Wife, mom of 3 beautiful children, dog lover, creative sole and children's book Author. Sharing my journey with depression and anxiety through blogging in hopes of educating and ending the stigma.
What a sweet and kind gesture I received upon my arrival at work this morning from one of my collegues.
A gentle reminder to help motivate me as I begin a new week.
Although my job itself has been extremely overwhelming and stressful for me, I am truly grateful knowing that I have a wonderful team of supportive women by my side to help empower me and remind me that “I matter”.
It’s International Women’s Day this Wednesday, March 8th. A perfect time to remind ourselves that we need to celebrate, lift one another up and support the incredible women in our lives because we all matter, not just today but every day ❤️.
I’ve been really struggling this weekend. Too many triggers are feeding off of one another.
Dealing with the symptoms of my depression and anxiety on a daily basis is hard enough to manage but having to also manage so many other unbearable physical symptoms as well is just getting to be too much.
I’ve had an unrelenting flare-up of all my neurological symptoms this weekend, most likely in response to an increased amount of stress lately. It’s also caused sharp pains to coarse through my veins, muscle aches, nausea and debilitating exhaustion.
This is my life. It’s not easy but I need to remember that I don’t always have to pretend to be strong. I just need to be gentler and kinder on myself because being vulnerable takes alot more courage and strength than pretending to be strong. And the same goes for you too. A struggle is a struggle; not a competition.
Letting go of what no longer serves you is only the beginning. Be your own advocate. Practice self-acceptance and forgiveness. Give yourself grace and compassion. Be your unapologetic self.
And when you feel your life start to snowball into an avalanche, take a deep breath and release that feeling by tossing it away.
New design now available @gentlereminderproject #unapologeticallyme
Why have I been feeling so incredibly anxious since late last night?
It’s taken me to a whole new dimension.
Our anxiety is usually trying to alert us that something isn’t right.
It’s an indicator that we need to realign something.
It’s very intuitive.
I just can’t seem to pinpoint its actual cause.
All I do know is that my energy is in really short supply right now and I’m just trying to make peace with my anxiety tonight by leaning into the discomfort and practicing some selfcare as the blizzard of 2023 causes chaos right outside my window.
When was the last time you really laughed; I mean like roll on the floor til you pee yourself or your belly aches kind of laughter?
What was so funny?
Learning how to laugh, especially at yourself can help maintain positive mental health during stressful times and gain a clearer understanding of what is and what isn’t important.
Being able to laugh at ourselves is truly valuable and especially at times when life feels really hard.
I know in my heart that suicide is not my only option. It’s the feeling you get though when you believe that you’ve exhausted all other options or are driven by such despair.
It muddles my better judgment.
It consumes me day and night.
It overwhelms me.
It drowns out everything and everyone who tries to stand in my way.
It’s stubborn and persistent.
These very vivid thoughts and pursuits of suicide I’ve been experiencing more and more of late are incredibly loud, confusing, scary and so excruciatingly lonely.
They don’t leave me alone.
I’m conflicted though.
They keep showing up in my dreams lately, like ALOT. I see myself standing alone, in the aftermath and filled with regret; these images are probably a good thing, right?
I just want peace.
But even if there are still other options to pursue, I’m simply burnt out. How long is a person supposed to wait until they find some kind of relief?
I spoke with my Psychiatrist this afternoon and caught him up on everything that’s gone on since our last appointment a couple of weeks ago. Like I said above, it’s been ALOT.
In the meantime though, since our last appointment he’s been working diligently to expedite those “other options” with specialists whom I’ve been waiting months to see and it seems that both his persistence and belief that those “other options” do still exist for me paid off because I received notifications for not just one but TWO appointments this week.
One such appointment is unfortunately still 2 months away with a specialist who last December when I had an initial consultation with his assistant said he was uncertain if he could help me but he is at least willing to meet me to do an actual examination. He specializes in pelvic reconstructive surgery and urogynaecology (it will be exactly one year at the time of my appointment that I’ve been waiting to see him!). The other appointment I received notification for just this afternoon via an email is set for the middle of this month. It’s with the Neurologist who is in charge of the “Deep Brain Stimulation” research trial that my Psychiatrist asked me to explore near the end of last year (if you missed it or are interested in learning more, click here: https://wheredidmommyssmilego.com/2022/11/29/consultation-with-doctor-for-deep-brain-stimulation-clinical-trial/).
My purpose of meeting with him is to discuss the clinical study in more detail in relation to my treatment resistant depression, but I am also hoping that he can give me some more insight and options to help me with my Neurological issues as well.
I know in my heart that suicide is not my only option and for now, I promise you that I will continue to keep all options on the table.
Feel free to follow my Blog at: youareenough712.wordpress.com
I’m struggling alot today since hearing the news that someone who had been admired by so many in my community has died by suicide. He was just 53 years old.
He was a true beacon of light and a pillar of strength to so many in our community and spent much of his time volunteering on so many different projects and non-profits. He was dedicated to our community and did so with such pride. He made an impact on every life he touched, both young and old alike, especially during his time volunteering as a crossing guard at a nearby school and running his own hockey league.
Everyone he met along his neighborhood travels will remember him for his friendly hellos and welcoming smiles; but what most of us never knew was that in more recent times, he was smiling through a battle with depression. “Smiling Depression” can be one of the most deadliest forms of depression because a person often feels as though they need to keep up appearances and power through their daily commitments as per usual, leading them to suffer in silence.
He and I were friends on Facebook but I didn’t know him very well personally. We’d only had some brief encounters over the years through Facebook where he’d engage on my posts from time to time as well as when he had reached out to me several years ago to ask me to be an admin on an online community website.
I certainly cannot speak to his suffering which ultimately led him to take his own life, nor do any of us on the outside looking in know the extent of his pain but today as I struggle to make sense of this tragic loss I’m feeling like I failed him somehow. I’m left wondering if he ever thought of reaching out to me for an empathetic ear like so many others do. I’m left wondering if I could have helped support him or made him feel less alone.
I know that I always have a strong urge to “fix” everyone. I want to save everyone around me before I even think about saving myself. I know in my heart though that it’s unrealistic and simply not possible. But for now I will keep on writing and sharing my story for as long as I am able to with the hope that I am saving lives.
RIP. You will be sorely missed by your beautiful family, friends and an entire community ❤️
I thought today was a good day to do a mental health check in. Feel free to add a heart or two. And remember I am here if you ever need to reach out.
Trigger Warning ⚠️ Very sensitive material, may be too difficult for some people to read; talk of M.A.I.D (Medical Assistance in Dying), suicidal thoughts
I just got home from seeing my therapist. I really needed her help today navigating my way through a number of moving parts in my life, mostly the ones which aren’t currently working for me that is.
To say my life is complicated at the moment would be an understatement and I’m not gonna lie but M.A.I.D continues to still be top of mind for me.
Earlier this week a Facebook memory of a Blog I’d written a year ago popped up. It completely triggered me; those darn memories can be both a blessing and a curse. That particular post has since become a curse.
It was a year ago this past week when I received a date for when I was to begin the clinical research trial for Psilocybin (aka: Magic Mushrooms). The date given was April 2, 2022. I had so much hope in my heart ❤️ for the next 5 weeks as I anxiously awaited my turn.
I titled that Blog “Uncharted Waters” (feel free to click here to read it:
“Uncharted waters or uncharted territory can refer literally to places not yet explored, but it can also be used figuratively to refer to unfamiliar situations in general.“~Webster Dictionary, which is exactly what this trial was, given that it was the first of its kind in Canada and I was about to be one of approximately 15 lucky little lab rats to participate in unexplored and unfamiliar territory.
Most of you reading this already know what followed next and the neurological damage that occurred due to the treatment which has continued to make my life completely unmanageable for close to a year now with daily bouts of brain zaps, constant tingling in my hands and feet, numbness, muscle aches and shooting pains in my arms and legs, an intolerance to any type of noise, near blinding vision during severe flare-ups, tics and tremors throughout my entire body all day long and unrelenting and debilitating sensations, throbbing and spasms day in and day out in my nether regions (if you would like to learn more about this last one click here: https://youareenough712.wordpress.com/2022/09/20/tmi/).
What I have been dealing with physically over the past year has only added to the further demise in my mental health which is why I recently began exploring medical assistance in dying (M.A.I.D) because I just can’t live like this anymore, especially after what I went through last month while in crisis. I’m exhausted and I feel trapped. Medication is no longer an option for me and I continue to fail every treatment I try for both my mental and physical wellbeing. Over the last year I’ve left many specialists speechless and many others unwilling to even see me, turning down every new referral my Psychiatrist makes as they do not have enough knowledge or expertise in treating my very rare, incurable nether region’s condition. I’ve continued to try and keep some hope in my heart that if one part can be treated, then maybe, just maybe it would help to settle down the other moving parts as well. But at the same time I no longer hold out for much hope at all ever since one Neurologist said to me last summer, “A circuit broke in your brain the day of my treatment and ‘hopefully’ it will fix itself one day!” I just wanna know when the heck “one day” will be?
My emotions are running quite high right now, as are those of my loved ones, friends and care team too. But for my own peace I really need to take the necessary steps at this time to see if this is what I want or if it’s even an option for me at all which is why earlier this week I made the initial phone call to speak with an intake coordinator after my Psychiatrist had forwarded me a direct link to the M.A.I.D program at the Ministry of Health a few days prior. I didn’t know what next steps looked like exactly but the kind lady on the phone guided me through to the next step, asking me some general questions, then created a chart for me and told me that a nurse practitioner would call me over the next day or so. She called around 7pm that same day. We spent about a half an hour on the phone asking me a more indepth list of personal questions in order to find out more about my reasons for calling. She reviewed the entire process with me and told me that because of my physical symptoms that have caused further ‘grievous’ and are ‘irremediable’, intolerable and cannot be relieved under conditions that are considered acceptable she would submit a request for a “Care Connector” to call me next to see if there is a Clinician available to take on my case.”
I received another call the next day from a “Care Coordinator”. She started off by apologizing to me as she informed me that my case is considered what they call a “Track 2” case which simply means that although my “illness, disease or disability or state of decline causes me enduring physical or psychological suffering” death is not imminent and that due to their enormous backlog right now they are only taking on cases at the moment where death is foreseeable and certain to happen soon. She told me to call back in mid to late April when she hopes their “Assessors” will have caught up by then. I suddenly felt like Dorothy from the Wizard of Oz when she finally reached the palace in Emerald City for the first time.
In the meantime though she told me to keep fighting and keep building my case by having my care team continue to find new specialists to see and asked that I speak with my GP to also see if she has any other networks or colleagues who may be involved with M.A.I.D.
I hadn’t told my GP as of yet that I had been considering M.A.I.D., that was until we spoke late Thursday afternoon and like with everyone else, I caught her completely off guard but also like with everyone else she was very respectful of my wishes even if like with everyone else, it’s not what she wants to see happen to me.
She made several suggestions and promised to call some other specialists, a Neurologist she knows being one of them as well as a Professor who I had been emailing with back in the summer for advice. She is a Professor at a very prestigious University in Kingston, Ontario, has her PHD and is an expert in the area of care I am so desperately in need of right now and basically the only one who seems to exist in Canada so my GP is hoping she may actually see patients but I am not certain she actually does. She wants to speak to her in particular about nerve blockers.
Before we wrapped up our nearly one hour phone call I mentioned to her about a world renowned Guru I’d found through lots and lots of research, testimonials, a Facebook group I now belong to and several specialists I’ve seen who have all referred to his 100’s of research papers (through their own Google searches) he’s published on the topic of my nether region’s condition (well people call him the Guru but he is an actual doctor of sexual medicine). I can see from the Facebook group alone just how many women he has helped throughout his very lengthy career. Women just like me. The main problem however is he lives in San Diego, California (but ironically he got his initial medical degree at McGill University in Montreal) and the cost involved to go see him would be unattainable for me. I know it’s a real long shot though but my doctor told me that OHIP (Ontario’s health coverage) will sometimes pay for expenses and/or treatments like mine (which has been deemed a persistent neurological condition) through their “compassionate care program” for specialized treatments not available here in Ontario so I decided to give his office a call that night and book the 10 minute free consult with him that he offers on his website. I was able to get an appointment for next month with one of his colleagues who they promised have all been trained extensively by the Guru himself.
I am truly blessed to have such a wonderful, caring team of healthcare professionals supporting me every step of the way. I can’t honestly tell you where my steps will take me next but I do know it certainly makes the path I’m on right now feel a whole lot easier knowing I’m not walking it alone.
“Sometimes it’s the saddest people who smile the brightest all because they do not wish to see anyone else feel the pain they feel.” ~ Anonymous
It’s been a really long week for me even though, technically it’s actually been a short one due to this past Monday having been a holiday in Ontario.
I’m beyond overwhelmed and trying desperately to hold it all together most days right now and the constant demands I’m facing during my workday are only adding to my fate.
I found myself needing an escape from my office several times today in order to reset and try and collect myself again.
As it is, I have to force myself to take a lunch break most days because there just aren’t enough hours in the day. I feel like I’m constantly bailing water out from a sinking boat.
Taking mini-breaks throughout the workday or in any stressful situation for that matter I know is ok; even if I feel really guilty doing so and can sometimes feel an increase in my anxiety level.
But in not doing so when feeling the overwhelm or when learning to walk away when needed will only create further burnout and decrease one’s level of productivity in no time.
So today I took the necessary mini-breaks I needed. I had a good cry in the washroom, I did some breathing exercises, I reset my brain, put a smile back on my face and pulled myself together long enough to continue my day all because I chose to remove myself from my workspace for a few moments at a time.
I’m wearing this gentle reminder hoodie today to honour every child who has ever felt the devastating impact of being bullied. Let’s honour them by wearing pink today on “Pink Shirt Day” and send a message to the world that our words matter.
YouAreEnough 
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