a bit more of an update.

This morning, while Joe was catching up on some extra sleep, I left the room to brush my teeth. When I returned, Joe was awake with an extremely concerned look on his face. I looked up and Joe's father had a similar expression on his face. I braced myself, because I thought surely I was about to receive news about Joe's condition that I did not want to hear.

Let's go back in time a few minutes. Joe wakes up and discovers that I have disappeared (I didn't want to wake him.) Shortly after, his father stops by for a visit...and then a Pulmonary doctor (fellow) shows up to check on Joe. They go through what is now a normal daily routine check. However, before the doctor leaves the room, he suddenly says, "I have some bad news for you." So you can imagine, Joe and his father were bracing themselves because they thought surely they were about to receive some news about Joe's condition that they did not want to hear.

Instead, they were told (and then, when I returned, I was told) that hospital security had discovered that someone had broken into my car. Now, you can imagine how each of us, when given this bit of information, did a kind of simultaneous sigh of relief and "grrrrr...we don't need this right now!"

The blessings are of course that the bad news was about the car, and not about Joe. Also, nothing appeared to be stolen (although if someone had to go and smash in my window, I almost wish they had taken something. That would at least make a little sense.) And finally, my insurance will cover the damage and my window will be fixed on Thursday. Oh, and of course the final blessing is that it is summer, not winter...so I was able to avoid duct taping a garbage bag over my window. The drama never ends.

Now, about Joe. On Friday morning, Joe woke up feeling a little short of breath. Joe also noticed a blurred spot in his vision from his left eye. A CT scan from the previous day showed some faint nodules and ground glass opacities in Joe's lungs. The possibilities for this seemed endless...fungus, cmv, pneumonia, bleeding, etc. Joe was started on oxygen through a nasal cannula. Joe was also given a bronchoscopy. The last time Joe needed a bronchoscopy was a nightmare, because Joe ended up with a cough that lasted six weeks. Obviously, none of us were excited that he needed another one, but we also wanted to make sure that anything serious could be determined and treated. The actual bronchoscopy didn't end up being too bad. What was discovered was a lot of blood in the lungs. This sounded scary, but if the blood was "simply" from hemorrhaging and not from some type of evil infection, then it could be considered a "best case scenario." The treatment involved large doses of Solu-medrol and increased platelets. In the meantime, Joe was also (and still is) being treated for a possible (though seemingly unlikely) fungal infection, the possibility of CMV pneumonia, CMV itself, and some other nasty infections. I've never seen such a fancy and packed IV pole. The photo really doesn't capture that craziness. As for the eye, Joe showed signs of hemmorhaging in his eyes. This will resolve on its own, unless it is found to be CMV related. So far, it does not seem to be CMV related. Praise the Lord. If it is, Joe will get medicine injected into his eyes.

By Friday evening, Joe's breathing was really labored. He was breathing around 52 breaths per minute. Normal, is 12-20 breaths per minute. Joe was switched to an oxygen mask which would deliver more oxygen. Joe also started getting chills, which was treated with a mini-shot of Demerol. It was a really crazy time. Crazy enough that the ICU doctor was sent up and we were forced to discuss things like intubation, just in case.

Things calmed down for a bit. Then Joe started having trouble breathing again in the late evening. A chest x-ray showed that Joe was overloaded with fluid. His lungs were so wheezy. Joe was given two separate doses of Lasix. (Joe says the name is because it "lasts six hours.") The Lasix helped Joe get rid of the excess fluid, which helped his breathing. The drawback was NO SLEEP. Joe had to go to the bathroom every 15 minutes. This would be torture for anyone. But imagine being short of breath, and being attached to a crowded IV pole, oxygen, and a pulse oximeter. It was like an obstacle course.

Fortunately, by Saturday Joe was feeling better, although his sides were sore from breathing so hard. He was switched back to the nasal cannula. Joe is still using it now. Each day since Friday has been a slight improvement. Joe was feeling pretty dejected on Friday and Saturday. He was sick of the hospital, sick or being sick, sick of a lot of things. But his spirits have improved since Friday as well. Obviously, Joe still isn't having fun, but he'll crack some jokes here and there, and then I know that all will be okay.

Today is supposed to be the day that the CMV results come back. When I left the hospital this afternoon, the results weren't back yet. Hopefully, oh hopefully, the result is a big fat negative!

That is the main stuff we've been going through. Joe has had about 9 platelet transfusions and 8 units of blood since last Monday. The good news is that each transfusion seems to make a little bit more of a difference and bump up Joe's counts just a little bit more than the previous transfusion. Also, Joe's WBC was higher today that it has been in weeks. We are still praying each day for a a full recovery. It will happen. It is just a matter of timing.

Hopefully, my update wasn't too confusing. There is just too much jumbled in my brain. It is hard unjumble and make it digestible :)
~~~~~~~~

So we have a million people to thank...
Thank you to everyone who has been continuously praying for us and loving us. So many people told us that they were praying for us last night, and that was really wonderful. Thank you so much.

Thank you to our parents for being the most wonderful parents.

Thank you to James Miller and S & T Bank for the sweet letter and donation to Marrow Trek in memory of Bob Duggan. What a beautiful gesture and loving tribute.

Thank you to Jim & Jesse for continuing the Marrow Trek. (There's a new blog update everyone!) You are such an inspiration. We are so blessed by your friendship and willingness to do all that you can to make a difference!

Thank you Myra for all of your calls, and visits, and book recommendations! You rock.
Thank you Sha, Patrick, and Ray for visiting and cheering up the room with balloons & giggles! Thank you also, Sha for the CD!
Thank you Jay for driving so far to see Joe. It always means so much to him to see you and spend time with you. Thanks also for the book!
Thank you Auntie S.B. for stopping by with the fun balloon.
Thank you to Auntie S.B., Sue-mei, and Auntie LihJen for being such prayer warriors and encouraging those around you to keep praying for Joe!
Thank you to Kitty, Neeta, David, Ariel, & Lilly for visiting Joe and making him smile.
Thank you to 2nd Auntie & 3rd Auntie for sending us hugs from Taiwan!
Thank you Nancy Baird, Caryn, Marcus, Alan & Joyce, Shelley, Cousin Lilly, Yi-Ting, 1st Auntie, Michael Chang, Albert, Eric Wu, and Victor for your phone calls!

Oh, and the cards...wow. There are still some that haven't been opened yet. We are so thankful for every single one. Joe just lights up seeing that physical evidence of love and encouragement. Joe has received love from all over the states, Canada, Taiwan, Japan, Afghanistan, and Papua New Guinea. Pretty cool.
Thank you...
Akiko
Anonymous
Anonymous
David & I-Ju
HSB (I was pretty impressed that Joe knew who you were immediately. Good radiology resident, I guess!)
Joanna
Kun-Tse
Lauren & Eric (happy happy anniversary!!!!!!!)
LihJen, PCC, & PCC Dawning Sisters
Cathy Liang
Jocelyn & Peter
Cousin Lilly
Joanne Maier
Mom & Dad
Evonne, Thomas, and Leah
Alan, Joyce, Allison, & Jason (sorry we missed seeing you when you were in town!)
Emily, James, & Alivia (We are praying for you, so much!)
Gretchen and the rest of the Allen's
A.M.
Yohko Shinozawa
Rune, Van, Hannah, and Noah
Frank & Janet
Kelly Tonkin
Sheena
Osamu, Yi-Shan, Yi-Ting, 3rd Uncle & Auntie
Mookie! (arf, arf!)
Peggy
Pei-Chen
Phyllis Miller (We got the snail mail card too! You are so sweet.)
Rachel
Roger & the SPHS AP Chem Class
Sha
TC & Yuen Chan
The Interventional Radiology Gang – Gordon, Rick Foster, Shelley, Linda, Rick Woods, Vinnie, Sue, Zahra, Nancy, & Val
Tina & John Bonney
Uncle Timothy & Auntie Grace

Also, big thank you's to Erica, Ann & Chris, and Nancy for your love and encouragement. Each of you have also been through so very much. We've never met, but we share an undeniable connection. You're in our daily prayers.

one more thing...

This is from an email sent out to the Pittsburgh Taiwanese Bible Class (and quoted in the comment below), but I think that everyone can join the fun from wherever you may be this evening at 9:00pm. (Thank you Auntie Shiow-Bih!)

Dear brothers and sisters of Pittsburgh Taiwanese Bible Class:
Please join me in praying together for Joe at 9:00 PM Monday night May 28, 2007. He really needs our prayers and support when he is struggling with oxygen, fighting for pneumonia. We will also pray for Karen, Dr/Mrs. Luke Lin and Dr/Mrs. Victor Lan at this very difficult time.
Shiow-Bih
~~~
p.s. It hasn't been confirmed for sure that Joe has pneumonia. So far it is just a possibility that he is being treated for. So please pray that it is confirmed that Joe does NOT have pneumonia.

Mini update.

It has been a rough few days. To be honest, I don't have the energy to recount all of it right now. I just wanted to say that we most definitely appreciate all the continued prayers. And after a super rough Friday, Joe is showing little baby steps of improvement each day. We rejoice in any bit of improvement we can get. We are still staying strong - which is not the same as not crying and not going through bouts of frustration. But it does mean that we are most definitely not giving up any time soon, and we know that we will get over this ridiculously humongous boulder we've encountered. After all, God is good and he has helped us over other ridiculously humongous boulders. For Him, this is nothing.

Eventually, I will share a more proper update and of course we have loads of people to thank.

Much love (keep praying!),
Karen

MDS sucks.

One of our worst fears was confirmed this evening. Results from Joe's bone marrow biopsy were back already. Joe's donor cells decreased to a mere 35%. The rest is mostly bad stuff - evil, awful MDS stuff. We were prepared for the news. But you can bet that we were hoping and praying and hoping and praying that what we heard would be the opposite of what we were prepared for.

So here is the current revised plan as I understand it. Joe's CMV takes first priority, because it can cause huge problems if left untreated. Once the doctors get one CMV negative, they will start treating Joe's MDS. It is still unclear what that treatment will entail. So far, it sounds like Joe will either be treated with Decitabine or Induction chemotherapy. The "good" news is that a second transplant, although likely, isn't as 100% as we first thought. That means there is still a ray of hope that we can cling to. Some patients, after being put back in remission following a relapse are fortunate enough to find that the donor cells suddenly come back. Wouldn't that be wonderful! It is a possibility, so that's what we're praying for now.

Send Joe some love! He could use it now more than ever. It just seems like after everything he's been through already, he's back at square one. Love him! (I know, you all already do - so very much.) Thank you. :)
Patient e-card greetings. (West Penn, Rm. T-715. )

Thank you to the Breast Center for the super awesome card. All of you are always so creative and funny. We love it!

Many thanks also to:
Caryn
Sha
Karin & Bryan
Shelley
The Miller Family
Daddy
Sylvia
Katy
Lilly P.
Deb from CT
Cousin Ben, Kristin, Alex, & Lauren (pulling out all of Ben's old tricks really worked to make us laugh!)
Gretchen
2 more "Anonymous people

for the cards! They really put a smile on Joe's face.
Joe also got two of the cutest cards decorated with crayon. We don't know who they are from (a class project maybe?), but they are SO cute. One from "A special friend" and one from Luke.

Day +134

"This ain't no thang!"
This is Joe on Morphine, Ativan, and Benadryl.













Last night, I forgot to mention that we learned that Joe is CMV positive yet again. So far, no other sources of infection have been found. It is possible that the CMV may be responsible for the fever, and maybe even all of Joe's other crazy lab reports. Time will tell. Between the Infection Diseases doctors and the Hem-Onc doctors it was decided that the Ganciclovir and the Cidofovir just aren't working. An executive decision was made to put Joe back on Foscarnet, despite the fact that it worked at the expense of a very un-fun side effect. As soon as Joe feels any indication that the un-fun side effect (for Joe's sake I'd rather not go into detail here...) is returning, changes will be made. In the meantime the doctors have done what little they can to try and prevent that un-fun side effect.

This morning Joe finally had the BIG bone marrow biopsy. Joe was given Ativan and Morphine before the biopsy which made him very calm. I think the doctor doing the procedure was far more nervous than Joe was. (Although the doctor did a good job.) Joe's platelet transfusion ended up happening after the biopsy. He is always pre-medicated with Benadryl to decrease the chance of a reaction. With that morning cocktail of Ativan, Morphine, and Benadryl, you can just imagine how lovely Joe's afternoon was! Every single time Joe blinked he would end up snoring. When something would wake him up Joe would grin a bit, occasionally utter a word or two, then resume his snoring. When Joe actually had to physically get up to go to the bathroom he would say, "I'm happy..." It was really cute.

By late morning, we learned that the platelet transfusion brought Joe's platelets up from 17 k/mcL to 19 k/mcL . Generally, the cut-off for transfusions is 10 k/mcL (on Monday, Joe's count was 6 k/mcL ...normal range is [145-445] k/mcL), but with Joe experiencing fevers and being CMV positive, the cut-off became 20 k/mcL . So Joe had yet another platelet transfusion in the afternoon.

It usually takes a few days for the results to come back from a bone marrow biopsy. Please pray that no matter what the results show that we are prepared to proceed with grace and faith.

That is about it for today. Joe was happy to see that a contestant from Monroeville, PA was on Jeopardy this evening, and he won! Interestingly enough, last week we saw a contestant on Jeopardy who was from Indiana, PA - he also won, the night that we watched. Nice to know that there are such smart people from our old stomping grounds. :)

Thank you so very much to:
A.M. & A.D
Cousin Lilly
April & Paul
Phyllis Miller
Frank & Janet
Alice
2nd Auntie & Uncle, Li-Ming, I-Ju, & David
Indiana Mom
Shiu-Bi & Jsiang-Jung Kuo
TC & Yuen Chan
Evonne, Thomas, & Leah
The Baird Family
Vince
Sara M.
Shelley
Louis
Ariel, Kelly, & Walker
and 2 "Anonymous" people

for sending cards to Joe. It really brightens his day, when he is at the hospital, to receive a pile of cards. So thank you for showering Joe with love! (p.s. Even though you fill out sender info, if the card is not signed in the message area, we don't know who it is from. We still appreciate the love though!)

Dear friends, do not be surprised at the painful trial you are suffering, as though something strange were happening to you. But rejoice that you participate in the sufferings of Christ, so that you maye be overjoyed when his glory is revealed.
~1 Peter 4:12-13

Still here.

Not that we expected to be discharged yet. That would have been exciting though! So last night, Joe had a platelet transfusion around 3:30am and he had to tell his whole post-transplant story to the intern on call at 4:10am. Such is the life of a patient who decided to get himself admitted to the hospital in the late evening!

This morning we waited, and waited, and waited to see the doctor and for Joe to get his bone marrow biopsy. Joe didn't end up seeing the doctor until around 4pm. By that time with the pathology lab about to close shop it was decided that Joe's biopsy will take place in the morning when everyone is bright eyed and bushy tailed, following a platelet transfusion. So the big bone marrow biopsy is now tomorrow...I don't think that is going to change again.

Today Joe received all kinds of antibiotics and two units of blood. His fever went away in the afternoon, presumably from the pre-blood transfusion Tylenol. This evening Joe has a mild fever compared to last night. He is doing well for the most part. His appetite decreased a bit starting Thursday. Now that he's on a bunch of IV meds his taste buds are affected, which doesn't help the appetite. Everything tastes bitter. Fortunately everything sweet still tastes pretty good! And obviously Joe is already missing the comfort of his own bed far away from the clicking and clacking of his IV machine. Otherwise, all is as well as can be.

Thank you for your continued prayers!

Back in the hospital

This really hasn't been our day. Today was to be the day of the big bone marrow biopsy that will determine what our next year will look like. It was postponed until tomorrow because Joe's blood draw showed that despite our bit of hopeful news on Friday, all of Joe's counts had dropped. Joe had a platelet transfusion and a shot of Neulasta.

We went home and planned to return in the morning for another platelet transfusion followed by the bone marrow biopsy, and possibly a blood transfusion. Unfortunately, sometime after dinner Joe spiked a fever. You know what that means. It means he was admitted to the hospital. We just arrived about an hour ago, and Joe has been giving samples of everything to be tested. I just got kicked out of the room for a bit so that they can give Joe a chest x-ray. Joe's most recent temperature was 101.6. Joe isn't feeling so great right now. He's still being calm and positive, but the fever understandably has him feeling uncomfortable and light-headed.

Obviously, we could use everyone's continued prayers and positive vibes. Also, please pray for Baby Livi, Ann, and Amy Wilhoite. (Links to the left.) They each are having their own kind of prayer-welcoming week.

If you want to send Joe another not-so-attractive card filled with lots of love and encouragement, here is the link again...Patient e-card greetings. Joe's at West Penn, Rm. T-715.

Thanks for looking out for my Joe!
~~~
Pssst. Happy birthday to Alice, Vince, Donna (bowlergirl!), and Baby Ethan. :)

Evolution of a PICC Arm Band

Today I share with you the evolution of a PICC Arm Band, and the innovative nature of my husband! When Joe had his PICC line placed last Thursday, they sent him home with this long folded up tube of "stuff." The idea was to snip off sections as needed and use those sections to cover his PICC. As you can see from the first photo, the material is cheap, kind of ugly, and it kept falling off. Plus, no matter how long we cut the material, once it was on Joe's arm it seemed to be too short.

Being the loving wife that I try to be and a joyful newbie knitter, I decided that it would be fun to knit Joe a PICC arm band. In fact, months ago, I remembered that I had come across a free pattern at KnitPicks.com. I even had the yarn that they recommended - one that they said "minimizes pilling and stretching." It really is a lovely yarn. And I knitted up the band in no time. It looked absolutely beautiful! (not that I'm bragging or anything) For the first five seconds that is, then it proceeded to prove that it in fact, maximizes pilling and stretching. At least when knitted up by a newbie like me. It looked perfectly snug when Joe put it on. Even a little bit tight. But once those first five seconds passed it proceeded to stretch enough it could have fit around his thigh. *sigh*

Being the innovative person that he is (and loving - Joe was really intent on making the arm band work!) Joe suggested using bicep bands to hold the arm band in place. PERFECT!

But then, my innovative husband came up with an even more perfect idea that will have PICC line wearers everywhere running to their nearest sports store. Joe was watching basketball, and noticed that a bunch of the players were wearing these sports sleeves (they are actually called shooting sleeves in case you are sports illiterate and curious.) They looked like they had just the right amount of stretch, and because they are made for athletes, we figured they had to be comfortable and breathable as well. Yes, yes, yes. Joe is a genius. Maybe Nike will hire him to create a line called "NikeChemo." (Are you listening Nike? huh, huh, huh? We LOVE YOU!) The sleeve works like a charm. It also has the added benefit of creating instant long sleeves, which is perfect for Joe since he has to cover up when going outside to protect his skin from the sun. The nurses at the BMT office were so impressed, they said that they were going to share the idea with all of their patients with PICC lines. Apparently, patients have come up with some pretty crazy excuses for arm bands. Joe's so smart. He's also a wannabe athlete. (shhh...don't tell him i said that!)

We received some hopeful news today! After a bit of a delay, we finally got Joe's CMV results from both this past Tuesday and this past Thursday. Both were NEGATIVE. We were so excited. Joe talked to one of the doctors on the phone today, and he could practically hear the doc jumping up and down with joy! This was a nice change from yesterday. Yesterday, Joe and I went to the hospital for his Cidofovir. Joe also ended up getting another platelet transfusion. When we met up with the doctor he sounded so serious and concerned about Joe's progress. We're still gunning for a miracle as far as Joe's next bone marrow biopsy. Another thing that gave us a little bit of hope today is that Joe's WBC has inched up a bit more. It is actually higher than it has been in weeks. Hopefully this is a good sign. Keep on praying!!!!!!! Second transplant - pshaw!

Don't forget. There are still a few more days to take advantage of the "Thanks Mom Marrow Donor Drive." You can register to be a donor for FREE if you sign up before May 21. Please, please, please, help us spread the word. It would mean so much to us. (Thanks Tina! We saw that you posted about it. :) )

Day +126

We had a pleasant weekend. On Saturday, my cousins stopped by to visit us. It had been a year and a half since we had seen Yi-Shan and Osamu. It had been close to three years since I had seen Yi-Ting...Joe was able to meet her for the first time. We had great fun hanging out. My mom came over too.

Sunday was Mother's Day. After calling our moms, Joe and I went to the hospital to have his blood drawn. We decided to wait for the results in case he needed anything. Joe's parents so kindly offered to meet us at home with lunch. Joe ended up needing another platelet transfusion which meant some waiting, so Joe's parents ended up bringing lunch to the hospital! It was nice to spend time with them even if it was in the hospital. After Joe's transfusion, he decided it would be fun to go visit my parents. We would see my cousins too, since they were staying there. It had been over a year since we went back to my parents house. So off we went! It was fun, and we stuffed ourselves silly!!!! As a rule, I like to have our moms over for a meal on Mother's Day. But we have the greatest moms ever and they were more than happy to each provide us with a good meal this year. Thank you!!!!!!

Today we went back to visit the doctor. After the platelet transfusion on Sunday, it seems that Joe's count only went up a little bit. We were excited on Sunday because Joe's WBC had gone up a bit; by today it had not gone up or down. And Joe's hemoglobin went down slightly. As of Sunday's blood draw, Joe is also still CMV positive. Joe's doctor said that it is pretty amazing that after so many weeks of being CMV positive Joe has shown no symptoms. At least 80% of patients who test CMV positive for a few weeks exhibit symptoms like pneumonia. We are so grateful Joe has not shown any symptoms, but it sure would be nice if Joe were negative again so we wouldn't even have to worry about it. For now, Joe is going to be continuing Ganciclovir twice a day for another week, and getting another Cidofovir treatment on Thursday. Pretty much, we heard two good things today: 1.) Joe doesn't have any symptoms from CMV. 2.) Joe's rash really and truly seems to be getting better.

Then the serious talk began. As noted before, Joe will be getting another bone marrow biopsy next week. Now it looks like it will be on Monday, May 21. This biopsy will determine much of what our next year will be like. If Joe's marrow shows improvement as far as a decrease in abnormal cells and an increase in donor cells, we will continue with monthly Vidaza. If Joe continues to show signs of relapse or no change at all then a second transplant is definite. Joe's treatment would follow that of patients with AML (acute myelogenous leukemia.) Joe would be admitted to the hospital for 7-10 days for induction chemotherapy and low-dose radiation. The intent would be to bring him into remission. Following induction, Joe would recover for four weeks and then go into transplant with a different donor. Joe's doctor is an extremely positive person, and for him to discuss all of this so seriously showed us that it is a very real possibility. In fact, one of the doctors on the team was already prepared to start Joe on induction chemo before finding out the results of Joe's next bone marrow biopsy.

It is feeling very surreal. Pretty much we would be starting everything all over again. We're just being ourselves right now. Who knows what kind of miracle God may have in store for us by next week. The thing is, although I'm the opposite of thrilled about the possibility of that "second option," Joe has proven to me that he has the strength, stamina, perserverance, and faith to handle anything that comes his way. He has said himself that physically, mentally, and spiritually he feels great. It is his insides that seem to be wreaking havoc. If I had any doubts before, I certainly do not have any doubts now that Joe will overcome any obstacles in his way. Everything just might take a bit longer than anticipated. That is okay. God has perfect timing, and who are we to interfere with that?

p.s. There is a sweet boy named Shane who has ALL and is collecting birthday cards! If you get a chance, send him one. Click on the links for more info, or visit http://www.shaneswish.com/.

~~~~
Thank you to both of our moms for never taking breaks from being moms - even on Mother's Day!

Thank you to Yi-Ting, Yi-Shan, & Osamu for coming to visit us!!!! We loved hanging out with you.

Thank you I-ju for calling us from Taiwan. Sorry, we missed your call, but we loved hearing your voice!

Thank you TK for your company!

Thank you Roger for the beautiful, beautiful card. We heard your had great talent and creativity, now we know it is so true!

~~~
It is not for you to know the times or dates the Father has set by his own authority. But you will receive power when the Holy Spirit comes on you; and you will be my witnesses in Jerusalem, and in all Judea and Samaria, and to the ends of the earth.
~Acts 1:7-8

Don't stop praying!

Yesterday, Joe had a PICC line put in. So far it seems to be far more comfortable than the ones in the past that jutted out from his neck! At times there is a little bit of pain or weirdness in his arm, but nothing too bad. Joe was started on Ganciclovir at the hospital yesterday morning. In the afternoon all the doses for the rest of the week were delivered to our front door. Just like the first time, the Ganciclovir comes in these cute little containers that look like baby bottles. Inside is what looks like a balloon filled with the medication. All we have to do is hook it to Joe's line and it runs for a little over an hour. The last time, Joe was getting his morning dose at the hospital and his evening dose at home. This time both doses can be done at home. This morning, Joe had an appointment so we brought the Ganciclovir so Joe could get his dose while we were waiting for our appointment. The nice thing is that Joe was given a kind of "Fanny Pack" so that he can just slip the bottle inside and continue on with his day.

Joe also received platelets yesterday. Today's results show that his platelet count didn't go up very much. Joe will go back to the hospital on Sunday for another blood draw to determine whether or not he needs another platelet transfusion.

Our next appointment with the doctor is on Tuesday the 15th. Joe's next bone marrow biopsy will probably be on May 22. Here is the part where we need EVERYONE to pray, and pray, and pray, and pray, and pray. We are all praying that the Vidaza is doing its job and Joe's abnormal cells are being suppressed and his donor cells are completely taking over. This is the ideal outcome. If this happens, then Joe will continue to receive Vidaza treatments monthly as maintenance. (Not sure how many months yet.) We don't really want to think of the alternative, but I must share so we can all pray more effectively! If the bone marrow biopsy shows that the donor cells are not increasing, then Joe will likely need to have a second transplant with a different donor. The second time (which of course we are praying never happens!) Joe would be getting low dose radiation in addition to all the other pre-transplant conditioning he had in January. Surely this second transplant business will never happen.

Joe and I are remaining hopeful and optimistic. All we can do is take one day at a time. We've found a kind of balance between expecting the best and being prepared for all things that are less-than-the-best.

We read a very inspiring article this week.
Teen cancer patient's blog celebrated life.

also, you must read this beautiful blog entry that was mentioned in the article... Whatever life we get is bonus. It is amazing that an 18 year old could be so wise.

Though the fig tree does not bud and there are no grapes on the vines, though the olive crop fails and the fields produce no food, though there are no cattle in the stalls, yet I will rejoice in the Lord, I will be joyful in God my Savior.
~Habakkuk 3:19

Day +120

Joe's rash is definitely looking better. It still covers a large part of his body, but it is lighter now. It's also dry, but Joe does not have the intense flakiness that he had to deal with the last time. Today his steroids were tapered slightly. We are thankful for this, and just keep praying that the rash continues to get better. Steroids can be great, but they can be really awful as well.

Joe's counts are still very low of course. And his blood draw from Monday morning shows that he is still CMV positive. Not really surprising considering his level of steroids. (Oh, but we were hoping for a negative!) Tomorrow we go back to the hospital and Joe will be getting a PICC line. After that he will be getting a platelet transfusion (today's count was 11 g/dL.) Joe will also begin a one week treatment of Ganciclovir twice a day. This will not help his WBC at all, but hopefully in combination with Cidofovir every other week Joe's CMV will be negative again. Having a line put in will give Joe's arms a break from being poked all the time.

That's about it.

~~~
Thank you Sheena for hanging out with us yesterday! We'll miss you.

Let us then approach the throne of grace with confidence, so that we may receive mercy and find grace to help us in our time of need.
~ Hebrews 4:16

Day +118

Today we had a relatively quick hospital visit. We did have a little bit of entertainment in the waiting room in the form of a disgruntled patient loudly whispering to a couple near him about his long wait.

Joe's WBC and platelets are still low, although this time it was expected since he just had chemo last week...

Normal Ranges
WBC - [4.4-11.0] k/mcL
Platelet Count - [145-445] k/mcL

Joe's Counts
WBC - 0.5 k/mcL
Platelet Count - 18 g/dL

Joe was given a Neulasta (pegfilgrastim) injection today, which is esentially a longer-lasting form of Neupogen (filgrastim). Joe is not experiencing any bleeding or petechiae from his low platelet count. We figure each one of his platelets must be as strong as ten platelets from a "regular" person! We are going back to the hospital on Wednesday, so Joe was able to avoid a platelet transfusion today. It is very likely he'll need one on Wednesday, but who knows? We may experience a miracle. On Wednesday we'll also find out if Joe's blood draw from this morning is CMV negative or not. You can bet we are praying and praying and praying that it is negative. If it is positive then we'll be back in the hospital on Thursday for the six hour process of Cidofovir...and probably Ganciclovir as well.

Since Joe does not have a line anymore (and his platelet count is low) he is acquiring quite a number of lovely bruises from all the needles and IVs. The rash continues. It still has not reached the intensity that it did the last time, and we are praying that it won't. Today it does look a tiny bit lighter than yesterday. The doctor estimated that the rash is currently affecting about 54% of Joe's body.

That's about it. We are grateful that Joe's GVHD has stayed away from all of his internal organs. We are grateful that Joe still has a pretty healthy appetite. We are grateful that besides some (although sometimes a lot of) itchiness, symptomatically, Joe is feeling quite well. It is really a weird thing when you look at Joe, to realize that things are pretty chaotic on the inside.

For in this hope we were saved. But hope that is seen is no hope at all. Who hopes for what he already has? But if we hope for what we do not yet have, we wait for it patiently.
~Romans 8:24-25

Day +117

Thursday, Joe and I went back to the hospital for his third round of Cidofovir. If Joe is CMV negative on Monday, then we party! If he is still positive, then there is talk of giving him Ganciclovir and Cidofovir. There is a hope that the two together might effectively take care of the CMV.

Thursday, we knew would be a long day. The whole Cidofovir process takes 6 hours. (Joe also got platelets again, but that was relatively quick.)In the past, we usually went home around 2 or 3 in the afternoon. But last week was the Week of Waiting; we went home at 7pm. Still, we are blessed that Joe is able to go home. (Dear Baby Livi and her mom have been living at the hospital since her transplant two months ago.) Not only that, but we were blessed by a visit from our dear friend Sheena. You might remember that when Joe was admitted to the hospital shortly after being diagnosed, Sheena let me stay at her place many nights so that I wouldn't be as far from the hospital. Sheena started attending our church and fellowship the same time that Joe and I did. In the past four years she has become such a good friend. Unfortunately for us, she is finishing up dental school and leaving Pittsburgh this week. We're going to miss her so much!!!!!! Sheena has such a huge heart, and she is also just about as silly as I am. Actually, she may even be sillier. In any case, she made our long day at the hospital on Thursday feel much shorter. Thanks Sheena!!!!

Since Thursday, we have had a bit of a break from the hospital. Unfortunately, also since Thursday, Joe's rash has become increasingly worse. On Saturday, after a call to the doctor, Joe was put back on Cellcept - the immunosuppresant that was stopped when we first learned Joe's graft had dropped. This whole treatment process is so crazy. Lower the steroids and immunosuppresants and the GVHD starts to flare. Increase the meds and Joe's CMV becomes positive again. Then there is the chemo which initially lowers blood counts that are already low. Crazy.

When Joe starts to scratch he always gets a lecture from me...or a little slap on the wrist. This time around though, he is getting pretty smart. Joe will seemingly vanish into thin air, and the house will become very quiet. Then he will emerge again, looking a bit sheepish and with some patches of especially red skin. Very suspicious...

Our friend Sha invited me to go to the symphony with her on Saturday evening. I almost declined. I'm not with Joe all the time. But I am with him most of the time. Up until last night, all of my excursions were either during the day or they were only a very short distance from home. What can I say? I'm an overprotective wife. But Joe convinced me that he would be fine and that I should get out of the house - not only for my own sanity, but so that nice friends like Sha still love us once Joe is well enough to be out and about! Well, I had a wonderful time with Sha. It was a really fun night of music. Plus, I got to see my Uncle Kao. When I got home in the evening, I reenacted the whole experience for Joe. I'm not sure that the conductor or the musicians would appreciate my impressions, but Joe seemed to get a kick out of it. :)

We go back to the hospital in the morning. I'll keep everyone updated. Speaking of updates, check marrowtrek.org sometime this week. Jim & Jesse should be putting up an update on their progress soon!

~~~~
ANNOUNCEMENT

If you look at our links to the left, you will see that one of the girls in our prayers is named Kailee Wells. She is only ten years old and has already had two bone marrow transplants. Six years ago, her parents had an idea for a "Thanks Mom" bone marrow campaign. Since then they have been able to work with the NMDP to run a national bone marrow drive each year in honor of Mother's day. There are drives being held all over the country with a goal of 20,000 new registrants. You can also register online for free while funding lasts. The event runs from May 7-21. You can learn more here. Please, please, please SPREAD THE WORD!
~~~
Thank you Sha for the lovely card that you sent!!!!

Thank you Indiana Mom & Dad and Monroeville Mom & Dad for visiting us this weekend and bringing food!

Again, I tell you that if two of you on earth agree about anything you ask for, it will be done for you by my Father in heaven. For where two or three come together in my name, there am I with them.
~Matthew 18:19-20

Keep up those prayers!!!!!!! (please)

Saturday...
Joe was started on Vidaza once again (a quarter dose like the last round). This was day two of round 2, post-transplant. On weekends the BMT office is closed, so Joe has to go to short stay. All of the nurses in short stay know us very well. It wasn't a very eventful day. For the last round of Vidaza, Joe had a line and thus he took advantage of the fact that Vidaza has been approved for IV administration. This time, since Joe doesn't have a line anymore, he has gone back to getting subcutaneous injections. With the quarter dose it is just one shot...not so bad, says the wife who isn't getting poked!

Sunday...
Joe had his blood drawn. Being a chemotherapy, Vidaza made Joe's counts even lower. Plans were made for a platelet transfusion to take place on Monday.

Monday...
The plan was to go to the BMT office. There we thought we might wait for 15, maybe 20 minutes for Joe to be called back to receive his Vidaza shot which would take a good 5 seconds. Then we would head up to short stay where we would wait about an hour for Joe's platelets. Platelets are fast, so the transfusion would take at most 15 minutes, and then we would be on our way home. We figured everything would take 2 hours...maybe 3 if things were really crazy. This is what we THOUGHT, because after months and months of going to the hospital and being given the opportunity to take full advantage of the WAITING rooms...we still haven't learned our lesson.

What really happened is that we went to the BMT office and waited for two hours before Joe was called back to receive his Vidaza shot which took all of 5 seconds. Then we headed up to short stay where we only had to wait about 15 minutes before Joe was taken to his room. At this point we were told that his platelets would arrive in an hour. Well, an hour came and went with no sign of platelets. Then a lovely nurse came and told us that they were informed that the platelets would arrive in 20 minutes. Apparently they were to arrive with the 2pm driver from the Central Blood Bank. Joe's platelets were not with the 2pm driver. We had to wait for the 3:10-3:15 driver. The 3:10-3:15 driver did not arrive until about 3:40, at which point the hospital people had to process it and such. Joe finally received his platelets at around 4pm. And yes, the transfusion took about 15 minutes. We waited over 5 hours for two procedures that took a total of 15 minutes and 5 seconds. The positive thing is that I was able to do plenty of reading and crocheting, and Joe was able to do plenty of reading and napping. The Benadryl that Joe was given before his transfusion did a great job of making him drowsy. The other positive thing is that Joe didn't have any reactions to his transfusion.

Today...
Today Joe had another blood draw. Everything was low again, which was expected. We also met with the doctor. Joe is going to be getting Vidaza each month again as a sort of maintenance. This sounds like a good idea right now. The not so great news is that after two negatives, Joe's Sunday blood draw showed that he is CMV is positive once again. That darn CMV loves to pop up and cause trouble all the time! Joe was already due for another dose of Cidofovir on Thursday. That will go as planned. Hopefully that will work to make that pesky CMV negative once again. If not then Joe might have to begin a combined therapy of Ganciclovir and Cidofovir.

The other thing is that Joe's rash started to flare up again. It is not too bad yet, but everyone would like it to stay "not too bad yet." So Joe's steroids were increased yet again. Not too high, but it already seems to be helping.

We are still smiling. In fact, on Monday one of the nurses said, "I think the two of you look happier every time I see you." Today, Joe's doctor said, "The two of you are always so positive." He thinks that all of this positivity has helped Joe to not look or feel as bad as many patients would during the "downs" of all the "ups and downs" Joe has been through. I think that it's true. One of the big things Joe and I have learned during this journey is that there is no point in worrying before you have to worry. And actually, with each "down" we experience, we are learning that there really is no sense in worrying then either. Worrying makes you feel miserable, it causes you to lose sleep, it gives you wrinkles, and in the end none of your problems are solved. Being positive makes you happy, allows for plenty of beauty rest, makes a better impact on others, and allows you to enjoy life despite all odds. :)

Thank you everyone for all of your prayers and all of the positive energy you've directed our way. Knowing we have so much love and support really helps us to continue to stay postiive.

Who of you by worrying can add a single hour to his life?
~Matthew 6:27

We could really use some prayer right about now...

This past week, we really felt like we had rounded a corner in our journey. Joe was feeling better, the rash was fading to nothingness, the sun was shining. All we needed was for Joe's counts to start moving in the proper direction. Well, today we learned that if we did round a corner - it is a detour, and we've hit a major pothole. Fortunately, we are from the 'Burgh. And if there is anything that people from the 'Burgh can handle, it is detours and potholes (and a weird new mascot...). Nothing can stop us from reaching our intended destination.

Joe started off the day with a blood draw and a dose of Pentamidine. The results from the blood draw showed that his WBC is still low and his platelets are creeping down. His hemoglobin is still holding steady. Later in the morning we had an appointment with the doctor. We were just doing our thing, grumbling about the long wait, talkin' about the weather, remarking on Joe's peach fuzz five o'clock shadow, and doing some reading. Then we received some results from the bone marrow biopsy Joe had on Tuesday. It showed that 30% of Joe's cells display chromosome abnormalities - those abnormalities that put us in this predicament in the first place. The FISH for donor cells has not come back yet. But if we assume that the cells with abnormalities are Joe's, and the cells without are any combination of Joe and the donor, then Joe's marrow is now no more than 70% donor. This was not the news that we wanted to hear today. It just seems impossible that such a drastic change could occur in two weeks. The doctor is concerned, as one should be in this situation, but NOT worried. Remember, Pittsburghers know how to navigate detours and potholes. Joe was started on another round of Vidaza today. It worked really well the first time his graft dropped, so there are high hopes that it will do the trick again this time. To further discourage Joe's cells from getting out of control and to encourage the donor cells to fight harder since they are still in the majority, Joe's steroids have been tapered even more, and he has been completely taken off of one of his immunosuppresants. Please pray that the donor cells take over once and for all, and that Joe's GVHD doesn't flare uncontrollably.

Amazingly enough, even after receiving this news Joe and I seem to be handling it very well (if I do say so myself). We're a little more quiet today, but far from mopey and not quite discouraged. I can't speak for Joe (although from our conversations and our day, I can say that I continue to be amazed by his strength), but as for me I feel this strange peace about everything. My mind and my heart seem unable to waver from being completely positive that everything will be fine and that God will provide Joe with complete healing. Some might say that I'm in denial, or it hasn't hit me yet, or I'm being a bit naive. I don't think so. I can't think so. This whole MDS thing has been horrible. Yet, so many positive and wonderful things have blossomed from the muck and mire that is MDS. Joe and I have grown in so many ways. Joe in particular has developed unbelievable strength and grace in dealing with the ups and downs of his treatment. Then there is the support from family and friends, the stories of people inspired by Joe's story, and the people who have stepped up and registered to be donors, or donated cord blood. I think that there are a lot more wonderful things in store for us...not the least of which is complete healing for Joe. Currently, I refuse to believe anything else.

Here's my theme song for the day.

God will make a way
Where there seems to be no way
He works in ways we cannot see
He will make a way for me
He will be my guide
Hold me closely to His side
With love and strength for each new day
He will make a way
He will make a way

By a roadway in the wilderness
He'll lead me
And rivers in the desert will I see
Heaven and earth will fade
But His word will still remain
He will do something new today.

Day + 106

Today, I present to you a photo of Joe and his college roommate Jim. It was taken on our wedding day. Jim is really tall. And not that it matters, but that isn't what he wore to the wedding. Jim was just making sure he was in the right place. Speaking of Jim, Joe got a call from him four days into the Marrow Trek. Jim and Jesse are doing well, although they are starting to get some blisters on their feet. When Joe heard from them, they still had a good 3,000 miles to go...but they are still super excited. Now the dogs...they are excited too, but they are also falling asleep every time Jim and Jesse pause for more than half a second. The trail and the heat may be a bit much for them, so the dogs are going home for now. Meanwhile, Jim and Jesse seem to be collecting some crazy stories...already. Like having a small town librarian call the cops on them. You would be nervous too if two big guys with four days of chin stubble, who smelled like they had been hiking and sweating for a hundred miles in warm weather were sitting in your library. Fortunately, the cops were very kind...

Joe is doing very well. Monday's blood draw showed that he is now CMV negative. YAY!!!!!!! This means just one more dose of Cidofovir, which will take place next week. The down side is that Joe's WBC is still very low (yup, he had another filgrastim injection). Yesterday, Joe had bone marrow biopsy #7 to ensure that everything is as it should be in his marrow. We are praying hard that the results are good. Joe has been feeling a bit better each day now so it only makes sense that everything else follows. Amazingly enough, Joe had his biopsy without any morphine. Is he brave? Is he crazy? Is he stupid? Maybe a bit of all three? I don't know. But the fortunate thing is that the nurse practitioner who did the biopsy did a wonderful job. Out of the six different people who have had the privilege of doing a bone marrow biopsy on Joe, she ranked in the top two...oh, but one of the six was eliminated from the ranking since morphine was involved. :)

Another thing is that the Mepron (the yellow paint stuff) and Joe's stomach just were not agreeing. Joe has lost a lot of sleep in the last couple weeks because the Mepron has caused a lot of discomfort and rumbling and such. So...Joe is going back to the monthly Pentamidine. We are trusting that the techs who administer it are fully aware of the proper methods now. Please pray that this is true!

~~~
Thank you Sheena for bringing us food. It was all so yummy. You better be eating well too!!!!!

Praise the Lord, O my soul, and forget not all his benefits - who forgives all your sins and heals all your diseases, who redeems your life from the pit and crowns you with love and compassion, who satisfies your desires with good things so that your youth is renewed like the eagle's.
~Psalm 103:2-4

One Hundred Days!

Joe has officially hit Day +100. It has been 100 days since his PBSC transplant. It seems like just yesterday that our families were seated around a long table talking to Joe's doctor about the upcoming transplant. It was mentioned that Day +30 and Day +100 were big milestones. At the time, Day 100 seemed so very far away. And now we are here. Some days, when Joe was admitted to the hospital again, or while Joe was enduring the seemingly-never-ending-rash, each day seemed to pass SO VERY SLOWLY. Other days, we would look at each other and say, "wow! it's Friday already...again." The wonderful part about today is that the seemingly-never-ending-rash is barely visible now. Yes, there is a bit of redness here and there, but nothing even close to what it was. In fact, during the days of the seemingly-never-ending-rash, Joe would wake up in the morning and his face would look all hairy from the skin peeling on his head, eyelids, cheeks, chin...basically everywhere. Now, when Joe wakes up, he actually has some oil on his face. Remarkable. The doctors were really excited when they saw how much Joe's rash has faded. It feels as though we are rounding a corner and finally heading in the right direction. Hopefully we'll be encountering far fewer bumps along the way.

Joe had another dose of Cidofovir today. As of this past Monday he is still CMV positive, but that was expected. We're hoping next week, and each following one will be a CMV negative week! While Joe was hooked up to his IV pole, I decided to trek downstairs where there was a blood drive and get punctured with a giant needle. It was the least I could do after all Joe has been through. I felt really good afterwards, and then a couple hours later I felt like I had been run over by a truck. I gained even more respect than ever for Joe and all the other people we pray for each day. One pint of blood had me all woozy, and here Joe's counts have been low for months and months, and he has been poked with so many needles, big and small. Overall, I had a really positive experience and am really anxious to donate more regularly. Speaking of Joe's low counts, he did need another shot of filgrastim today. Fortunately, those needles are really tiny. Let's go counts, think UP!

Today is a monumental day for another reason. Jim and Jesse made their way down to the Mexican border today and will officially begin the Marrow Trek tomorrow. We are really excited about what they are doing, and so blessed by their energy and spirit. You can track their progress by clicking here. They will also be keeping a blog which they will update each time they encounter a computer! Please keep Jim and Jesse, and their beautiful dogs Whistler and Scooter in your prayers. Also a gigantic thank you to the people who have made pledges or donations to Marrow Trek so far. The support that has poured in for CLLF and Dana-Farber has been overwhelming. We are so amazed and encouraged by the generosity of both friends and strangers. Thank you.

Now for those curious minds who don't read Chinese, and saw my dad's comment the other day...Essentially, he was teasing me for writing such a lengthy blog and using a well known Chinese saying to equate my post to the cloths that were once used to bind the feet of women in China - long and smelly. Thanks dad, I love you too! :P

~~~
Thank you Cousin Lilly, Ben, Kristin, Alex, Lauren, and 1st Auntie & Uncle for the postcard!!!!! (Bet you didn't know that I just started teaching myself how to play ukulele and learning a song that mentions the humuhumu-nukunuku-a-pua‘a. I laugh every time I get to that word. So the postcard was perfect!)

Thank you Gordon & Julie for the food. It was so sweet of you. We appreciate it so much!

Thank you Nancy for sending such great photos. I can't stop looking at them. They are great.

Wait for the Lord; be strong and take heart and wait for the Lord
~Psalm 27:14

Ten ways YOU can help.

So often, when friends, families, and acquaintances learn about what we are going through, they want to know how they can help. Every so often, I like to post specific ways people can help. Although I know these posts can get long and tedious for some, I urge you to please read through the list. Everyone is different, and everyone has a different gift. I tried to take that into consideration as I compiled my list. Together, we can make a difference. We really can. And honestly, the best way you can help us is by helping others.

1. Pray. So many of you have been praying for us, and I cannot emphasize enough how much that has meant to us. I firmly believe that each of your prayers, happy vibes, and virtual hugs have kept us strong on days when we should have been weak, helped with the overall smoothness of Joe’s recovery process, and have all around enveloped us with the best of warm fuzzies. I would also challenge you to add one or two other people to your prayer list from our links to the left. Or go to Asians for Miracle Marrow Matches and pray for the patients there. There are too many people who are battling these awful cancers, and each one of them could benefit from the power of prayer.

2. Spread the Word. It is all about spreading awareness. We knew virtually nothing about bone marrow failure, blood cancers, and bone marrow transplants before our journey began. Now that we have been forced to come face to face with the awfulness of MDS, it has challenged us to arm ourselves with information so that we are able to educate others and promote awareness. Go out there and spread the word. Tell people about this list! Getting information directly from a human being can be much more effective than getting information from a flyer.

3. Register to be a Donor. If you are in good health and are between the ages of 18-60, you can register to be a donor. Registration is simple and doesn’t hurt. Just fill in some forms and swab your cheeks. Most people will never be called, but if you are – honey, you’ve won the lottery. What can be more fulfilling than an opportunity to save a life and be an answer to prayer. Click here to get started.

4. Pregnant? Make plans to donate cord blood. If you have already decided to make arrangements for personal storage, that is a personal decision and totally cool. If not, then the umbilical cord and placenta are commonly tossed after birth. Consider making arrangements to donate the blood. It could help save a life! If you will be giving birth in a hospital that is not affiliated with a cord blood bank (for example, Pittsburgh does not have a cord blood bank yet) you may call Cryobanks International, and visit their site for more information. The number is 1-800-869-8608. They accept donations from all over the U.S. You must register between the 28th and 35th week of your pregnancy. You can find more information here.

5. Donate blood and platelets. Patients with cancer often have to have multiple blood and platelet transfusions throughout the course of their battle. Donating blood and/or platelets is a wonderful way of helping to make sure they get the transfusions necessary. Look up your local blood bank or Red Cross for more information.

6. Support a charity.

• 
  Marrow Trek – Thursday, April 19, 2007 is Joe’s Day 100! Friday, April 20, 2007, Joe’s college roommate Jim and another college friend Jesse will be starting a 3,000 mile hike over 4 months. The purpose of their trip is to raise money for the Dana-Farber Cancer Institute and Cammy Lee Leukemia Foundation (CLLF), and raise awareness and sign up donors for the National Marrow Donor Program (NMDP). Amazingly enough, the pledges have already exceeded their goal of $15,000. However, Jim always hoped that the goal was a conservative amount. You can still donate. And you can be sure that every penny of your hard earned, tax-deductible donation will go straight to Dana-Farber Cancer Institute or CLLF. Visit the site for updates on their progress.
• 
  Aplastic Anemia & MDS International Foundation, Inc. – AA&MDSIF is a wonderful group that provides support to patients and does research related to treating and curing bone marrow diseases. The bravery bracelets that some of you have are from AAMDS!
• 
  Leukemia & Lymphoma Society – This is another group that funds education, research, and support. You may recall that our friend Louis ran a marathon to help raise money for the Leukemia & Lymphoma Society.

7. Knit, crochet, or sew. I know that there are many people out there who are crafty. Here are two organizations that are dedicated to turning craftiness into charity. Check out the pages for more information.
Project Linus - providing security through blankets.

Head Huggers - providing hats for those who have lost their hair due to chemotherapy or other medical situations.

8. Shop through iGive.com – For all you shoppers out there, you can shop at many of your favorite online stores through iGive.com. Go shopping, and a percentage of your purchase will go to the charity that you designate. CLLF, AA&MDSIF , and The Leukemia & Lymphoma Foundation are all charities that you can choose from.

9. Use GoodSearch.com to Surf the Web – Love to surf the web? If you use GoodSearch.com as your search engine, money will go to your designated cause. I know that you can choose AA&MDSIF as a charity.

10. Contact your congressperson. This message was in the most recent AA&MDSIF e-bulletin.

Dear Friend, On March 6, 2007, Representatives Jim McGovern (D-MA) and
Mary Bono (R-CA) introduced H.Con.Res. 81, the Bipartisan Bone Marrow Disease
Resolution, to encourage the federal government to fund research and engage in
public health initiatives that give patients greater access to more treatment
options and, ultimately, cures for bone marrow diseases.

The Aplastic Anemia & MDS International Foundation played a key role in drafting, presenting, and securing the introduction of this resolution before Congress.

Now it’s your turn to help!

For this resolution to pass, we need to have a broad level of support from individual Members of Congress. Now is the time to contact your U.S. Representative to urge them to cosponsor H.Con.Res. 81. If you do not know who your Representative is, or need contact information, please access [the U.S. House of Representatives site] and enter your zip code under the heading "Find Your Representative."

For your convenience, we have attached a sample script that you can use when you contact your Member of Congress.

Members of Congress do not cosponsor these types of resolutions unless they hear from their constituents. Spread the word and contact your elected Representative today!

Sincerely,

Sherrie Van Vliet

Acting Executive Director Click here for Script

If you have read this far, THANK YOU. I know for a fact that many of you have been doing your part to help as much as you can. How can we begin to thank you? I want you to know that every time we hear that someone has helped in some way, Joe and I literally jump up and down with joy. It is important that we make every effort to turn something negative into a giant positive for others. We are grateful for each one of you who is helping us with that effort!

You are the light of the world. A city on a hill cannot be hidden. Neither do people light a lamp and put it under a bowl. Instead they put it on its stand, and it gives light to everyone in the house. In the same way, let your light shine before men, that they may see your good deeds and praise your Father in heaven.

~Matthew 5:14

Quick update.

Just a quick little update to let everyone know that Joe is still doing well! We went to see the doctor today, and Joe's steroids were tapered a bit more. His rash is very faint now and only itches a little bit at random moments. Not too bad. Joe's WBC is still low, so there was another filgrastim injection today. That's about it. We return to the hospital on Thursday for Cidofovir. That will be a pretty long day. Tune in tomorrow. It has been awhile since I have blogged about ways to help. I'm making a list, so be prepared. :)

Please pray for all the students, faculty, and families affected by the tragic events at Virginia Tech.

99%

Three lovely photos have been posted for your entertainment. First, we have Joe smiling because his mind is far away from the Mepron he will soon be taking. The second is a photo of the Mepron. Didn't I tell you that it looks like bright yellow paint? The third photo needs little or no explanation - but it is Joe's reaction to taking Mepron. Apparently though, things could be worse. Poor Baby Livi has to take a medication that smells like skunk.

We went to see the doctor yesterday. Joe's rash is definitely looking better and better each day. He is not shedding as much skin, and his skin is not as red. Joe was given permission to taper his steroids slightly. Today was the first day of the taper; so far so good.

The results from the chimerism test earlier in the week show that Joe is 99% female. Yay! Those donor cells are doing just what they are supposed to be doing. The fact that they are doing what they are supposed to be doing largely contributes to why Joe's rash was so ugly. High price to pay, but in the end it should all prove to have been worth it.


Joe got another Neupogen shot on Friday because his WBC are still stubbornly low. The positive CMV result isn't helping either. Praise God though, because Joe is feeling well overall. Monday we return to the hospital. Mostly just a routine check. Thursday will be round two of the Cidofovir.
~~~
I keep forgetting...thank you Susan H. for the lovely card! It was really fun to read.

Great is the Lord, and most worthy of praise, in city of our God, his holy mountain. ~Psalm 48:1