Good evening everyone! I can’t believe it has been a week already! Last Tueday, Jen had posted a picture online about this might be the last time she did her vest. One week later, she looks great! I think she is almost ready to take over the blog again. Hope she doesn’t completely though. This has been a good outlet for me through this process. I bet I sleep much better tonight than I did last Tuesday!

Today was another great day here in Seattle. I am really not sure about the weather, but room 5328 was awesome. The morning started off early. Really couldn’t sleep so I headed over early to the hospital. Jen was sleeping, so I quietly slipped in. It takes a good 15 minutes to get acclimated to the temperature in her room with the gown, gloves, and masks. Finally got comfortable and the nurse came in to get blood or give meds. After she finished I grabbed a pillow and slid my chair up the bed. We were both out in just a few minutes. Woke back up about 9:00.

Jennifer’s goals today were to stand up, take a few steps to a chair, and sit down. That happened about 12:00pm. Physical therapy came to do all of that. It seems like it takes longer to get all the cords, wires, tubes, and hoses ready to move then to move Jennifer. She hugs the pillow, since she can’t use her arms. She sat in the chair for an hour and a half this afternoon.

On the second Tuesday of every month they have a support group for people in the lung transplant program. Teresa and I went. There were probably 20 people there today. Jennifer and I attended in November and there were probably 50 people there. There really was no agenda for the group, but it started with introductions. I got to introduce us first and everyone clapped when I said Jen was upstairs recovering. This entire process just blows my mind. I find it completely amazing that just last week, the lungs that are in Jennifer were in someone else. I hope that family is finding peace with their loss and I hope they know that we are very grateful. As everyone in the group was introducing themselves, a common theme was their donor family. Jen and I had talked about what that process might look like, but today really firmed that up. Before being discharged from the hospital, we will register with the life center for the northwest region. Basically, we will send a note to this organization and they will get it to the donor family. If the donor family chooses to respond, we will get a note back. Some people in the group have heard back from their donor families while others have not. Angela, the social worker, mentioned that in last month’s group a gentleman had finally received a note from his donor family 12 years later. Kinda crazy to think about.

It’s crazy to hear everyone’s stories as each one is so very different. I really enjoy listening to the other stories of this journey! From how long they waited (or still are…33 months for one gentleman), to when they got the call, to life after transplant (the good and the bad). One experienced a condition and now is re-listed. The interesting part here is that he only received one lung the first time and the native lung began taking from the transplanted lung. Long story short, when he gets his second transplant he will have two different lungs from two different donors. Another lady, just celebrated her 2nd lungaversary and she is doing amazing. Crazy how the body works.

Another of Jennifer’s goals was to cough! She did a good job getting stuff up. There is still just a little bit of mucus build up that needs to clear. Hopefully that happened today, or it will mean bronchoscopy tomorrow. I don’t want that for her!

This evening she ate her first meal post transplant. Chocolate pudding and a milkshake! They are beginning to wean the tube feed and move to oral nutrition. Tomorrow she should be able to order when she’s hungry and they can supplement at night, if needed.

Finally found a place to call home! Moving in tomorrow. We had some issues with apartments. The biggest issue is…everything is full!!! I found a extended stay hotel that offered suites and a UWMC discount! It is a two bedroom, two bathroom suite. I will let you know how it is!!!!

I was talking with Jennifer tonight and asked if there was anything I could tell the readers. I bet you all know what is coming but…

Her response, “It feels good!!”

I read her the comments from last night from people again this morning. She also says, “Thank you to all of you for the continued support.”

Teresa washed Jen’s hair tonight before heading back to the hotel. She really enjoyed that! She felt good enough before I left so that I could get a hug! I also snuck a kiss too!

Until tomorrow…

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22 Responses to Day 6 – Post Transplant

  1. Rick says:

    Great post tonight. Got me a little teary eyed with the, “It feels good!” Very happy for all of you 🙂

  2. Lindsey Stanton says:

    Love the progress! Everyday is filled with so much change! The body, Jennifer and your family are all truly amazing! Continue positive thoughts and prayers!

  3. Tammy says:

    I’m so happy for you Jen……and so happy hat it “feels good”……I bet you can’t wait to get home…..I know thisis a long recovery….but just think of the wonderful summer you and your family will have….woohoo……Maybe even a bike ride…..I will never forget Jay Starr telling me about his first bike ride…so cool…..Stay strong…..and I love the post…..

  4. Ronnie English says:

    Jen, I’m so happy for you! God is Good!! Emily has been keeping me posted and I’ve been reading Kerry’s blog posts…he’s doing a great job! Thank you, Kerry, for keeping the good news coming. Prayers are continuing daily for all of you and especially for you, Jen! Love and hugs, Ronnie (Emily’s Aunt in Alaska)

  5. Judy Bishop says:

    Hi, Jennifer and family. I am Stephanie Bishop’s mom. I’m very interested in your progress and enjoy the updates. It sounds like it’s going as expected. I have a question for you. Why will you never be able to raise your hands above your head? I don’t understand. My grandson, Jaxon, has cystic fibrosis so I’m trying to learn things as you go through it. I’m really glad you’re doing so good!!

    Take care of you.
    Judy

  6. Vi Jobb says:

    Great news keep hitting those benchmarks ( had to get the education jargon in) one small step at a time and you will be off and running beforebyou know it. Love and prayers
    Vi

  7. Jessica says:

    Wonderful news. Brings tears to my eyes . You are both amazing and have so much love for each other and so much love around you. God is good never forget that ! Keep up the fight Jen.

  8. Doug says:

    The progress sounds incredible… While we know it will be a long while, we are so looking forward to having you two back home…We miss our great neighbors!!!! Go Jen!

  9. Gail says:

    The little milestones are huge everyday. I remember the pillow hugging with Rex’s heart surgeries. Noah and Eli made Grandpa his own Duck’s pillow the second time. Hug that pillow tight, Jen!!! Rex remembers the coughing – the hurt is so good. Sleeping in the chair next to the one you love, holding their hand. So many memories come back from your blog of other surgeries. Thanks so much for your details, Kerry. Times that you are so extra close to the one you love. Treasure every moment you spend with her, even if they seem forever to change to the next milestone. This time will seem short when you both are back in Roseburg playing with your dogs and Jen is healthy!!

  10. Debbie Tuttle says:

    Great news!!! I love reading all the updates and how Jen is improving daily. Greg and Theresa you are amazing parents. Jen couldn’t have had anyone better to go through this lifelong journey . Kerry, Jen is lucky to have you by her side through all this healing. Through all this your love for each other has grown stronger. Jen, you are a trooper. You have so much love surrounding you and so many prayers for you. Some from people who don’t know you, but know your story. Thank you for sharing your story! Keep the courage to continue healing.

  11. Kevin Miller says:

    This is awesome progress!! It is great to hear Jen is doing so well. I hope you are both getting enough rest and the healing continues. Everyone that asks me for an update I tell them to “Read the blog, it is the best place to find out what is going on.” 🙂 Keep up the good work, and don’t hestitate to sneak a kiss and hug when you can, both have amazing healing powers!! 🙂

  12. Doris says:

    Each day you’re able to post miraculous news. Thanking God for continually answering prayers. I’m amazed at all that Jen is able to do ALREADY! Wow!! Keep on “blogging”! It may be therapeutic for you, but its comforting to all your readers. Hugs!!

  13. Lisa Dickover says:

    Congrats Jen and Kerry! So glad you are doing well. Keep it up! Thanks for the updates.

  14. Debbie J. says:

    This is just soooooo AWESOME! Robert and I pray for ALL of you daily – in gratitude for everything you all have been blessed with as well as prayers for continuing strength to carry you through this journey. You are loved!

  15. Amy Peach says:

    You got me teary! Keep working hard. Thinking of you very often. Thankful for donars and their families

  16. Mo Nichols says:

    I so enjoy following this blog and seeing your wonderful progress! You are so awesome! Virtual hugs to both of you,
    Mo
    PS: I’m assuming Kris’ place did not work out?

  17. Vickie Shuey says:

    I’m so glad you are doing so well. My love and prayers are with you both.

  18. Julie Stoffal Weaver says:

    Thank you Kerry for the great updates. Bless you Jen. You are so brave and strong. I cried while reading tonight’s update. We are so happy for all the wonderful things happening. We pray that all this greatness continues.

  19. Rita Dale says:

    So happy to hear such great news. Keeping you in my prayers and sending positive thoughts to you Jen in Seattle.

  20. Carol says:

    Thank you for keeping everyone informed. We are so very excited for you all. May God continue to bless Jen with strength.

  21. Linda Williams says:

    So happy for you, Jen. Kerry, you are an amazing husband. God’s blessings on you both.

  22. Marlys Hobson says:

    Great news. So happy that her time came for this transplant and that it is going so well. I really appreciate the blog as it keeps us posted on all the good news. Thanks for taking the time to do it each evening when I know you are exhausted.

    Glad you found a place to stay that meets your needs. Since they have discounts for UWMC, is it walking distance to the hospital and UW medical facilities or are you still going to be driving back and forth? Allen and I stayed in one over close to a lake when we were up visiting my brother, but it is quite a distance from the hospital.

    Both of you stay rested. Jen to heal and you to stay healthy.

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