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  • Summer Meltdowns, Loss of Control and Missing the Hospital

    Today was one of those days. It’s been coming for a while. The type of day where I recognize my mental health is in a precarious state due to many circumstances I have zero control over and I’m all at once slowly and rapidly losing my shit to the point I miss the hospital. I want the hospital. I meet zero criteria for the hospital, but the hospital is controlled, with rhythms and routines and predictability. My life presently is not. My brain and my body are seeking it in any way possible.

    I’m not sure when I began to recognize the tides were turning. Was it when my two “best” friends turned on me inexplicably and iced me out without word? Perhaps. That wound is still bleeding from lack of understanding and closure. There are three sides to the truth. All I know is my truth is I was always kind, always there when asked, willing to lend a hand when needed, there for every child birthday party or major event invited. I am not perfect, so sometimes I was needy with my mental illness and needing someone to listen at perhaps inconvenient times. Or just needy. Maybe that’s what did it. I’ll never know. I do know that my children’s birthday party is not prioritized the way I would and one person was supposed to have a major role in the surprise twist to my children’s birthday party. But not anymore, I think they actually forgot.  BOTTOM LINE IS: take all that away, my heart hurts, I still lack closure and a major portion of my mental health support system is gone. Poof. Just like that.

    I did learn I had another support system around me, subtler, less in your face but equally precious. One that I’m grateful this ‘ice out” has given me the opportunity to grow and blossom, though not healing the wound any less. 

    Perhaps the tides were turning when we grew more and more suspicious with the behavior of one of our children. Despite extensive evaluations, our guts kept telling us it was something more than what every doctor had told us. We kept watching and tracking and adding up symptoms. No sleep. Limited food intake. Irritable aggression. Going on for over a week. My faulty genetics being passed down the line and parental guilt kicking in as I never wanted to pass this wretched disease onto one the boys. It has been and always will be my worst nightmare and my worst day as a mother: diagnosis day for my son. 

    I already feel a bit like a parental pariah with his other diagnoses, and now to add this to the pile. I can’t publicly advocate for him, loud and proud the way I do for myself. He has to understand his disorder first. Then, when he’s older, it will be his story to tell. In the meantime I need to figure out to fill up my fuel tanks for puberty for this will be a loathsome combination.

    Perhaps the tides began to turn when I did publicly advocate for my children. One in particular was subject to racial slurs two years in a row by classmates and as a family we took it public to bring about community awareness and change. Being a maven and fomenting change is exhausting and uncomfortable at times while being exhilarating at it’s best. I am confident not everyone is on board with my loud message of preaching diversity be it skin tone, mental health, or being neurotypical/atypical.

    Then we have my grade in my current class for my doctoral program. I am used to being a very high achiever. I graduated UVA with masters summa cum laude. To get punched around in a doctoral level class and be one point below a passing grade is humbling. It’s not reflective of the hours of work I put in each week and my capabilities as a student. It wears on my psyche week after week after week.

    I needed to ugly cry today. I needed to get it out. I needed to ask my husband to hospitalize me. I needed to hear from him that it wasn’t the right thing to do, that I have better choices (and days) ahead of me whether I have the ability to recognize it or not. Right now, I need stability, routine, calm, and peace. I need the chaos, lack of control, zero predictability and no sense of routine to stop. Most of all, I need to my support system is there when I need it.