Showing posts with label allogeneic bone marrow transplant. Show all posts
Showing posts with label allogeneic bone marrow transplant. Show all posts

Wednesday, October 26, 2016

October 24-25, 2016. On our own; Out of the Hospital

I can brag now that we made it through the first night out of the Hospital, October 24! We survived one full night outside the hospital with no fever! Thank God. I was afraid to post last night that Todd was discharged from the hospital; there was a slight delay as he developed a rash on his torso. After examinations, the doctors thought it was a reaction to the oral antibiotics they started him on before discharge. So, they changed the prescription and we were off out of downtown Houston and onto a 5 lane highway going 35 miles per hour heading towards Pearland, a suburb south of Houston.

Our hotel is great! The beds so comfortable. We got dinner and slept in late. No fever!

We learned yesterday, October 25, 2016, that the Bone Marrow Transplant Team/Lab processed the blood from the kids and Todd's other brothers for the bone marrow match. All of the kids were a match, but Abby was the closest match.  Todd's half-brother Paul was also a good half match, but not quite as close as Abby.  At first the Transplant Team wanted Abby out here this week! As soon as we started making plans to fly her out, they informed us that they had not received the needed insurance approval to run the tests on Abby, the donor. So we are hoping to get her out here early next week. Thanks to all who have donated to the Go Fund Me Account; now we can fly Abby out here and house her with us.

Our second day at the hotel, Todd did not get out at all.  I had a difficult time getting him up or awake in the morning and afternoon, so I called the nurses' line.  They told me to keep an eye on him and bring him in if I felt uncomfortable with his excessive sleeping.  By early evening, he ate some dinner and sat up in bed the rest of the night to watch TV, including the first game of the World Series in Baseball (cheering for the Cleveland Indians over the Chicago Cubs!). 
Leaving the Hospital after being admitted for Fever.



Wednesday, October 5, 2016

Acute Myeloid Leukemia with MDS Diagnosed; Treatment Decided Oct 4, 2016


 Induction chemotherapy -
Chemotherapy given to induce a remission. 
      This term is commonly used in the treatment of acute leukemias.     Chemocare.com 2002-2016

After 6 days at MD Anderson Cancer Hospital, the doctors finally had enough information from the test results to make an official diagnosis and propose a game plan for treatment.  On Tuesday, October 4, 2016, Dr. Benton came by in the morning with the much anticipated bone marrow results.  Todd's blast counts were at 21% which officially puts him into the diagnosis of MDS with Secondary Acute Myeloid Leukemia (blasts > 20% in the bone marrow).  While the full genetic panel was not back, the bone marrow flow cytometry report revealed a positive major genetic mutation marker known as CD56, also known as NCAM1, Neural-Cell-Adhesion-Molecule 1.  This mutation stems from a translocation of the 8 and 21 chromosomes [t(8;21)].  Having this mutation puts Todd at risk of the Leukemia infiltrating the blood/brain barrier and entering the central nervous system.  The Transplant Fellow explained it as follows:  There are very few or no cells in the spinal fluid sac that surrounds the brain and spine.  You usually don't find any white or red cells in there.  With this mutation, the blast cells CAN penetrate this barrier and can be found in the spinal fluid.  AS A PRECAUTION, they will do a "lumbar puncture" or spinal tap to collect spinal fluid for testing, to see if it tests positive for blasts.  As an additional precaution, they don't wait to get the results back to treat this area.  Instead, they need to replace the fluid they remove with something else to avoid a spinal headache, so they insert a type of chemotherapy into the spinal fluid to kill any potential blasts cells there.  Of course, we already know that Todd has the TP53 genetic mutation that makes it more resistant to treatment and he has the IDH1 mutation. 

To treat the AML, Dr. Benton and his colleagues recommended using a study trial regimen available only at MD Anderson. (Trial #2012-1064).  Instead of the standard of care treatment given everywhere else, known as the 7 + 3, where they give 7 days of cytrabine and 3 days of daunorubicin, they will use four drugs in a 5 + 5 day trial treatment called Decitabine + CIA

The first 5 days they will give him a drug called Decitabine a Hypomethylating Agent (HMA) used to prime the leukemia cells to accept the other drugs.  Then they will give the CIA:
Clofarabine 5 days, Idarubicin 3 days, and Cytarabine (Ara-C) 5 days.  The Idarubicin is given less days because it poses the most toxicity, especially to the heart. 
According to the Trial information posted on clinicaltrials.gov, the following regimens are possible:


Drug: Decitabine     Purpose:
Other Name: Dacogen (DAC)
Purpose: Designed to damage the DNA (the genetic material of cells). This may cause cancer cells to die. 
Phase I and II - 20 mg/m2 by vein daily for 5 days (days 1-5)

Drug: Clofarabine
Other Names:
  • Clofarex
  • Clolar
Purpose: It is designed to interfere with the growth and development of cancer cells.
Phase I Starting Dose - 15 mg/m2 by vein daily for 4 days (days 6-9)
Phase II Starting Dose - Maximum tolerated dose from Phase I (number of days selected based on Phase I portion).

Drug: Idarubicin
Other Name: Idamycin
Purpose: Designed to damage the DNA (the genetic material of cells). This may cause cancer cells to die. 
Phase I and II - 10 mg/m2 by vein daily for 3 days (days 6-8)

Drug: Cytarabine
Other Names:
  • Ara-C
  • Cytosar
  • DepoCyt
  • Cytosine Arabinosine Hydrochloride
Purpose: Designed to insert itself into DNA and stop the DNA from repairing itself.
Phase I and II - 1 g/m2 by vein daily for 5 days (days 6-10).  Clinicaltrials.gov, 2016.
                    
    We have not been told whether he will be part of Phase I or .  The whole intention of this "induction" chemotherapy is to get the Leukemia into remission.  The most upsetting revelation of this remission is that with AML, remissions are short-lived, and each time there is a relapse of disease, another remission will be harder to achieve and will be of a shorter duration.  The first remission after the first induction usually lasts <6 months.  According to Texas Oncology, "If a complete remission is achieved and no further therapy given, over 90% of patients will have a recurrence of disease in weeks to months."  (Texas Oncology.com 2016).  Because of this realization, we have agreed with Dr. Benton that Todd will have this induction with the intention of pursuing a Second Bone Marrow Transplant as soon as possible. 

    It can be difficult though to get a non-related donor lined up in a short period of time.  When Todd had his first transplant, he was fortunate to have a perfect match with his brother Tom.  However, since Todd relapsed so quickly after the transplant, they would rather use a non-related matched donor this time.  Dr. Benton brought in a transplant doctor and a fellow here at MD Anderson to consult in the matter.  They came by today to discuss transplant options.  It was his opinion that finding a non-related donor from the National Bone Marrow Registry who would be ready to donate, (Be the Match) may take up to 3 months!  It was his opinion that we did not have that long to wait if at all possible. 

    After the first induction, they like to wait for the bone marrow to recover but not long enough for the cancer to return.  In this case, they could do a second round of chemo called "consolidation" until the bone marrow donor is found and ready to donate.  For this reason, he was very interested in screening our three kids to see if one of them would be a haplomatch (half full match).  Abby, was screened at registered when S.A.M./Sharing America's Marrow came to the University of Cincinnati to recruit donors during her freshman year.  She actually volunteered with Sam and her sister during their visit. 

    Consolidation chemotherapy -
    Chemotherapy given once a remission is achieved. 
    The goal of this therapy is to sustain a remission. 
    Consolidation chemotherapy may also be called intensification therapy. 
    This term is commonly used in the treatment of acute leukemias. Chemocare.com 2002-2016

    We would have the option to have the transplant here at MD Anderson or back at the Cleveland Clinic.  However, traveling after induction can be risky.  In addition, MD Anderson has more options here than Cleveland does.  They may have different pre-transplant conditioning and/or suppression therapy after transplant than Cleveland.  Also, if Todd was to relapse once again after transplant, there are more trial and treatments options here for him.  For this reason, we have asked Dr. Hamilton at the Cleveland Clinic to transfer the donor search from there to here.  The team here will continue the search, including sending screening kits to our three children. 





    I took Todd downstairs today to the MD Anderson Hair Salon for Patients.  He wanted to have his head shaved before starting the chemotherapy.  The Salon is ran by the Volunteer Services Department, but the wonderful hair stylists there are paid by the department.  They will wash and style hair, or trim or shave hair and they assist with wig selection and styling.  Todd is still handsome without his hair!

    After getting the insurance approval today, the trial nurse came by to discuss the treatment with us and have Todd sign the consent.  We knew we would work well together when she asked Todd if he was a Bengal's fan!  Her husband is from Cincinnati and she has been converted too! 

    The thing I found the most upsetting when discussing Todd's treatment was the topic and discussion of putting Todd is "Protective Environment" after the first round of chemotherapy induction.  It is something that is only done here, because they have always done it this way.  They gave us two options: the Protective Environment or Discharging him on the Fast Track.  From one extreme to another.  PE is when they put patients  50 years or older with AML just off of induction therapy in a special room for over 20 days, where there is no bathroom, a special HEPA filter, no family allowed inside, etc. to help protect the patient from getting infection and being able to detect and treat a fever or infection right away.  I would only be allowed to come visit in a visitor's room connected to Todd's room where I could speak to Todd only through a glass window between.  I could not touch him or help him.  But, doctors, nurses, cleaning people, and the food service people would be allowed to come and go with proper attire (shoe covers, protective clothing covers, masks, and gloves) but not any family!   There is no real research or data that "proves" that PE is more effective. Even though Todd is only 47, he is close enough in age for them to think PE was a good idea.

    I thought it was a bad idea, because of the lack of mental and physical support the isolation would cause.  Todd and I have been through a lot together and I can't imagine not being there to help him, comfort him, hug him, and encourage him.  He felt the same way.  If he goes into transplant after treatment, he will have to stay in the hospital another 30 days. 

    On the other spectrum, the Fast Track program would allow Todd to be discharged right after chemo induction and then he would have to return every two days for treatment like transfusions, check-ups, etc.  We would have to stay within 10 minutes of the hospital in case Todd spiked a fever over 100.9; he would have to brought in within 30 minutes even if it was just a neutropenic fever and not an indicator of an infection.  Apparently, an infection can take hold fast. Any fever over 100.9 would always necessitate being admitted.  It is not uncommon for these patients to be admitted several times during the Fast Track process.  He would have to be readmitted at some point when the transplant conditioning begins and/or if consolidation therapy was needed (not sure about this). 

    This made the decision difficult.  Finally, we got a social worker to come in and talk to us.  She said that we had the right to say what we wanted to do and that some patients in the past was able to do a "modified environment" where we could just stay in a regular room like now on the leukemia floor.  She said she wishes she would have been here when the doctors were rounding and she could have told them of this other option.  Today, when the doctors rounded, we just told them that we didn't want Todd to go to PE; instead we preferred a modified environment.  So, hopefully, this has been accepted.  We will see. 

    The social worker gave me a substantial list of places to stay nearby.  I have to start calling right away to get on several waiting lists.  Even if we don't do the Fast Track option, we still will need housing post-transplant. 

    I know I am probably forgetting to include so many other things but that is all I have time to blog now.  I will say that Dr. Benton hopes that the size of Todd's spleen could start going down soon after he begins the induction therapy.  This would be a big bonus!  He would be able to get off some of the major pain medicine he has been on the last couple of weeks, just to cope with the pain of the enlargement. 

    It is late, and Todd was able to start his first round of Decitabine tonight about 9:00 p.m. DAY 1 Cycle 1. They started him on 42 mg (amount adjusted according to Todd's weight) at 50 ml/hour.  No transfusions were needed today, Wednesday October 6, but he had one unit of blood yesterday, Tuesday, October 5, 2016. 

    References:

    Chemocare.com  2002-2016.  "Chemotherapy Terms." Cleveland Clinic. Web. Retrieved from: http://chemocare.com/chemotherapy/what-is-chemotherapy/chemotherapy-terms.aspx

    ClinicalTrials.gov.  April 26, 2016. "Decitabine Followed by Clofarabine, Idarubicin, and Cytarabine in Acute Leukemia." Trial Identifier: NCT01794702.  Web.  Retrieved from: https://clinicaltrials.gov/ct2/show/NCT01794702

    Texas Oncology.  2016. "Acute Myeloid Leukemia Induction; Overview".  Web. Retrieved from: http://www.texasoncology.com/types-of-cancer/leukemia/acute-myeloid-leukemia/acute-myeloid-leukemia-induction

    University of Texas, MD Anderson Cancer Hospital Webpage.  2016.  Trials.  "Study #2012-1064 Phase I/II Study of Decitabine (DAC) followed by Clofarabine, Idarubicin and Cytrabine (CIA) in Acute Leukemia." Retrieved from: https://www.mdanderson.org/patients-famiy/diagnosis-treatment/clinical-trials/clinical-trials-index/clinical-trials-detail.ID2012-1064.html



    Thursday, December 11, 2014

    Day + 86: MDS is back after Transplant

    We received the sad news today from Todd's doctor that the preliminary bone marrow biopsy showed that Todd's MDS has relapsed, finding 6% blast cells. The doctor has recommended that he start Chemotherapy on Monday, December 15. 2014. 

    They will be giving him Vidaza, the same chemotherapy he had before going into the hospital for the transplant. He had good results with it then. Those four rounds were able to get him into remission before the transplant. So this is encouraging. 

    It is easy to be frustrated when his condition is right back where it was in March 2014, except at that time  he had about 8% blast counts. It's disappointing to go through the entire transplant process, only to relapse before the crucial 100 days post-transplant period. 

    We are trying to arrange to have the chemotherapy administered locally like before, but if they can't get him on the schedule on such short notice, we will have to do it at the Cleveland Clinic all of next week. 

    What happens beyond this first round of chemotherapy is not known. The doctor is still planning a strategy. It is likely that he may still need a second transplant from his brother's stem cells if all goes well. 

    Meanwhile, we are back at the Cleveland Clinic tomorrow for blood work and possible treatment. His blood counts dropped this past week close to the threshold of requiring  transfusions. His white count went as low as 1.45 or 1,450. His hemoglobin was as low as 8.7 and his platelets dropped to 23,000.  Transfusion thresholds: Blood is given at <8 Hemoglobin and platelets given at < 10,000. 

    The last few days he has felt achy and nauseated. This could be because of his low blood counts and being off the immunosuppressants. His hip seems to be more sore and achy than any of the past twelve times he has had them done. 

    We are trying to stay positive in light of this unfavorable news. Please continue to pray for healing and guidance for us and the doctor. While we still have confidence in her and the transplant team, we are not ruling out a second opinion. There are several treatment options that the doctor can recommend, so we pray that God will guide her choices. 

    Tuesday, December 9, 2014

    Day +84: Biopsy scheduled Today Dec. 9, 2014

    On Sunday afternoon, December 7, 2014  Todd received a message from his online "My Chart" that the BMT Team finally scheduled his bone marrow biopsy for Tuesday, December 9. That meant we were going to have to be at the Cleveland four days this week!  This was too much since we have been trying to drive home in between appointments on Mondays and Fridays. This week, however they had scheduled his doctor's appointment on a Wednesday instead of a Monday with 3 treatment appointments Monday, Wednesday, and Friday. I think the schedule was changed due to his doctor's schedule. He hasn't needed a Wednesday appointment since the first week he was out of the hospital. 

    Todd decided he wasn't going to go up for his Monday treatment appointment, so I called the doctor's office to rearrange this week's schedule. We decided to drive up on Tuesday for the biopsy and spend the night so we could be there early for his Wednesday treatment and doctor's appointment. 

    We won't get the results of the bone marrow biopsy for about 4-7 days and then the cytogenetics will take a few more days longer. They are looking for a few specific things. 

    First, that there is bone marrow from the engraftment. If there is no significant amount of engrafted marrow this would likely indicate a failure in the BMT. 

    Second, they will look at the chimerism of the cells present: how many are from his own original bone marrow and how many are from his brother's donated marrow that has engrafted. 

    Third, they will look to see if there is any disease present (MDS). They can determine this by looking for blast cells and/or the type of blast cells, and how many there are. 

    It looks like they are going to do a CBC today and/or tomorrow to check his counts. 

    We are expecting good news. We have been praying that God would bless us, and Todd's body specifically. We are praising God in advance for his wondrous mercy. Please continue to pray on his behalf. 

    Friday, December 5, 2014

    Day +80 Good end of a discouraging week

    Monday's doctor appointment (December 1, 2014) and blood work left me discouraged. His white counts dropped to 2,440; hemoglobin dropped to 9.9; and platelets to 32,000. This news combined with last weeks' chimerism results left the doctor concerned too. She said they were going to schedule a bone biopsy, but as of this posting we have not heard from the scheduler. The doctor also discussed using a dose of steroids if his chimerism continues to show increased cells from the original bone marrow and dropping counts. She said this treatment is "somewhat controversial" but didn't say why. 

    While the latest chimerism results were not back that day, Todd received a call on Tuesday from his nurse coordinator that his cells from his original bone marrow had increased to 60% which means his brother's donated cells were only at 40%. On Monday, the doctor told Todd to cut back on his Tacrolimus/immunosuppressant to every other day starting Wednesday. However, after the chimerism results were back the nurse instructed him to terminate the medication starting that day. It is the doctor's hope that removing the immunosuppressant will stop suppressing Todd's new bone marrow and allow it to take over and increase. 

    Tuesday night I had hit an all time low. I was so concerned that these results were indicating a bone marrow transplant failure or a relapse in his disease within the 100 day critical period. But after pleading with God to turn things around I began to believe it would happen. By morning, Todd and I were both on the same page. We were going to expect the best to happen!! We decided to ASK God for healing and a change in his numbers, we agreed to BELIEVE it, even visualizing Tom's donated marrow engrafting in Todd and seeing it make healthy cells. Then we both decided to have FAITH that Todd was going to be healthy again; that God was going to answer our prayers. 

    Every day since I have been enjoying living life with Todd to the fullest. I decided that I would do whatever it takes to get Todd the best care and treatment even if it meant going to another Hospital for a second opinion (if it comes to that).

    We drove up to the Cleveland Clinic for treatment on Friday (December 5) praying for good news with his blood work. We were not disappointed! Not only were his blood counts stable but we saw a slight increase in all three cells. White counts were 2,700. Hemoglobin at 10.0 and platelets at 33,000. No transfusions were needed. 

    We are going to stay positive and expect the best!  We continue to pray. 

    This week the same word keeps coming up from the scripture:

    Be of good courage. And he shall strengthen your heart, All you who hope in the Lord. Psalm 31:24




    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. 

    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!

    Tuesday, October 7, 2014

    Discharge Date Set as Platelets go to 13,000: October 8, 2014

    Before leaving the hospital last night to go spend the night at the hotel, I put my hand on Todd and said a prayer that his platelets would come up today.
    "I do set my bow in the cloud, and it shall be for a token of a covenant between me and the earth." Genesis 9:13


    Day +21, October 7, 2014  Total Days in the hospital: 30

    I gave praise when he texted me this morning saying: 13,000!  What an answer to prayer!  His other counts were steady even though his white count had dropped slightly to 1,070 from 1,810.   No transfusions were needed at all today!

    Last night he did have a couple bouts of loose stools and he took 2 Imodium tablets to help.  This caused a bit of concern today when the doctors came by during their rounds.  While Todd has not had a fever, they are still cautious about any type of infection or Graft versus Host of the intestines.  They don't want to discharge a patient with an infection, only to have to bring them right back in for re-admission. So, today they were just going to keep an eye on it. They decided that he would get an IV bag of Neupogen, a medication which helps stimulate the bone marrow to increase the production of neutrophils (what I refer to as ANCs)  in white blood cells. 

    The discharge papers were prepared and Todd's bone marrow transplant nurse coordinator stopped by to discuss the discharge process tomorrow.  So far, Todd has not had any diarrhea or loose stools today.  He walked a mile in the halls and ate two full meals and a banana for breakfast today.  This is the most he has ate in a single day since the chemotherapy.  He has lost a lot of body hair, but has just started loosing some of the hair on his head this week.   Overall  he is very healthy and they are not concerned about the 20 pounds he has lost from lack of appetite. 

    We had to compare our own thermometer and blood pressure cuff to that of the hospital, so we could check their accuracy.  I had to show the nurse I knew how to change his Hickman Central Venous Catheter dressing and flush his lines.  We discussed diet, symptoms, and how and when to call or take him to the emergency room if there is a concern. 

    He noticed a small patch of red irritation on his left arm after his nap this afternoon.  The nurses have made a note of it and we all have to keep an eye on it in case he is developing Graft versus Host of the skin.  Her first reaction was, a little Graft versus Host isn't a bad thing.  While I have blogged about GvH and have mentioned it numerous times as something that is bad, there is truth in the nurse's statement.  This is called the Graft versus Cancer Effect.  Essentially, if any of Todd's bone marrow survived the chemotherapy, it can be attacked by the newly grafted bone marrow that came from his brother.  Todd's new bone marrow will think the old bone marrow is an invader and work to kill it, keeping the chance of relapse to a minimum.  As a matter of fact, they will periodically test to see how much of Todd's blood cells are from his old marrow versus the new.  The doctors can then manipulate the amount of immunosuppressants they give him to increase the Graft versus Cancer Effect if they feel there is too many cells from the old marrow that has survived.  This effect will work to eliminate or keep those cells to a insignificant trace.

    I brought a small suitcase today to start packing up some things to take back to the hotel tonight.  Tomorrow will be a busy day.  We will need to finish packing up, meet with the pharmacists who will go over all the medications Todd will be taking on a daily basis, go over discharge instructions with the nurses and the nurse coordinator, and say our goodbyes to everyone, etc.  We already have a three page schedule of appointments set for the next three months to put in our calendar!  Finally, I can drive him back to the hotel and get him settled in.  By then, he will likely need a nap!

    Sunday, October 5, 2014

    Moving, Exericse and Walking are essential in Healing process

    Todd stands outside his hospital room ready to go on a walk for the first time without his IV pole! If you walk the "L" shaped hallway of the11th floor round trip, the distance equals 1/6 of a mile.  Todd usually likes to walk all six laps at once, but sometimes he will just walk three laps in the morning/afternoon and three laps in the evening so he can get at least a mile of walking in.  Sometimes he will also go to the exercise room afterwards to use the sit-down elliptical machine or treadmill.

    If there is one thing I have learned from the bone marrow transplant process (from observation and from talking with other families here) it is this:  the patients who get up out of bed and walk and/or exercise are the most successful in getting out of here and sooner!

    For those who lay in the bed because they are having difficulties or who just don't have someone close to them to gently give them a prod and a push to get moving, their progress and length of stay is much longer and harder.  There comes a time when the family and/or caregiver have to exercise some "tough love" and insist on getting the patient moving.  Enabling and pitying them does them NO favors.

    While I understand that every person's situation is different: the type of cancer they have, their age, their health prior to admission, the type of chemotherapy, the type of transplant, and how their body heals and recovers, I still feel that getting up and getting moving is essential for recovery. 

    The bone marrow transplant binder that is given to patients prior to transplant recommends that the patient "Walk in the hallways 4-6 times a day" in addition to sitting in a chair for all meals, walking to the bathroom, using the exercise room on a regular basis, and to going to the family lounge to visit, use the computer, etc.  (Cleveland Clinic, 2011).  While every patient can have a bad or "off" day from time to time and just cannot get out of bed, these shouldn't be everyday.  Exercise keeps the patient from developing hindrances like pneumonia while promoting muscle and bone strength, stress relief, and better balance.  Personally, I think it can help work up an appetite and provide a change of scenery from the same four walls!  It is a great way to meet others who are going through the same process and compare recovery strategies.

    Difference in Transplants regarding length of Hospitalization time:

    Autologous bone marrow transplants use their own stem blood cells harvested prior to chemotherapy  to be transplanted or infused on Day 0/Transplant Day.  There is no risk of Graft versus Host Disease since they receive their own cells, so these patients are not required to stay hospitalized as long, nor are they required to stay near the hospital for the 100 days after transplant.  From my observation of the patients on the floor with us, those with Acute Lymphoblastic Leukemia (ALL) or Non Hodgkin Lymphoma often have this type of transplant.  These patients have their Hickman Central Venous Catheter removed before discharge from the hospital. 

    Allogeneic bone marrow transplant, like what Todd had, is when the bone marrow is from another  donor who is either related or unrelated, a partial match (where 4 key HLA matches are found) or a full match (all 8).  Todd's brother happen to be a full 8 point full match.   According to the National Marrow Donor Program:

    Each brother and sister has a 25%, or 1 in 4, chance of matching you, if you have the same mother and father. It is highly unlikely that other family members will match you. Under very rare circumstances, family members other than siblings may be tested...About 70%, or 7 out of 10, patients who need a transplant do not have a suitable donor in their family.  (National Marrow Donor Program.  1996-2014.)
    We feel so blessed that out of two brothers, only 1 out 2, was a match for Todd.  It is believed that full matches have less chance of developing Graft versus Host disease or other complications.  We have met about four other families who were only able to find a partial match; most where children or siblings.  We meet two other patients besides Todd who received a full match donation.  One patient received his bone marrow donation from someone in Germany.  In his case, the bone marrow was collected from the donor in Germany and then was frozen and flown to the Cleveland Clinic.  In Germany, it is MANDATORY that ALL German Citizens become donors!  The majority of the patients we have met on the floor have had Acute Myloid Leukemia (AML) or Chronic Leukemia.  Because of the risk of Graft versus Host Disease, these patients have to remain within an hour drive of the Cleveland Clinic for about 100 days and take immunosuppressant drugs to prevent GvH.  These patients have to keep their Hickman Central Venous Catheter in place through the 100 days in case treatment or re-admission is needed.

    Some other setbacks that can happen include: fever, infections, infection in the Hickman Catheter (Central Venous Line), nausea, severe diarrhea including C-dif, vomiting, severe headaches, mucositis and esophagitis (which can be so severe that morphine or another pain medication must be administered). These complications or the age of the patient can also make exercise difficult. They are often identified with a sign outside their door as a "fall" risk because they are at risk of falling down. This is obviously a major hindrance to walking.  One of the elderly patients in the leukemia side of the floor had such a hard time walking that she pushed a walker while her son held her up from behind.  I think they too realized the importance of walking and moving, no matter what it took.

    Todd has been so fortunate not to have any serious side effects or setbacks.  Yes, there have been several days that he didn't get out of bed at all.  Yes, there were days he needed to be prodded to get out of bed by me or his doctor or nurses, but in pushing himself on most days, he has recovered so well that he is almost ready to be discharged!  Will I still have to push him to walk?  YES!  Everyday! It is still important that once he is discharged to continue to get his exercise.  Then we can walk at the mall, grocery store, in a museum (during non-busy times), a park, or neighborhood.

    As I have gotten older, I have learned how important staying active is to having good health.  This experience has reinforced to me that we need to make exercise part of our everyday routine, for the rest of our lives.   

    References:

    Cleveland Clinic Foundation. 2011. Staying Active During Your Hospital Stay. Index #14676.

    National Marrow Donor Program.  1996-2014. Web. http://bethematch.org/For-Patients-and-Families/Finding-a-donor/HLA-matching/

    Thursday, October 2, 2014

    No Platelets for Todd on Day +14--Cleveland Blood Bank cites shortage

    On Day +14, September 30, 2014, Todd's CBC blood counts were:
    Hemoglobin: 7.8, White Blood Count: 70, and Platelets: 8,000.   Technically, he needed a platelet transfusion since his platelet count was under 10,000 and a blood transfusion since his Hemoglobin was below 8. 

    Unfortunately, the Red Cross Blood Bank located within the Cleveland Clinic denied Todd platelets because of the platelet shortage they are experiencing.  (Did did receive a blood transfusion).  I was upset by this news and asked the doctor on call to come by his room to discuss this me. 

    First, let me say that the doctors here are great advocates for their patients and argue our case for whatever they need to the blood bank.

    Q.  I asked him why they denied him platelets?
    A.  His response:  They denied him based on the concern that they have been giving him platelets daily, but that he wasn't retaining them.  In light of the shortage, they felt they didn't have enough to spare if his body was going to remove them and/or his body wasn't retaining them.

    Q.  I asked about using the HLA matched platelets that he had requested?
    A.  Apparently, they still were not able to provide them. 

    Q.  Next, I asked if I could donate blood for platelets or if his brother, who was the bone marrow donor, could give blood/platelets that way? 
    A.  He said that this was  not easy to do because it is very cost prohibitive and that there are too many clerical errors made in labeling and getting the donated blood to the correct patient.

    Q.  I asked him how low did his platelets have to drop for it to be critical if he didn't get a transfusion? 
    A.  His response: He stated that there was no set number they had to drop to where the Blood bank could no longer deny him platelets.    He explained that Todd's body would eventually be able to make and retain his own platelets once the new bone marrow is more engrafted. The decision is based on their own judgment.

    The next day, Day +15, Wednesday, October 1, 2014, a new doctor was on rotation.  Todd's CBC was HBG: 8.5 (so no blood transfusion was needed) and his white count finally hit triple digits: 130, but his platelets were down to 6,000.  There was talk about giving him the HLA platelets, but not until next Monday, October 6.  I'm not sure the reasoning, either they felt he would be in a better place to keep them then or that they wouldn't be able to get them until them.  We were surprised when his nurse came in late in the morning saying he was getting regular platelets that day.  We asked what had changed, but she didn't know.  The doctor on rotation came in and explained that as the advocate for the patient, they argued again and did testing to prove that Todd's body was not creating any anti-bodies that was killing the infused platelets (This can happen because the body thinks that the platelets are a foreign invader and try to kill them).  Since the blood bank had this proof and reassurance, they were more receptive to the request for platelets. 

    Yesterday's transfusion must have worked, his platelets went from 6,000 to 9,000 today (Day +16) October 2, 2014.  His white count jumped to 300! But his Hemoglobin was down only slightly at 7.9, which meant he needed both platelets and blood today, but thanks to the great doctors on staff here and the tests they did, he received both with no problems.  We are hoping the white count will start doubling at this point.  This gives him greater immunity to infections. 

    We are all hoping to be released from the hospital one day next week, October 6-10th, Days +20-+24.  While this are the number of days since the transplant, we have actually been at the Cleveland Clinic for 25 days already.

    Sunday, September 28, 2014

    Staying at the Cleveland Clinic

    While Todd is on the Bone Marrow Transplant Floor at the Cleveland Clinic's main campus, he is not allowed to leave the floor.  So, I have taken some photos of what the floor is like, to give everyone a better idea of his surroundings.
    Todd's room.  
     Views from his window:





    View from the family lounge area:



     Yes, the Heliport is on top of the Emergency Building right outside his window. 
     Partial picture of the family lounge:

     The Exercise room:
    The view out the window of the Exercise room looking towards University Circle.  The Intercontinental Hotel in the foreground.
     The Kitchen area.



    Wednesday, August 27, 2014

    Nurse Visit part 2: Graft versus Host Disease (GvHD)

    Graft versus Host Disease in a condition that can occur after an allogeneic transplant in which "the donated bone marrow view the recipient's body as foreign, and the donated marrow attack the body." (Cleveland Clinic Foundation, 2014).

    It can be either Acute (aGvHD) or Chronic (cGvHD). Todd could get one, both, or experience neither. 

    Since Todd is receiving his bone marrow donation from his brother, who is considered to be a "perfect" 8 of 8 point match donor, the risks of developing GvHD are somewhat lower. His young age also helps decrease this risk. 

    If  acute GVHD occurs, it will usually show up when his brother's cells have "grafted" into Todd's body (within weeks).  Chronic GvHD can develop anytime, even years after the transplant. 

    Acute GvHD usually develops in the skin, liver, eyes, or gastrointestinal tract.
    Symptoms include:
    Skin: rash or reddened skin
    Liver: abnormal blood tests (liver) and/or yellow discoloration of the skin/eyes
    Gastrointestinal: nausea, vomiting, diarrhea, or abdominal cramping. 
    Eyes: increased dryness/irritation. 


    Chronic GvHD can manifest itself in these same areas, but in additional places too including the mouth, lungs, neuromuscular system, and/or genitourinary tract (bladder/sexual organs).
    Symptoms for these areas include: 
    Mouth: dry mouth, white patches inside the mouth, pain or sensitivity to spicy foods. 
    Lungs: Shortness of breath, changes in chest X-rays. 
    Gastrointestinal: difficulty or pain in swallowing. 
    Neuromuscular: fatigue, muscle weakness, or pain. 
    Genitourinary: urinary frequency, burning or bleeding with urination, or penile dysfunction. 

    Many of his medications can cause similar side effects making diagnosis difficult. Detailed tests and consultations with specialists will help distinguish the difference. Checking current results with baseline test results taken prior to the transplant can be helpful.

    While GvHD can be deadly in some rare cases, most cases can be counter-acted with medications, though some can cause long-term side effects. Since Todd's brother is a perfect donor match, we are praying that the chances for developing GvHD are slim.

    On the flip-side, GvHD does have some good benefits.  A slight case can be positive.  "The same immune response responsible for attacking your normal cells is also monitoring and destroying any surviving cancer cells."  (Cleveland Clinic Foundation, 2014). This is called the Graft versus Tumor Effect. In other words, Todd will have his brother's bone marrow in place of his own: normal, healthy bone marrow.  If any of Todd's original unhealthy bone marrow is still left, then Todd's new immune system from his brother will attack these old dysplastic or cancer cells.  Also, patients who develop GvHD have been shown to have lower disease relapse rates. 

    So how can he avoid GvHD?  Using a perfect or best match donor's cells and giving him preventive immunosuppressant medicines after transplant.  Constant monitoring of symptoms is also imperative to diagnosing and controlling GvHD symptoms. 

    A major time of developing or confronting GvHD is when the doctors take Todd off his immunosuppresant medications.  Some patients have to continue these medications for longer than the initial treatment time, sometimes for months, years, or indefinitely. 

    I have done the best to describe GvHD as simple as possible.  I have used the information handout (Revised 2/27/2014) provided to us by The Cleveland Clinic Foundation in our transplant information binder.  Please follow this link to find this information online: http://my.clevelandclinic.org/services/Bone_Marrow_Transplantation/hic_Graft_vs_Host_Disease_An_Overview_in_Bone_Marrow_Transplant.aspx