To Read Tami's Story from the Beginning

Just CLICK HERE. Her blog begins on March 12, 2009 with a post titled "Tami's Myelodysplasia Diagnosis." Then at the bottom of each post, click on the words "Newer Post" located just below the comments section on each page.

Wednesday, December 2, 2009

A Message from Tami Day +155

Hi Everyone,

I just wanted to share a belated Thanksgiving message with all of you from Tami:

Happy Belated Thanksgiving to all my family, friends and supporters,

These past months I have been overwhelmed with all of your love, support and messages in person, by email, on the phone, through the mail and through my blog and website. I am so thankful for each of you and I'm hoping the best for each of you in the coming year.


Stacie here, I am happy, no, make that thrilled to report that Tami is finally feeling better! Her back isn't perfect but continues to improve. Her body also continues to recover from the transplant. And big news, her hair is starting to grow back! At day +155 post transplant she's almost halfway to her half-year mark! That will be a reason to celebrate for sure. Maybe it'll catch on, celebrating half birthdays with a cupcake :)

Other patients we know are also reporting good news.

Matthew: Is recovering from his transplant and has moved out of the hospital and into an apartment near his hospital, very similar to how Tami did. Read his blog by CLICKING HERE

Zyreal: Is 7 years old and received his transplant and is recovering, still in the hospital. Read his online journal by CLICKING HERE

Jonathan Haupt will be receiving his mini haplo (a half matched) transplant from his sister Lynn on Dec. 8th. To learn more you can read his blog by CLICKING HERE

Our friend Roger, who also had MDS just like Tami, is continuing to recover from his transplant in Texas. He received it in March of this year but is having some complications now. It took Roger a year to receive his transplant because he had no insurance. Now he cannot work and is stressed about finances. If you would like to help Roger you can purchase a $5 "Cancer Sucks • I HAVE MDS" wristband or can make a donation to a fund I started for him here on Tami's website. Just CLICK HERE to place an order or make a donation.

On a sad note little Jasmina Anema is not doing well post transplant and it is feared that she has in fact relapsed and her Leukemia is returning. Recently the Make a Wish Foundation had arranged for her to meet and talk with President Obama as well as attend the annual pardoning of the White House turkey last week, but instead was rushed to the hospital due to a seizure. Her meeting with President Obama has been postponed for now. You can read more and watch a news video about Jasmina getting ready to leave for Washington D.C. by CLICKING HERE

There is now a follow up video to that story that you can view by CLICKING HERE


  1. Hi Tami and Stacie-

    I am so glad to hear that you are doing well Tami! Half a year down, that's awesome. My doctor always tells me that relapse usually happens in the first 6 months so that is a great milestone to hit. I am coming up on my first birthday, Jan. 7th. I'm cancer free but a little GVHD. Gotta keep that cancer away, right? I enjoy following your blog. I started a blog myself a couple month ago.

    Stay strong- Julie Rando

  2. I love the updates from Tami. I'm so glad too that she's making her way out of it and kickin'! It is amazing what an individual can do to "will" themselves to continue fighting! I will be seeing Tami at the marathon finish line!