KAT-Walk & Karo-5K Events 2012

Even before yesterday’s 4th Annual KAT-Walk and 1st Annual Karo-5K started, I knew it was going to be a special event. The number of strangers effected by brain aneurysms that have contacted us this year about the event was astonishing. I think it also meant that our advertising efforts were finally paying off.

People from Maine, Massachusetts,  New Hampshire, Rhode Island, Maryland, and as far away as North Carolina informed us they were coming to the Walk/Run andKim and Heidi let us know WHY they were coming and with whom. Sharing their stories of loss, strength, courage, and survival  – our original tribute to Kimberly Tudor’s memory has now become a tribute to anyone touched by brain aneurysms. I’m beginning to think that’s an even bigger tribute to Kim because of her desire to help people and comfort them. I constantly see her smile on these days and I know she would be proud of all of us and the hard work we’re doing.

As a survivor of a ruptured brain aneurysm, and living with another aneurysm, I love meeting other survivors. Our stories are all different and our paths of survival are also very different. Some are more successful than others and all of those examples were represented yesterday.

Trailer PicDave and I arrived earlier than others at the venue to set up the main display. We wanted something to greet the volunteers as they started showing up to get them excited about the event. The trailer that transports all of the signs, banners, posts, poles, tents, boxes and forms from our house in Augusta, also doubles as a beautiful display of flags. Dave decorates is differently each year. Last year, because the walk landed on the 10th anniversary of 9/11, he decorated the trailer to remember those fallen that day.

This year, because the run was in honor of another family who lost their young daughter last year, the Karo-5k was run and new banners, signs and directional materials had to be created. The trailer included a photo of Karolina and Kim and new signage that Dave and I created.

The committee also decided to solicit for sponsorship this year to help defray the cost of the event and we were highly successful with the venture and could not have done it without them!

Setup for the event, as usual, was extensive and beautifully displayed. There was a brief rain shower that was significant enough to get everything wet, but not enough to dampen anyone’s spirit.

The rain stopped, the sun came back out and the winds picked up. Being on the coast allows for stunning views, the sounds of the water along the shoreline and high winds! We had all of those.

I was joined in the Brain Aneurysm tent by a fellow survivor, Julie. Dave and I had gone over to her aneurysm event in NH last month and she repaid that favor, but also provided a two-pronged attack in our tent to reach out to other survivors or those effected by aneurysms. Julie is a fervent advocate for early detection and fighting for your rights as a patient and demanding your own self care. She is also a breast cancer survivor. Very proud of her.

Two young woman who attended the event yesterday had flown into Maine from Baltimore on Friday night. Sarah had just lost her mom a month ago to a ruptured brain stem aneurysm. At 27 years old, we were impressed she decided to use our event as the way to honor her mother so soon after losing her. It was emotional and comforting for her and I believe everyone who attended welcomed her with open arms and knew how difficult it would be for her.

Both of the mother’s of Karolina and Kim took Sarah under their wings during the day and gravitated towards her, which was understandable, sad, and sweet all at the same time. They lost their young daughters who were both about the same age as Sarah, and Sarah had just lost her mother. Two mothers without daughters and a daughter suddenly without her mother. Touching and heartbreaking.

My own personal heartbreak for this year’s walk was honoring my sister Dori who we lost in May to a ruptured brain aneurysm. She had always wanted to come up for our walk and had met Kim when I had my rupture in October of 2006. How awful, ironic, and heartbreaking is it that Kim  and Dori were both lost to ruptured brain aneurysms and I was the one who basically “introduced” them to aneurysms and got them interested and involved. It’s just not right and basically sucks. I find that word one of the best to describe it.

So, I decided to relinquish my duties at the aneurysm tent since Julie was helping me and complete the 3-mile walk in Dori’s honor. The last time I did the walk, was in 2009…in honor of Kim. I recalled a beautiful rainbow appeared that day and we knew it was Kim. Yesterday, I started the walk and about a mile into the walk I realized a little butterfly was flying in front of me off to the side.

I was walking by myself and kept seeing the butterfly, then it reminded me of the butterflies that were placed in the beautiful flower arrangements at Dori’s memorial service and the emotions took over. After trying to walk and cry at the same time, I realized I needed to get off the path, so I stepped aside and let it all out for a bit. Then I resumed the walk. Perhaps this beautiful monarch butterfly was Dori joining me for the walk finally.

Heidi and Dori on boatAs I went around the Back Cove and up onto the bridge, I looked across the water and saw the many flags and tents flying in the wind from our event. It was a beautiful sight and I felt very proud. Then as I rounded the corner and neared the 2.5 mile marker, I was looking at the chop in the water and remembering the one and only time Dave and I took Dori out onto the harbor on his sailboat when she came to Maine for a visit. Dori was scared too death, but we had fun. LOL It was a good memory.

I didn’t have anyone greeting me, but as I dragged my weary bones and feet across the finish line, I blew a kiss to the heavens above and told Dori that was for her. A few minutes later I saw another survivor, Leray, cross the finish line and made sure I ran (well, walked!) to greet her and congratulate her for completing the walk. I was very proud of both of us and Leray will be going in for a recoiling next week, so I wanted her to know how proud of her I was.

This year was also the first time some members of the local medical community participated. My own doctor, who did my stenting and recoiling in 2011, came with his family and Julie promptly made him wear one of the Brain Aneurysm Foundation baseball hats, which he did. He even ran with a baby stroller in tow. We’re hoping to have more medical events in the future so that local EMTs are educated to the symptoms as well as the general public. As I have mentioned before, if I had not gone to the ER and had myself checked out and the Dr. there hadn’t been suspicious of an aneurysm, I may not be here today. Many people have brain aneurysms misdiagnosed, and many are not here today as a result.

We don’t have the exact numbers yet, but it appears there were over 450 people at the walk and run. The run was very well attended and I know that meant a great deal to Karolina’s family and friends. Karo was an avid athlete and had just completed a triathalon a week or so prior to her rupture last July. I’m sure she would have been proud of all of the hard work her family and friends put into supporting this event.

There was a silent auction and this year I finally won those tickets to the Portland Symphony Orchestra’s Christmas concert in December. We had a magician and face painting for the kids and donated food and water to keep participants nourished. This year we rented a sound system with a wireless microphone and were lucky enough to get a fantastic announcer who was a close co-worker of Kim’s. Larry did a wonderful job. I also put together a playlist on my iPad that kept the crowd upbeat and happy.

Unfortunately, I was so busy I do not have any photos of the event myself. But there are some terrific photos of the run and walk HERE-››: Maine Running Photos. Once I receive more photo of the actual venues and tents, I’ll post more links. These are mostly of the run and walk itself and not of the fantastic setup and the new “Honor Board” that was a hit.

Not only is the Back Cove location a stunning venue to hold an event such as this, there is a real sense of community when family and friends meet to support one another and share stories and memories.

Brain Aneurysms don’t discriminate. Young, old, men, women, black, white….doesn’t matter. The sudden and shocking destruction of a rupture CAN be prevented in most cases if the aneurysm is discovered before it ruptures and that’s the word we’re trying to get out. If you’re “lucky” enough to have symptoms before a rupture (some do not), it’s important to get it checked out and insist on getting a good CT-Scan or an MRA. It could save the life of a loved one, or yourself.

Touching More Lives

We attended the first Mystery Ride in New Hampshire over the weekend where we joined the Alton, NH American Legion Riders, Chapter 8, a charitable veterans group, to solve a murder mystery and raise funds for The Brain Aneurysm Foundation. Participants followed the clue map to each stop around scenic Lake Winnipesaukee and picked up clues to solve the mystery of who murdered Hugh Mann Body.

Dave and I were in charge of the last stop (and clue) on the map and set up our Brain Aneurysm tent. It was a beautiful day out and we welcomed the bikers and some other civilians in their cars as they went in search of clues for a wonderful story written by an aneurysm survivor (and event organizer), Julie.

We have to admit hearing and seeing the 15 or so motorcycles turn into our stop all at once was quite a sight. As much as we wanted more to participate, it was still pretty exciting to see those that DID participate. They all seemed to enjoy the mystery and their help in bringing awareness and money to Brain Aneurysm was greatly appreciated.

The Silent Auction was a huge hit and all of the money raised from that, as well as individual donations, and a 50/50 raffle will go to genetic research for familiar aneurysms. Julie decided to give that money to the Brain Aneurysm Foundation in my sister Dori’s name. I was very moved and touched she did that.

They were also able to connect with at least two other survivors and that is really what part of the events like this is about. The more people you can connect with, the more of a community you can build. One woman had survived a pretty awful rupture just a couple of months ago. She was doing GREAT! And an older woman discovered she had 3 brain aneurysm and an aortic aneurysm, but was there ready to to kick butt in the silent auction!

As with our KAT-Walk event, in some years it’s not about the quantity of the people who participate, but the quality of the people and I’d say we had some top-notch, salt-of-the-earth folks who cared about a cause that was very near and dear to their friend.

Thank you to EVERYONE who participated, contributed, and cared. For a few PHOTOS from the event, CLICK HERE>>

Aneurysms Be Damned….

Aneurysms be damned…we’re taking that trip to the UK finally!

Although Dave and I had planned on waiting a year after our wedding to take our official honeymoon to the UK, we hadn’t planned on my large aneurysm raising it’s ugly head, the discovery or a new aneurysm and the addition of more coils and a stent to my brain. Those little item resulted in a longer delay for the honeymoon and we had to put it off for another year.

Well, the “one-of-those-days” moments is about to arrive and we’re really going to do it. Tickets, hotels, guides and flights are all booked and ready to go. We’re as ready as two people can possibly be for an overseas trip. Hell, we’ve had long enough to plan for the darn thing!

And even though I know it won’t happen, I can’t help but think all of that metal in my head will set off the metal detectors going through airport security. LOL I know it won’t, but I’ll still think about it for sure.

I love that we’re taking this trip with so much love, support, blessings and prayers from our families, friends, and co-workers. I am truly thankful for it all and for the Dr’s who have provided their expertise and skill to prolong my life and give me another chance to LIVE! So many aneurysm survivors are not able to enjoy living their lives to the fullest, but the majority of us DO try and this is a big step for me. I haven’t flown since 2005 when I flew to visit my friend Gwen in Canada. Little did I know during that trip that I had a 1/2″ diameter aneurysm waiting to blow.

Now I DO know what’s going on and I’ve been given the “Green Light” to travel by my Dr. So…LETS GO TO LONDON BABY!

Christmas Memory

As I was finishing up wrapping Christmas gifts for Dave and I today, I was reminded of five years ago and how frustrating Christmas was for me. Yes, I was thankful I was alive, but I was frustrated because I couldn’t enjoy Christmas like I previously had.

Just wrapping gifts was exhausting and I most certainly wouldn’t have been able to wrap gifts all afternoon like I did today. A simple task for most, but at that time, two months after my rupture, it was daunting…and frustrating.

I look back now on my blog entry from that year (2006), and have to smile because I’ve come so far since that day and I am so lucky to be here wrapping gifts at all.

For those of you still struggling, don’t give up. It WILL get better. Baby steps. Just take it day by day and celebrate the small victories…like getting ONE gift wrapped. You’re doing great!