February 8, 2026 

Hello Family & Friends!

I know it has been a while since my last post about Matt. I apologize for the wait. So, here goes (I pray I can remember everything). The last day of Matt's 3-day testing, he had two pretty easy tests, compared to the two days before. The same day, we met with Matt's Pre-Transplant Coordinator. She went over his vaccines and informed him that he will have to be vaccinated for Hep B and will have to receive an annual Covid vaccine with his Flu shot. He also needed to start taking vitamin D. She said she would be calling us after the transplant committee met, the following Thursday. After meeting with her, we met with an incredibly kind, soft-spoken and caring social worker. It was wonderful having both Isaac and Megan there. We learned quite a bit from her. One thing she told us that we didn't know is that we are required to have at least $5000 in savings for Matt to be added to the waiting list. We have to provide proof of it. We can do it with fundraising or by selling things. Hence, our trailer and a few llamas, Megan and I had hoped to keep, being for sale. She suggested an organization called Help Hope Love. I am waiting to hear back from them. Some of you have asked about donating. I will let you know as soon as I know more. Matt received the call at the beginning of the week, following the committee meeting. He was told that he had a few things to have checked out, but he has not been excluded. This was a step in the right direction. She said that Matt tested positive for Tuberculosis and would have to meet with an Infectious Disease doctor. He would have to meet with a Cardiologist and wear a heart monitor for 10 days. This is because Matt passed out on the treadmill at Pulmonary Rehab. The Cardiologist who did his Cardiac Catheterization said that everything looked great, he saw nothing that concerned him and that he was saying Yes to transplant. (Yay!) The Endoscope test showed that Matt has a slow esophagus and that if transplanted, he may have to have a feeding tube for recovery. The doctors won't know for sure until he is in surgery. On his full body scan, Matt had possible signs of cirrhosis of the liver. We said he rarely drank alcohol. Unbeknownst to us, there is a cirrhosis Wawa that is not alcohol related. He would need an ultrasound to confirm or dismiss the possibility. If he has it, he can be put on medication. There is also a need to continue losing weight. We are working on that. He has already lost 83 lbs., but he has another 60 lbs. to lose. He is taking it seriously. Matt and I met with the Cardiologist and the Infectious Disease doctor this past Monday. We really liked them both a lot. The heart doctor believes, like we do, that Matt's passing out was due to asphyxiation, not a heart issue. He had a heart monitor put on Matt for the 10 days that the transplant doctors requested. He is wearing it as I am typing this. It is adhered to his newly shaven chest. The Infectious Disease doctor is a silly woman. She actually chose to move up here because she missed the snow she experienced growing up in Pennsylvania. She had been living in Nashville, TN. Indiana certainly welcomed her with a good amount of snowfall. We informed her that she was crazy and that we would have loved to trade places with her. LOL! She said that Matt could have contracted TB as a child or during his time in Marine Corps boot camp, in 29 Palms, CA, or schooling, in Camp Lejeune, NC and that it has been and still is dormant. Matt is not contagious in any way. To prevent it from "rearing its ugly head," he would be started on medication just before or just after transplant. He will go ahead and have bloodwork done to make sure it is not another issue that can cause a false positive. Matt has his liver ultrasound this coming Friday. The Pre-Transplant Coordinator also informed us that the committee is now requiring that we have $8,000 in savings before they will add us to the list. This is because I am self-employed and plan on not working during Matt's recovery. This basically means that if Matt ends up being cleared medically, it could be money keeping him from a transplant. So...does anyone need a trailer or any llamas? Thank you all for your continued love, support and prayers. This would all be so much harder if it were not for every one of you. We can never have too many prayers. I will continue to keep you all updated. I will do my best to do it sooner next time. Take care of yourselves and God Bless you all.

Matt & Erin

Another Update On The Same Day ~ 10/24/25 

Hello Family & Friends!

Dr. Jha just called Matt, personally. He believes that Matt definitely has Rheumatoid Arthritis and that is what is making his scarring in his lungs worse. Dr. Jha is going to go ahead and start Matt on a long round of Prednisone plus another steroid called Cellcept. He will be on them for at least 2-3 months. Unfortunately, the Rheumatologist is booked until May. We are hoping that maybe Dr. Jha can get him into another specialist or get him a much earlier appointment.

Until our next update, take care.

~Matt & Erin

https://www.caringbridge.org/site/d748b785-b463-11f0-9946-1147d21a3fd1/post/1fcf3b8b-29c3-4de7-a52c-5a5e2d7d7eaf

New Problems To Face ~ 10/24/25 

Hello Family & Friends!

On 10/24/25, Matt had blood drawn for 9 blood tests. Dr. Jha's nurse just called. Most of his results were normal. However, his rs factor number is very elevated. He is now going to be referred to a Rheumatologist to find out if he has Rheumatoid Arthritis.

He also had an echocardiogram done that day. Here are a few of his results:

Technically difficult study. (Who's surprised, it is Matt after all...hahaha)

Left Ventricle:

Left ventricular systolic function is low normal with an ejection fraction of 50%. There is grade 1 (mild) diastolic dysfunction and normal left atrial pressure.

This is not a big concern, right now, but it is something Dr. Jha is going to keep a close eye on.

IU has responded to Dr. Jha's referral and should be calling Matt sometime this week to make appointments to start his medical work-ups for the transplant list.

Matt's condition has been given a name. He has Chronic Interstitial Lung Disease (ILD) With Worsening Fibrosis. He is going to start taking a new drug, named OFEV (nintedanib). It has to be mailed to him. It took a long letter from Dr. Jha to get our insurance to cover it. We count this as another blessing. The OFEV won't reduce or eliminate the scar tissue already in Matt's lungs. Hopefully, there will be a decrease in the progression.

One of the most difficult changes Matt is facing right now is that he just got his first pair of glasses, ever. They have progressive lenses, too. I think they make him look quite distinguished. After he kept acting as if it was a horrible thing, I reminded him that he needed to be careful because I have been wearing glasses since Middle School. His mom was four when she got her first pair. Many of you know how it is. Well, except for Isaac. He tried to tell us that he "lost" his $400+ pair of glasses within the first week of having them. It's funny now.

Don't hesitate to reach out and ask questions or just to chat. Please continue to keep Matt in your prayers. This is all a lot for him to take in and work through, mentally and emotionally. I am trying to keep his spirits up and remind him that he is in the right hands now, but we all know how well he listens to me. Lol! We truly appreciate your continued prayers and support.

~Matt & Erin

https://www.caringbridge.org/site/d748b785-b463-11f0-9946-1147d21a3fd1/post/aa514797-b973-402a-a2cb-4eea8655f70d

Meeting The New Pulmonologist ~ 10/8/25 

On 10/8/25, Matt underwent a new High-Resolution CT Scan, from under his chin to his waist. This was for his new Pulmonologist, Dr. Jha (pronounced jaw). We really like him. He is very blunt and honest and we appreciate that. Unfortunately, Matt's lungs are getting worse. Dr. Jha said that Matt is too young to be dependent on oxygen 24/7/365. He wants to do better for him. So, he is referring Matt to IU. This is a great thing. Matt will get more extensive testing and the doctors there should be able to do more to help him. That is also where he would have to go to be put on the lung transplant list and Dr. Jha wants him on that list as soon as possible. It all sounds very scary, but it will give Matt a much better quality of life. Dr. Jha says all of this is going to be a lot to handle and it will be absolutely exhausting. We are praying that we will hear from IU within the next month or so.

Matt was put on Ozempic for his type 2 diabetes. As of his last appointment, he has already lost 80 pounds. Dr. Jha says Matt will need to lose at least 20 more pounds to improve his chances of getting new lungs. He should be able to lose at least that much.

Please keep Matt in your thoughts and prayers. Prayers of thanks are always appreciated, too. We count all of this another blessing. We will continue to keep you all updated. Thank you all for your support.

~Matt & Erin

https://www.caringbridge.org/site/d748b785-b463-11f0-9946-1147d21a3fd1/post/a6b7e968-a964-4931-8792-5c601dc56580

In Case You Didn't Know ~ 10/8/25 

Hello Family & Friends!

Matt and I believe this is the best way to keep all of you updated on Matt's health. This is much easier than calling everyone and explaining everything, over and over.

For those of you who may not know, or are too "afraid" to ask, Matt is on oxygen because his left lung is more than halfway full of scar tissue. Who would have ever guessed that pigeon dander could cause so much damage and scarring?

We have included pictures of his CT scans, one year apart (click on it to see both). It's also a reminder of why he's on oxygen 24/7/365. He is more than likely going to need a lung transplant. We have been together for more than 30 years. Like everything else we have faced in our lives, we will face it hand in hand and side by side.

We will continue to update you as we learn new results and plans. We thank everyone of you for your kind words, positive thoughts and continued prayers.

Matt & Erin

https://www.caringbridge.org/site/d748b785-b463-11f0-9946-1147d21a3fd1/post/d7e2c14a-b463-11f0-8e5f-916287ba3049