A few days ago I wrote a post called ‘What’s not difficult, what is.’
I kept thinking that—after I got over the fact that Elvis Stojko has not returned my telepathic messages—I would tell you what’s different.
[Delightful Canadian neighbors, get that boy to give me a call. I give the go-ahead. Talk to your maple-happy peeps and see what you can do. Tell him I can skate backwards, but I look like a hippo in heat as I do it. A CUTE hippo in heat. Props where props are due.]
*****
What’s different: I’m on a new, necessary road now. What’s different is that I am the one saying, yes, this is necessary. I need help. I need your help and your help and your help.
I am almost 40. This is not where I expected to be. If you’d asked me when I was 24 what my 40-year-old self would be up to, my 24-year-old self would have been her optimistic self: happily predicting all sorts of theatre success, plays being produced constantly across the state, acting roles coming in by the day, material riches, a great marriage, a big farmhouse with a big farmhouse table, rescue dogs, and terrific kids. And no acne. And great hair. (And no cellulite, because by the time I got to be That Old, there would be a cure for that.)
I’ve had some plays produced. I haven’t acted since the girls were born, unless you count the acting that comes as self-survival in a small town: Why, yes! Fine! Hanging in, how about you? Great! Great! Didn’t you go there for vacation last year? Skiing again? Whistler! Terrific!
The truth is more humble: I have wonderful rescue dogs, and terrific kids. And great family and friends. And you.
It’s not what I pictured at 24, but I am grateful for what I have.
My illness and its treatment play funny tricks with a mind that’s already addled. The meds…if you are new to this world, try to imagine NyQuil, with four NyQuil chasers, and maybe a shroom or two. This will pass, the doctors assure me. I go along with it. I asked for aggressive treatment this time. The big guns have been brought in, and they are aimed at my head. I catch their bullets in my teeth, laughing, wiser now.
The potential side effects are gory: diarrhea, stomach pains, nausea, vomiting, skin rash, hair loss, weight gain, acne flareups, thyroid screwups. I need blood tests for a while, weekly. I need some hands to hold and chew on for those. I almost broke my poor mom’s hand in the ER before I was admitted to the hospital—just from the blood they needed to draw as simple protocol.
I try to take a lot of deep breaths during the day, these days. I have never been a good breather. It makes me hyperventilate, thinking about my breathing.
I could not navigate my way through this time alone. My mother bought a host of pill cases. She divides the medication, she oversees the meds so I don’t have to think about it. Thinking is spotty right now. Thank you, Mom.
My father sent some money for heating oil and clothes for the girls. Thank you, Dad.
My brother and my sis-in-law write loving letters and reach out from across the country, and it makes such a difference. Thank you, J and K.
Gorgeous loved ones Ali and Molly and Wil and Rebeccah and Maude check in regularly. They, and people I don’t know well, feed me, hug me, hold me. Thank you so much. If you have extra food, don’t hesitate. It’s welcome here, and will be for a while.
This is a slow process, this getting well. I have found it incredibly difficult to ask for help. I am asking now. I can’t do it alone anymore.
What’s different is that I wound up in the hospital after an event that frightened me, after my illness got the better of me. I can’t quite talk about that yet. Too hard. Still making sense of it myself.
I recognize it will do that at times, get the better of me, no matter what I do. Medicines always need tweaking, especially over time. But I can do my best to stay on top of it, to stroke the beast, to feed it cookies, to learn to live with it.
Am I scared? Sort of. My brain spins too fast or not at all, and plunges into darkness. I am tired of sobbing beside the washing machine, tired of my grief at my situation taking over all that is good in my life.
Yes, I am tired of the dark. It is time for light. Time to take my elbow and rub a bit of clean into the panes of glass, so I can see out.
Help me see out, if you can. I extend my hand. This is new for me. But in a way, it feels right to come clean, to say, Hey, no, I’m not all right. Yes, it’s a little embarrassing. Okay, it’s really stinkin’ embarrassing. But I am working hard to get better. Please, don’t judge anyone in your life. Who knows how hard they have it? I mean, really truly have it?
Bless you all most kindly. You have no idea how much you mean to me. That hasn’t changed.
And those rescue dogs and baby girls of mine? They haven’t changed either, but how I hold them, well, that’s changed some. Hugs are tighter now. Yes, indeed.

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Dear Lori,
How lovely that your words, “There is always Hope”, were the words my mom often said. She was a very special lady and loved Jenn a lot. Today, November 30, is the anniversary of her leaving us 23 years ago.
I feel like she prompted you to write that message to Jenn. And, thank you, for your kind comment at my blog too.
It is amazing and comforting to see how many readers have reached out to Jenn. And equally amazing is how Jenn’s journey is resonating in other’s lives. Thank you all!
I wish I had some advice to give. I’m no expert. But I do believe that taking lots of deep breaths is a start. And asking for help is the first step to getting better…how can I help?
((Hugs))
I think of you often. Last week, I thought of you extra hard when I drove by Emily’s Lebanese Deli and remembered how much you loved it. I’m sending you Virtual Tabouli, baby.
Soooo…. your medication side effects are kind of like pregnancy, huh?
How very cosmic.
You’re so smexy when you’re basking in your emotional nakedness.
Sending you tender thoughts and images of light today. I haven’t been following this blog but dropped by yesterday via fern. Blessings.
Hi,
Delurking to say that I know about the dark and am right there with you regarding the medications making everything fuzzy and trippy.
I know I am a stranger but I am sending you much positive energy and light (isn’t it funny how it is easier to do that for others than ourselves).
Thank you very much for writing your blog.
I like what Kelli, your very first commenter on this post said. I believe in you, too, Jenn. I do, and I’m reaching out to hold your hand. It’s hard, though, and I’ve stayed around the hand guns side of mental medicine, not even looking in the direction of the big guns. So for you to be this candid with something so deep and scary is a tribute to your strength.
But I believe in you, and I agree that yes, it’s a good time to let in some light. Because when it hits your face, it shows you to be the beauty you are, and not what the shadows would have you believe.
You sound a lot better today than you were. I think of you often, and am glad you’re being so strong.
You are very brave and strong. I hope the healing light shines on you. Your truthfulness is a gift to me. Thank you.
sweet. i will be dropping helpful stuff off at your place.
Debbie Meyer’s green bags? don’t knock’em til you try’em.
you are a really brave badass. it is hard to ask for help and really easy to wave it away, even when you know you would like it. i’ve done it many times, but i am always glad when let myself accept help.
~what can you do for us when we bring home boy #2? uh, well, honestly, you can make us some easy dinners, so we don’t have to cook. that would be the best gift EVER!~
there was a great interview on wamc this morning with a woman who’s husband has dementia. she had some really wonderful words of wisdom that i would totally share with you if i could remember any of them.
something about not trying to change what can’t be changed, but learning to love what is… she said she was just trying to manage her life as best she could.
there was a very distinct and lovely ring of optimism in her voice.
at first she thought her husband was curable, but then realized that was not the case and she was going to have to figure out how to make the best of what was dealt. she wrote a book, so maybe after you are through with all that mormon vampire porn…
In tears at my desk at work. You are a remarkable person, Jenn. Thank you for asking for help, for sharing so much of yourself with us. For trusting us with your truths.
Who was it that said out of your darkest struggle comes the seeds for your greatest victory?
Like you, I am not where I imagined I’d be at 40. As my own daughters grow older, I’m going to teach them to live in the present, embrace it, squeeze the life out of it, and hope that they will spend less time than I did daydreaming about the future and thus…perhaps…setting themselves up for unnecessary disappointment. Or is that wishful thinking on my part?
I love your posts. I have gushed here before and I will gush again now. You are helping so many. Your writing is beautiful, you are beautiful, and as another commenter already said, you have created community. Brava!
Who knows what comes next? What awaits you down the path? Life is long and the reality is that 40 is still quite young. We have many more years, more adventures ahead. You’ve started on your dreams. There will be time to continue them. Your opus awaits.
sending you warm thoughts and positive energy too.
Jenn
It sounds like you could use some clif bars. I have a market five miles west of your town and I will leave a credit worth 10 clif bars under your last name.
You have been giving unidirectionallly for so long, it is great that you are asking us to give as well. You have an amazing ability to make others feel close to you. Very few people have this gift and it is much rarer than being great in theatre. You are a modern version of a travelling bard…a stationary bard who instead of travelling has more time to make a story-worthy life.
If anyone would like to send groceries, please give them my email and I will create more store credit for you from their donations.
here with you. I have been there.
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