Reminders

Our monthly brain aneurysm support group meetings are a wonderful way for survivors, their supporters and for those who have lost loved ones to come together and discuss this horrible thing that connects them. The fantastic medical professionals who have come to speak with us have opened the eyes of those who haven’t been educated themselves and have helped supporters gain a better understanding of what their loved one has gone through. I rarely come away from the meetings feeling anything other than positive energy and proud of the group, but tonight was different.

Dori and I in Maine Three years ago tomorrow, we had to say goodbye to my sister Dori. Her rupture was massive and deadly. She ruptured on Mother’s Day and was kept on life support until the 29th of May. No signs of life and no signs of recovery were recorded. They had shaved her long, thick, mostly gray hair from her head completely. She was on life support, a ventilator, and had a drain set up to alleviate and remove fluid on her brain. It’s an image that still haunts me as the last time I saw her.

Some of our discussions this evening at the support group centered on drains and locations of brain aneurysms. Dori’s aneurysm ruptured on her brain stem, which was catostrophic. As these discussions took place tonight with a survivor who had a drain and a rupture, the image of Dori in that hospital bed was running on a loop in my head. I’m glad we flew back from London immediately to see her at the time, but it technically wasn’t her in that bed. She really was gone the day of the rupture but I see her in that bed this week and my heart hurts because I miss her so very much.

I know for those who have lost a loved one, the support group can be sad, educational and scary all at the same time. Usually I’m naturally focused on the survivor side of it because I am one, but unfortunately, I also have the flip side as part of my life in losing my sister and Dave’s niece to massive ruptures. The successes (me surviving I guess) don’t quite balance out the failures (losing Dori and Kim) but life still goes on around us and I’m still alive to try and help others if I can. If we’re able to get one person scanned or help one survivor understand their situation better and offer comfort, then those lives lost will always be with us as a reminder at how precious life is and how we all can DO something.

8 Years And Counting

20141004-230625.jpgI say it every year around this time but Happy Annie-versary to me! 8 years ago today I suffered a ruptured brain aneurysm at home. I believe I was guided by God’s hand to go into the ER when I did. I KNEW it was something I had never experienced before and wanted to get it checked out because it scared me. I was only vaguely aware of the term aneurysm because a cousin had one coiled a few years earlier. I had no idea just how serious it was for her and just how my life, and my family’s life, would be changed.

No, I wasn’t sent to Boston for my surgery. My particular aneurysm was a good candidate for the relatively new procedure called coiling. What I know NOW, but didn’t know then, is that the rather large, 1/2″ diameter brain aneurysm is actually sitting on my optic nerve and the head of neurology was nervous about doing the more invasive procedure of a craniotomy and clipping (which I just went through with my un-ruptured aneurysm). Thankfully the staff right here in Maine at Maine Medical Center were more than capable of handling that procedure and are now in 2014 even MORE prepared to handle all of the new treatments available.

16 coils and four additional coils, a stent, a craniotomy, and now a metal clip, and here I still am. It was a frustrating recovery in 2006 and I am now meeting, and hopefully assisting, recent survivors at our brain aneurysm support group. We’re all lucky. We survived.

I’ve given up asking “why did I survive” and why didn’t Dave’s niece Kim or my sister Dori survive their ruptures. There is no answer. God had other plans I guess.

I mentioned to my mother earlier in the week that I had finished the first round of layouts for the ENTIRE catalog for next year’s book. Ironically, 8 years ago, I remembered celebrating that milestone and one or two days later, the brain aneurysm ruptured. I’m still working just as hard, still stressing just as much, but a little bit more tired this year because my UN-ruptured brain aneurysm was clipped in January. One of the side effects from THAT surgery is when I’m overly tired, my left eye lid gets droopy and even though it doesn’t look it, I feel like my brain and skull are swollen when I’ve worked too hard. Yes, I still push myself. It’s my job, it’s my responsibility. I do have limits though….you’d think I would have learned that 8 years ago. LOL

I still don’t eat as well as I should and I don’t get enough exercise. Perhaps that part of my brain that activates motivation has changed. Who knows, but I’m here. No special celebration today, just making home made chili in the crockpot, working on the catalog (yes, on the weekend!) and hanging out with my Maine Man and my kitty cats. That’s more than I was doing eight years ago in ICU.

If I’m able to help any other survivors and help spread the word about the symptoms and treatments of these silent killers, then I’m hopefully turning something bad into a more positive thing. There are days I don’t want to talk about brain aneurysms. There are days I don’t want to think about them, but I can’t get away from them. That’s the sad truth. So, I’m trying to make the best of it and try to help others LIVE in whatever way they’re able to. They are a part of my everyday living.

For those of you still struggling, you’re not alone and things will get better with time. Just treat yourself right, enjoy life, and celebrate the people around you. You just never know.

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Photo taken on my first walk outside after craniotomy in January this year.

It Has Been A Week

I have been close to tears about five times this week. None of these times actually produced tears, mostly because two of the times were at work, so I really kept it in, but the other times certainly could have produced tears….but nothing.

Since my brain aneurysm rupture in 2006 I noticed whatever mechanism within my brain that triggers tears, just isn’t the same. I would feel sad about something, and knew I would normally be crying over it, but the tears would not come. I’d be curious to know if any other brain aneurysm survivors have experienced the same thing. However, when those tears DO start flowing it’s difficult for me to shut them off and they completely drain my body and brain of any needed functionality.

Tonight I opened that valve and the tears are flowing. This Sunday is Mother’s Day. Normally a happy occasion for families to celebrate their moms with gifts and spend time with mother’s, granddaughters and grandmother’s. Unfortunately, for my family, it’s a sad occasion and doubly so this year. No, my mother hasn’t left us, but both my sisters have. So not only has a mother lost two daughters, but I’ve lost both my sisters and my niece and nephew have lost their mothers.

My sister Dori had a massive ruptured brain aneurysm ON Mother’s Day in 2012. My husband and I were in London, England when we found out. We cut our trip short to join my family in a two-week, hopeful vigil praying for a miracle that never happened. Technically, we had already lost her on Mother’s Day. I don’t know how my mother or my sister’s son, can ever replace that memory. I know I can’t. Because she died of a brain aneurysm, I’m also tormented by my own demons about how she was misdiagnosed and how I should have pushed her more to insist the Dr’s look closer. Having the “urgent care” president where she was treated admit in a letter, after her death, that aneurysm signs were missed, makes it even more heart wrenching.

My “Family” mailbox in my Email now only consists of my husband and my niece. No other relative emails me. In fact I didn’t even know my cousin’s husband had died because she didn’t email me and none of her brother’s or sisters did. I miss my emails from Dori and Rhonda and Mom. Since mom had to switch to a laptop from WebTV, she hasn’t been able to understand and grasp using a computer, so we no longer have that convenient form of communication. She doesn’t call me, due to the cost, but I call her two times a week. And as I sit here typing this, I am bawling and feeling horribly pain in my head, that is just short of 4-months out of open brain surgery to repair my 2nd aneurysm.

Searing pain around the side of my head that is made worse by the stress of crying…and I can’t stop. I want, and desperately need a day off of work to get some sleep and rest, but there are meetings I must attend. Why I’m asked to attend some of these meetings, when my ideas and recommendations are met with a giant eye-roll and dismissed, is something I don’t understand. Even though I was apart of developing the program that’s being discussed and am very familiar with how it works, being treated that way in front of many others (for a 2nd time) can lead to tears, but I held it together…until now. So on top of grieving again for my sister, I’m dealing with being dismissed at work and just getting there on a daily basis while I’m still recovering.

Then there is my darling niece who will have to endure her first Mother’s Day without her mom because my other sister Rhonda died just 4 months ago. My poor mother has lost two daughters and I’m all she’s got left. And even SHE is having issues right now with horrible pain in her back, which brings back many memories of my sister Dori. She had horrible back pain for months before finally having surgery a few weeks before her death and I’d talk to her on the phone as she was in that pain and knew she had been crying due to that pain.

So when I hear my 87-year old mother talk about getting to the point where the pain makes her cry, how can I NOT think about my sister. I don’t know what to do to help my mom when she’s in NY and I’m in Maine. She’s been to two doctor’s and they’ve given her patches and some meds and told her to stop lifting things. Great. That’s great advice…but do they know what is actually wrong? I doubt it.

So, that crying thing is very difficult. We’re told it’s good to cry every once in awhile to get it out of your system….they say it’s a “good cry”. Well, for me, a cry is never good. My head feels like the skin and muscles are being pulled away from my brain right now. And it won’t settle down, until I settle down. Poor Dave has tried to console me, but I don’t even know what I need. I guess a “good cry” and venting in my blog will have to suffice for now even though I know I won’t feel any better physically or mentally afterwards.

Bad form Facebook. Just bad.

There is a birthday calendar reminder on Facebook. I normally like it as it sends up a reminder a few days before one of your “FRIENDS” has a birthday coming up.

However, I was unprepared for the reminder email I got tonight reminding me that my deceased sister’s birthday is coming up and I should remember to send her a Birthday Greeting.

Excuse me? What? Is this from the same account that we worked with Facebook on in memorizlising after her death? We had to send a copy of the death certificate and proof she had died complete with date, year, and obit to get her account distinguished like that.

Wouldn’t one think if they had received that type of very personal and devestating info, they’d automatically remove that account from being sent out on birthday reminders? Well, that makes sense.

Now, if we want to delete or deactivate the account we’re forced to go through the same damn procedure AGAIN. Ridiculous.

Obviously, I knew Dori’s birthday was coming up this Friday and I was already not looking forward to the day, then to be reminded of it in such a careless way is inexusable and thoughtless. Tears flowed and my heart broke…oh, I’d LOVE to wish her a Happy Birthday but a ruptured brain aneurysm killed her.

Thanks, but no thanks, for the lovely email reminder Facebook.