Thursday, October 4, 2012

T-Shirts... continued


















Wow! I'm pretty speechless after looking at all these again. It's nothing short of amazing to see all of the support from you all pouring in! I swear I am like a little kid on Christmas each time I get on Facebook and see a new picture. (Just ask Matt or my mom..lol). It's hard to explain just how much this means, and how much it helps me want to fight this nasty thing even more. I know Kalen had mentioned in his previous post that they are all on Facebook, but I figured I would put all of the ones that I have to date for you all to see as well. :) And the even better part? There is still more support coming! Some of out friends from Alaska are getting in on this next order (can't wait to see those pics!), friends from NC and SC, and even friends that I ,unfortunately, haven't talked to in years are joining in to support- Ania Terry you made my day the other day by ordering one!

I think that is an awesome idea that Team Bullers has to have a Team Meghan profile pic day if y'all are up for it, and having it as a celebration day once this chemo is over sounds fantastic! (Just a side note, I am 33.3% done with this nasty stuff... for those of you that know me, I'm terrible at math, I didn't do that calculation on my own, a fellow colon cancer fighter figured it out for me. haha) But none the less, 4 down, 8 more to go, and then I would love to see your profile pics supporting Team Meghan.

I also would like to thank all the faculty and staff at Francis S. Grandinetti Elementary School. Yesterday Matt and I received a heartwarming note with a very generous donation from their CARE days at the school. Thank you all so much for your help!

Now for a quick update- We are rounding the bend leading in to treatment #5 on Monday. I am hoping it will go as well as #1,#2, and #4....#3 was a little bit hairy and a pain in the ass. But I am going in positive! Side effects haven't been too bad this time, thank God, and I have been able to maintain my weight so far. Matt is in Alaska for a few weeks, which is somewhat of a double edged sword. It's great that we finally know he will be here with me in Annapolis for the next year, however, it is a real bummer that he is stuck up in Alaska for so long and will be missing the next treatment. I'll be missing him for sure, as this will be the first treatment without him. I don't think the nurses will know what to do without him sprawled out in the bed sleeping next to me. lol Luckily, Jim (my step dad) has been flexible enough that he is okay with me stealing mom for a few extra days, and she will take me to treatment and hang out for a few days after until Matt gets home. I will be wearing my Team Meghan T-shirt to this treatment to get some autographs from my nurse Joanne and my doctors.

On a note aside from all the medical bs- mom has been here "visiting" since Monday. I say it like that, because my mom doesn't really know how to visit or vacation...haha She has been working since she got here, which is a complete godsend for me! We now are no longer living out of totes and boxes, our house actually looks lived in, and we have a freezer stocked full of food for treatment days where we don't feel like cooking. Tomorrow, I am giving her the day off and we are getting out to at least do some "window-shopping". Also, Dad, Nancy, Jenna, and Luke are coming down Saturday morning. It will be great to see them again finally, and to show them around Annapolis! :)  I am one lucky girl to have such great family and friends willing to come visit and put up with me so I am not too lonely while the hubbs is away.

Please do take a minute to send some good thoughts and lots and lots of prayers Gary Gerber's way. This whole situation is such a nasty one to deal with, that I wouldn't wish upon anyone, and my case was even fairly straight forward. Some of the bumps and hurdles that I have heard he has had to overcome, he certainly deserves some love and support! Great news that he is home though, speaking from experience, hospitals are no place to recover, and there is nothing quite like the comfort of your own home when you're feeling down. Keep your chin up Coach, keep fightin' and it'll get better! Also, I know I mentioned this on Facebook and Kalen did as well, but if you can, please stop by Bill Mitchell's fundraiser on October 14th. He and his wife could really use your support, plus it is spaghetti- who doesn't like spaghetti!? Bill and Lara, you have all the support in the world coming from Matt and I, and we are keeping you in our prayers daily. Stay strong, and defy the verdict!

Thanks again for all of the love, support and prayers- can never have too much of that! Maybe someday, as the article from MD Anderson put it, dying from cancer will be as common as dying from pneumonia. We just have to keep searching.  Hope all is well with everyone and you all get to enjoy a wonderful weekend!

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