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Help Hope Live for Jill Ottow

November 21st ~~ The simple sound of the words “double lung transplant” can spin your head around!  As we approach Thanksgiving, I think we all need to be thankful that such a life saving procedure is even possible AND that is has been performed on our precious Jill.  This knowledge gives hope to us all. I, for one, feel honored to know Jill and to share in this journey with her.  I also feel empowered by her story; like no matter what life throws my way, I’ll be filled with hope and up for the challenge. I will think of Jill’s incredible strength and her ability to move past her fears and charge forward toward resolution.  I will also remember the amazing medical team that has saved her life, allowing her to breathe again.  The team that continues to provide guidance throughout her long bumpy road to recovery.  ~  A Friend

Updates (77)

January 18, 2025

A new year, a new life.Well, here I am just under 4 months out from my transplant, walking more than a mile and a half, cooking, doing some housework, driving and visiting with friends and family in small groups.  No oxygen, no cough to speak of.  Slow and steady progress to gain weight and build muscle/strength, good test results and monitoring.  The miracle continues as does my gratitude for every moment, every day.Organ transplant patients are not allowed to receive any information about their donor...the person, age, gender, background, circumstances of their passing or where they came from.  Lung recipients are given a packet where they can write to a donor’s family to express their thanks, which goes through a third party organization passing it to the family. It is up to them to respond or not, something I completely respect..  Apparently, donor families receive the same packet.I have the privilege of belonging to a lung transplant support group with people waiting for transplant and those who have had them. I have been thinking a lot about thanking my donor’s family but worry about being the most respectful I can of their grief and not writing at the wrong time for them.  This week I had asked the support group if any of them had sent a letter and how long after their transplant, getting various answers, boiling down to “it all depends on what is in your own heart.” (of course)  One member said he had not yet written after more than 6 months but then received a letter from the mother of his donor who said she wanted him to know about her 31 year old daughter who died in a tragic accident and that he was the SIXTH recipient of her organs donations.  They live in the same state and are now friends. It is the most incredible thing I’d ever heard.  Just think about the large impact her choosing to be an organ donor has had.  Shortly thereafter, I told my pulmonologist the story, and he reported that he has a patient who wrote every month for a year to their donor family and never heard back.  In the 13th month, when he stopped the letters, he received a letter from the donor’s family asking “where’s our letter?”  The patient continues to send periodic letters updating on his progress and new life.  I think he still does not hear back but now knows that gifts have two very spectacular benefits, what both the receiver and the giver get.John is doing well, adjusting well to not having me so dependent on him.  He enjoys breakfasts and lunches with his friends, his wood projects and his invention of a remote control system for at-home oxygen concentrators, another great thing that is coming out of my illness and transplant.  I’m sure he’ll update you on that soon.  He’s going to Big Bend National Park with some Wisconsin guy friends next month.    We are in the process of adopting a dog and are planning a hopeful trip to Florida in April and a Wisconsin family wedding in May.Life is beautiful.Love and gratitude to each of you,Jill, Jilly to some?

December 4, 2024

December 4, 2024We went for our now bi-monthly Lung Transplant Clinic appointments on Monday.  The first appointment was for the 6 minute walk test.  In the pulmonary world this measure of how much ground you can cover in that time is an indication of lung function.  Jill did great, covering 1200 feet in 6 mins, nearly a quarter mile. All without stopping to rest or oxygen use. This was no surprise to me as this was our first visit to MGH where we did not use a wheelchair to get around the massive hospital. We walked 6 blocks back from a restaurant dinner the night before, then from the hotel to the hospital in the morning and then to 3 different locations within the hospital for tests and consults.The tenor of much of Jill’s questions with the doctor were different from previous clinics.  Rather than only talking about her current health status, many questions were about the future. When can I drive? Can I be left alone? When can I travel?  A side benefit to the clinic was meeting fellow lung transplant recipients and caregivers in the waiting area. There were two recipients who received their lungs shortly after Jill.  Like many of you reading this update, they too were impressed and inspired by Jill’s progress. It is hard for me to fathom that all this took place exactly 10 weeks from the day she was wheeled into the operating room while new lungs were being flown in from Maryland. Amazing!

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Guestbook

November 21, 2024

Jill & John!!!! So glad to hear that the last few days have provided beautiful naps, meals and cards :) Jeremy and I are just back from CO and some busy months so now catching up and wanted to say we have been thinking about you, telling your story to others and gobsmacked by your continued strength, determination, and love of each day...inspirational. From a snowy East St in Fort, we both send our love to you and the fam and hope the coming days include more meals together, Packer wins, Jill winning at cards most days, and plenty of smiles and laughs. xo xo Cynthia & Jeremy

Cynthia & Jeremy

November 12, 2024

Always in our thoughts hoping you are doing well and getting ready for some cards and wine

Ronald Lepri

November 12, 2024

Ron

Ronald Lepri