I have always
been the type of mom that was great with bee stings and skinned knees. I could
make a fabulous paste with baking soda and toothpaste to put on a bee sting and
I always had a kitchen cabinet stocked full of Little Mermaid band-aids just in
case of an emergency. I remember once after one of Erin’s surgeries, at St.
Louis Childrens Hospital, she had shared a room with a kid with chronic issues.
When the doctors came in the room for a history, her mother rattled off a long
list of medications and side effects as well as past admissions. As the mother was
verbally going down the painfully long list of awful things that her daughter
had been dealing with, I couldn’t help
but feel a little guilty. I was feeling like I was carrying such a big burden
watching my toddler in pain when this mother seemed to never catch a break.
Dave and I looked at each other as we sat shocked on the other side of the
privacy curtain and mentally thanked our lucky stars that we were not “that
mother”. Our daughter was only staying because anesthesia made her throw up a
gazillion times no matter what anti nausea drugs they gave her.
Fast forward to present day and today was just plain shitty. Driving home from
the Aphasia Center today I looked over and saw the back of Lauren’s head. I
immediately knew something was wrong. I could tell she wasn’t just looking out
the window, her head was turned too much to the right, it was actually turned
so much it was almost facing the head rest behind her. I called her name several
times and unsuccessfully tried to nudge her head back towards the center. I was
driving at the time so it wasn’t easy. I pulled over in front of a stop sign, I
didn’t care if I was blocking traffic, I have a rental car and have no clue
where the hazards button is. Luckily a
policeman was at the stop sign going the opposite way. I rolled down the window
stuck out my arm and motioned him over. When he pulled up I quickly told him
that she was seizing and turned my attention back to her.
This seizure was
different; her beautiful face was still contorted like all the seizures in the
past but the convulsions seemed less severe. I looked at the clock as soon as I
noticed her head turned, from start to finish it was only about 2 minutes. Of
her 6 seizures since the accident this was the shortest. She did foam at the
mouth a bit and her lips and area around her mouth turned a bluish color. (I
think my heart may have stopped for a bit) That was a symptom that I hadn’t
noticed happening before. I have
medicine to give her that I ALWAYS carry with me that will prevent her from
having seizures back to back. I asked the policeman if he had any water so I
could give her the medicine. He let me
know that they have to wait for medical professionals. I looked down, and luckily
Lauren never goes anywhere without her lemon flavored Vitamin Water. (I wasn’t
waiting) She was lethargic but responding, she was able to swallow the pill without
issue. I asked her to take out her
invisalign, I didn’t want her to choke on them if she had another seizure. She
was worried about finding the case before she took them out. At that point I
was pretty confident that her cognition was good. The ambulance showed up and I
started making calls to her epilepsy specialist’s office. We just weaned her
off a medication so I was kind of expecting this. As crappy as it is, it is
part of our world now.
While in the back
of the ambulance they were taking her vitals and checking her blood sugar I was
rattling off her lengthy history and hospitalizations, medication lists and
past medications and past seizures etc. Then
it hit me, Oh my God, I AM “That Mother.”
It is an exclusive club that no one wants to be a part of. No amount of
Little Mermaid band-aids or baking soda paste can fix this. This is big time
boo boos and many times I would like to run away, but I can’t. I don’t have to like my set of circumstances
but I do have to look for the positive because, as in everything in life, there
is always something positive. Sometimes my take away can be the simple fact
that I have mastered silent crying. Often times I can be grocery shopping or
sitting on a plane or even watching TV and slow tears are rolling down my face.
Not a soul even notices, this is something I have perfected in the last two
years. But on the flip side, I can still laugh and I laugh a hell of a lot more
than I cry.
I even laughed tonight. After dinner, (2 hours post seizure) Lauren got up and started
cleaning the kitchen. I sent a pic of her loading the dishwasher in a
group text to reassure the family that she was back to her old self.
When she saw the pic (a while later), we were sitting on the couch
watching TV. She said, "Oh My God my ass is huge." then she zipped up
the bag of chocolate covered pretzels and put them in the kitchen.
Everything
happened pretty quickly today and I am pretty proud of how I handled
everything. Unfortunately I am becoming an expert. This seizure didn’t seem as
bad as the others. Maybe it was milder, or maybe I am just getting used to
them? The frustrating part for me is getting a specialist to call me back. I
understand that they see seizures daily but come on….is it really Okay to tell
a mom, “the doctor will call you back tonight or tomorrow morning by the very
latest? Seriously??
This isn’t the
first time I have had this issue, I even looked at switching doctors once when
a different doc was slow at returning calls. My options were finding a less
knowledgeable doctor that calls me back or going to a top rated doc that
returns calls when he gets a spare minute. Sometimes being the one in charge of
medical decisions, medications and doctor appointments is just too much
pressure. For now, I wait….and watch her like a hawk. It's 11:00 pm and I'm still waiting for that call. This is a new doctor and I have yet to get out
my bear claws, the others have seen the claws and have learned to return my
calls quickly. No worries, this one will learn as well. I will spend the night
watching Lauren sleep and carefully and meticulously, sharpening my well manicured claws.
1 comment:
I realize Doctors are very busy but they just don't always understand what it is like to wait and wait. They deal with their practice on a daily basis but WE don't! When it is a family member, especially your child, you don't want to wait! I hope you get your call soon with some helpful information. Good Luck!
Post a Comment