Author Archives: breathingwithcf
Today marks 5 years since Dan got his transplant. The time that has passed feels long and short at the same time.
I’ve been thinking about how time keeps going lately. It’s hard to accept that this month will be 2 1/2 years since he passed away. I’ve never liked the idea that time keeps growing since that day.
I have also been thinking about this summer… specifically the Great Strides Cystic Fibrosis Walk here in Redmond. The first year after he died, I totally skipped out of town for it. The second year, I attended but could not help lead Team Meyer. This year, I feel I can be more involved again.
So… please join me and mark your calendars for June 3rd, 2017. Walk with me in memory of Dan and his two brothers; and walk to support his living brother and others living with cystic fibrosis.
Here is our Team Meyer site for the Great Strides walk.
I don’t really feel like posting on here anymore (I’m not sure if that will ever change). I don’t really feel like sharing my feelings with the world. But… I am surviving. I am trying to keep busy. I am trying to do fun things. I have some fun things planned. …That’s enough sharing for now.
Tonight, what prompted this post, I was going through some pictures, so I wanted to share these.
Daniel Lee Meyer
February 5, 1979 – September 21, 2014
Daniel passed away at the age of 35, with his loving family at his side. Dan had a strong fight with Cystic Fibrosis.
Dan was born in Eugene, Oregon, to Chuck and Martha Meyer.
Dan grew up in Redmond, Oregon. He received a Bachelor’s degree from University of Portland and Paramedic degree from Central Oregon Community College. Dan was a career firefighter/paramedic with Redmond Fire & Rescue.
Dan married Jessica (Wilken) Meyer on May 14, 2005. He was a member of St. Thomas Catholic Church and the Knights of Columbus. Dan was devoted to his family and friends. He led an active life, played rugby in college, loved to hunt and traveled the world.
Dan is survived by his wife, and son, Jackson (5); parents, Chuck and Martha Meyer; maternal grandparents, Bud and Alice Sizemore; and four siblings, Patrick, Katey, Stephen, and Cheryl (Meyer) Palmer. He was preceded in death by his brother, Jeffery Meyer and paternal grandparents, Nel and Vernon Meyer.
In lieu of flowers, contributions may be made to his surviving wife and son. Contact Redmond Memorial Chapel for information. Services will be held at St. Thomas Catholic Church in Redmond, Oregon. Rosary will be held on Friday, September 26, at 7:00pm. Funeral will be held on Saturday, September 27, at 10:00am.
I miss him so much.
Jackson and I are back home. And it’s quiet. It’s a big change from being in the hospital and constantly having nurses and doctors coming in all the time.
I can’t even describe how I feel. I feel like I’m holding back tears the whole day. They do come out, but I don’t want to be crying all the time. Thank goodness some family stocked my fridge before we got home, cause Jackson and I might have starved this morning. Everyone has been amazing. I am overwhelmed with feelings of love and support. I am so thankful and blessed that I am surrounded by such wonderful people. Thank you everyone for all the comments on the blog and Facebook. Please forgive me for not responding back. I want everyone to know I appreciate the comments, it’s just hard to write back sometimes.
I met with the funeral director today and made some of the funeral arrangements. That’s not a fun meeting, but thanks to Dan’s brother, his wife and the funeral director, it wasn’t too bad.
I have been asked by many, if there is a way to help with expenses. So I have added a “Contributions” tab up top on the blog website, on that page there are three options to make contributions to Jackson and me.
Services for Dan will be held at the St Thomas Catholic Church in Redmond, Oregon. There will be a Rosary prayer on Friday, September 26th at 7:00pm. And the funeral will be Saturday, September 27th at 10:00am.
If you have any questions, please email me.
Yesterday was filled with friends and family visiting us. Dan was able to spend some time outside, it was wonderful. This wasn’t even half the visitors that came yesterday.
A counselor through the hospital came by yesterday and we made this. I know it will be cherished for years to come.
Last night, Dan’s breathing has gotten a little more difficult. The nurse was great and gave him some more medications to help. Today, he has been sleeping quite a bit more compared to yesterday. It’s caused by both using more comfort meds and his body just being more tired. The doctors don’t know for sure, but estimate Dan has anywhere from one to a couple of days left.
Thank you everyone for all the wonderful comments. I know it’s hard to find the right words in times like this, but for me I really appreciate anything you find to say. Knowing so many people support us is so overwhelming, but does help me know that I’m not alone. This is so much harder than I ever imagined.
Today has been very tough. After talking with the doctors yesterday and again today, Dan has decided that he wants to only have comfort care.
That means that only things that are needed for his comfort will continue. They already disconnected his IV nutrition, he will not get his regular night medications, they have taken him off of telemetry (EKG monitoring), they will no longer do vital sign checks or blood sugar checks. He will no longer have to suffer through dialysis.
The nurses and doctors will still be here for him for his comfort. That means he can still have pain meds, it is his choice right now, he has a button to push to immediately get them. He can have medicine for anxiety if he needs it. He can have oxygen still. And they will keep the NG tube in and keep it on suction because it is relieving lots of pressure in his stomach. And tomorrow the Hospice team will come evaluate him and most likely put him officially on hospice. Which just means things will continue as above, they will just monitor and ensure he is comfortable.
We will stay in this same room. We all agree that is the best option too. It’s not the biggest room, but the best thing and actually what Dan prefers too.
Everything we are doing right now is what Dan wants and we (his family) are fully in support of it. We agree with him and are confident that this is the best decision, it’s just not one that anyone ever wants to make or go through.
Please keep him in your thoughts and prayers over the next few days. I don’t know how often I will post right now, sometimes it’s too tough to even think about, but sometimes it’s even a little therapeutic.
Yesterday, Dan has been in the hospital for 5 weeks now.
Today, we will be having a meeting with his doctors.
I will post more once we have some things figured out.
Nothing really new to report. Just going slow. It’s hard to tell if there is any progress, seems like more little steps backwards than forward. The doctors started the golytely yesterday afternoon after Dan finished a 6 hour round of dialysis. Around midnight he started having a tough time. Was getting short of breath and feeling very full and uncomfortable. So they stopped the golytely and then this morning put him back on suction to let his stomach rest some more.
Dan’s mom and sister Katey brought Jackson back to Seattle last night. They had been at home for five days, so it was so good to see them all. It was good to have more familiar faces around. The hospital staff is nice, but they are not substitutes for friends and family. It was especially wonderful seeing Jackson.
Well instead of getting a good nights sleep, the doctor came in at 3am concerned about Dan’s ct scan. The radiologist is reading it as a complete bowel obstruction. The night time doctor was concerned enough that he thought Dan needed a nasogastric tube placed (through his nose down to his stomach). They gave him some ativan to help relax him to get the tube in. They got it in fine and confirmed it with an X-ray. It’s been just under 10 hours and has suctioned out about 500cc’s (half a liter) of gross stomach contents (gross – my very precise medical terminology). An internal medicine team came and examined Dan to see if he needs surgery or not. They have agreed to just let the NG tube suction and give the stomach some rest, so no food at all now. And then will start a medicine maybe tomorrow called Golytely to help clear the obstruction. The doctor said it might take some time to see if that will work. If it doesn’t, then surgery might have to be an option. They aren’t wanting to do surgery because he is at higher risk for major complications, so we are hoping the Golytely helps and it will resolve without surgery. Dan has been resting most of the day so far, the ativan helped. He wakes up occasionally asking what the plan is. He asked for the tv remote once, but was so drowsy he fell back asleep after attempting to change the channel.