September 14, 2017 Bend, Oregon

Sunrise, the Palouse, Washington (24" x 16" Acrylic on linen)
Sunrise, the Palouse, Washington (24″ x 16″ Acrylic on linen)

Still Just Killing Time in Bend

Yesterday was the start of Round Five of my chemo treatments, just one more round to go after this one and maybe I will be able to hit the road again by the end of October and head south for the desert, since Florida and the coast of Texas are now out. I had planned on returning to Rockport, Texas and Goose Island State Park, one of my favorite winter stays, where I  spend my time shooting Whooping Cranes and other birds, but I’m sure the hurricane has made this and  all of my favorite stops along the Texas coast ( such as the beach at Aransas Pass ) something I need to pass on this winter.

So, not sure where I may head but am sure I will eventually end up going back to the BLM areas around Yuma and then maybe on to Tucson, an area I have only visited once before and that was back before retiring, so I didn’t get to explore that area thoroughly.

Am continuing my attempts at acrylics and just finished the painting of the Palouse in spring, as seen from the top of Steptoe Butte. As you can see from the photo of that painting at the top of this post ( you can right click on it to see a larger version ), it didn’t come out too bad, every painting presents me with an opportunity to learn a bit more about these acrylics and this one was no exception. Am beginning to figure out how to blend a little better with these paints as there was a lot of blending to be done on this painting. One of the nice things about staying here at the Family Stay Area at Saint Charles Hospital is the free Wifi signal from the hospital. Not having to worry about my $10/GB Verizon signal, I have discovered  a ton of uTube videos on acrylic painting lessons, and, while most are not all that great, mostly because I am looking for realistic painting styles, there are several that have been quite helpful.

Having little else to do to combat boredom here, I am grateful to have resumed this intense interest in the challenge of learning how to master these acrylic paints. I have to stay here to have these continuing chemo treatments but the treatments themselves, including blood draw, oncologist visit, and infusion treatment for the one drug that is administered via injection, takes only about an hour and a half one day a week. That leaves me with most of the treatment day and all of the other six days to find something to do. Bend is a very nice little city with wonderful surrounding mountains to the west, but extensive forest fires have raged in the area all summer and smoke is everywhere, leaving me with what would have been a debilitating case of cabin fever if not for this resurrected interest in painting. It seems odd to not be out photographing birds and other wildlife after doing so almost every day for the past 4 plus years, but the only use my photo gear gets these days is to take a shot of my latest painting to post on this blog.

But it now does appear that I will be able resume travel, and wildlife photography sometime before winter, and for that I am grateful.

Myeloma Update

Not being able to come up with a “caregiver ” to assist me for a couple of weeks after the hospital stay for a bone marrow transplant has left me ineligible for that transplant procedure, the best hope for an extended period of remission for this relentless disease. However, my oncologist continues to insist that he has never been completely sure that a transplant would be best for me anyhow, saying I may have an equally decent chance of remaining in remission for at least a couple of years or more on a maintenance drug routine. With or without a transplant, this cancer always returns, it is just a matter of how long one can stay in remission and thus off the most powerful drugs ( that eventually take a toll on the body ) that gives you the best chance at a longer survival and a better quality of life living with the disease.

Every thing I read, and he agrees, at this time says that the transplant procedure is the first line of defense in terms of length of remission. However the procedure is no walk in the park and there are some, though still relatively small risks of complications that can be life threatening. Recovery from the transplant can take from a couple of months if you are are lucky, to as much as a year, it varies greatly from patient to patient. And often there are lingering problems from the procedure that never go away such as loss of taste or continuing  fatigue. He points out that some recent studies have shown that the difference in length of time in remission between transplant patients and those going on a maintenance drug regiment only is just a matter of nine months to a year. Since the procedure  essentially robs you of the first three to as much as twelve months of that first year of remission, some oncologists are beginning to lean towards no transplants for some patients, especially for those that have had a robust positive response to their initial drug therapy. And, of course, that is a category I happen to fit in.

After reviewing blood work test results, in yesterday’s conversations with him, my oncologist says he remains amazed at the continuing strong  positive results of this treatment plan. He says everything looks good and progress continues to be made in all realms to getting this thing into remission. He definitely plans to finish up this course of treatment after one final, sixth round and switch me over to an oral maintenance regimen, at which time I can leave the area and resume my travels. I will be required to have monthly blood tests at a hospital or medical facility wherever I happen to be, with the results emailed to him so he can monitor my progress and be able to make whatever changes to the regimen  that may be required. As long as I can be reached via email, he has no problem with my being off wandering anywhere and he will be able to keep up with me via email. He states that he would anticipate no new problems arising during the first two or maybe three years ( with no guarantees of course ) and that when new problems do arise, he says at current, there are eight or nine alternate drug cocktails that can be implemented to get the disease back under control.

But, and this he is most optimistic about, there are so many new, almost daily, updates on treatment and even possible cures for this cancer, that as long as a patient is able to remain alive, there are new ways of combating this coming down the pipeline, the most encouraging, being new T-cell therapy. So, of course, I had to go on the internet and Google T-cell therapy. The links below are a couple of results of this search, interesting reading if you have the desire to do so ( and it spares us from having me attempt to describe exactly what this is all about ),

https://www.cancer.gov/about-cancer/treatment/research/car-t-cells

and

https://www.seattlecca.org/treatments/immunotherapy/immunotherapy-facts/t-cell-therapies

Guess that’s about it for now. Weather here has begun to moderate and turn toward cooler autumn temps, actually is quite comfortable today and is supposed to drop to forty degrees tonight, my kind of weather, still patchy smoke from the fires though.

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9 thoughts on “September 14, 2017 Bend, Oregon”

  1. Keep up the beautiful painting! I do believe you definitely have the hang of your use of acrylics. So glad you are doing well health-wise with your treatments. You are continually in my prayers.

  2. I’m glad to hear the treatment continues to go well and that you have such promising options for the future. And thank you once again for your photos, paintings, and this site (especially the quality of your writing). I just spent over an hour learning more about the Palouse and checking out your annual travel maps.

    1. I have done the Palouse in the fall and in the spring and believe the view at sunrise from Steptoe Butte should be on everyone’s bucket list, it is one of the most breathtaking sites I have ever witnessed. I have always hesitated to visit there when it is at it’s most spectacular, when the heat and rapeseed fields are at peak color in summer because of the 100 degree temperatures, but hope I still get the chance someday soon.

      Thanks for the compliments!

  3. Really nice painting Bob. Have you been using any of the various acrylic mediums or the open acrylics which make them act more like oils? Glad to see that you are still plugging along and that the cancer is not getting the best of you. Looking forward to seeing your next painting!

    1. Using only Golden fluids and water. Have tried several mediums and retarders, etc. but am finding with a little experience, just water will do the trick. Also have just started a couple new paintings using some inexpensive Liquitex Basics and the Golden fluids and kind of like the versatility of that combo. Think I am starting to get the hang of it with these acrylics, just takes some patience. The cancer thing just is what it is, eventually it probably will get me, but who knows when. I remain realistic despite my oncologist’s very optimistic opinion of my chances.

      How goes it in the Upper Valley art world?

  4. Thinking about you and hoping you are going to enjoy yourself with your difficult times. I love your paintings. Hard to find the correct words just wish you all the best in the future.
    Brita,

  5. I love the Palouse painting; it really draws you in and keeps you there.
    Great ongoing news on the chemo and not really having to have the transplant.
    You could look for horse activity up on Steens Mt. Loop Road or Palomino Buttes. They have a brochure you can pick up at the BLM office as you drive into Burns describing the different wild horse areas with maps.

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