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4yrs; Day 1565 – from Corey

hi everyone it’s corey,

today was a good day i started out with seeing dr. Yalamancheli. it was a really early morning appointment, 6:30am. he was happy to see me and talk to me. he said my head is fine but i probably will have headaches for a really long time. i asked how long is long. he didn’t have an answer. he also said 1st they didn’t think i would live and 2nd they didn’t know how much better i would get. look at me now, wonder if they are still wondering?

the second appointment continued the day with seeing dr A.

dr. A helps me with mental therapy. i don’t know if there is another word that describes it better but it’s what you think and what it causes you to do.

i am afraid that my mom will up and leave me or people would get tired of taking care of me. i don’t know if that’s true but it’s what i fear anyway. dr. A and mom told me mom is not going anywhere. i’m happy but still scared at the same time. so what does that even out to?

if people are busy doing other things i’m afraid they will forget about me. i know
that people will stop coming to help so i would like to work even harder towards not needing any help, if it’s possible. Again, more of a reason to keep working?

i don’t know what to do for any of this, so i hope i can learn, xoxo

4yrs; Day 1563 – from Corey

hi everyone it is corey

today i went to bryn mawr and i worked out with natalie. first of all, i rolled over onto my stomach to do matte stretching. then we went on a long walk. i walked 403 feet in only 6 minutes.

that warmed me up. next i worked with anne on AB’s by twisting for tennis balls. the big exercise was working with 2 and 3 pound weights. i was doing tricep work with them as well as bending over to punch down to the floor and lifting my elbow up like i was starting a lawn mower. hope mom doesn’t get any ideas?

all in all i am glad about todays achievements, xoxo

4yrs; Day 1460 – celebrate life

Hi Everyone,

Tonight I attended a memorial for the father of dear friends. I had the privilege of meeting this man several times. His energy, kindness, sense of humor and smile are just a few of the images that come to mind when I think of him.

I was driving home thinking of how we chose to celebrate special days in our lives; birthdays, holidays, weddings and various special occasions.

The gathering tonight was also special. It was truly a celebration of life. There was joy in the room as we all shared and listened to the stories of how each of our lives were enhanced not only by this man but his wife and his children too.

The common thread in all the stories was this mans ability to make each person he met feel welcomed whether it was at his place of business, his home or on the sidewalk. It was a great reminder to be present, celebrate today and the people we share our lives with.

Every day is special because we make it special, no matter what the calendar says. Celebrate life every day, xoxo

4yrs; Day 1557 – from Corey

hi everyone its corey

a good friend of the family has asked me what i did today to keep moving forward?

first of all, today i told my mom that i did not feel like exercising anymore. so then my mom gave me 2 choices.
1. my mom could hire someone to come and watch me when i was in my chair because not exercising will not get me stronger
or
2. i could start exercising so i could stand up from the chair and start taking care of myself.

so i decided that having helpers around me 24/7 was not quite my idea of improving, so i got up and started to exercise.

i walked 2 laps around my house with my cane, rode the bike for 20 mins and did the matte stretching exercises

even though the exercises were very important it was mostly my attitude that motivated me to do them. i guess that is the secret to exercising, staying fit, and keep moving forward, xoxo

4yrs; 3 months

Hi Everyone,

One of my dearest friends once told me, “I can guarantee one thing about life…it will always change”.

We are at a new crossroads with therapy…AGAIN. Evaluations and another round of botox are on the docket for this week.

Needless to say, I am worried. As my internal cheerleader plays tennis with my thoughts, I’m trying to process my emotions and regulate my fears of ‘NOW WHAT’?

I remember hearing our ICU nurse telling me it was time to visit acute care rehabs and felt panicked. What did she mean; it’s time to leave the ICU? Corey didn’t ‘wake up’ yet?

7 months later, Corey was nearing the end of her inpatient stay. I was terrified at the thought of leaving the acute care facility and moving home. I was worried about the next step of recovery and how we would manage.

It seems like a lifetime but, 3 1/2 years later, we are facing the next transition.

Sometimes change is welcomed because you know it can make life better. Sometimes it causes concern because the change can be challenging. Most often change is feared because of the unknown outcome. The unknown is an uncomfortable state of mind. Rationally, we know things cannot get better without change. Corey’s temperament improving with her new medication is proof of that.

Change can bring new opportunity. The direction it takes can either initiate success or failure. Truthfully, the only opportunity that fails is the one never tried.

Change will happen if we accept it and it will still happen if we fight it. We must be open to it. We must be willing to be willing. It’s success will take effort. Effort to change our attitude, change our perspective, change our thinking and change our actions.

Change will require letting go. It will take courage, faith, confidence and perseverance.

As I write this entry I feel as if I’m in the challenge round of the tennis tournament of internal thoughts. Let me serve one more shot…we take risks everyday, we live minute to minute most days, we have no timeline for recovery and we’ve managed to figure out how to stay in the game and advance to each round without the rules being explained to us. We haven’t won our Grand Slam but I’d say so far it’s Game, Set, Match…what’s next? xoxo

4yrs; Day 1551 – blank page

We will open the book. Its pages are blank. We are going to put words on them ourselves. The book is called opportunity and it’s first chapter is New Year’s Day ~ Edith Lovejoy Pierce

Corey,
It’s New Year’s Eve. most people prepare for the celebration by looking back over the last 365 days to reflect on what went wrong, what they wish they had achieved or started and never completed. Try to remember to look at what life gives us each day and maintain the hope in the possibilities that will continue to unfold. It’s up to us to make a choice to look for the opportnities that will direct us towards that end. My New Year’s wish is to recognize them.

The next year is not a time to hold onto the past and focus on the negatives, but rather look forward to another year learning how to grow, love and contiue to work towards the person we were meant to be. The days that lie ahead have not yeat happened and we can make them whatever we want them to be. This is not a wish; it’s a blessing, xoxo

4yrs; Day 1545 – Xmas Steps

Merry Christmas Everyone,

“Where there’s life, there is hope” ~ Stephen Hawking stated this simple yet profound thought. If you haven’t seen the movie, ‘Theory of Everything’, it should be on your TO DO list. Hawking struggled throughout his adult life to ‘live’ life to its fullest potential. What an amazing example of never give up and never give in.

Coincidentally, I asked our neighbor to film Corey’s newest accomplishment. I debated as to whether it was an appropriate time to share it with all of you because she is in the infancy stage of her latest challenge. But after seeing the Theory of Everything and thinking of the meaning of this holiday as well as remembering to appreciate and make the most of TODAY, it is a perfect gift to share with all of you at Christmas.

Corey, never give up Hope on the dreams you have for your life. May God continue to give you strength, determination and courage to keep walking towards them, xoxo

Corey Beattie Xmas steps 2014

4yrs; Day 1542 – falls

Hi Everyone,

Sorry for our recent absence, it’s been an eventful week. Corey’s headaches have been bad again and unfortunately, a fall in the kitchen didn’t help. Corey is still unaware of her physical limitations. She does not understand why she can’t just stand up and walk around the house or drive a car? When I remind her that her brain is healing and her left side is still weak, she often asks, “with all the medical technology invented, how come no one has technology that tells them how to fix the brain”?
My magic 8 ball doesn’t have that answer…

Corey was sitting at the Kitchen table on her IPad, I was sitting on the couch watching the end of a show. She wanted to come in and join me. I said no, the shows almost over and it’s almost time for bed. She didn’t like that answer so she tried to stand up and come into the family room to join me and fell backwards. This is one of the moments that you look forward to (her standing independently and walking) but it’s also the most terrifying at the same time (the potential for falling is always present)

Falls are a common ‘accident’ when a survivor gets more mobile. The nurses and I checked for signs of concussion for two days. Corey never lost consciousness, I didn’t see her fall and couldn’t find a lump/bump on her head, her speech and vision remained the same, appetite didn’t change, physical stamina didn’t change and she appeared unaffected cognitively. Thursday night she mentioned her eyes hurt with or without her glasses. Friday she had a headache, Saturday it was a bit worse. By Sunday, she was nauseous, tired, had a raging headache, couldn’t wear her glasses. I called my girlfriend, an ER nurse, for a consult. We agreed it couldn’t hurt to go get checked out. When I asked Corey if she wanted to go to the hospital she said yes,

The ER at Christiana Hospital is very good. She was seen immediately, had a CT scan and x-rays to look at her VP Shunt and her skull plate to make sure the plate hadn’t shifted and the shunt was working. She had IV fluids, blood work, and slept through most of the testing…that’s how I knew she was REALLY feeling poorly.

The Doctor’s confirmed NO brain bleeds, no change in the ventricular’s proving the shunt was functioning, blood work looked good but she was borderline dehydrated and had low potassium (she wasn’t drinking or eating much Saturday/Sunday) and they ruled out post-concussion syndrome. Given her history, they decided to keep her for observation.

As you can imagine, I was relieved on several levels. No concussion and thrilled my worry about the plate shifting and shunt not working were put to ease…for the moment. Unfortunately, with a VP Shunt, we are always a bit guarded because it can become infected and/or unexpectedly stop working…but for today…it is.

The end result; Corey had a REALLY bad headache. Another unfortunate fact, most survivors suffer chronic headaches for years if not forever once they have sustained a TBI. My next search will be to find a headache specialist that may help us manage them without drugging her. There’s got to be something or someone out there that can help so Corey doesn’t have to live with daily headaches.

As my mother and I would often say, ‘I’ll worry about that tomorrow Scarlet’, xoxo

4yrs; Day 1536 – within the silent moments

Hi Everyone,

The ride to DC roundtrip was fine; the visit with Dr. G was very difficult.

Working through Corey’s anxiety is as exhausting as fighting our appeals. Fortunately, Dr. G has the expertise we have been searching for. Corey had several meltdowns today. At one point, Dr. G asked me to leave the room. So many emotions rushed through me as I sat in the hallway outside his office listening to Corey scream. I was unable to hold back the tears of fatigue. We are in the center of a new crossroad. Dr. G ended the session with a strategy we can practice this week. He also warned us, “it’s going to get harder before it gets easier”.

Corey was tired and quiet as we listened to the hum of the rush hour traffic on the way home. It was the white noise we both needed to release the stress of the day.

In the silence I was thinking of all of you. I tried to imagine myself following our story from an outsiders perspective. The physical accomplishments can be riveting, virtually watching the heroine, Corey, fight for the happy ending. Then there’s the details not highlighted and often overlooked. The day to day details of life after brain injury.

It’s not unusual and won’t come as a surprise to most of you, you only know what you know. I never heard of Traumatic Brain Injury before I was called to the ICU. I was familiar with concussions but never truly understood how a concussion can leave residual side affects, let alone what a severe injury can do to affect a survivor and their family. If we’ve never experienced caring for an elderly parent, a sick child, a personal illness or something as simple as a broken bone, why would we think of the complexities that face the person it affects or the affects on their family?

Friends would share the announcement of a life changing challenge and I would add them to my prayer list but until our experience I never realized the depth of what I should have been praying for…the day in, day out, minute to minute life they were dealing with.

Looking at our story from an outsiders perspective, I would wonder how do ‘they’ handle the moments that are unspoken? What are the moments that fill the spaces ‘between the lines’ of the message recorded day after day? What are the details of the heroine’s untold story?

Glancing at the driver of the car riding alongside of us, I wondered what their challenge was and how are they coping? Are they riding in silence or is their radio filling their space with the distraction they need to break the worry? Or are they searching for answers in the silence too?

Despite the rainy commute, the ride brought clarity; there are no answers. Our message and the strength to keep moving forward comes from within during the silent moments. My internal voice repeated, ‘be still, find comfort in the quiet, rest in the quiet’.

Corey, there’s a moment we all face when a challenge is presented. When that moment is presented, pause. Within that pause, you can decide to react or respond appropriately. Sometimes that pause gives you a moment to regroup and regain strength to take another step forward. Don’t be discouraged. Most times that pause is not easily recognized, but taking time to let the moment of silence speak to you can make the difference in choosing the direction to take on the crossroads you’re facing, xoxo

4yrs; Day 1531 – from Corey

hi everyone it is corey and my family seems to be getting in the christmas spirit. our house of course has a tree and stockings hanging on the staircase.

caitlin took me christmas shopping for my family; however, i don’t remember what i got for everybody. it seems that short term memory loss is not so bad after all because for 1. i can keep a secret and 2. it will be a surprise for everybody including me.

physically i am feeling well. my headaches have bean iffy. they are mostly bad when the weather changes, which lately has been a lot, so they’ve been bad again. i guess that answered that.

i am looking forward to this weekend because we will go and see the christmas lights at Longwood Gardens with my family. that will definitely keep us in the christmas spirit.

i hope you all will be doing something fun this weekend with people you love, to feel the christmas spirit, too. isn’t that what this time of year is about after all?

i think so anyway, xoxo