As a speaker who shares her story of mental illness and recovery, I’m often asked what helped me most when I didn’t want help. What benefited me most when I was struggling and pushing people (and their assistance) away? What worked I call the “Crazy Naked Truths” (CNT).

CNT are principles healthcare providers, savvy friends, and my parents, in particular, embodied. They are strategies they utilized which facilitated my wellness journey. Eventually, I lived into these tenets– allowing me to flourish on my own. 

I was learning to manage bipolar disorder, anxiety, psychosis and the aftermath of a spiritual emergency. But these pointers encourage wellness in general. They’re applicable to many situations where someone is in distress or for anyone wanting to increase their ‘contentment quotient’. The guidelines transcend condition and illness, gender, age, ethnic background, socio-economic status, sexual orientation, religious affiliation, even political persuasion. Darkness knows no bounds. Neither does light. 

The 20 Crazy Naked Truths 

1. You can’t get well for me. You can’t change or control my behavior, reactions or choices. You can create conditions and options to help me accept my illness and make positive choices.

2. Acceptance is my greatest liberator; denial my greatest barrier.

3. Who you are and how you show up, matter as much as what you do and how much you know.

4. Find support and skills for yourself so you have the strength to say ‘no’ to me and offer me alternatives I may not welcome.

5. Learn to set boundaries with me so I can learn to set boundaries for myself.

6. Stay calm in conversations. Practice responding rather than reacting. Before you get to your “wits’ end”, walk away. Take a time out.

7. Show me how to use my anger not lose my temper.

8. If conversations always escalate into arguments, consider family therapy.

9. Learn to empower, not enable. As consistently as you can, offer me choices that work for YOU. Incorporate your needs and wants. IE: In exchange for living with you (the parent), I (your adult child) needs to get up by 9am and do a chore everyday. If I don’t want to do that, then you can still be there to help me and explore ways to find subsidized housing. 

10. Slowly, in small steps, create a reciprocal relationship with me. A relationship that is based on respecting the needs of others. Julie Fast has two excellent articles about this: The Hijacked House  and Reciprocal Relationships: Parenting your Adult Child with Mental Illness While Meeting your Needs

11. Sometimes I need a kick in the butt more than a pat on the back. Sometimes, the opposite.

12. Don’t protect me from the privilege of failure. 

13. You may never know which of your words created my tipping point into wellness; but know our conversations matter. 

14. I will rise to your expectations.

15. Hold a vision for me until I can hold it myself.

16. Explore what helped me in the past and focus on those strengths and tools to help me in the present.

17. Help me discover what I yearn for most deeply, and you will have helped me find the intrinsic motivation I need to participate in my wellness journey.

18. Push back indicates that fear is afoot. Model and teach me tools to manage and articulate my anxiety and needs, and I will move forward.

19. Respect my timetable. It is likely different (and slower) than yours. 

20. Once I’m well, support me to make ‘a good thing better’.

What do you think? In the comments section, let me know which one you’d like further information on. Who knows, it might appear as a future blog post.

© Victoria Maxwell




Ok before anything. Let’s take a deep breath. I’m serious. Do this with me. Inhale 1 – 2 – 3. Pause. Exhale 1 – 2 – 3. A little better? 

Like many of you, if you subscribe to newsletters, many are focused on information about the unusual times we are in and what we can do to prevent the spread of the COVID-9 virus and the anxiety that surrounds it. 

I’m not going to repeat what you probably have in your inbox. Instead I’m going to share with you my experience and what I’ve unexpectedly gleaned from this collective situation. I realize many aren’t as fortunate as I am: a privileged middle-aged white woman, not working the frontlines, with some small savings in the bank, in my home country and healthy. The following “COVID19 Silver Linings” might not be relevant to you – but I offer it in the spirit of kindness and support.

1.It’s OK to go slow: I have felt strangely comforted by this surreal global experience. Let me explain. It’s put the brakes on my work – allowing the pace of my life to sloooooow down. Three of my speaking events have been cancelled and I expect more. Although this comes with financial consequences, I’m ok with this. Everyone is facing uncertainty. Businesses everywhere are having to make changes. I know I am not alone. We’re all going to be given time and wiggle room as we find solutions to support ourselves and each other. On my day off, like last Sunday, I made banana bread. For the life of me, I can’t remember the last time I baked banana bread! The more I slow down, the easier it is to breathe deeply and calm myself.

2. Perspective: A global pandemic puts things into perspective. Like any illness, it can help us reprioritize what’s really paramount and recognize what we thought was important (finding a better fitting pair of jeans for instance) maybe isn’t so important after all. I’ve phoned (yes, phoned not texted!) people I haven’t in awhile. A friend’s mother who I knew had fallen, a writerly friend (ok I did text her), good friend who’s been facing other life bumps.

3. One thing at a time tactic: What used to be urgent isn’t. I don’t feel the pressure to be busy-busy-busy and get my usual to do’s done. I identify the ONE thing I know needs to be done today. Then I take one slow, gentle step at a time to get it done. This ‘one-thing-at-a-time’ focus helps me soften into the present moment, allowing surfacing anxiety to pass on its own. If I get that ONE thing done, I identify the next one thing that needs to be done and so on. This is also a great antidote for fuzzy thinking.

I hope some of my experiences spark an insight or small gentle sense of ok-ness for you while we ride the waves of this. Share with me what you have discovered to help you stay grounded and connected. We really are in this together.

© Victoria Maxwell



I love this initiative. Rob Osman from Bristol in the UK, who has struggled with social anxiety and depression, created a dog walking group for guys to gab about their feelings and struggles (if they so choose). He did so after he found walking his dog, Mali, was such a huge help for his own mental health. 

For anyone, but for men especially, ‘let’s go for a walk’ is so much more appealing than ‘let’s have a talk’. 

Dudes & Dogs Walk & Talk he calls it. Don’t you just love that? 

The program is there to make it easier for men to talk or, even just to join in and go for a walk with another dude and a dog. No pressure or requirement to say a thing.

In a Somerset Live interview, Rob Osman says “”It [walking a dog] is a good way (for people to relax and drop their barriers) because you do not have to look at each other in the eye and are in an open space.”

I talk about how to create an encouraging space for folks to talk in my most recently developed “keyshop” (combo of a keynote and workshop) Creating Comfortable Mental Health Conversations at Work

When you’re talking to someone about a potentially delicate issue (like mental health, or simply feelings), you want the individual to feel safe. You don’t want them to feel cornered (as in a hallway) or too exposed (in view of co-workers in the break room) or threatened or defensive (like sitting across a table or a desk even).

I suggest the very initial ‘how are you doing?’ questions happen while casually walking through the parking lot away from others. Strolling from one job site to another is another good place to start a conversation. 

Osman continues: “It is at their pace and there is no expectation for them to have to talk – it could be that they just listen the first few times.” 

Men and women relate and express their feelings in very different ways and environments. We women sit across from each other, looking supportively into each other’s eyes, drinking tea or coffee and talk, and talk and TALK. 

I can call a girlfriend who I will be seeing that same night, talk on the phone for an hour or more during the day, and still have things to say to her in the evening. My husband just shakes his head and wonders how on earth could we have so much to say to each other. That’s women for ya.

Men on the other hand, so I’ve been told, open up when they are side-by-side doing things together. None of this eye contact kind of stuff. They watch ‘the game’, sit around a fire, go for a hike, or as Osman knows, go walking with a dog. Then talking flows from the activity.

We need our men to talk. The stoic ‘I-can-tough-anything-out’ is killing them. 11 people die every day by suicide In Canada. Most of them are males. That doesn’t even capture the individuals who attempt it. 

We need to normalize talking and explore ways of sharing that’re comfortable so men are willing to participate. Having women suggest ways ain’t gonna fly too far. Role models are the best way to create change. Rob Osman is one of those who is pioneering new methods to get his brothers in arms to stop suffering in silence and instead get into nature, with dude and dog, and share some of the tough stuff. 

When men find healthy ways to express themselves and their struggles it positively impacts their families, their workplaces, and their communities. And THAT is something definitely worth talking about! 

© Victoria Maxwell


How do you support an adult child who has a mental illness? How do you as a caregiver hang in there when your adult child, who so clearly needs help, refuses it? I get requests from parents and caregivers just like this every week.

Some of you reading this right now may be facing these very situations. Your adult child may be struggling with addiction, maybe it’s a severe chronic mental illness, or maybe it’s both.

I wish there was a simple three step solution. Do this, this and this and your adult child will accept the help they’re being offered. Put these five strategies in place and the rehab program they’re in, the out-patient program they’re involved with will, all of a sudden, turn things around once and for all. 

But it doesn’t work that way of course. Recovery is possible. Recovery should be the expectation. But the cold truth is recovery isn’t guaranteed. Recovery is also relative. Recovery varies for each individual depending on myriad factors – especially how chronic, how severe the mental illness is that the person is dealing with.

There is still reason to hope. There are solutions, though the road may be arduous. 

With this in mind I want to share with you an issue of the Canadian Mental Health Association BC Visions Journal: Supporting Adult Children: Helping Them Find Their Way.

You’ll find first person experiences from parents and caregivers. Like Holly Horwood, whose daughter lives with severe schizophrenia. She describes what they have gone through as a family and explains what has helped and what hasn’t. 

You’ll read about the pivotal part support groups play in the lives of caregivers. Other articles offer strategies for setting and reviewing boundaries, how to hang in there as a parent when your adult child doesn’t want help and tools to support them when they do. 

You can learn about additional resources, and communication strategies to help your adult child in this Psychology Today post: “Help Your Loved One with Mental Illness with These Resources”.

In particular look at #6 and watch Dr. Lloyd Sederer’s TEDxAlbany talk ‘When mental illness enters the family’, where he describes key steps to help someone who doesn’t want help.

Watch how my parents coped and navigated my unwillingness (or perhaps better said my inability) to accept help in my theatrical keynote (available for purchase here should you be so inclined).

If you love an adult child with a mental illness and/or substance use issue, my wish is that you realize you’re not alone and as a result feel some relief and hope and also discover some new resources for your journey.

Visions Journal is a free magazine produced by the British Columbia Division of the Canadian Mental Health Association. Electronic subscriptions are free to anyone. Print subscriptions are free to anyone in BC. The cost is $25 for a yearly subscription outside of BC. Click here for more info.

You can view past editions here.

© Victoria Maxwell



September is fast approaching. In light of this, I thought it apropos to write a post regarding accommodations for students with mental health issues in a post secondary setting. 

Creating accommodations help students who have mental illness reach their academic potential. Whether you’re advocating for yourself, or helping to advocate for someone else here are points to keep in mind.

1. Accommodations are a right, but are negotiated.

2. Determine what changes would be most effective for your specific illness or illnesses. It may take some experimentation.

3. Role-play asking for the accommodations to gain confidence before actually requesting them.

 With few exceptions, teachers and schools are very amenable and experienced in accommodating students with disabilities. As part of the American Disabilities Act and the Canadian Human Rights Act, they have an obligation to fulfill reasonable accommodations requests.

Dr. Sarah Helm, Diversity and Inclusion expert, cites “according to the National Center for Education Statistics, individuals with depression, mental, emotional, or psychiatric conditions now represent approximately 24% of college students with disabilities and have become the largest cohort of post secondary students who identify having a disability” (Helm, 2012; NCES, 2009).

Despite this, fellow students and teachers still can lack understanding, sensitivity and patience. The more comfortable you are with your mental health needs the easier it will for you to communicate with teachers. In the classroom, you are not required to disclose what illnesses or disabilities you have. But you will need to be able to discuss what accommodations will be helpful. You can, if you choose, to disclose voluntarily. But that is a decision that is very personal, and should be made carefully.

There are both informal accommodations (strategies students can implement on their own) as well as ones that are formalized through disability services on campus. Two people with the same condition may not need the need the same classroom strategies. Here are a few examples of formal accommodations:

– Due date extensions

– Time extensions on exams

– Quiet and/or alone place for taking tests

– Ability to complete work at home

– Advance notice of course expectations

– Study buddy or academic coach

– Alternative forms for assignments

– Alternative types of study resources

– Pre-arranged breaks to get fresh air and move around

Dr. Helm explains “counseling centers and disability services offices have been increasing their level of support for students with psychiatric disabilities; yet despite these existing support structures, students are not seeking assistance from disability services offices due to fear of disclosure and the negative stigma” (Collins & Mowbray, 2005; Helm, 2012).

So it is imperative students with psychiatric disabilities understand they have a right to reasonable accommodation as well as protection from discrimination stemming from stigma. Colleges need to recognize that insidious stigmatizing attitudes towards those with mental illness have subtle yet far reaching ramifications. On-going dialogues about mental health and mental illness on campuses are crucial so stigma and it’s consequences are lessened. In doing so, students can be propelled from the fear of disclosure and requesting support to the freedom of accommodation and academic success.

 An excellent resource is the Higher Education Support Toolkit: Assisting Students with Psychiatric Disabilities from Boston University Center for Psychiatric Rehabilitation.article continues after advertisement

© Victoria Maxwell


 References:

Helm, Sarah PhD Career Development Experiences and Employment Concerns of Job-Seeking Students with Psychiatric Disabilities PhD diss., University of Tennessee, 2012 http://trace.tennessee.edu/utk_graddiss/1304

National Center for Education Statistics (NCES). (2009). 2007-2008 National Postsecondary Student Aid Study (NPSAS: 08). Computed by the Data Analysis System (DAS-T) Online Version 5.0 on June 29, 2009

Collins, M. E., & Mowbray, C. T. (2005). Higher education and psychiatric disabilities: National survey of campus disability services. American Journal of Orthopsychiatry, 75 (2), 304-315.


Diagnosis doesn’t equate acceptance (as many of you well know). I certainly took my sweet time in accepting my conditions. Mental illness, particularly psychosis, wasn’t something I had been striving for in my 5-year life plan.  

Below are questions and approaches my family, psychiatrist, other health professionals and my friends could have used to help me become more aware and more accepting of what I faced.

A caveat however. If someone is experiencing a psychosis or a severe lack of insight (anosognosia*) these suggestions may not be appropriate or at the very least will need to be adapted. For tips about how to communicate with someone in a psychosis these videos might be helpful. Though neither is a psychiatrist they have good information (suggestions start at 6 minutes 48 seconds).  I don’t like his finger pointing (which you’d think he’d know isn’t a good way to communicate). Some advice and examples are a bit flip and graphic, but some information is excellent.

Another video to watch is: https://www.youtube.com/watch?v=_ss_CMUdH2U She makes an excellent point about being a ‘comforting force not a challenging force’.

Here are 10 strategies that could have helped me feel understood, empowered and more willing to investigate the treatment and help being offered:

1. I wish…someone asked me exactly why I didn’t want to accept the diagnosis. Why I didn’t want to take medication. When the reasons for resistance are shared, erroneous assumptions can be discussed, potentially corrected and new actions can take place*. E.G: I believed medication was a ‘cop-out’ and meant I was weak. I believed if I did enough therapy and got to the ‘root’ of the psychological reason I was depressed, I wouldn’t experience it anymore.

2. I wish…someone validated and empathized with me regarding my resistance to medication instead of trying to get me to see it their way. That doesn’t mean agreeing with me but it meant acknowledging my position. Arguing with me and telling me to take it only made me feel more misunderstood, and forced me more into myself.

3. I wish…someone validated and empathized with me regarding my resistance to medication instead of trying to get me to see it their way. That doesn’t mean agreeing with me but it meant acknowledging my position. Arguing with me and telling me to take it only made me feel more misunderstood, and forced me more into myself.

4. I wish…someone helped me understand the truth about mental illness, and showed me how to investigate those objections, allowing me to come to my own conclusions. That is, do some basic stigma busting with me.

5. I wish…someone asked me if I wanted to talk about my psychoses. Because I did want to talk about it. I wanted to, needed to make sense of it.

6. I wish…someone validated and explored with me the profound, life-changing spiritual elements of my psychosis. It’s important to note, not all aspects were negative and not all were meaningful. Instead, what happened was my insights and experiences were labelled as pathological and part of the illness, something to be discarded and forgotten. It wasn’t until I met my psychiatrist, Dr. Dillon, who discussed my experiences with neutrality, curiosity and compassion.

Questions like these would have helped:

  • What did I learn?
  • What was it like?
  • What happened?
  • What aspects did I want to talk about, but was afraid to? And why?
  • What am I sad about? What did I lose? What do I need to grief?
  • What am I afraid of, concerned with and how can it be addressed?
  • What am I confused about?

7. I wish…someone could have helped me integrate a medical model with a spiritual perspective sooner and explained to me that it is possible to have both a spiritual experience and a mental illness; that one does not negate the other.

8. I wish…more people praised my scepticism; it meant I was deciding things on my own and the choices I made were intrinsically motivated.

9. I wish…someone informed me sooner the severe negative and anxious feelings I was experiencing could be part of a mood disorder not just a set of emotions and low self-esteem.

10. I wish…someone had explained cognitive therapy more clearly. When I was told my thinking creates my feelings, I felt I was being blamed for my depression.

Kay Jamison states in her book ‘An Unquiet Mind’ that we don’t know why some people walk through the door of acceptance or walk through it easily and others don’t. We also don’t know when people will do it. What I know for sure is, when we meet people where they’re at, when we’re curious and respectful, it helps people feel safe. People who feel safe are more willing to take risks and try things. That’s what happened for me at least.

© Victoria Maxwell


*NAMI defines anosognosia “when…someone is unaware of their own mental health condition or they can’t perceive their condition accurately”. Click here for information about it in the context of mental illness.


Anxiety has been giving me a run for my money. Diagnosed with generalized anxiety disorder, I’m used to dealing with my uber easily triggered flight and freeze response. But in the last year anxiety has been screaming at a high pitch for long periods of time in my body and my mind. It is UNCOMFORTABLE. Side note: Having an anxiety disorder it’s rather ironic I chose to be a self-employed public speaker.

Working for myself, which consists of on-going financial uncertainty, and doing the one thing people fear more than death. However, that isn’t driving my current state of dread and sweat. Among other things, menopause has kicked me in the butt.  Since I’ve entered that oh so lovely transition, anxiety has spiked more than I’ve ever experienced it. I didn’t know anxiety was a symptom of menopause. I didn’t know a lot of things about menopause. It’s not exactly a sexy cocktail party topic. Regardless, my husband has been suffering through it with me.

Anyway…the big ‘M’ and other life ‘stuff’ has ratcheted up my adrenals and kept my system revved up for far too long. My usual wellness tools haven’t been working as effectively either. To find some relief, I signed up for a 6-week ACT group course at our local mental health and substance use centre. An ACT group. Sounds like it would be right up my alley, yes? ACT. I’m an actor (or actress depending on your preference) right? Well it’s not that kind of acting group. ACT stands for Acceptance and Commitment Therapy. It’s developed from Cognitive Behaviour Therapy (or CBT). Its basic premise is using mindfulness to become comfortable with (ie: accepting) your uncomfortable physical sensations and difficult thoughts and distressing emotions. Then use your core values to guide your actions so you can live the life you want.

What’s important to understand is that accepting them does not mean liking them. It means I give them room to ‘be’ without trying to change them. It was a mind stopper this one. Allow myself to be ok with feeling this intense anxiety? Not try to change it? Fix it? Fix me? One of the meditations recommended in the group was the 3-minute breathing space meditation. Three minutes of meditation. That I can do. At the outset it was wonderful. Each time after doing it, I felt peaceful, like a gentle parent holding me. But then weeks later, some proverbial crap hit the fan and I experienced unrelenting anxiety.

This 3-minute breathing space felt more like a 30-hour jail cell. I’d sit and immediately want out. Breathing, and allowing my anxiety, seemed only to magnify it. My heart beat faster, louder, or wait was that a skipped beat? No now all I could hear was the blood rushing in my ears and feel my stomach tighten – even more. I. AM. OFFICIALLY. GOING. CRAZY. Again!!! When the tail starting wagging the dog, and my anxiety overwhelmed me, this whole letting it be and noticing seemed like, well, a really bad idea. Until I listened to a podcast reminding me of one paramount ingredient I’d forgotten to include in my mindfulness practice.

A dear friend sent me a recording of a talk from Thich Nhat Hanh, a Vietnamese Buddhist monk and peace activist, and author of over 100 books. I’ve never been much of a fan of ‘Mr. Hanh’. Not that he isn’t wise, or walks his talk. He definitely is and he definitely does. It’s just that I’ve never quite jived with how he expressed his wisdom. Until this talk. Until, I guess, I needed it. Maybe it will help you. Using metaphor, he describes how mindfulness works. It broke open my heart and changed my practice.

Paraphrased from his dharma talk ‘You are Both Depression and Mindfulness’. This segment starts at around 18 minutes. “When depression manifests, we should invite mindfulness. The energy of mindfulness will recognize the energy of depression. There is no fighting between the two kinds of energy. Because the job of mindfulness is to just recognize things as they are. Then to embrace whatever is there in a very tender way, like a mother would embrace her child when the child suffers.” That is what got me. “The mother is working in the kitchen, but she hears the baby crying. She knows the baby suffers. She goes into the baby’s room and picks the baby up and she holds the baby tenderly in her arms. The energy of tenderness of the mother begins to penetrates into the body of the child. And after a few moments the child feels better. This also happens with the practice of mindfulness. With the practice of mindful breathing or walking we generate the energy of mindfulness. With this mindful energy we recognize the other energy (depression, anger etc.) and we can embrace the other energy with tenderness.

There’s no fighting. There’s only supporting, helping.” When I practice mindfulness, I simply watch what is going on inside of me. But instead of a clinical dispassionate watching, I add tenderness. The watching becomes an embrace of kindness. This way the sensations and thoughts are easier to stay with. A softening usually happens (not always, but often). This loving kindness I practice generating soothes those other energies within me. Like the wise ol’ Mr. Hanh said it would!

Try the 3-minute practice with the pointers from Thich Nhat Hanh yourself. Share your experience and thoughts. I always love hearing from you.

© Victoria Maxwell

Supporting a loved one with mental illness can be trying. I’ve witnessed the toll it takes on my husband. I’ve experienced it as a daughter of a mother and father who both had psychiatric conditions. A chronic mental health condition is like addiction. Even when well managed, its presence is still felt in the relationship.  

My husband has taught me a lot about what it means to support someone. With practice, I do it more and more for myself. Some I already knew, some I only discovered by being with him at my most vulnerable, my most messy.

Think psychosis. Think oozing self-loathing. Think unrelenting anxiety. I know. Yuck.

What Works

Someone who…

  1. Walks beside me on the journey
  2. Watches a movie with me
  3. Can stand my company even when I can’t
  4. Listens without fixing
  5. Listens and helps me problem solve
  6. Sets boundaries and let’s me know when he’s reached his limit
  7. Reminds me it’s ok to take my beta-blockers; that I DON’T always have to tough it out
  8. Talks with me about ‘trivial’ things that have nothing to do with how I feel
  9. Requires honesty
  10. Tells me to un-pretzel myself when I’m in my most challenging yoga pose. You know that one of navel gazing and head up my butt. It’s surprising how long I can hold that posture.
  11. Helps me name things I’m ashamed of – like when he asks ‘peeled grape’ day? Yes – that’s how I feel, frequently, more frequently than I’d like to admit.
  12. Explains naps are good medicine and gives him a break too!

What does your partner do that helps you when you’re in struggle mode?

What do you do as a partner to help your loved one?

© Victoria Maxwell



There are many reasons why people don’t accept a diagnosis of mental illness.

I received an email the other month from someone whose spouse had psychotic experiences and was later diagnosed with bipolar disorder. However, the spouse believes they had a powerful spiritual experience.

The spouse has agreed to see a psychiatrist, and continues to see their counsellor, but won’t take medication.

I’ve been in that very position, refusing both the diagnosis and medication. Understandably. The experiences I’ve had (two, quite recently) from a science approach typically are called psychosis. I like to call it non-shared reality. Regardless how you describe them, elements of these experiences are profound for me.

I’ve always had difficulty with the ‘either/or’ perspective. Either my experience is an illness as seen through the medical model OR it’s strictly a spiritual experience as seen through alternative perspectives such as the anti-psychiatry movement or transpersonal psychology.

What I experienced was more nuanced. To cavalierly categorize it as either only alienates me from potential help.

But what to do?

In my case, I encountered a brilliant psychiatrist who helped me understand what I experienced could be both. Or, more accurately, they could exist simultaneously.

I had undergone (and continue to undergo) spiritual experiences meaningful to me. While at the same time I have a mental illness that would benefit from some medical assistance.

I’ve come to understand the diagnosis of bipolar disorder, anxiety and psychosis does not diminish the importance of these personally transformative events. Mental illness and spiritual awakening are not mutually exclusive.

This was life-changing for me. It allowed me to embrace the spiritual path I held so dearly while also accepting much needed treatment for psychiatric disorders which were, in no uncertain terms, ravaging my life and relationships.

I am of the belief, for some people, we need to blend both approaches, spiritual and medical. If either one excludes or denigrates the other, it won’t be helpful. For me, the litmus test is this: does the person have the quality of life they want? Is the approach they are using causing them more suffering or less?

I wanted to be someone who didn’t need to take medications. But I’m not that kind of person. Some people don’t need to or can manage without. For me, I needed to be open to the possibility of needing meds and not needing them. I needed my support circle to be on board with that too. Or to be honest with me about any bias they had. That built trust. Trust in the end is the best bridge to help build a life worth living.

Allowing for ‘Both’ rather than forcing an ‘Either/Or’ stance made getting better, well…better. I am able to comfortably hold both my spiritual and medical model perspectives. It’s a fine line, but that’s fine with me.

The following are resources to help those of you grappling with the ‘either/or’ situation. Whether you are supporting someone who identifies only with the spiritual, even to their detriment, or for those of you given a psychiatric diagnosis and trying to reconcile it with your profound experiences, I hope these shed some light and offer insight.

1. Visions Magazine – This edition focuses on spirituality and how it related to mental illness. Visions is an award-winning magazine that brings together many views on mental health and substance use.

https://cmha.bc.ca/wp-content/uploads/2016/07/visions_sprirituality.pdf

The following I wrote or created in partnership with others. Each describe in different ways my journey integrating both a spiritual perspective and medical model approach to help my life come into balance so I could begin to flourish.

2. Bridging Science and Spirit – a 7-minute documentary https://www.youtube.com/watch?v=sXq9B9a3sOI

3. Does God* Have A Place In Psychiatric Treatment Plans? – blog

https://www.psychologytoday.com/ca/blog/crazy-life/200910/does-god-have-place-in-psychiatric-treatment-plans

Note: I use the word ‘God’ but don’t mean it in the strictly religious sense, per say. I use it interchangeably with Love, the Divine, Universe, Spirit, Goodness, what-have-you. Please replace it with what you are most comfortable with.

4. I Went Off my Meds to be More Spiritual: Spiritual Growth and Psychiatric Medication – an oxymoron?  https://victoriamaxwell.com/i-went-off-my-meds-to-be-more-spiritual/

5. Crazy for Life – My theatrical keynote (aka one-person stage show) focusing on my struggle to reconcile the mental illness diagnosis with profound spiritual experiences. In it, I describe how medication, for me at least, needs to be part of my wellness tool box. Not the only one, but one nonetheless. View a clip from the show here (watch at 1min 25sec): https://www.youtube.com/watch?v=z-CU5DaOl74&t=7s  Also available for download purchase. https://victoriamaxwell.com/product/crazy-for-life-a-story-about-accepting-help-for-mental-illness/

Have you had spiritual experiences within your mental illness? Do you think it is one or the other? I’d love to hear from you to learn about how you made sense of it.  

© Victoria Maxwell

In a previous post, I described the O.A.R.S. framework (Observe, Ask + Actively Listen, Refer + Support).  A simple protocol outlining how to approach someone in the workplace who may be struggling with a mental health condition. The 4-step system along with the ‘do’s and don’ts’ helps make difficult conversations more comfortable and effective. For a copy of a handout click here .

Besides good communication strategies, employers and co-workers need resources – resources beyond your typical EAPs (Employee Assistance Programs). Mental illness, a multi-faceted issue, needs multi-faceted solutions.

These are some workplace resources I recommend. I’ve chosen not to list the well-known and well-respected Mental Health First Aid or the Mental Health Commission of Canada’s workplace webinars. Likely you’re already aware of them. If you’re not, please do check them out.

I’ve decided to highlight ones that may not be on your radar.

Please note: I am not affiliated with any of the following organizations or individuals. I know them as reputable resources offering services and information to effectively help employers and co-workers address difficult mental health issues.

Mind: A UK based non-profit providing advice and support to empower anyone experiencing a mental health problem.  Included is a free download about how to support staff experiencing mental health problems: www.mind.org.uk/media/550657/resource4.pdf  

Visit www.mind.org.uk  to find other good resources.

 

Job Accommodation Network (JAN) is a free on-line resource that offers expert and confidential guidance on workplace accommodations and disability employment issues.

Unique to JAN is their Searchable Online Accommodation Resource (SOAR) system and their A to Z listings by disability, topic, and limitation. The databases lets users search for a specific disability (IE: anxiety disorder, ADHD) and then offers disability-specific accommodations, case studies and questions to consider. https://askjan.org/a-to-z.cfm

 

Not Myself Today: A fee-based program developed by the Canadian Mental Health Association for employers to help create mentally healthy workplaces. It’s evidence-informed, with practical solutions, focused on building understanding, reducing stigma and fostering supportive work cultures. www.NotMyselfToday.ca Visit https://cmha.ca/programs-services for other programs.

 

Mary Ann Baynton & Associates: Mary Ann Baynton and her staff offers various services to improve or resolve workplace issues related to individual or organizational mental health issues. Well-respected across Canada and beyond, she has been a pioneer in workplace mental health consulting since 2008. https://maryannbaynton.com

 

Deborah Connors offers training to develop psychologically healthy workplaces and transform culture. https://deborahconnors.com/

 

 

Hayley Peek Consulting: In partnership with Kim Sunderland, Hayley Peek offers programs that teach people how to have a supportive conversation with someone who may be struggling with a mental health challenge or illness. www.hayleypeek.com

 

Provides various free resources such as tools, training, strategies, assessments for employers, staff, managers to improve workplace mental health. https://www.workplacestrategiesformentalhealth.com/

What workplace mental health resources do you recommend? Send me your go-to websites or resources and I’ll list them in a future blog post with your suggestions.

© Victoria Maxwell