) feeling better than I have felt in roughly 20yrs. I’m learning a lot about all this mess, and am happy to share what I’ve learned. If you or steve would ever like to share research, or even just chat about common woes, please do feel free to give me a call or email. 510.922.1900
Health and Happiness to you. The mind is an amazing machine,
Oscar
Great to have a plan! You are lucky to live so close to great medical facilities. When I would go with my Mom to Boston there were people in the waiting area from w-a-y far away, going through treatments by themselves and showing photos of their kids at home to me. So much better to be able to stay near your family. And I read the comment from Oscar - isn't it wonderful that complete strangers reach out to help?
the news continues to sound better and better on the Plan and about the doctors etc...how very lucky to live close enough to drive and get treatment etc...wish I could be part of the volunteer efforts...I know what it meant to my mom to be driven for chemo rather than fend for herself.
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