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Hallelujah Day!!!
Today is transplant day! My mom started calling it Hallelujah Day and it has caught on. It is also considered my new birthday. So I now celebrate my actual birthday (June 6, 1956), my spiritual birthday-when I gave my life to Jesus (Oct 25, 1980) and now my new cell’s birthday (Sept 23,2022).There are a couple of rough weeks ahead so prayers appreciated.
I have no white count, my hemoglobin is below 8 (normal is 12-16). I will get red cells when that hits 7. My platelets are 5 (normal 140-400) so more platelets today.
These numbers are supposed to drop as they are as this is part of the process. In a few days, the stem cells will start to mature into white, red and platelet cells. Then those numbers will start ti go up and I will feel better. This could take 7-10 days. Until then you might hear from David not me. I love you all and so appreciate your thoughts and prayers! Please continue to pray!
Godbless you! 💚 Kay

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An Update
Fun Fact Day: While waiting for the stem cells to be infused tomorrow, Friday, called Day Zero. Did you know today was not only the first day of Fall (where we broke a record here in Houston of 98 degrees)? But it is also NATIONAL ICE CREAM CONE DAY.
HERE IN HOUSTON, we truly are staying and being treated in an International City – literally all nationalities are present. And this diversity is readily apparent in the truly caring people we meet here every day at MDA in the form of nurses, PCTs, doctors and even food service and housekeeping personnel. It is quite fun to meet and share with so many who are special in each their own unique and wonderful ways, as God intended. Esperanza is the Spanish word for hope. That is what we are doing alot of these days. Encouraging and being encouraged with the Hope that God continues to give us. Esperanza has almost a musical ring to it, don’t you think? So we thought we would share the beauty of that.
Last but not least. We are giving you this tidbit that we learned about Dr. Champlin recently that we did not know before. Kay’s transplant doctor. In 1986, during the Chernobyl, Russia nuclear radioactivity explosion where many were exposed to the life threatening radiation, Dr. Champlin and a couple other doctors went over to Moscow to see if he (they) could help save some of those (28 or so) who suffered the worst exposures.The story is told here at this link, https://time.com/5826461/chernobyl-doctor/ and in a 5 part HBO miniseries produced back in 2019. https://www.hbo.com/chernobyl Please take a look. Thanks for following us during this exciting, yet scary time, in your prayers, thoughts and well wishes.
Love,Dave and Kay
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Rest Day
Today (Wednesday 21st) is called Rest Day #1. But let me fill you in on yesterday first. Was a pretty good day. The final day of pre-transplant conditioning (fancy words for strong chemo). I felt pretty good; got in a mile walk; did my exercises; read for awhile (sometimes with chemo focusing is hard) and played a game of Scrabble with David, my most excellent caregiver!Today and tomorrow are Rest Days-no chemo. Though my body will still be processing the chemo. So still side effects to deal with. Besides needing a nap each day, my biggest side effect is no appetite. My caregiver is making sure I eat something and drink my Boost supplements. I am hoping to do a little craft I brought with me today and tomorrow.Then Friday morning,(my mom calls it Hallelujah Day!), I get my donor’s cells. From what I hear it is almost anti-climatical because it is just like getting a transfusion but I am super excited to get them, get through the post- conditioning and get out of this hospital!As always, I/we are so very grateful for your prayers, thoughts and cards. Much love to you all! Kay/David

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Sunday Update
Yesterday(Sunday) was a bit rough. Very tired in the morning but felt better after my afternoon nap. Then was nauseous at dinner time so did not eat. Think I might exist on Cheerios for the next month! A friend who went through a Stem Cell Transplant told me to find a food that tastes good through the chemo and eat it. So Cheerios it is!!! Also supplementing with Protein drinks. Finally done with three showers a day and can wear my own pjs and clothes now. Today (Day-4) I am hooked up to my chemo now (early morning) so will see how the day plays out. I will need Platelets again. I am so thankful to any of you (and really anyone) who donates blood and or platelets. It takes 3-4 donors of platelets to give me one infusion. David brought my family photo banner to my room yesterday. I am enjoying having ‘the fam’ here with me. 😉💚
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Day Two of Chemo
Day 2 of chemo done (day -6)!!! Feeling pretty well. Walking a mile each day so far and doing in room arms, legs and core exercises. Food doesn’t taste too good but making myself eat what I can along with supplemental protein drinks. Three more days of chemo (they give it at 5am!), two days of rest then Friday is the Transplant Day! I am needing platelets every few days. Haven’t needed blood (hemoglobin) for a few weeks. That is expected to change as the chemo does its job of killing cells both bad and unfortunately good ones too. God is in control and we see His hand in so many ways here. Our inpatient doctor, Dr Khouri, is very good, lots of experience and knowledge. He is with me through the next week. The nursing staff become friends quickly. The support staff has been amazing-from patient care techs to food service to housekeeping. Truly such a caring team of people. Truly a God ordained thing that I am here at MD Anderson for such a time as this. Thank you for all your prayers and support. I feel it all the time! Kay


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Thank You

To My Stem Cell Donor,
Thank you! I know very little about you other than you are a young man living in the US and are my perfect match for my transplant. What I know about you without even knowing you is that you are a kind, selfless and caring man. After a few weeks delay, I should get my transplant next week. The road ahead is going to be rough but because of your donation to me, I have a chance at more years of life. For that all I can say at this time is THANK YOU!
Maybe we can converse more personally in the future but for now, please know that I, my husband of 40 years, my five children and ten grandchildren, family and friends all thank you from the bottom of our hearts for your willingness to be a donor for me. May God bless you!Your Stem Cell Recipient
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Angel Nurses

Today God provided two angel nurses.
The one for my platelets- I told her I needed someone who would be able to place the IV in one stick. She did it in my hand – hurt like crazy – but she got it in!
Second after platelets I had to have a blood draw so the doc tomorrow would see a good number. I saw that this older black very thin phlebotomist (she has curly white hair) was working. I have had her before and remembered her. When she called me back, I told her my situation And she said – “no lymph nodes, no tourniquet.”
She poked once and got what she needed. I was almost in tears!
- Love Kay
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The Plan – 9/13/2022

As of today, the plan is to admit to the hospital on Thursday the 15th in the afternoon. 1st chemo is scheduled for Friday. Then Kay will undergo chemo Saturday, Sunday, Monday, and Tuesday.
Wednesday and Thursday will be rest days and the transplant will take place on Friday, September 23rd.
Pray for no fevers or infections as either will delay the schedule.
Today (9/13) Kay will get platelets (go donate blood!) and tomorrow (Wed 9/14) she’ll get a new central line put in.
Extra prayers around the placement of the central line as the last line placed (at the end of August) caused incredible discomfort, swelling, pain, and difficulties before it was removed to try again.
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September 11, 2022

Almost 4 years ago, Dr. Wang (Kay’s MCL lymphoma doctor at MD Anderson) got Dr. Champlin on the phone and said in our hearing.
“Richard, I have a very strong lady here”. “She will need to come to you soon for a transplant”.
She has come along way since then. Although she could not qualify for a transplant (auto type) back then in 2018 and 2019, she does now qualify and need a transplant (allo type, from an unrelated donor’s stem cells).
Dr. Champlin has been, for nearly 30 years, the Dept. Head of the Stem Cell Transplant program here at MDA in Houston, TX. He is world renowned; wrote the book on SCT so to speak and has taught hundreds of other doctors the art and science of the effective Stem Cell Transplant to save people’s lives. We are very blessed to have him as Kay’s primary care doctor.
And now, having virtually conquered the MCL, she has a different cancer called MDS, which again is very serious and life threatening. The B cells in her blood are no longer able to identify and bring about cell death to the cancer cells that might appear in her blood stream. This also is related to her entire immune system being able to keep her healthy from any bacteria, virus or fungus which might try to gain entry to her body and make her sick in some other life threatening way.
She already has in her system a bacteria that is drug resistant. Her only hope is to kill off her entire blood forming system found in her bone marrow, and start again with healthy stem cells engrafted into her system which will come from a blood donor. This person, a 27 year old male, has already donated his blood and they have taken several units of just his stem cells during a process called apheresis. His stem cells are here in the freezer at MDA waiting to be infused into Kay’s body on a day they call DAY ZERO.
DAY ZERO is currently scheduled for Friday Sept. 23rd. Much needs to take place successfully before then, otherwise this date will continue to slip backward. She is needing transfusions for red blood cells and platelets. She has received these now twice in the last 2 weeks. She will have a new CVC or PICC line inserted this week into her left shoulder or arm to receive the infusions she will need. DAY ZERO will also be the day, according to Dr. Champlin, when her donor’s blood cells will go after any remaining cancer cells that are hiding in her body, on a last ditch search and destroy mission, which is what healthy blood cells are designed to do!
She has remained strong until recently, and will need these next 2 weeks to remain in a stable condition, in order to allow the process to move forward. This Thursday she will be re-admitted to the hospital so her care and condition can be closely monitored as she is prepared for the infusion of the new stem cells into her blood stream, which will quickly move into her bone marrow where they will need to mature there (like an incubator for new baby chicks), before it will be able to move into the rest of her body’s circulatory system. She likely will need many more blood transfusions until that ENGRAFTING of the new cells takes hold. They will know within about 2 weeks after day zero, or what they call DAY 15, whether the ENGRAFTING has successfully taken place.
There is no other plan in place for her at this time. She has committed herself to seeing this through. We have no other options but to support her in this decision, and pray that it will be a successful outcome. Nothing is guaranteed. She remains, as always ultimately in God’s hands and under his watchful eye. He loves her even more than any of us will ever be able to.
We will try to do bi-weekly news/status updates, or no less than once a week, if we can. Please understand that she will not be able to respond to texts/calls in person soon, as much as she would like to if she could. But she will continue to grow weaker over the next several weeks, which is to be expected, and then God willing, she will begin to emerge from the treatment and grow stronger later in October and November. She will be in isolation for 90 to 100 days after DAY ZERO, as that is the period that her new cells are maturing and she begins to grow a whole new immune system inside her body. Our activities will be very limited during that period, and no visitations should be planned. She very well likely may be in-patient at the hospital for up to a month or so after DAY ZERO. Then we will come back to stay here at our tiny house through the end of the year.
Kay loves to get cards. They do encourage her heart. She reads each one. Please do not send flowers or plants to the hospital. There is danger of bacteria coming in on them that is too risky for Kay at this time. And not to the tiny house for the same reason. You can continue to send cards to us here at our Tiny House location at the Lakeview RV Resort.
The address is:
DAVE AND KAY LAFRANCE
11911 SOUTH MAIN ST. OFFICE
HOUSTON, TX 77035I will be stopping back here at this Houston address at least twice a week, and taking any items I can back to Kay while she is staying in her hospital room.
We appreciate the prayer support and have felt the prayers of all of you holding us up over this time.
May God continue to richly bless each of you and your families, as he already has for us,
Dave and Kay
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September 4, 2022

A very delayed but necessary update. To my family, friends and fellow warriors: My Stem Cell Transplant is delayed. My donor cells are chilling in the freezer at MDANDERSON waiting for my body to get ready for them. I have been inpatient since Aug26 with fever of unknown/undetectable cause. I have been on strong IV antibiotics all week. We are hoping to go home to our tiny house on Tuesday. The doctors want me to have a week of rest before hitting the re-set button on Transplant.
Though not our timing, we trust in God’s timing. Though we don’t understand, we believe His ways are higher than ours. Our care team has been excellent! Just the right people to care for me. We keep looking up- unto the hills from where our help comes is from our Lord! We appreciate your prayers, support and love during this time. If you happen to see one of our kids or grandkids give them a hug from me. They have been great. They need support too. God bless you all!!!






