Friday, November 28, 2014

Day +73: Mixed Chimerism Still an Issue


Todd with his Great Nephew Jeffrey at Thanksgiving, November 27, 2014
To follow-up to last week's post, we saw the bone marrow transplant doctor on Monday, November 24, 2014, with no real new news or progress.  After reviewing Todd's CBC blood counts, she concluded that they were stable with no significant decreases.  She had ordered another chimerism study to be drawn that day too.

It was difficult for her to hide her concern.  She recommended that Todd drop down another Tacrolimus pill, from 3 per day to 2 per day immediately. I asked her to give us some indication of her level of confidence that reducing the immunosuppressant would be effective.  She really hated to put a number on it, but I got her to say about  50%.  She tried to encourage us that she was really stepping up the process of removing the immunosuppressant (starting Day+62), because normally, they don't start tapering patients off this drug until they have reached Day +100 and even then they taper it slowly for months.

I confirmed that Todd did have a full intensity, myeloblative allogeneic bone marrow transplant and not Reduced intensity chemotherapy (RIC) which is more common with bone marrow transplant failures.  Additionally, she confirmed that even the timing and the type of medications used in the trial regime wouldn't have necessarily had anything to do with the mixed chimerism that Todd is experiencing. 

She also reiterated that she wants to move the date for a bone marrow biopsy.  Normally, this is done around Day +100, but she wants to do it around Day + 80, which would be around December 5.  She said then they could look to see how many cells are actually in the bone marrow, what their chimerism would be, if there was any presence of the disease (meaning his MDS or blast cells), and if so, at what percentage.

I also implored her to talk about what would happen if removing the immunosuppressant didn't work, and she did somewhat reluctantly.  The most likely scenario would be to harvest stem cells from Todd's brother again, but this time it would be done peripherally,which means they would remove the stem cells from his brother's blood instead of from actual marrow in the hip.  This process would require Todd's brother to receive medication injections prior to the harvest to boost the number of stem cells they could obtain.  However, the process would be much easier on his brother Tom than before.  This 45 second video shows the process: https://www.youtube.com/watch?v=2bTCSslVmKs or this 4 minute video: https://www.youtube.com/watch?v=pZgee5RWccs.  She did not say whether or not he would need additional chemotherapy prior to this transplant, but that they would use a different kind of immunosuppression therapy that would work to suppress Todd's bone marrow right away and not the donor's stem cells like  normal. 

I asked if Todd would be required to be admitted and stay again under close monitoring at the hospital for 30 or more days like before, but she just stated that the process wouldn't be quite as "strict."  She then responded that I didn't need to worry about it; that it was her job to worry about it.  I agreed that it was out of my hands and that she was the professional, but that I would like to have an idea of what might in store just in case, especially since I was planning on going back to work, or finding a job.  If all of this happens, I may not be able to work at all for some time. 

After his appointment, we headed home to spend an entire week there!  We were allowed to cancel his Friday appointment (since it would be the day after Thanksgiving) and return on Monday.  Todd did receive a call from the doctor though late Wednesday night, November 26, 2014, asking him to take away another immunosuppressant/Tacrolimus pill starting that day (cutting them down to 1 tablet/day). She was able to review the levels found in his blood from Monday's results and described the amount found in his system, as "therapeutic" and that this was still too high for him. I imagine she will likely take the last pill away sometime next week. 

Todd's chimerism results showed up on his MYCHART app today: 57% of the cells being from Todd's original bone marrow and only 43% of his brother's donated cells.  This was likely what she saw when she called on Wednesday.  Chimerism results from this week may not be in until Saturday or Monday since much of the staff was off for the Thanksgiving Holiday on Thursday.

Despite this discouraging news, we were so Thankful for Life, Love, Friends, and Family this Thanksgiving Holiday.  We spent Tuesday afternoon with our dear friends Chris and Lynda, with my family on Thursday, and we are planning a dinner tomorrow with Todd's mother.

We are still praying that the removal of the immunosuppressant will be effective.  We go back on Monday, December 3, 2014 for: blood work, an appointment with the bone marrow transplant doctor, and a physical therapy appointment for his frozen shoulder late in the afternoon. 

Friday, November 21, 2014

Day +66: New Bone Marrow Not Engrafting; risk of Transplant failure

Todd's treatment appointment today, Friday, November 21, 2014 started out a bit disappointing. His blood counts have not been going up like they should. As a matter of fact, they have dropped. His whites went down to 3,080; his hemoglobin to 10.6, and platelets down to 37,000 (a few weeks ago they were up to 58,000).

Then the doctor called us about 5:00 p.m., while we were driving home from Cleveland with the results of Todd's latest chimerism numbers from the blood tests they drew on Monday.  More bad news. Instead of his original bone marrow going down to the 0-5% they need to be, they went up!  To refresh every one's memory: The day he left the hospital (October 8) his original bone marrow was at 49% and his newly donated bone marrow was at 51%. The next set of results at Day+49: Todd's original marrow had dropped to 28% and his new marrow increased to 72%.  These results were slow, but good. At least they were headed in the right direction. This week's results:  Todd's original marrow went up to 50% and his new marrow decreased to 50%.  This is not what the doctor had expected.  This is a serious indicator that his newly donated bone marrow is not engrafting. Instead, his original marrow is growing back and taking over.  This may lead to a bone marrow transplant failure.  In this words of his doctor, this is not a rare occurrence, but it is not the common result, which should be full engraftment (New marrow at 95-100%). 

So, what does this mean?  That's what we are unsure of.  Unless they can get his original bone marrow to go back down and his newly donated marrow from his brother to engraft, Todd will likely relapse and have to have further treatment. 

While this development can be fatal if it happens earlier after transplant, this isn't the case at this point.  In that situation the body thinks the new marrow is a foreign invader and tries to kill it not knowing that the chemotherapy would have likely wiped-out all the original marrow, leaving the patient with no marrow and therefore no way to make blood cells.

What's likely happening now in Todd's case is that for some reason Todd's body may have developed some kind of anti-bodies or resistance against the new marrow and is attacking it and taking over (or many other possible reasons that are too technical to understand and explain here).   At least Todd's original marrow is producing some blood cells and the new marrow is producing the other half the blood cells.  The whole purpose of the intensive chemotherapy was to kill Todd's marrow which is not healthy, cancerous, and can't produce enough mature healthy cells.  The purpose of the transplant was to replace the bone marrow that would produce new healthy blood cells with normal blood counts.  If this doesn't occur it is considered a Bone Marrow Transplant failure and can result in a relapse of his disease: MDS.

There are several things that can be done for Todd, but at this juncture, the doctor is opting for the simplest solution: to ween him off  the rest of his immunosuppressant medication (Tacrolimus).  Last week his doctor changed his medication from 4 capsules per day to 3, because his numbers had dipped some.  Tonight, she told him to cut it down from 3 capsules per day to just 2 per day.  She will likely drop them down again next week when we go back.  She said there is still hope that this will allow Todd's body to develop some Graft versus Host Disease to suppress the existing original bone marrow and allow the new to engraft. (See posts on Graft versus Cancer/Leukemia Effect).  So far, Todd has been doing great, maybe too great.  He has had little side effects, little to no symptoms of Graft versus Host Disease, no rashes, no digestion issues, no severe eye dryness, no infections, etc.  He needs some for the Graft versus Cancer Leukemia Effect to work.

This is where God comes in and how you can help!  We desperately need your prayers, that this simple reduction in medication will be the answer to this problem.  This is a critical time.  This needs to work in the next few weeks or it may be back to the drawing board for other, more difficult solutions. 

To gauge how the re-development of the former marrow is effecting his counts, his doctor has also suggested moving up the post-transplant bone marrow biopsy from the +100 check-up point to about Day +80.  She wants to see if the re-growth of his original bone marrow has developed any cancerous blast cells.

To think about the possibility of further re-treatments after everything he has been through is just too much for us to wrap our heads around.  The possibilities could include: another transplant of his brother's stem cells with another new 100 day period of watching and treatments; a new round of different chemotherapy and another transplant from his brother's cells; or another round of chemo and/or transplant with an unrelated donor's cells with the same 100 day follow-up.  I'm trying not to worry about these possibilities and neither is his doctor. 

While it has only been +66  days since the initial transplant, we were in Cleveland for 8 days before that.  Todd spent 31 days in the hospital, endured intense chemotherapy, isolation, nausea, diarrhea, fatigue, lack of appetite, and lack of friends of family.  I have spent around 68 days living in an hotel room/suite, driving to the hospital for 12-14 hour visits or some days overnight visits, away from our home, our three daughters, friends, family, and yes my dog!  Our children have had to be away from their parents and worry about their dad, my poor mother had to be away from her home and my dad while trying to fill my shoes all that time (a job well done, but not for the faint of heart).  Todd and I have had no ability to work or earn an income but instead have had multiple households and expenses to pay for. The thought of doing this again would be too difficult to put into words here.

I guess we will learn more on Monday when we go back to see the doctor.  They will draw blood for another chimerism study in addition to checking his regular CBC counts.  We are blessed that the dropping counts have not yet resulted in the need for any transfusions. 

In the meantime, will you pray?  This journey has been full of ups and downs and twists and turns.  I feel like God is asking us to let go of everything else and trust him completely.  I have been applying for jobs, with no response. The one job interview I had scheduled (for seasonal work) was canceled tonight because they had just finished filling all their openings.   I want to cry out to God: "Why we can't we catch a break!  Why are you allowing things to go wrong? Why are we suffering such financial losses and the loss of things that make us feel secure?"  I want to tell God that "No, I really can't handle anything else!"  But, I know he is trying to teach us through these trials to solely rely on him.

Next week is Thanksgiving.  I want to give Thanks for the lives of those I love and the good health that he has blessed us with.  I understand that every good gift surely does come from above.  Thank you Lord. 

Tuesday, November 18, 2014

Change of Mailing Address:

Now that we've been coming home on the weekends, it would be easier from now on to receive all cards and mail at our home address. Even though Todd will continue to have two appointments per week at The Cleveland Clinic we are anticipating coming home through some weekdays and/or holidays as we enter the final stretch. 

Thanks for your support!

Todd Cade
2984 Kings Gate Blvd
Beavercreek OH. 45431

Thursday, November 13, 2014

Financial downturn: Major side effect of Cancer

One in five American adults will struggle to pay medical bills this year. A sudden accident or frightening diagnosis can touch virtually anyone, unleashing mountains of bills even on the insured. In fact, medical bills are the leading cause of personal bankruptcy, a last resort after millions of families have drained their savings, maxed their credit cards and even refinanced their homes.  - Christina LaMontagne. 2014
Someone recently told me that "Cancer can financially suck the life out of you."  I never thought that would be us, but I'm finding it to be true.  If you are like us, we are not used to being on the asking or the receiving end of the situation. Seeking assistance can have an unfortunate stigma attached to it, but that is why there are programs, organizations, and people who are able to help in a time of crisis.

Loss of Income
First, you have to deal with lack of income.  When Todd began out-patient chemotherapy every 21 days back in April 23, 2014, he left work and went on disability.  This disability was a private insurance policy that he had paid for years while employed.  At first his private disability insurer deemed this as temporary, short-term disability, with a monthly payment at a minimal rate.  During this time, we had the assurances from his employer that we could maintain our family health insurance policy at his normal employee rate.  After 12 weeks, Todd's private insurance policy moved him to a long-term disability status, which meant his disability payment went up by about $500 per month.  I worked as a substitute teacher until almost the end of the school year, the third week of May, 2014.  Of course, there was no work for me during the summer since school was out.  I  haven't been able to work during this school year yet because I left to go to Cleveland with Todd on September 7 and I'll be here through the 100+ days his transplant requires.  We have had to rely on the private disability payments and savings to get us through.

Social Security Disability
I have to admit, I was pretty ignorant about applying for social security disability.  Todd paid the maximum amount into Social Security for years while he worked, but the first time he applied for benefits, he was denied.  We appealed the decision and the request was finally approved, but not retroactive to the original filing date (April 2014), but as of the date he entered the hospital for the transplant (September 2014).  The private disability insurance company was insistent that if the Social Security Disability was approved retroactively, we would have to pay back every penny of benefits he received from them, because there is a rule about not receiving both at the same time.  (We didn't have to do this after all since Social Security did not make it retroactive).   Regardless of when you get approved, you have to wait a mandatory five months before you can get your first monthly payment.  So, that means we will have to wait until March 2015 before we can receive any help.  As frustrating and embarrassing as this may seem, if you have paid into the system and are qualified for benefits, it is a benefit you cannot do without.  Just be prepared for the five month waiting period with no payments! 

Medical Expenses and Insurance Premiums
Second, you have to cope with increased medical expenses. Although we had the assurance of his employer that our health insurance premium would stay the same, things changed unknowingly.  Without any notice, we were "accidentally" cancelled from all of our health insurance on July 31, 2014, unbeknownst to us.  Todd went in for a daily chemotherapy treatment and was turned away because of no insurance. (See blog post http://toddsmds.blogspot.com/2014/08/treatment-halted-due-to-insurance.html)  He did not get to finish that 7-day round of chemotherapy at all.

After sorting it out with his employer, we had to sign a Right to Elect COBRA Continuation Coverage Form asking us to say that Todd had voluntarily terminated his employment and that he now had to go on a COBRA policy (Note: He did sign it, but he wrote that he left due to going onto disability).  Apparently, his employer justified this action saying that Todd was taking leave under the The Family Medical Care Act and not because he was disabled, which doesn't make any sense because No Family Medical Leave was requested by Todd,  nor did any of the appropriate paperwork get filed).  See: https://www.tasconline.com/biz-resource-center/plans/family-medical-leave-act/
We signed and agreed that our insurance premium would only go up from $585.86 to $597.82 which equates his normal employee rate plus a 2% processing fee.  We were surprised by this amount, and asked his employer to verify this, because we were under the impression that COBRA payments should be higher.  But they confirmed it. 

After making two months of payments at this rate, we noticed that our third monthly payment did not cover the new balance of $1,195.64 per month  Once again, we were not told or notified by his employer that our rate had doubled because we were supposed to pay both the employee premium and the employer's share.  When making inquiries, we learned that his employer had a made a mistake and didn't charge us enough those two months.  Instead, they had to "eat" those two months of their half, because they incorrectly charged us.  By law, apparently, they are not allowed to over-bill us to recoup their payments.  At this point, we had no choice to continue our health insurance policy.  Todd was post-transplant and still needed to be in the hospital for several more weeks needing the post-care treatment.  Our children still needed coverage back at home.

After discussing financial issues with other transplant patients in the hospital, we learned of some grants and programs that may be available to us by several leukemia and cancer organizations.  So, we contacted our social worker at the Cleveland Clinic to start the paperwork.  I'll share these organizations later in the blog, but back to the insurance premium story for now.  By October, 2014, while Todd was still in the hospital, we had learned through the another source that our premiums had now been raised to $1,480.66!  We later received a letter from my husband's employer stating that due to the open enrollment period premiums had been raised for the upcoming year to $656.43 per month per employee, and since we were on COBRA, we would have to pay both the employee and employer portion which made the amount $1,312.86 effective November 1, 2014.  This explained some of the increase, but not the $167.80 difference.  After talking to the COBRA administrator, we asked if the employer had raised it to try to re-coup their lost portions from the prior months, and he said they were not allowed to do this, but he would call the employer to confirm the amount.  In the meantime, we called the insurance agent for the employer and learned that since his employer's policy offered the Health Savings account option, which allows for out-of-pocket deductible reimbursement, our policy total was now $1,510.27 per month ($1,480.66 plus 2% processing fee).  In essence, our health  insurance premiums had almost tripled in three months!

So, we experienced the 1-2 punch!  First, lack of income, then triple insurance premiums.   Thank God that the insurance we had was great insurance.  We had already met our deductible by the time the chemotherapy and the transplant procedure began, so we fortunately did not have huge hospital bills like some of the other patients we met.  We did have some co-pays on some of the more expensive drugs/medications Todd needed post-transplant, but they are manageable since we've met our deductible for the year.  Next year, may be a different story.  Starting January, our deductible ($6,000 per person/$8,000 per family) will start over and that is on top of the $1,510.27 monthly premiums.

And we are fortunate.  Most families end up in bankruptcy with medical bills after such procedures.  After talking with some of the other patients we met in the hospital, some received bills of $700,000. just for the transplant day alone!  Total bills for the entire procedure were near $1,500,000.00.

Now the good news and agencies that you can check into:

What help is available: Grants, reimbursements, organizations:
"Be The Match" Patient Services offers various grants depending on the patient's specific circumstances: whether the donor is related or unrelated, whether the transplant is autologous or allogeneic, and whether the transplant takes place at an approved transplant center or not.  Autologous transplants are not eligible.  Unrelated donor transplants are eligible if the donor was found through the National Marrow Donor Program.  Related donor transplants are eligible. There is a criteria that has to be met including a statement of income and expenses.  We contacted our assigned social worker at the Cleveland Clinic who gave us an application for the Hendrick Marrow Program Grant for transplants using related donors.  Contact a social worker at the hospital in which your transplant will take place at for assistance in getting the grant application processed.  For more information visit their website: www.bethematch.org/patient.  This grant is usually a one-time payment/award.

A second source of assistance is through the Leukemia & Lymphoma Society and their co-pay assistance program.  This program can provide assistance to qualified applicants in paying their treatment co-payments, insurance premiums, and medication co-payments.  Go online to www.LLS.org/copay or call 1-877-557-2672.  I will warn you that most of the application process for this program is online.  There will be some verification that will need to be processed, like proof of diagnosis from your doctor, but they handle this directly.  You do have to provide a copy of your insurance card, citizenship/residency proof, and proof of income.  This nice thing about this program is that the award given is usually available for your co-payment claims for a year from treatment.

Another source, believe it or not is the hospital!  First of all, many large hospitals or cancer treatment centers have their own charitable foundations that can assist those in need of financial assistance.  Second, these same hospitals may be able to assist you with your insurance premiums during chemotherapy, transplants, and post-transplant treatments because it is beneficial to them for you to maintain your health insurance.  They can collect more money from an insurance company for these large ticket item procedures than from a person with no health insurance.  And, as a last resort, many people fail to realize that you can negotiate with the billing department of the hospital on final bills.  Many times they are willing to settle for an amount they can collect, than for collecting nothing at all. Options include establishing monthly payment plans and/or negotiating a lump-sum settlement amount. 

Don't forget to exhaust all available national and local sources.  A social worker is your best advocate in this situation.  Even the American Cancer Society can be of some help.  For example, discounted hotel rooms for caregivers and cancer patients are free for a few days and thereafter rates can be reduced to $12 per day.  While I have heard some negative stories about some of the facilities, it may not be the case everywhere.  In the Cleveland area, The American Cancer Society has agreements with some of the Extended Stay Hotels with this type of arrangements. The Marriott Towne Suites we are staying in is subsidized with significantly reduced rates and offer extras such as free shuttle service to the hospital and/or free parking passes for the Cleveland Clinic parking garages which can save up to $100 per month.

I have talked about the Hope Lodge in prior posts, and would like to mention it here.  It too is an excellent resource for transplant and cancer patients and families going through treatment.  The Hope Lodge here in Cleveland provides FREE lodging for the patient and an adult caregiver going through treatment at the Cleveland Clinic.  There is often a waiting list, so you need to have your social worker help get you on the list.  They provide a private room, freezer and refrigerator space, community space with TVs and computers, and a community kitchen for all the patients and caregivers to use.  In addition, various groups (church, fraternities and sororities from Case Western Reserve) come in at least once a week and cook meals for those staying there.

While we were tempted to seek out a second opinion and have the transplant procedure at the Ohio State Center so we could be closer to home, we are glad we stayed with the Cleveland Clinic.  Not only for their great doctors, nurses, staff, and awesome social workers, but for their facilities that allow for visitation from friends and family due to the state-of-the art filtration system and because they are an approved transplant center that has the financial ability to help with subsidies.

Local sources include Cancer Support groups, your church family, friends, and neighbors. A fellow transplant patient was fortunate enough to have meals brought in from church families, and their neighborhood even organized a golf scramble with all the proceeds benefiting the family!  Don't forget to contact your local chapter of the American Cancer Society or American way to see what help they can provide.

Here in Cleveland they have an organization called Touched by Cancer that provides two locations called The Gathering Place, where cancer patients and families can go for counseling, exercise programs, art classes, nutrition classes, music therapy, meditation and relaxation therapy, and other activities at no cost.  http://www.touchedbycancer.org/

I'm sure there are more organizations you can find online or just by making connections with other cancer patients. 

 "How are we doing now?"  
Well, without going into personal details, we are making serious changes.  We are cutting our monthly expenses.  I am looking for a full-time job with benefits so we can get rid of the high cost insurance we have after Todd's treatment period is over.  We are looking into The Affordable Care Act (Obamacare) which is something I never thought we would have to do.  Unfortunately, we are finding that the policy we would qualify for or need would still cost us about $1,000. per month!   I will go back to substitute teaching until I can find something better. Todd's ability to go back to work at this point is not known.  Sometimes it can take up to 18 months for a transplant patients to get their energy level back to normal.  Beginning in March 2015, Todd will finally get his first Social Security Disability payment which will be a huge help.  We've talked about selling our home and downsizing in the Spring to something smaller or renting a home or apartment in Beavercreek so our youngest daughter can continue to go to school there.  Whatever happens, or however discouraging things may seem, we don't want to lose sight of the precious gifts of life and love we are blessed with.  We are trusting in our Great God!


References:
LaMontagne, Christina. March 26, 2014.  Web.  Retrieved from: http://www.nerdwallet.com/blog/health/2014/03/26/medical-bankruptcy/

Day +55: Half way through and a Weekend trip home.

At Todd's Day +55 treatment and doctor's appointment, on Monday, November 11, 2014, everything was on schedule and there were no problems.  His counts overall were good and on the rise, but there was a slight drop in his Platelets.  Two out of four of his CBC counts are now in the normal range.  Here are the results:

White Counts:     4.43 or 4,430. Normal range is 3.70-11.0
Hemoglobin:       11.5                 Normal range is 13.0-17.0
Platelets:              47,000             Normal range is 150,000-400,000
Absolute Neut (ANCs) 3.44 or 3,440  Normal range is 1.45-7.50

We were a little concerned in the drop in his Platelets (went from 58,000 to 47,000), but after talking with his BMT nurse coordinator, she said that they typically see a slight drop in the Platelets from day 50-60 (Not sure why). 

That day, we ran into another former patient that Todd was in the hospital with.  He said he experienced the same drop in his numbers and even had to have a transfusion of blood due to lower hemoglobin at the 50-60 day point.  When asking him about his chimerism or percentage of donor vs. self bone marrow left, he said he had gradual drops in his own bone marrow and that he was now at 100% of his donor's bone marrow cells and 0% of his own.  He had his transplant about a week before Todd.

We also had breakfast with another former patient and friend we meet in the hospital.  She was at a similar chimerism as Todd, but her CBC counts were a bit stronger.  They started reducing her other immunosupporessant, Tacrolimus, just that week.

When Todd saw his BMT doctor later that morning, she said that they would probably begin reducing his Tacrolimus next week.  They also drew blood work for another chimerism report, but it will likely take 1-2 weeks to get the results as usual. 

The best news has been that Todd has not seen an obvious signs of Graft v. Host Disease since he was taken off his first immonosuppressant, Cellcept, last week.  Todd's magnesium results were also steady after reducing his magnesium supplements from 6 to 4 tablets per day. 

I still take his vitals twice per day, and there has been no sign of fever or high/low blood pressure.  Todd is doing so well!  We have no complaints!  Well...except to go home.

Speaking of home, we had the doctor's permission to go home for a weekend visit the first time in two months!  We arrived in Cleveland on Sunday, September 7 and got to go home for our first visit on November 7, 2014!  It was so wonderful.  I was able to cook using my gas range and oven!  We were able to stretch out in our king size bed and sleep with our favorite pillows.  The greatest thing was getting to see our daughters and parents.  And of course, my dog!  I'm sorry to say I didn't take one photo the whole weekend!  We were living in the moment, every moment of everyday!  We didn't get to go to church, because that is frowned on by the doctor (too many people, shaking hands, hugging, etc.), but we hope to go soon. 

55 days down, 45 more to go!

Thursday, November 6, 2014

Day +49: Doctor stops Cellcept immunosuppressant

Todd got a call the next day after his appointment, Tuesday, November4,2014, from his bone marrow transplant doctor with the results from his chimerism study. The cells from Todd's own bone marrow is at 28% which is down from the 58% result from October 8, 2014 but still not to the 0-4% they need to be. 

So, to help the new bone marrow from Todd's brother to engraft better, the doctor instructed Todd to stop his immunosuppressant Cellcept that day.  She hopes this will help by allowing a little  Graft versus leukemia effect to happen. Unless Todd's old marrow dies out there will be a risk of relapse in Todd's MDS. 

That same day I received a phone call from another BMT patient we got to know while Todd was in the hospital. She had a related-perfect-match donor 

I'm transplant a few days after Todd's.  She too received a call from the doctor (we use the same one) to discontinue her Cellcept too. Her original bone marrow cells were at 30% which isn't too different from Todd's. 

Although the doctor is pleased with both recoveries, she is concerned about that percentage being a bit higher than she would like to see. Both Todd and this other patient/friend were part of the clinical trial where they received the reduced amount/experimental regime of pre-transplant chemotherapy. This is a little concerning. We hope that the trial regimen was strong enough to kill off the patients own bone marrow to allow full engraftment of the donor's marrow. 

At this point, there is no reason for alarm. We still have to be on the lookout for any signs of severe Graft versus Host disease and hope that the Graft versus Leukemia Effect will take care of wiping out Todd's original bone marrow which still has MDS. 

I'm sure the chimerism test will be repeated in a few weeks 

Monday, November 3, 2014

Day +48: Numbers Increase and Medication decreases

At today's doctor's appointment, Monday, November 3, 2014, Todd's doctor did not have his latest chimerism study results back yet.  It could be as late as Friday before they come back.  So, we won't know the results until next's week's Monday appointment.

The good news is, that even though these results aren't back, his doctor is ready to remove one of his immunosuppressant drugs named Mycophenolate Mofetil (Cellcept) from his medication regime beginning this Friday.  Under normal conditions, this medication is stopped between days +50 and +60.  So, this Friday, will be Day +52.  The removal of this medication will allow for more engraftment of the new bone marrow, but it can also allow Graft versus Host (GvH) Disease to surface.  A little of GvH is good because it allows for the Graft versus Cancer/Leukemia Effect to take out any remaining original bone marrow.  However, a lot of GvH can be dangerous and/or problematic bringing about a host of secondary problems which I have discussed earlier.

We feel good that the results of the chimerism study will show higher percentages of Todd's newly donated and engrafted bone marrow from his brother, because his CBC blood counts continue to increase at a steady pace as shown in his last three results:
                              Hemoglobin       White        ANC        Platelets
October 27                 10.9                3,110        2,190        50,000
October 31                 11.3                3,840        2,740        57,000
November 3               11.6                4,610         u/k           58,000

His potassium and magnesium results have also been high enough not to need infusions.  As a matter of fact, he is allowed to cut back to only 4 slow-release magnesium tablets per day instead of 6.

While any symptoms of GvH would take a week or more to show up, his doctor thinks he may be ready to go home for a weekend visit very soon.  I'm ready!

I'm getting so tired of hotel living.  The noises, thin walls, weird smells coming from neighboring rooms, and the train that decides to blow its whistle when it comes through about 2 am!  Not to mention that I am terribly missing my family and my dog Charlie!  I miss my bed, my pillow, my kitchen with an oven that works properly, and all my kitchen tools that make cooking so much easier!  My poor mom is ready for some relief too!  (God, please  help her to hang in there!).

We praise God for Todd's good health.  We ask that you remember us in your prayers.  This week specifically: That Todd's body will respond positively to the withdrawal of the medication.  That God will give us all patience and forbearance to endure our living situations a few more weeks.  That God will give us direction in our finances, job opportunities, and affordable health care in the months to come.  Thanks.