Showing posts with label American Cancer Society. Show all posts
Showing posts with label American Cancer Society. Show all posts

Monday, May 11, 2015

AG-221 Drug holds off Blood Transfusions for 3 weeks!



Todd Celebrates his 46th Birthday!
As of today, Monday, May 11, 2015, Todd has gone three weeks without a blood transfusion, thanks to the trial drug AG-221 that Todd has been taking now for 19 days.  His blood counts have not been in the normal range, but they have been significantly higher than they have been in months. 
On Monday, May 4, 2015, his white counts were up to 1.5; hemoglobin was at 9.0!; and his ANCs or neutrophils were at 1.2; and platelets at 53,000. 

We went to the Cleveland Clinic on Thursday, May 7, 2015 for his Day 15, Cycle 1 assessments.  We drove up on Wednesday and stayed at the Hope Lodge, sponsored by The American Cancer Society, for two nights and three days.
Our room, Hope Lodge, Cleveland, Ohio
This is the first time we have been able to stay there, since there is typically a waiting list for cancer patients and families that need to be there for treatment or transplant.  The best part of staying at the Hope Lodge, is that you can stay at NO COST.  You are required to clean-up after yourself, like wiping off your table in the dining area, removing your sheets, and straightening up your room, taking laundry down to the laundry area, change trash, etc.  We were eligible to stay after Todd's transplant last year, but decided not to because no children under the age of 18 are allowed to visit there. 


When we arrived on Wednesday night, volunteers had prepared a dinner for the tenants.  This was so nice; we didn't have to go out to eat, leaving us to go to bed early.  There are no TVs or food/drink in your room, so it's easy to go to bed early!  We had to be at the cancer center at 7:30 a.m. the next morning.  Blood work, urinalysis, and an EKG are done before Todd takes that morning's dose of AG-221, which is always taken around 9:00 a.m. every morning.  This also was the last day he could have the drug with food.  Starting Day 16, he will be required to fast two hours before taking the medication and for one hour after. 
Dining and Kitchen Hope Lodge

Since this was Day 15, the half-way point in the first cycle, Todd had ten hours of blood draws, more EKGs, and a bone marrow biopsy on the schedule.  This makes for a very tiring day.  There isn't much to do in between those hourly blood draws.  Todd tried to nap and I worked a puzzle.  We got lunch in one of the cafes in The Cleveland Clinic.  We wrapped up the day about 7:00 p.m. making it really almost a 12 hour day.  We were able to go to Little Italy (which is near the Hope Lodge) to eat dinner and to Presti's to have dessert.  We sat outside Presti's enjoying the beautiful warm weather (it's about time!), thanking God that Todd was healthy enough to do this (especially knowing our friend Rick lay in hospice).

Cream Puff and Crème brûlée
  We  hit the bed, did our chores in the morning, and ate breakfast at the Lodge prepared by volunteers, Helping Hands, before checking out and making the long drive back home to Beavercreek. 

I don't have the numbers from his counts that day, but they were holding steady, although they were not as high as that Monday before.  He did have a few blast cells in his bloodstream, which was a bit concerning, but the research nurse assured us that this is expected during treatment, since the medication often pushes the cells into the bloodstream.  His overall bilirubin was still high, but nothing they are concerned about.  The trial study research nurse assured us that they don't get concerned enough to change the dosage until they see levels up to 5 times higher than the normal level.  We all are anxious to see what the bone marrow biopsy results are.  Hopefully, we should get a preliminary report tomorrow or Wednesday. 

Todd with daughter Ellie
On Saturday, May 9, 2015, we celebrated Todd's 46th Birthday!  Unfortunately, we didn't get to celebrate as much as I would have liked. I woke up with a case of Vertigo, which necessitated a visit to the doctor.  I haven't been worth much since!  We went to Todd's mom's house for a birthday dinner and had a great visit.  We didn't really do much for Mother's Day either.  We had too much to do around the house to prepare it for listing and I still was suffering from the vertigo.
We received some sad news early Saturday morning that our friend Rick, from the transplant floor, lost his battle with Acute Myeloid Leukemia at 6:45 a.m. that morning.  They had moved him to Hospice in Ashland, Ohio, so he could be near to family and friends.  He had one good day while he was there: he was happy, ate food, went outside twice, and was able to visit with family.  Unfortunately, that was his last good day.  He was in terrible pain the following days and had to be medicated hourly.  Please pray for Lisa, his girlfriend and caregiver, who is deeply mourning his loss.  He had a 28 year-old son, who drove in from Colorado the day before he died, but didn't get to interact with him at that point.  He also leaves behind a mother and a brother. 

I have to admit that I was afraid that Todd wouldn't make it to this birthday last December/January.  His condition and prognosis was so poor then.  Thank God this trial drug is really making a difference.  Not only is he not needing transfusions, but he has energy to do things!

Family News
Our eldest daughter Abby finished her finals and moved out of her dorm room, wrapping up her freshman year at the University of Cincinnati.  Our middle child, Hannah Lewis, is finishing the senior year off.  Ellie, our youngest, finished Club Volleyball Season and Track.  She qualified to go to the GWOC Conference Final Track Meet, where she threw her personal best in shot put. 

God has answered prayers here too.  Abby found two jobs: one at Texas Roadhouse in Beavercreek as a hostess and the other at Steak and Shake as a server.  Hannah Lewis found a job at Graeter's Ice Cream and both are starting work soon. 

We continue to work hard on getting our house ready to sell.  We have been blessed with many friends and family who have volunteered to come over and help us complete some projects and clean up our house.  The real estate market here is very good right now, and we need to get it on the market as soon as possible.  No family going through the stress of cancer should have to worry about having another major upheaval like moving from their beloved family home, but we really don't feel we have another choice.  At this point, I think it will help cut our expenses tremendously and allow us to live more simply.  Please continue to pray for the right home for us to move into and for the right buyer to buy ours. 

Hannah Lewis has decided to accept an offer from The Columbus College of Art and Design in Columbus, Ohio.  We feel it is financially the best choice and we were impressed with their program.  Graduation and party will be at the end of the month. 

I hope my vertigo goes away soon.  I start my summer class June 8.  I can't imagine trying to move and do homework at the same time!  Haven't thought that far ahead; too much to do now. I need to finish this year if at all possible so I can start working full time.

What's next:
We go back up to Cleveland again this Thursday, May 14, 2015 for routine tests.  No long day!  They will check his blood counts and make sure that he doesn't a transfusion.  Hopefully, we will be able to discuss the bone the results, even though Todd is not scheduled to see his doctor this week.  The first cycle of the drug trial treatment ends on Wednesday, May 20 and we will go up for another long day of testing for Day 1, Cycle 2, on Thursday, May 21, 2015.

Thanks for your support.

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/