I guess it has been just over thirteen years since my life changed. It was a cold, grey, and wintry morning in December 1996 when Sam and I were on our way to do some errands. As I was walking towards the car to put him in his car seat, I slipped on a patch of black ice on our concrete driveway and smashed the back of my head, hard. The next thing I knew, Sam was sitting on my lap crying, everything was very fuzzy, and my head and neck really, really hurt. This is how my mild traumatic brain injury (MTBI) occurred. Natasha Richardson suffered an MTBI and her outcome was quite different than mine. I will take my post-concussed life, rather than the alternative.
Somehow I managed to get to the phone and call my dear friend and neighbor, Gisele. I think I was able to remember her number because I dialed it everyday. Frank her husband answered and said Gisele wasn't around. He later said I "didn't sound right" and the next thing I remember was being in the car with him driving to the hospital. Sam had finally calmed down in the car, but Frank said he couldn't walk very well. It turned out he had a sprained ankle. From what we can piece together, I must have held Sam so he wouldn't get hurt and took the brunt of the fall. I protected his head, but my "ample" hips landed on his ankle - hence his sprain. In retrospect it was a good thing, because we lived on a fairly busy road at that time, and if he were able to walk away from me... well the outcome could have been very different. It gets even more sketchy here, because when we arrived at the hospital, I wasn't sure who Frank was. He later told me I asked him if he was my husband!
At the hospital I have no recollection of being examined, changing into a hospital gown, or having my vitals taken. The next thing I do remembered was having a doctor ask me to touch my finger to my nose. My CT was negative. With those results in hand, but loads of head and neck pain, nausea and amnesia, plus Sam's sprained ankle, we were sent home. What was offered was rest for the next 48 hours and a referral to see a neurologist in two weeks.
The next few months is, to this day, pretty blurry to me. Gisele and my ex-husband Michael kept our household running. I was pretty much out of it from what I've been told. My head and neck hurt all the time, I was so very tired I slept most of the time Gisele said, and I had a hard time concentrating on basic daily tasks. Packing lunches, getting Sarah ready for school was too much to handle, so Michael made sure Sarah had everything she needed in the morning. In the afternoons, Gisele would be there to help get Sarah off the bus, tend to her homework, dinner and basic tasks that any mom should be able to do. Thank goodness for their help!! My poor kids, Sarah was in Kindergarten and I missed most of her year. Sam, well, he had lots of cranky issues at that time anyway, so we just added this one to the pile!! (But he is turning out just fine, thank you.)


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"Clumsy girl."
Words can't come out of my mouth. I don't remember what happened, except that I'm back in the ER again, begging for them not to cut off my shirt.
Yes, my CT scan is clean, as is my MRI. My husband leans over me to ask what I said, but I don't remember. And I close my eyes. Isn't this the 4th time this has happened?
I'm a genius. A flipping MENSA genius, yet, for once, I can't process ideas. I cry. They ask what hurts.
He points to my neck. I'm glad he's there. It's only taken 5 of these, but I'm so glad he's there. The C-collar is made with latex, and I'm swelling by the minute. I scratch like an ape. He says something for me.
No, they can't take it off until my c-spine is clear. But I can't breathe. I take it and fling it across the room, not caring anymore. It's not like they can help me anyway. I'm going to have to go see my headache specialist to get words back in my brain.
The doctor yells. He yells back. "If you're not going to treat her correctly, we're leaving AMA." I very nearly lost my life this time. Yet, this is the best I've felt after a MTBI.
The time before, it was a backwards fall, trying to protect both my camera and my head. I lost 10 minutes multiples of time. For months, I lost words, lost days, lost dreams, lost friends, and eventually wound up on a plane to my Migraine Specialist.
That MTBI was the worst of my life. Not the one that scared the most people, or looked the most dramatic... Just the one that changed me- even now... 'Cause while I look ok, and feel ok, and act ok, it affected the OTHER side of my neck. And that's a definite change. While meds have given me my life back, I still feel like something changed that day that I don't think I'll fully see again- but who knows.
I'm lucky that the Aphasia's gone away from the last MTBI, and I can concentrate again... but I still get tired, and multi-tasking... Meh. Once it was a joy- now it's a bit of a struggle- but I can DO it again. Is that where the story leaves off? No. But it is for right now.
I'm really lucky to be alive, have such great medical care, friends, and allies. They'll help me continue writing chapters in this book, until hopefully, there's a "happily ever after" ending.
Thanks for shedding light on this, Nancy!
Again, the "bubble" and where do we get one for you!!
hi theree im a teenager and i have been suvering from migrains since the early age of 7 the acttackedd started off small but they got worsee i have benn to lots of hospitals because of deese ..when i was in sixth class 12 yrs old i got an attack and wass rushedd to hospital and stayed there for a week ... the pain is so badd that id rather diee than have migrainss i get all the symtops beofree the pain act comess the burly eyes the nomb hand nomb face every thingg .... in september 2009 after bein on a waitin list to see a migrain specialist ... i had an MRI scann but there wass notin when the results camee i dont eat choclate i dont eat dairy foodss my last option was medication ... my mam didnt want me to take medicatoin as i am very youngg!. we had no optoin i had missed 56 school dayss because off this.. the docter gave me medication called SANAMIGRANE! i was on 0.5 of this every day still no use.:( i was told 2 increse it two 1.0 still no usee i am now on 3 milligrams of this medicaation a day which isnt gudd .... i dont get the attacks as offenten but i still get themm .. they run in my family .....
Hello, and welcome to MyMigraineConnection.com!
Migraine is a genetic neurological disease thought to be caused by overactive neruons in our brains and genetics - yup runs in families. It sounds like you doctor isn't helping you now, so it may be time to consult a Migraine and headache specialist. It's important to note that neurologists aren't necessarily Migraine and headache specialists. Take a look at the article Migraine and Headache Specialists - What's So Special? If you need help finding a Migraine specialist, check our listing of Patient Recommended Migraine and Headache Specialists.
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