Tag Archives: Special needs

The Elephant in the Room

I watch Haley. Alert and anticipating. Ready to spring into action at any moment. That intensity isn’t lessened by the fact that she went 10 hours seizure free. That tension wouldn’t be lessened if she went 10 months seizure free. That expectation, that worry, that awareness that a seizure could strike any second, is prevalent in my mind. Always. At any given moment.

When I make a grocery list. When I weigh whether it’s safe enough to drive 10 minutes to the larger grocery store or whether I should stay in town. When I work. When I visit a friend. Even in the rare moments that I take time for me. It’s always there. Niggling, nagging, present.

It is the elephant in the room. Those seizures that might occur at any given second. The seizures that are unpredictable and relentless. Those seizures that steal pieces of my baby girl one minute at a time. Even when she’s not seizing epilepsy is stealing her life from us. The caution, the worry, the fear. The seizures that don’t happen but could.

The side effects of the 17 medications that she has tried in various combinations have taken their toll. The side effects we were never fully informed of or that were brushed off as rare or necessary risk. The question of whether the pharmaceuticals have done more damage than the seizures is the elephant in the room. Unanswerable. But the question hangs there, persistent in my mind.

The words cannabis, marijuana, pot, weed. Whatever you call it. I call it medicine. I call it hope. I call it our last chance. But every conversation where we skirt around it, where we call it cbd, where we don’t speak openly about the government patent on its neuro-protective properties, where we don’t admit that we are victims of decades of manipulation and lies, where we don’t acknowledge that it’s just a plant makes it another elephant in the room.

SUDEP…and the 50,000 seizure related deaths that occur in the US every year. The fear the grips my heart any morning I awake before my daughter. The anger and fear that coils in my stomach and throat, that wraps around my lungs and makes me unable to breathe through those moments. The acknowledgement that my child is at high risk of becoming a statistic is an elephant in the room.

The moments we lost, the memories we didn’t get to make, the hovering question of who would Haley be if she had access to cannabis from the beginning. Who will she become if she could get access to it now? I hope we get the chance to find out. I hope we leave behind the elephant in every room and learn to live. Cannabis gives us hope that someday we might…

I am a Mom

I am a Mom. For over half of my life now it’s how I’ve identified myself. But something changed after my youngest daughter was born. I suddenly entered the foreign world of being a special needs mom. Suddenly I went from pshht, I got this Mom thing down, to a foreign country filled with therapists, evaluations, neurologists, IEP meetings, attorneys, advocates and community.

I am a Mom. Above all else. It transcends everything else I might be and that title defines me unequivocally. And for 5 years now I have been a special needs Mom. An epilepsy Mom. Epilepsy invaded our lives with dramatic flair on 9/11/09 leaving my otherwise healthy 2 year old crumpled, unresponsive and blue. That was my initiation.

I am a Mom. I cook and clean and work and wipe noses and help with homework and taxi the kids around. I also hug and listen and love my children with a ferocity I didn’t believe myself capable of.

I am a Mom. I am fighting for my child’s right to try a medicine that could be her miracle. I am fighting for the opportunity for my daughter to be healthy. I am fighting for options when the medical community has left us without any. I am driven by love and fear equally. Fear that I may lose my daughter before she gets this chance. Fear that it may not work. Fear that we may never get the opportunity to meet her beneath the haze of pharmaceuticals. Love of her soft cheek snuggled up for a story. Love of her funny quips and imagination. Love of her very existence.

I am a Mom. But I have become an activist. Fighting to end cannabis prohibition for all patients in need and for adults who believe that cannabis is a safer alternative to alcohol.

I am a Mom. Just trying to save her daughter.

Welcome

Welcome to my blog! This is where I hope to chronicle my journey as a single special needs Mom. This is my little corner of the internet to share my life lessons and raw feelings sometimes in real time, sometimes upon reflection.

Either way grab a cup of coffee, expect it to be flavored with salty tears at some point, and let’s share this brutal, beautiful life.

Open hearts, open minds…