My name is Miles, and I am now almost 7 years old. This is me and my Daddy, my Daddy was very sick, he had leukemia. We found out in June 2009, and since then, my Daddy has been to the hospital for lot's and lot's of treatments. He got better for a little while, but then he had to get a Bone Marrow Transplant! It has been tough for my Daddy, for my Mommy, and for me! My daddy still has lots of hospital visits, but he has gotten much better, and has not been sick for almost 2 years now!!! Mommy used to make digital scrapbook kits, but had to stop since she didn't have time anymore, with Daddy being sick. We thought we would give all her kits she has made away for free, but if you like them, maybe you can donate to help my Daddy's medical expenses. Thanks for reading!

Saturday, July 27, 2013

Long time ...

On September 9th of this year, my husband will be marking his 2 year anniversary post Bone Marrow Transplant.  It has been a long battle over the last 4 years, since he was first diagnosed in 2009 with AML - Acute Myeloid Leukemia.  We have been through chemotherapy, remission, relapse, more chemotherapy, transplant and recovery.   Are there still issues?  Yes. GVHD still pops up, sun allergies, meds, and such, but all in all, life is back to "normal" or at least the new normal.  So to all those who have visited in the past, I am happy to give you this update, and hope it is encouraging to anyone out there facing what we have been through the past few years.

Besides all that, I am redoing the site a bit and adding all the scrapbook kits to the front page, and also I am going to be adding in some recyceld craft projects here and there as well.

Thanks for visiting, and keep on checking in!

Saturday, February 18, 2012

Day +170 just an update....

It seems my reports have gone by the wayside since we have been home. But I thought an update was in order for any who are still following to let you know we are all alive and kicking. We have made 1 return visit for a checkup to Karmanos so far, and actually were scheduled to leave tomorrow for the next, but we post-poned it for the beginning or March due to some testing Frank will be doing this week and next on his liver. Oddly enough, it has nothing to do with the leukemia or transplant, but during the rounds of genetic testing, it was discovered he carries a very uncommon gene hemachromatosis, in other words, his liver stores excessive amounts of iron. This led to a round of phlebotomies back in 2010 while he was in remission, but was left on the wayside after the relapse. However, the gene is doing it's thing again, and some more tests and phlebotomies are on the agenda. Just another "little" thing. The only good part is so far, everything can be done here in Laurium, so no excessive travel is required. Other than that, everything has been going well. Fatigue is still an issue, and Frank's hair has just now returned to a state where you wouldn't know it had been gone, although indeed it is a completely different texture than before. Miles is also doing well, and has been enjoying all our beloved snow activities, shoveling, snowshoeing, sledding, and our wonderful neighbors gave him a child's set of x-country ski's they had from ther own children. We have been out once with them, but have not had another opportunity yet as he has been a bit under the weather with a cold. Luckily, Frank nor I have picked it up, but he has been indoors all week, and is just about ready to bust a seam. So all is good for now, and that is all we can ask for :)
Happy President's Day everyone!

Saturday, December 10, 2011

Day +92 Home!!!


We arrived home on Wednesday! It is great to be back home, we left Tuesday after Frank's clinic visit, and spent the night in Muninsing. Once we crossed the Mackinac Bridge, we knew we were "home", what a difference from one side to the other. Frank held up very well over the trip, and we have been settling back in, getting our stuff unpacked, some Christmas decorations up, and just enjoying being home! Frank will see our oncologist up here in 2 weeks, and then it will be back to Detroit the second week of January for the first check-up, but so far so good. One feels so much better being just being here.

We have seen a few of our friends and neighbors so far, and wil get to everyone eventually. But the lights are back on in the Ryan household, shining again on Tamarack Street!

Email

You can email me at: tmfscraps@gmail.com

About Me

My photo
United States
My husband, son, and I live along America's North Coast in the beautiful Michigan UP. Our life was turned upside down in the summer of 2009 when my husband was diagnosed with acute myeloid leukemia (AML). One minute he was in the ER for what we thought was a nasty case of bronchitis, the next thing we know, he was diagnosed with blood cancer, and was rushed by ambulance to the "big" hospital 3 hours away where he underwent induction chemo for almost 5 weeks. After 6 months of chemo treatments, he went into remission, but his AML relpased in April of 2011. He has been through induction chemo again, and 1 consolidation chemo, and now we are starting the long journey of a bone marrow transplant. As far a digi scrapping goes, I used to run desertscraps.com, but I kind of had to "close shop" when my husband was diagnosed, and am just releasing all my kits I made here as freebies.