I’m making it easy for you to donate in my team’s name this year! Just click on the link, enter my name (Kim Smyth) in the Box (find an individual) and your donation will count towards my team fundraising goal.
Thank you all in advance, by now you know that my mother passed in 2014 from complications of her PKD and that I also have it. Luckily, I am not symptomatic yet, and take preventive measures to stay that way!
Millions aren’t so lucky though and have to have transplants or suffer through years of dialysis like my mom did. She was on it for over 18 years!
Please give whatever you’re comfortable with, every little bit helps and again, thanks so much, I appreciate it and so does the foundation!
Today I am not going to do my normal Throwback Thursday instead, I want to thank everyone who has given to my PKD walk or otherwise supported the Foundation and ask that you join me again this year as I prepare to walk again this fall. This is one of several posts you can expect before October, I will try to make future posts more exciting and fun!
Those who know me and follow my blog have all heard my story, but for those that might be new here, PKD stands for polycystic kidney disease. Currently, my status is that I have too many cysts to count, yet they are not bothering my kidney function and I am otherwise healthy. I may have bad knees and arthritis and normal aches and pains, but that’s no different than any other 56 year old! However, as far as insurance companies are concerned, my condition is considered fatal therefore, I cannot get life insurance. Thank goodness that right now I am covered by my husband’s insurance or I might be up a creek.
It is because of you and your generous support that important research has been able to take place, research that will one day bring a cure to this debilitating and potentially fatal disease. My mother had it and died from it, I also have it, but currently, I am not in any danger and my labwork looks wonderful, praise the Lord!
You can help me by joining a walk close to you, volunteering your time serving at one of the walks or donating money for research so that we can someday find a cure. My local chapter will walk again this October and we are currently taking donations. Be a hero again, help us beat last year’s goal and know that your dollars go 100% to projects like the ones involving 5+ potential PKD treatments now in clinical trials. Last year you helped us reach the goal of 2.5+ million dollars in science and research funding and walked the road with thousands of patients and families in 60 local US Chapters.
Register today at walkforpkd.org and if you choose to support my team, great! I am in the portal North Texas Walk for PKD as Kim Smyth (I don’t actually have a “team” yet but I will by Oct.!) Thanks in advance for any help or donation you are able to give, I realize there are many causes to support out there, I appreciate you considering ours.
If you have questions or comments, please feel free to let me know. See you mañana on the patio!
Well folks, I got my first email today from the PKD Foundation letting me know that it’s once again time to start thinking about the PKD Walk for a cure. Last year some of you were so sweet and helped me raise some money for this potentially fatal disease. I appreciate it and I want to do something this year to encourage you to help out again, whether that be a giveaway, a coupon or some other goodie I can dream up. Good thing is, I have until October to figure it out! Maybe some of you creative geniuses can even give me some ideas on the subject…you know, help me help you!
As you may or may not know, my mother passed away from complications of PKD after being on dialysis for 18+ years and I also have it. I discovered I had it when going in for testing to see if I could donate a kidney for her. Later on I found out that the disease is genetic and children of mothers with PKD have a 50% chance of inheriting the disease. You can check out my posts from last year to find out more, but basically, PKD is short for polycystic kidney disease. In my case, I have too many cysts to count, but they aren’t impeding my kidney function so far. I am monitored by a nephrologist (who I LOVE) and I try to eat healthy and take care of myself so the disease doesn’t progress any faster than normal.
Since you will be hearing more about this in future posts this year, I’ll cut it short and just tell you that I am already registered and can start raising money immediately. I myself will again be donating a personal pledge for myself and also in my mother’s memory. You can feel good knowing that 100% of the money raised goes to research! Go to walkforpkd.org to donate, whether you do it for my team or not is totally up to you, I do want to surpass last year’s goal however-I’m shooting for $500 this year. If you are a company, or know if one who would like to sponsor the walk, get sponsor info at: firstname.lastname@example.org or call 816-268-8462, or go to the sponsorship tab at PKD Foundation page.
This morning was finally the day for the PKD Walk, put on by the good folks in Southlake and was relatively well attended. Nothing compared to the walks to raise money and awareness for breast cancer, and not as organized, but I was glad to be a part of it. My hubby walked with me, after the balloon release, which was emotional for me. It makes me feel bad that I could have and should have been doing more to raise awareness and money since my mom was first diagnosed. So, I was thinking of her as we released our balloon and her name was on my back as we walked. Not that many were there to see it-my hubby and I were way out in front of the pack the whole way, our pace being much quicker than most. Thanks again to everyone who donated to my “team”, even if that team turned out to be my hubby and me. I also put in my own private donations, although I would have done that online as well, I would have been able to designate part for myself and part as a pledge in my Mom’s name. She passed away two years ago from the disease. As far as I know, I’m the only one of her five children to be diagnosed as well. Anyway, I hope next years Walk is bigger and better, and that the contributions for research keep pouring in.
Later in the day, he took our son Chris to play golf as part of his birthday present. While they were gone, Becky and I secretly baked him a kickass Banana Pudding birthday cake and, just in case he smelled something cooking when he arrived back home, I made some Paleo chocolate chip cookies so he wouldn’t get suspicious. I got the recipe from http://Www.ambitiouskitchen.com and they are delicious.
After all the activity in the kitchen, I subjected Becky to my taped recording of the Rocky Horror Picture Show remake-she wasn’t impressed. Then again, she is so young, she barely remembers the original. We had fun laughing at it anyway. See, I DO remember the original and I appreciated the music of both versions. The soundtrack and of course Tim Curry (the original Frank-n-Furter) made the whole movie. So I was happy to hear all the songs again, even if they weren’t exactly the same renditions as the first. I though the remade Riff Raff was awesome and Victoria Justice was very good as Janet.
It was kinda like the creators of this one forgot the whole point, originally, it was so outrageous for a man to be playing a transvestite with over the top makeup-just not the same with a female playing a transgender role. Although I must say, the acting and singing would have been fine had you never seen the original and had it to compare to.
All in all it was a very good day, and the night is yet young! I can’t wait to see if Becky chickens out on performing her birthday “rap” for Chris’s birthday! Stay tuned, results will be in tomorrow, on the patio 😉
Wow! It just so turns out that my Dad’s 82nd birthday is today and I’m also on my 82 post in the 365 day challenge! What a coincidence!
Also, today is the last chance to get a donation in for my team in the PKD walk. Of course, you can always donate or make a pledge, however, tomorrow is the actual PKD Walk, and I’m just halfway to my team goal. I’d appreciate whatever you can do to help me in this effort. And thanks again to the bloggers who have donated so far! I was reading some news today concerning future treatment options for my disease, and there are five new medications in clinical trials! Yea! Would it not be fantastic if me and hundreds of other PKD patients had the option of stopping the advance of the disease with a simple medication and not have to go on dialysis or have a kidney transplant? That is what we are raising money for, to make medications like this possible and other life saving treatments and research is ongoing in this endeavor.
I know y’all are probably “tired of” me talking about this and pleading for donations, I will soon be giving it a break for a while…til the next walk lol! But seriously, because it is a cause close to my heart, my Mom had it too, I will continue to educate myself and others and do what I can to support this cause. Wish me good luck and pleasant weather on tomorrow’s short walk. Luckily, mine is short, since the old back ain’t what it used to be. A mile ain’t nothin for a stepper though, and my hubby will be with me all the way.
After all that, I will be busy with preparations for the big birthday weekend. My Dad and my son have birthdays two days apart, and my friend’s is the day after my son’s. She is unfortunately out of town on business, so I already put her card and gift in the mail. My son and my Dad will be joining us for dinner Sunday and so far, that’s all I know, lol. Hopefully I get something figured out for their gifts before then. I, for one, think birthdays should be special. I’m sure I will get something worked out. 😉