Well, Well, Well.....I have met the minimum goal of $2300.00 as of 8/14/09 thanks to all of my wonderful friends and family!!! This walk means so much to me. Just to fill you in....2 weekends ago (8/1/09) I walked 7.5 miles with Jeanne & Lisa. The walk was good but also kicked my butt. Not too bad though. I even attended the Kenny Chesney concert that same evening and stood the whole time. Now thats what I call a trooper....LOL!! I will continue to do walks up until the weekend of the walk. I am so honored to do this event. It means the world to me!! I am not doing this for myself I am doing it for my friends & family who have been directly affected by Breast Cancer or any other form. I can't do much while you are going through everything, but I sure as heck can do something to try and help prevent our kids and family members from having to go through it. You all are HEROS in my book.
I have included the details of our walk so you all can see what we will be up to. I may be sore after but that will be my sign that I accomplished what I set out to do.
Thank you again for all of your generosity. You all mean the world to me!!!
September 11 - 13, 2009
The Seattle Breast Cancer 3-Day will begin with an emotional Opening Ceremony at Shoreline Community College, where we'll gather together to pay tribute to the many women and men who have lost their battle with breast cancer, and honor the survivors. We'll remember the reason we're walking as we make our way north into the Richmond Beach area, through the quiet, tree-lined town of Woodway and into scenic downtown Edmonds. We'll
enjoy great views of Puget Sound as we make our way back east into Lynnwood. We will explore Mukilteo before heading to our own private Breast Cancer 3-Day camp in Everett for the night.
On Saturday morning, we'll rise and shine, ready to hit the trail. This second day of walking will wind through historic neighborhoods and downtown Everett. Bask in the cheers from local shops and businesses along the route. Highlights will include lunch overlooking the Sound, before we travel down beautiful tree-lined streets and back to camp for another night of community, camaraderie and fun.
After a short bus ride, the final day of our journey will showcase many major Seattle landmarks, including Green Lake Park, downtown Wallingford and Gas Works Park. On the way to lunch we will pass by the quaint Portage Bay marina and walk through one of the most historic neighborhoods in Seattle. Lunch will be at a gorgeous park with plenty of shade. The route will travel through the fun, eclectic neighborhood of Capitol Hill before heading downtown. We will pass the famous Pike Place market and walk down the waterfront as we make our way to the Seattle Center for a celebratory Closing Ceremony.
Tuesday, August 18, 2009
Tuesday, May 12, 2009
It's been a while since my last entry.....
Well, I have been kind of bad lately about training. Unfortunately I had some life changes happen that I needed to get a grasp on first and now that I am moving by end of the month I will be more settled and have a more strict training schedule. I just thought I would let you all know what I have been up to. I haven't neglected this event, I have just been very emotionally exhausted. Things are looking up and I look forward to the next 3 1/2 months of training for the event. Will post more soon!
Love to you all!
Love to you all!
Sunday, March 29, 2009
1st 3 Mile Training Walk
Well yesterday (3/28/09) was our first training walk. The 3 of us drove up to Bellevue Square Mall to meet at the New Balance store by 7:30am. From there we preceded to walk 3mi around the Bellevue Square area, up and down hills in the rain/sleet. It was quite amusing. There were times in my head I was saying I just wanted to give up, but I just kept pushing through it. The only reason I was feeling that way is I have been suffering through a slight case of Vertigo for the past week. No fun, but at least I can say I did it!! I was proud of myself because I wasn't even at the back of the pack. We finished the walk about in the middle....literally! It was a great time and we totally felt pumped after. Then once I got home I crashed hard. Didn't help getting up at 4:30am on a Saturday. For those that know me....I love my sleep in days. :-) The rain kind of made it a bit easier to walk in because it made me feel the "hurry up and get this over feeling." All 3 of us bought new Pink ball caps that have the ribbon on them. Those helped keep the rain out of our eyes (or as Lisa put it, kept the rain off of her glasses).
As for donations, I can't complain. You all have been so generous. It is so great to see all my friends and family who want to help out. It means the world to me!!
Well keep checking back for more updates.
Love to you all!
As for donations, I can't complain. You all have been so generous. It is so great to see all my friends and family who want to help out. It means the world to me!!
Well keep checking back for more updates.
Love to you all!
Friday, March 20, 2009
Day 2 Since First Email Went Out, 3/20/09
Well, day 2 since I have sent the first round of emails out to my family & friends. All I can say is WOW!! It's people like you that make this so exciting for me to do!! I am at 8% ($230.00) of my goal as of now. That is FANTASTIC being that I only signed up this past Monday, 3/16/09!!!
It is so fun to watch the honor roll ticker on my personal page. You guys are the best friends I could ask for. If you have or are planning on donating my team and I are kicking around a couple of ideas for those who want to make donations in "Honor" or "Memory" of a friend or loved one. One idea was put all the names on the back of our t-shirt, but then another idea is to make a quilt of Memory & Honor. So if you want, please email me at tianamorton@comcast.net and let me know who your donation is in honor or memory of.
I probably won't update again until Monday, but have a great weekend and thanks again for all of your support, no matter how it's given!!!
It is so fun to watch the honor roll ticker on my personal page. You guys are the best friends I could ask for. If you have or are planning on donating my team and I are kicking around a couple of ideas for those who want to make donations in "Honor" or "Memory" of a friend or loved one. One idea was put all the names on the back of our t-shirt, but then another idea is to make a quilt of Memory & Honor. So if you want, please email me at tianamorton@comcast.net and let me know who your donation is in honor or memory of.
I probably won't update again until Monday, but have a great weekend and thanks again for all of your support, no matter how it's given!!!
Thursday, March 19, 2009
Aunt Debbie's Breast Cancer Journey
Before I begin this story of my journey through my experience with breast cancer, I have to say that without the love and support from my wonderful friends and family it would have been a lot harder journey. All of their love and caring helped to keep my attitude positive. One of my biggest inspirations to me was my cousin’s husband who had gone through years of pain and surgeries from his Crohn’s disease and I thought of those years and only remembered him always being so positive and smiling. Another great inspiration has been the people that I have met at the infusion center. A lot of them are going through a much rougher time than I am and they are all so supportive and encouraging. I think to myself that I’m lucky to have such a good prognosis and I know everything will be okay for me and I need to try and stay positive. The chemo nurses and my Oncologist are the greatest and have helped keep me going. When I first learned of my prognosis and treatments, family members had told me that I’m a strong person and I can get through this. The funny thing is, I’ve never thought as myself as a strong person. I have had days when I was really down and have had some pity parties for myself and that’s to be expected, but I found that you just need to pull up your bootstraps and do what you have to do.
It was late on a Saturday evening in March of 2008 and I had my PJs on and was watching a movie on TV. I was eating a snack and some of the crumbs fell down inside my PJs and when I was brushing these crumbs off my right breast I discovered a lump. On Monday morning I called my gynecologist office and they had me come in for an exam. I was then scheduled to go have a mammogram and an ultra sound. After the ultra sound the breast clinic scheduled a biopsy in a couple of days. My gynecologist office called on Monday afternoon and asked if I could come to the office at 4:30 that afternoon to discuss the biopsy results. When I expressed concern, I had been told that this was normal procedure. As you can imagine I was pretty darn upset when she told me I had breast cancer. The next couple of days were the most emotional trying to come to grips with the big “C” diagnostics. I was next scheduled to see a surgeon and he explained that I would have a lumpectomy and since I was in the early stages my prognosis was very good and that breast cancer today, if caught in the early stages, is not like it was years ago. I then met with an Oncologist and Radiologist and it was explained to me that they wouldn’t know until after the surgery what my treatment would be. After that I was scheduled for a breast MRI, chest x-ray, and PETScan. When the results came back from the MRI and PETScan, it looked like I had another spot lower on the same breast but smaller and deeper. The biopsy on this spot did not come back with good enough information so they decided in surgery to remove this 2nd lump first, freeze it, and then test it to see if it was cancer. If the tests during surgery showed that it was cancer I had agreed with the surgeon for him to do the mastectomy, and if it wasn’t then I was to have a double lumpectomy. The tests they did at the time of surgery showed that this was not cancer, so he performed the double lumpectomy. When I went in for the first surgery I was in the beginning of stage 2 of invasive cancer on the lump I had found.
A couple of weeks after this surgery I received a phone call from the Oncologist and was informed that after further testing, the second lump was diagnosed as DCIS or Ductal Carcinoma In Situ which is considered pre-cancer. It was explained to me that this pre-cancer can start growing at any time and is not easily detected so you would always be wondering if it was later developing into invasive cancer or growing. The “team” which included my Oncologist, surgeon and other doctors met and discussed my case and they recommended that I have a mastectomy. So after discussions with the Oncologist and the surgeon, I made the decision to go back in and have the mastectomy.
About a month after the mastectomy I started with my first round of chemo which was 4 treatments, one every two weeks, of Adriamycin. As most of you know, the worst side effects of this treatment are losing your hair, horrible nausea, and fatigue. When my hair started falling out I was pretty upset. I went to my hairdresser because she offered to be the one to shave my head when it was time and she really put this hair loss into prospective for me when she said “It’s only hair and it will grow back”. Boy, I thought she is so totally right and after that I was totally fine with losing my hair. The next round of chemo was a weekly dose of Taxol and Herceptin for 12 weeks. I was only getting 1/3 dose of each every week and shouldn’t have many side effects, but I seemed to have a few. My feet and hands were numb and tingling a lot, I was still getting nauseas, especially in the mornings or when I was tired, and the fatigue was still pretty bad. After about 6 or 7 Taxol treatments, my feet and ankles were swelling a lot. They took me off the treatments for a couple of weeks and put me on a diuretic to help reduce the swelling. I had a couple more treatments and the swelling was not getting any better and since this can be a side effect of Taxol, the Oncologist decided to stop the treatments in early October. I am still having some swelling in my feet and ankles and still cannot wear enclosed shoes. I started getting just the Herceptin treatments in October and will have them every 3 weeks for a year. Thank goodness …there have been no side effects from the Herceptin.
My hair is growing back and I’m feeling pretty darn good. I hope to start my breast reconstructive surgery in September. Wearing a bra now is not very comfortable at all. It had to be a man that invented the breast prosthesis, because I’m sure that a woman would not have made it so heavy. Since I’m having the reconstructive surgery, there is a lot of loose, folded skin and wearing this darn thing is very uncomfortable. Also my bra strap on the left hand side irritates the heck out of my port. My husband used to laugh when I was still wearing my wig because I would walk in the house after work and immediately remove the wig and take off my bra with a big sigh of relief. So for now, I’m having my Herceptin treatments every 3 weeks and a MUGA Scan every 3 months to check my heart, as the Herceptin can damage your heart. So far everything is looking very good for me and I strive to keep a positive outlook.
It seems like I’ve been through a lot this past year, but really there are so many people out there that are terminal and in so much pain every day of their life. I feel like I’m one of the lucky ones.
Thank you everyone for being there for me when I needed you the most. I feel so honored that my niece, Tiana, is walking in the 3-day cure race in my honor. Please support her.
Thank you,
Debbie Hendrickson
It was late on a Saturday evening in March of 2008 and I had my PJs on and was watching a movie on TV. I was eating a snack and some of the crumbs fell down inside my PJs and when I was brushing these crumbs off my right breast I discovered a lump. On Monday morning I called my gynecologist office and they had me come in for an exam. I was then scheduled to go have a mammogram and an ultra sound. After the ultra sound the breast clinic scheduled a biopsy in a couple of days. My gynecologist office called on Monday afternoon and asked if I could come to the office at 4:30 that afternoon to discuss the biopsy results. When I expressed concern, I had been told that this was normal procedure. As you can imagine I was pretty darn upset when she told me I had breast cancer. The next couple of days were the most emotional trying to come to grips with the big “C” diagnostics. I was next scheduled to see a surgeon and he explained that I would have a lumpectomy and since I was in the early stages my prognosis was very good and that breast cancer today, if caught in the early stages, is not like it was years ago. I then met with an Oncologist and Radiologist and it was explained to me that they wouldn’t know until after the surgery what my treatment would be. After that I was scheduled for a breast MRI, chest x-ray, and PETScan. When the results came back from the MRI and PETScan, it looked like I had another spot lower on the same breast but smaller and deeper. The biopsy on this spot did not come back with good enough information so they decided in surgery to remove this 2nd lump first, freeze it, and then test it to see if it was cancer. If the tests during surgery showed that it was cancer I had agreed with the surgeon for him to do the mastectomy, and if it wasn’t then I was to have a double lumpectomy. The tests they did at the time of surgery showed that this was not cancer, so he performed the double lumpectomy. When I went in for the first surgery I was in the beginning of stage 2 of invasive cancer on the lump I had found.
A couple of weeks after this surgery I received a phone call from the Oncologist and was informed that after further testing, the second lump was diagnosed as DCIS or Ductal Carcinoma In Situ which is considered pre-cancer. It was explained to me that this pre-cancer can start growing at any time and is not easily detected so you would always be wondering if it was later developing into invasive cancer or growing. The “team” which included my Oncologist, surgeon and other doctors met and discussed my case and they recommended that I have a mastectomy. So after discussions with the Oncologist and the surgeon, I made the decision to go back in and have the mastectomy.
About a month after the mastectomy I started with my first round of chemo which was 4 treatments, one every two weeks, of Adriamycin. As most of you know, the worst side effects of this treatment are losing your hair, horrible nausea, and fatigue. When my hair started falling out I was pretty upset. I went to my hairdresser because she offered to be the one to shave my head when it was time and she really put this hair loss into prospective for me when she said “It’s only hair and it will grow back”. Boy, I thought she is so totally right and after that I was totally fine with losing my hair. The next round of chemo was a weekly dose of Taxol and Herceptin for 12 weeks. I was only getting 1/3 dose of each every week and shouldn’t have many side effects, but I seemed to have a few. My feet and hands were numb and tingling a lot, I was still getting nauseas, especially in the mornings or when I was tired, and the fatigue was still pretty bad. After about 6 or 7 Taxol treatments, my feet and ankles were swelling a lot. They took me off the treatments for a couple of weeks and put me on a diuretic to help reduce the swelling. I had a couple more treatments and the swelling was not getting any better and since this can be a side effect of Taxol, the Oncologist decided to stop the treatments in early October. I am still having some swelling in my feet and ankles and still cannot wear enclosed shoes. I started getting just the Herceptin treatments in October and will have them every 3 weeks for a year. Thank goodness …there have been no side effects from the Herceptin.
My hair is growing back and I’m feeling pretty darn good. I hope to start my breast reconstructive surgery in September. Wearing a bra now is not very comfortable at all. It had to be a man that invented the breast prosthesis, because I’m sure that a woman would not have made it so heavy. Since I’m having the reconstructive surgery, there is a lot of loose, folded skin and wearing this darn thing is very uncomfortable. Also my bra strap on the left hand side irritates the heck out of my port. My husband used to laugh when I was still wearing my wig because I would walk in the house after work and immediately remove the wig and take off my bra with a big sigh of relief. So for now, I’m having my Herceptin treatments every 3 weeks and a MUGA Scan every 3 months to check my heart, as the Herceptin can damage your heart. So far everything is looking very good for me and I strive to keep a positive outlook.
It seems like I’ve been through a lot this past year, but really there are so many people out there that are terminal and in so much pain every day of their life. I feel like I’m one of the lucky ones.
Thank you everyone for being there for me when I needed you the most. I feel so honored that my niece, Tiana, is walking in the 3-day cure race in my honor. Please support her.
Thank you,
Debbie Hendrickson
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