Hope you all had a wonderful thanksgiving and weekend. We celebrated with a home full of great friends. A little football, a lot of food and plenty of relaxed conversation. Guinness joined in grabbing a Turkey leg off the buffet table. This after I was extolling his virtues as a dog that NEVER grabs food off the table. Luckily we had all eaten and gone back for seconds before Guinness joined the fun. Joseph was home which was great. Our thanksgiving crowd includes the kids close friends and I think they all had fun.
This past week was the point in my post chemo regimen (about 12 days out from the last day) when my blood counts drop fairly dramatically and I am back to visiting the clinic once a day for platelets and red blood as needed. Luckily I had thanksgiving off!!
Today (Monday) I am also getting a bone marrow biopsy in preparation for th donor cell infusion. The biopsy will tell us how much of the marrow is me vs the donor. It will also let us know if there is any leukemia lurking.
The infusion will introduce more healthy disease fighting white blood cells in an effort to both eradicate any remaining leukemia and boost my immune system. When someone relapses like I did in August, this is standard protocol to get then back to remission. Complications from August until now prevented us from doing the infusion earlier.
If all goes as planned in coordinating with the donor, we are looking to do the infusion within the next two weeks. will keep you posted.
That's it for now. Will post again when I get the results of the biopsy. In the meantime, thanks for checking in.
Love. Maureen
Maureen was admitted to Beth Israel Deaconess in Boston MA 12/16/14 with Acute Myloid Leukemia. She underwent two rounds of high intensity chemo followed by a transplant March 19, 2015. The leukemia was in remission for several months but returned late August '15. Since then Maureen has had several different types of treatment both as an inpatient and outpatient. Currently Maureen is in the hospital (10/17) receiving two different chemo regimens. She hopes to go home soon.
Monday, November 30, 2015
Sunday, November 22, 2015
weekend update November 20
What a few days! This week I have been unusually winded and short of breath. It was to the point where my friend Amy had to wheel me into my appointments Thursday. Thank goodness she was there! I never use the wheelchair but could not get more than a few feet without stopping to rest. Anyway that started a whole new series of tests (including an ekg, walking heart rate and echocardiogram) So here is where we are.
First the EBV...Per the pet scan the Epstein barr virus has not spread to my lymph nodes which is great news. That would have complicated my next phase of treatment (the donor cell infusion).
The shortness of breath and accelerated heart rate could be explained by inflamed lungs from either an infection or a reaction to one of the drugs. It could also be low red blood (leaving me anemic) I did get red blood during my 6.5 hour clinic visit on Thursday (again so grateful a friend was with me!) and feel much better today. I was back in Friday for the echocardiogram and also got platelets
The weekend has been great.
Friday Emma and her great friends Samantha and Caitlyn were in a county wide geography competition called jowdy. For the second year in a row this team won each round and ultimately won the competition. Congratulations girls. A hard one victory and we are very proud.
I was back in the clinic on Saturday and spent the time with one of my closest long time friends from Ohio, Tom. We had so much to catch up on and it was lovely to see him. Jim joined Tom for the Notre dame (Tom is an alum) BC game. What a game! Yesterday afternoon Emma had several friends over who will be joining us with their families on thanksgiving. Their work was complemented by a visit from even more Thanksgiving angels today delivering tables/chairs/linens and providing amazing set up service for the holiday we are hosting here later this week. They did a great job getting our house set up for Turkey Day.
Sooo grateful for our friendships and for feeling stronger. What a fortunate and blessed life I have.
Add to top it all all off Joseph comes home Tuesday and we cannot wait!!
Thanks for checking in
Love Maureen
First the EBV...Per the pet scan the Epstein barr virus has not spread to my lymph nodes which is great news. That would have complicated my next phase of treatment (the donor cell infusion).
The shortness of breath and accelerated heart rate could be explained by inflamed lungs from either an infection or a reaction to one of the drugs. It could also be low red blood (leaving me anemic) I did get red blood during my 6.5 hour clinic visit on Thursday (again so grateful a friend was with me!) and feel much better today. I was back in Friday for the echocardiogram and also got platelets
The weekend has been great.
Friday Emma and her great friends Samantha and Caitlyn were in a county wide geography competition called jowdy. For the second year in a row this team won each round and ultimately won the competition. Congratulations girls. A hard one victory and we are very proud.
I was back in the clinic on Saturday and spent the time with one of my closest long time friends from Ohio, Tom. We had so much to catch up on and it was lovely to see him. Jim joined Tom for the Notre dame (Tom is an alum) BC game. What a game! Yesterday afternoon Emma had several friends over who will be joining us with their families on thanksgiving. Their work was complemented by a visit from even more Thanksgiving angels today delivering tables/chairs/linens and providing amazing set up service for the holiday we are hosting here later this week. They did a great job getting our house set up for Turkey Day.
Sooo grateful for our friendships and for feeling stronger. What a fortunate and blessed life I have.
Add to top it all all off Joseph comes home Tuesday and we cannot wait!!
Thanks for checking in
Love Maureen
Wednesday, November 18, 2015
Quick Update Wednesday 11/18
Hi everyone
In a recent blood test I was found to once again have elevated levels of the Epstein Barr Virus. This happened once before. The virus is something that apparently lives in all (or most) of us at such a low level as to be undetectable. A complication of the transplant is elevated levels of this virus. Apparently the test shows my level is higher than the last time and I am having a PET scan to see if the virus has impacted any of my organs or other parts of my body.
My medical team fully expects to see the virus has not had any undo negative impact. So I am going with that expectation.
The above was communicated over the phone so I undoubtedly missed some things. In my mind the summation is - they saw something they did not like in a blood test but it does not appear to be too bad - I will get another test to be sure initial thought of 'this is not too bad' is confirmed.
We are moving toward the donor cell infusion (I am calling this a mini transplant - it is basically a boost of my donor's healthy white blood cells). If all goes well that will happen within the next 2 to 3 weeks.
Will update again tomorrow.
Thanks for checking in
Love - Maureen
In a recent blood test I was found to once again have elevated levels of the Epstein Barr Virus. This happened once before. The virus is something that apparently lives in all (or most) of us at such a low level as to be undetectable. A complication of the transplant is elevated levels of this virus. Apparently the test shows my level is higher than the last time and I am having a PET scan to see if the virus has impacted any of my organs or other parts of my body.
My medical team fully expects to see the virus has not had any undo negative impact. So I am going with that expectation.
The above was communicated over the phone so I undoubtedly missed some things. In my mind the summation is - they saw something they did not like in a blood test but it does not appear to be too bad - I will get another test to be sure initial thought of 'this is not too bad' is confirmed.
We are moving toward the donor cell infusion (I am calling this a mini transplant - it is basically a boost of my donor's healthy white blood cells). If all goes well that will happen within the next 2 to 3 weeks.
Will update again tomorrow.
Thanks for checking in
Love - Maureen
Monday, November 16, 2015
Monday November 16
Good afternoon! Well I did break out of the hospital on Wednesday of last week (Nov 11). I had some kind of virus that settled in my lungs but the antibiotics did the trick. How wonderful it is to be back home! Joseph was in this weekend and it was wonderful to see him. He and Emma spent the day together Saturday and we had a Staudt movie night on Sat evening. It is kind of nice having him home when all his friends are still at school so we are the only game in town!
I continue to go into the clinic daily for infusion chemo (Decitabine) for a course lasting 10 days. Since I started in the hospital my day 10 actually comes tomorrow! I am also back on the pill chemo (Sorafenib).
Next up in my treatment is likely a donor cell infusion - this is the infusion of white blood cells from my original donor. While the chemo has been very effective keeping my leukemia in check, my greatest chance for full remission is getting a 'boost' of cells from my donor. This will amplify the immune effect so any future recurrence of leukemia will be battled back by my new enhanced immune system.
We held off with this infusion until my previous rash cleared up thinking that rash was graph vs. host.
It does get confusing but I am confident I am on the right course of treatment. I am showing no leukemia in my blood stream which is great. Right now I am a bit tired from the Decitabine. This too shall pass.
Will keep you all posted on my progress and next steps.
Thanks for checking in. Love Maureen
I continue to go into the clinic daily for infusion chemo (Decitabine) for a course lasting 10 days. Since I started in the hospital my day 10 actually comes tomorrow! I am also back on the pill chemo (Sorafenib).
Next up in my treatment is likely a donor cell infusion - this is the infusion of white blood cells from my original donor. While the chemo has been very effective keeping my leukemia in check, my greatest chance for full remission is getting a 'boost' of cells from my donor. This will amplify the immune effect so any future recurrence of leukemia will be battled back by my new enhanced immune system.
We held off with this infusion until my previous rash cleared up thinking that rash was graph vs. host.
It does get confusing but I am confident I am on the right course of treatment. I am showing no leukemia in my blood stream which is great. Right now I am a bit tired from the Decitabine. This too shall pass.
Will keep you all posted on my progress and next steps.
Thanks for checking in. Love Maureen
Monday, November 9, 2015
Monday November 9th
What a gorgeous fall weekend we had. Joseph has started track practice at Bowdoin and is very glad to be getting back on the turf or asphalt or grass or whatever. The first meet is not until January but that will come soon enough. Jim and Emma watched the patriots game on Sunday with some good friends and had a wonderful afternoon. They came to see me at the hospital Saturday we had dinner and watched a few college games.
Yes I am back in the hospital for a quick tune up. In my normal clinic visit on Friday, I had a fever of 100·9. I tried every argument I could think of to get them to agree to send me home. They were having none of it. Periodically over the last 6 weeks or so when my white blood count was insanely low, I would marvel I had not caught a virus landing me back in the hospital. Anyway that time came Friday and while I am sick to pieces of always finding the silver lining, I must say that if I was going to get a fever I am so glad it was on a clinic day so they could act quickly and get me treated quickly.
Today is Monday and I may go home as soon as tomorrow. I also started my next round of chemo which I can continue as an outpatient.
So never a dull moment. I promise you this hospital stay is not a setback. It could have been if it was not treated so effectively. So hopefully I'll be home in the next day or so. Thanks to all of you for your support and prayers. And Thanks for checking in. Love Maureen
Yes I am back in the hospital for a quick tune up. In my normal clinic visit on Friday, I had a fever of 100·9. I tried every argument I could think of to get them to agree to send me home. They were having none of it. Periodically over the last 6 weeks or so when my white blood count was insanely low, I would marvel I had not caught a virus landing me back in the hospital. Anyway that time came Friday and while I am sick to pieces of always finding the silver lining, I must say that if I was going to get a fever I am so glad it was on a clinic day so they could act quickly and get me treated quickly.
Today is Monday and I may go home as soon as tomorrow. I also started my next round of chemo which I can continue as an outpatient.
So never a dull moment. I promise you this hospital stay is not a setback. It could have been if it was not treated so effectively. So hopefully I'll be home in the next day or so. Thanks to all of you for your support and prayers. And Thanks for checking in. Love Maureen
Sunday, November 1, 2015
happy Halloween and weekend update Sunday 11/1
Had a great visit with my brother John last week. Picked him up from the airport and we immediately went to a clinic appointment for a skin biopsy. Not quite the freedom trail for John but it was great for me to have the company. All is trending in the right direction with me. My counts are recovering meaning I do not have to go into the clinic quite as frequently for transfusions. Soon we will have a plan for next steps. I think the medical team would like to see the rash fully gone and my counts a bit stronger before taking the next steps in my treatment. All good stuff. Jim went to bowdoin this past weekend for family weekend. He and Joseph had a nice guys time together dividing their time between campus and the outlets in Freeport Maine. Nicely done boys. Next appt is Tuesday and I will update you shortly thereafter. Thanks for checking in. Love Maureen
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