Ok so I had planned on getting on here last night because we received BIG GIVES yesterday!!!! AGAIN!!!! we realize everyday we get one how very blessed we are to have been chosen for this wonderful thing. We are hoping to become a part of the BIG GIVE when we get back from our trip..... Obviously I didn't get on here last night

Taylor had her pre chemo blood check yesterday afternoon so after working half a day I picked her & Sami up then drove almost an hour to the hospital, gave blood, saw the dr, Taylor's blood levels came back as low normal, but at least they are normal, so no shot to boost her ANC & WBC before chemo next week!!!! We drove home, got home around 5, then we had to go pick up the poster pictures that we had made up for the press conference that was taking place today at the hospital.
WAIT!!! Did I tell you all about that? If not I will now, if I did just skip the next paragraph....
Rare Disease Awareness Day is Monday Feb 28th & as you all know I will be standing outside the Today Show with about 100 other people to promote Histio Awareness, since Histio is a rare disease. So when Taylor's doctor heard I was doing this they asked me if I would be interested in doing a press conference with them before it to help promote it. We spoke to Taylor first because after all it is her story to tell & she said yes. We were excited & the date was set for Feb 24 at 10:30 in the morning. I was ok until yesterday then I was like

what did I get us into!?!?!?!?!?! To say the least I was very nervous last night... ANYWAY back to yesterday & why I couldn't get on here....
So we go pick up the poster pictures, I grab the kids something to eat, go home, bathe them, laundry

~ look at the clock 9:00!!!!!!!!!!!

WHERE DID THE NIGHT GO????? I call Johnny to see where he is & he is still at work, ( work is crazy for him this week ) Now I am trying to get the girls settled down, finish folding laundry & I still have to write up some notes for the press conference so I am not unprepared....
At about 10:00, I sit down to write up notes & Taylor asks what I am doing (I know they were up VERY late last night but NO school this week

) so I tell her & she says she wants to write her own notes too.

so cute right?
She yells to me a few minutes later that she is done & says good night, I looked at what she wrote before I finally went to bed around 12:30 this morning & I was so proud of her... I will share with you at the end of this rambling post..... Oh by the way Johnny got home around 10:20 last night.... (in case any of you were wondering)
We received a few wonderful BIG GIVES yesterday that I can't wait to post the pics....

I still have to upload them.
We went to the press conference today & Taylor was wonderful, I am so very proud of her for what she is doing. We always ask her before we commit to any type of talking about Histio or her story because it is utimately up to her. She really wants to do it..... Sami was also at the press conference she absolutely did NOT want to talk to anyone

TOTAL opposites....
Oh & by the way I made her wear high boots because I didn't want her not matching socks showing on television.....
Here is what Taylor wrote for today's press conference & she actually read it to the whole room full of people into the mic ......

LOVE HER
My mom asked me if I wanted to try to talk about histiocytosis & tell people my story & I said yes. I want to tell people about Histiocytosis because if I tell people I have it they don't even know what it is. Alot of times they say that I look fine & don't look sick but I don't always feel fine inside. I know what it feels like to have histiocytosis & alot of the time it hurts. I have to have chemotherapy & I get really tired, I get bad mouth sores from chemo & then if I am hungry I can't eat, I get headaches, my belly hurts, I get alot of muscle cramps & I even throw up sometimes. I had to go to the hospital alot of times because I got sick with a fever. But the worst part is I can't do things with my friends or play soccer during chemo week & sometimes even when I don't have chemo because I just don't feel good. Sometimes I am afraid to go to sleep because I am afraid I am going to die. Dr. V tells me that I am going to be ok & I really love her for taking care of me. Even when I feel really bad I always try to keep smiling, I know that everyone worries about me & when I smile they smile. I know that histio is rare so that means alot of people don't have it but it doesn't mean that kids like me with histio don't matter. I really want to teach everyone about histio & help Dr. V find a cure so that it goes away & never comes back.
When I read that last night after she went to sleep I was so proud of her, she is my inspiration to try to make a difference. I have some pics from the press conference that I will post later as well if people would like to see them....
Well be back later to post pics, just wanted to check in & let you know what has been going on in this crazy place called our house......

oh yeah only 17 DAYS LEFT

that could also have something to do with why the girls are bouncing off the walls.....