October, Shocktober

October has always been a bitter-sweet month for me and my family.

The Sweet:

  • my nephew Ian was born (he’s now a handsome 19-year old!)
  • my step-nephew Adam was born
  • my sister Dori was born

The Bitter:

  • my Dad was diagnosed with cancer in October (lost him in 1994 – 6-months after diagnosis)
  • my Mom passed away in October last year (2014)
  • my brother-in-law Fred was killed in October
  • I suffered a ruptured brain aneurysm in October in 2006.

And I’m sure I’m leaving something out, but those are the biggies. I think that’s enough, don’t you?

October 25th is a bitter-sweet day for me as well. It was Dori’s birthday, but it was also the day I was released from the hospital after a three week stay nine years ago next week. I remember speaking to Dori on the phone after I got home and she told me my coming home was the best birthday present I could have given her. We were both crying.

How awful that six year’s later, I was crying in a London hotel room after findiing out Dori had suffered a ruptured brain aneurysm too and I never got a chance to say good-bye and let her know how much I loved, and adored her.

Brain aneurysms simply suck. They take the lives of young, old, healthy, joyful people, and devestate the lives of those they love. Granted, they don’t always kill, but they certainly can cause distruption and change the lives of all those around you forever.

October is also a stressful month for me at work. With my rupture happening in the critical last weeks of catalog production, it was left to our small crew and a poor graphic artist brought in to pick up the pieces to finish the book. They did the best they could. Three months later I returned to work part-time to find my office with calendar’s still set on October and reminders on my computer for jobs that needed to be completed…in October. A surreal experience for sure.

I am one of the lucky ones who #1, worked at a great company that allowed me the time to heal and recover and #2, I was physically able to perform my job full time after a 6-month recovery period. Soooo many are not so fortunate and the needs of survivors and their issues after a rupture are so varied, it’s difficult for employers and co-workers to truly understand the depth of recovery needed.

I suppose that’s one of the reasons I speak out about brian aneurysms and try to educate others. Although this blog as been theraputic for me personally, I have received a few comments from other survivors and those who have lost loved ones who tell me it has helped. That means more to me than any amount of money I could raise. Support is what we all need. I have survived a rupture, a coiling, a re-coiling and a stent, then a craniotomy on a 2nd un-ruptured brain aneurysm. And that first large brain aneurysm is STILL giving me issues. Look for updates on more potential “brain bling” in the New Year!

Every October I remember the day of my rupture. Every October I remember my mother’s death now. I remember my father’s diagnosis with cancer and I remember my sister’s birthday on October 25th. I still hate October, but I’m here. For whatever reason, I. AM. HERE.

 

Head Over Heels

A fellow brain aneurysm survivor posted on Facebook tonight that she had fallen and hit her head pretty hard. After a CT scan, she was given the “all clear”, but I know it must have been scary. She has been through multiple procedures and suffered a stroke.

This week I celebrated my 9th Annie-versary: nine years ago I suffered a ruptured brain aneurysm. The 11mm (almost 1/2 inch in diameter) aneurysm I didn’t know was growing inside my brain suddenly ruptured. The annie-versary day went by with little fan fare. My husband made me dinner, which is always a special treat, but beyond that, because I’m always so busy at work, I didn’t do much to celebrate.

The first couple of years, I would take the day off and have a spa day. I think I need to start doing that again…regardless of how stressful & busy things are at work this time of year…which it always is. They’re lucky to still have me.

Falling and hitting my head is probably my biggest fear. I hate it when I get to work late and have to park up on the very steep hill parking lot. I always fear falling down and make sure I grasp and have a good hold on the PVC pipe railing along the “side walk” up and down the hill. The railing is always covered with snow or ice too, so not sure how much of a help that is.

I probably didn’t share this with many people, but on our last night in Scotland in 2013, our tour guide dropped us off at a hotel near the Edinburgh airport. Dave and I enjoyed a lovely dinner in the hotel restaurant, then I REALLY wanted to take a long soak in a tub and there was a deep, soaking tub in our room at the hotel. As I was getting out, I misjudged the height of the tub to the floor and slipped on the tile floor as I got out, BARELY missing hitting my head on the tub and landing on my backside pretty hard.

Dave immediately ran in from the other room. I was laying on the floor with my head pretty much laying up against the tub. Once we both realized I was okay, we both shook in fear. It was a scary moment and one I hope never to repeat. And that was before I had my craniotomy on my 2nd brain aneurysm.

I suppose the fear is that a hit on the head could produce some sort of shock on the aneurysms and force them to bleed. Or that the surgical work that has already been done…could become “undone”. I’m not even sure how realistic that fear is. I supposed I should ask on my next visit with my neurosurgeon. Because I’m susceptible to aneurysms and bleeding, I would think any hard hit could be a risk. So, I’m very glad Lori got a CT scan after she fell and hit her head. I’d do the same thing.

I didn’t hit my head when my first brain aneurysm ruptured in 2006. No warning, no symptoms, that I recall. But I know that brain hemorrhages can occur when hitting your head. The tragic death of Natasha Richardson is a sad example of that.

So, nine years ago this week, I was in the ICU at Maine Med, then moved to the 608 Neuro-ward. I was in the hospital for two weeks then had six months of recovery before going back to work full-time. Only one person from work visited me and it was simply because she was in the area. I’m so glad Lori has such a wonderful group of friends to support her. I’m sure this fall scared her very much. I know her daughter and husband keep a close eye on her and I’m sure THEY were just as scared as she was. Her service dog Tober will make sure she’s okay. What a great dog he is. Love him.

I’m a NASCAR fan, and the race at Charlotte, NC is this weekend. I remember watching that race in ICU with Dave and my sister Dori (who died of a ruptured brain aneurysm in 2012). They were impressed I knew the drivers and was so responsive. I was one of the lucky ones. Some times I wonder WHY I was one of the lucky ones when so many beautiful, vibrant people who had children to live for aren’t here anymore. It just doesn’t make sense some times. Survivor’s guilt? You bet cha. I’m not a mother and I think I’m a very selfish person, so I’m not sure why God chose ME to live over all of the other beautiful, strong individuals who have lost their lives and devastated their families over ruptured brain aneurysms. It just doesn’t make sense to me some times.

So, yes…I walk slower in snowy & icy conditions. I drive slower in snowy & icy conditions. I don’t ride a bike anymore because of the fear of falling off and hitting my head. I don’t do any strenuous physical sports anymore…not that I ever did before. Falling and hitting my head can happen at any time…even slipping on some of the acorns in the driveway, which is like walking on marbles, gives me pause. I bought this fear up at a support group meeting, but I was on the only one who addressed it. I’m sure other’s have that fear. I’m so glad Lori is okay after her fall. Aneurysms survivors have another added fear. Goody….but I’m still here.

A H.E.R.O Among Us

On this past Labor Day holiday weekend, Dave and I attended the Nolan’s H.E.R.O. Foundation 1st Annual 5K Run & 3.13K Walk in Pittsfield, Maine. About a 40 mile drive north from where we live. We brought a Brain Aneurysm Awareness tent and information regarding brain aneurysms.

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Nolan’s H.E.R.O. Foundation is a non-profit organization formed to carry on the mission of Nolan Berthelette. who lost his life to a ruptured brain aneurysm just a little over a year ago in 2014. At the very young age of 14, Nolan’s death struck a chord in this tight-knit community and the outpouring of support his family has received is overwhelming and inspiring.

Last year, just a short time after we heard of Nolan’s death, our group contacted the family to see if there was anything they needed or if we could lend support and comfort. We were surprised when a group of over 160 people arrived at our KAT-Walk & Karo-5K just a few short months after losing their son, brother, friend and team mate to this silent killer. Emotions were still very raw and many had a difficult time, but we had hoped the support and comfort they felt from the local brain aneurysm community would help in some small way on their paths to healing.

When Nolan’s parents set up their H.E.R.O. Foundation and pursued holding an event in Pittsfield, we knew we had to have a presence in some form and show OUR support in return for their event. Sadly, it was just Dave and I from the group in the southern part of the state, but it was an honor to be there and help in any way we could. We provided almost off their tents and their fantastic crew of volunteers made setup and tear down an easy experience.

Ray, Amy and Nason are still grieving the loss of Nolan, but setting up the foundation and creating, what they hope to be an annual event, allows then to be able to DO something, where they weren’t able to save Nolan. I know that’s something that everyone struggles with after losing someone: if they only could have DONE something to save them or help. That helplessness and lack of control can linger for years.

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As we arrived in Pittsfield at the Maine Central Institute’s football field, the town was still waking up on a brilliant morning filled with blue skies, light fog, and the hangover of Nolan’s former football team kicking butt & taking names the previous night on that very field with a 64-0 win! How appropriate.

The number of volunteers and donated items was remarkable. Truly a community effort. So many parents knew Nolan because of his friendship with their children and they know and love Ray & Amy and wanted to show their support in any way they could. Cheerleaders from the school were there to cheer on participants, the entire football team, tired from the previous night, showed an amazing amount of energy and support and helped in any way they could.

Since we were in a tent representing what killed Nolan, we weren’t sure how many people would stop to talk with us, but it was a nice mix of curious adults and teens and those who knew someone else who had a brain aneurysm as well and I think they all appreciated us being there, even if it was a painful reminder.

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The most poignant moment for me was when a group of young ladies from Nolan’s school came to the table. I think they were mostly there for the free brain aneurysm awareness bracelets, but they did ask a few questions and seemed genuinely, albeit hesitantly, interested in exactly what had happened to Nolan. Dave tried to be very sympathetic and careful in explaining what an aneurysm was and how it effects the brain when it ruptures. At one point I saw one of the girls place her arm around another lovely young ladies’ waist for comfort. It’s those simple gestures of compassion that can mean the most to someone who has lost a loved one to brain aneurysms. I know…I’ve been there.

I think the family, Nolan’s classmates, and the community are moving in a good direction by honoring Nolan in such a positive way. I never knew Nolan, but the stories I hear about him indicate he was a very special young man and had an amazing life ahead of him. The number of orange items, Nolan’s favorite color, was evident throughout the event in his honor.

H.E.R.O. stands for Helping Everyone Realize Opportunities. “Being a hero doesn’t take someone that is superior to others or with an abnormal power. All it takes is an average human willing to do what is right for others.” Those are words written by Nolan in his last essay and they have inspired Ray and Amy to create the foundation.

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If you know someone who is “willing to do what is right for others”, let the world know and nominate them for a “I Am A H.E.R.O” bracelet on the Nolan’s H.E.R.O. Foundation website.

I think everyone knows an unsung hero in their life. Why not recognize them in a special way and let the world know they are a true H.E.R.O.

A Compelling Story

“You need to have a compelling story.“ That’s what we’ve been told our group (Maine Brain Aneurysm Awareness) needs in order to get some local television coverage. Webster’s dictionary’s definition of the word “compelling” is:

: very interesting
: able to capture and hold your attention
: capable of causing someone to believe or agree
: strong and forceful
: causing you to feel that you must do something

So, apparently no one feels the following examples are compelling enough to warrant at least one television or newspaper interview in the last 6 years?

  • A vivacious 32-year old died suddenly in her bathroom of a massive ruptured brain aneurysm three days after Christmas. She lived alone and was found the following morning by her devastated mother. (The KAT-Walk was created in her memory & honor)
  • The husband of a ruptured brain aneurysm survivor also lost his niece and sister-in-law to ruptured brain aneurysms.
  • A woman from New Hampshire was vacationing in Maine and suffered a ruptured brain aneurysm in Shaw’s Supermarket. After a misdiagnosis, she eventually went to Maine Medical Center where the only interventional radiologist in the state saved her life. A few years later, she also survived breast cancer and a double mastectomy.
  • A man suffered a ruptured brain aneurysm while home alone. After many hours, his young children discovered him after coming home from school. Two hospitals and a trip to Boston saved his life.
  • A 40-year ruptured brain aneurysm survivor had to be taken to Canada.  At the time of her rupture, no one in the northeast did brain surgery for aneurysms then. The original clipping failed and she was re-clipped. Which means multiple craniotomies. She is a walking miracle.
  • A much-loved 53-year old woman died of a massive ruptured brain aneurysm on Mother’s Day after presenting symptoms two previous visits to doctors, leaving a husband and a 15-year old son behind.
  • A beautiful 28-year young woman, who was an active runner and very physically fit, suffered a ruptured brain aneurysm while working out. She never recovered leaving her family devastated. She was to be married only a few short weeks after her death. (The Karo-5K was created in her memory & honor)
  • One woman survived a ruptured brain aneurysm that was filled with 11 coils, only to lose her sister to a ruptured brain aneurysm six years later. Then Dr’s discovered she also had a second brain aneurysm which was clipped via a craniotomy, but the original one that ruptured is still giving her cause for concern 9 years later.
  • A father of three survived a devastating ruptured brain aneurysm. The deficits he and his family have faced are life-altering and difficult but he IS alive and living life to the fullest.
  • A woman’s ruptured brain aneurysm at 4 a.m. left her with limbs numb, speech slurred, a rapid heart rate, sweating, and falling to her knees. The EMT’s who arrived at her home took her blood pressure and asked some questions. They determined it wasn’t a serious issue and left it to the patient if she wanted to go to the hospital or not. Thankfully she went on her own and the Dr. in the ER sensed what it could be and had her scanned and transported to Maine Med where her life was saved.
  • A young, talented, 13-year old boy fell victim to a ruptured brain aneurysm in his home. The outpouring of grief and support after his death was overwhelming. (Nolan’s H.E.R.O. Foundation)

I could go on and on if I knew I could accurately describe the situations of everyone that I have met. So many stories of hope, fear, disaster, strength, and courage.

So…apparently none of those stories are compelling? How many people have to die and suffer debilitating deficits before this cause it compelling enough to the local news media? To those whose lives have been touched by brain aneurysms there is plenty to hold one’s attention. Survivors HAVE to begin to believe they’ll be fine or they’ll crumble. And in many cases of those left behind, the desire to DO something is overwhelming after these silent killers attack without warning in some cases. Our fundraising events do more than raise money to help other families, they raise the hope and spirits of those left behind or those surviving.

We were lucky enough to have a lovely article written about Kim after her passing. It was written in the local sports section because she was a fantastic softball player, but beyond that, we have received little to no local media support focused solely on our cause. It’s not for our group’s benefit…it is to raise awareness and to allow others who have been touched by brain aneurysms to gather and support one another.

Our cause doesn’t have a specific color that we brand; doesn’t have a celebrity spokesperson that everyone adores; or a social media “challenge”. The more we’re able to talk about brain aneurysms, the more awareness will be raised and hopefully we can SAVE A LIFE.

I think that’s pretty “compelling” don’t you?

READ MORE About Us: MaineBA.org

It is estimated that up to 1 in 50 people in the U.S. will develop a brain aneurysm during their lifetime. Each year about 30,000 people will suffer a ruptured brain aneurysm. Almost half of the victims will die and of those surviving, only one third will recover without disabilities.