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Day 50

Out of all the side effects of the chemo, I would take exhaustion over the rest. Becca has had very little nausea, which seems to be a gift. She had several visitors today, which she enjoyed. Some were blasts from the past, others were family. It seems to help her get through the routine of hospital life.

50 days is a long time, who would have thought? It seems all a blur to me. We still have a long road and we will continue to rely on a lot of friends and family. I am very grateful for the love and generosity of so many. I know I have written this before, but Sunday seems to be a day of recollection and reflection. We are so truly blessed. A very close friend of mine asked me today about the tag line on the top of the page. It reads, “Our journey through the blessings of Cancer, the power of Prayer, and Faith in our Father in heaven.” I feel strongly that this has been a blessing. With great trials come great victories. Our family is closer than ever. My faith in my Father in heaven is eternal. With faith and prayer we can overcome obstacles. I, like my father-in-law, feel that my glass is half full. There is always a small light somewhere and we can’t sweat the small stuff as life is too short. Please keep your family close and do those things that keep getting pushed aside.

Please keep up the prayers 🙂

Day 49

I was able to take the boys to see Becca again today. They enjoy the opportunity to visit with her, even if it’s not a long time. Saturday seems to be the best day for everyone. She was teary-eyed and grateful for the visit.

We do have good news, we are 99% sure they will release her on Monday to be able to go home! So, until the next treatment (three weeks), she can stay with us now at my in-laws. We will have some home PT & OT come in, but they think she is strong enough and ready to do it. We are all so excited and thankful for the blessing, after so many long days, to bring her back to the house.

So for now, continue praying for her. She is in good spirits, but still very tired. Anyone that would like to visit will need to keep in mind she really doesn’t have an immune system. Don’t be alarmed if we turn it into a mini hospital with face masks and antibacterial wash 🙂 But trust me, any visits are good for her.

Day 48

Becca is doing well today. She is still sleeping a lot, but she still is working hard. We smuggled her today and went up to the 6th floor for lunch in the cafeteria to give her a change of scenery. We came down from lunch and was met by her physical therapist. We were headed out for some fresh air. He asked if we could work her outside and Becca was excited. So here are a few pictures of her playing, I mean working outside.

Becca wanted to do the stairs, but he was apprehensive as they are a bit big. She walked right up them like she had been doing that height all a long.

She is standing there without support. He tries to move her one direction, hoping that she corrects the movement…which she is doing well.

Is Becca actually dancing with another man? Hehe 😀

Day 47

Becca started chemo last night finally… I almost hate to say that. She is doing AWESOME and is just a bit tired, which is a side affect. She worked with PT today and was able to do more than at LDS rehab. The doctors are impressed she is still working out while doing the chemo. She should be on the drip until Monday night. A few have asked when the effects will kick in, she should loose her hair in about 10-14 days. Becca is just fine with that, she said “who cares? it’s only hair and it will grow back.”

By the way, these are the names of the drugs for you google scholors: Ifosfamide, Doxorubicin, & Mesna.

Keep praying for strength and that the tumor will completely dissolve with the chemo… she really doesn’t want surgery again unless she has to. Thanks again for all your love.

Day 46

For all of you keeping score on information from the doctors, we are still waiting for her chemo to start. They were supposed to have started it yesterday afternoon. Apparently the pharmacy received the orders yesterday, but questioned the dosage. They were unable to contact the doctor to verify the dosage by the time they closed. So, they say that they will be starting it now at 4:00 PM (they originally told us 8 AM today on the new schedule). I think it is important they get it right, it’s just a little comical now.

Becca has continued with her therapy, including working by herself in bed… a little bit of an over achiever 🙂 So I thought I would share a picture. Keep praying, she will need it more now than ever.

Becca getting her toes done by her mom… a little R & R.

PT working her out.

Relaxing, taking in the breathtaking view of the Salt Lake valley.