Showing posts with label HTLT. Show all posts
Showing posts with label HTLT. Show all posts

Wednesday, 12 June 2024

Navigating Mental Health Miles Apart: An Interview with the Co-Founder of Gum on My Shoe

Welcome to Gum on My Shoe, a platform dedicated to fostering understanding, support, and advocacy for mental health, particularly in relation to bipolar disorder. Today, we have the privilege of delving into the story behind this impactful blog and its companion book, High Tide, Low Tide: The Caring Friend’s Guide to Bipolar Disorder. Join us as we chat with Martin Baker, one of the blog’s co-founders, about the power of friendship, resilience, and breaking down barriers in mental health advocacy.

1. Can you share the inspiration behind starting Gum on My Shoe and writing High Tide, Low Tide?

The idea for our book High Tide, Low Tide came when I mentioned to Fran that I felt inspired to do something creative. I wasn’t thinking about mental health as such, more like maybe some short stories, or focusing on my photography. Fran had other ideas! “I know what you could do,” she said. “You could write a book about being friends with someone who lives with mental illness!” I realised straight away what a great idea it was, but it took a while to figure out the best way to approach it. Ultimately, it was a conversation Fran had a couple of months later with a mutual friend of ours, Laurel, which provided the insight I needed. It took us four years, from the original idea to publication, but we’re both proud of what we achieved.

Our blog, Gum on My Shoe, initially arose from wanting to develop a platform to showcase the book we were working on, and other content on the theme of mental health and mutually supportive friendships. In time, it took on a life of its own. We posted rather haphazardly in the beginning as and when we had something to share. After a while, we settled on publishing something new every week. That might seem a challenging schedule, but it works for us and we’ve only once missed a deadline!

2. How has the distance between you and Fran influenced your friendship and your collaborative efforts in mental health advocacy?

Great question! Fran lives on the east coast of the US. I live on the other side of the Atlantic, on the east coast of England. You might imagine that being three thousand miles and three hundred minutes (five timezones) apart would be a problem, but it’s not hard to stay connected if you want to be. We’re in touch every day, usually several times a day, on chat or video calls.

There are some negatives, of course. The most obvious is we can’t hang out in person. We’ve met once, in Southampton, when Fran called in there briefly en route to Germany for a three month trip around Europe with her parents. Those months were a massive challenge to Fran’s health, to our friendship, and to my ability to support her effectively, because technical issues meant we couldn’t keep in touch as much or as easily as we normally would. We share a lot of what we learned during those months in our book, which is filled with excerpts from our phone calls and chat conversations as we did our best to hold things together.

The five hour difference in timezones actually works well for us. This was especially true in the first months of our friendship. Fran was in an acute manic phase at that time. The time difference meant I could be available to chat or talk with her at times when it was inconvenient for her friends over in the US, such as through the night over there.

In other ways, the physical distance is irrelevant. I can chat and talk as easily with Fran on the other side of the world as I can with other friends much closer to home. Cloud apps such as Onedrive and Google Drive mean we can share documents and collaborate easily. That’s how we wrote and edited our book together. We’ve been interviewed about our book and other mental health work for podcasts and review articles. On one occasion, I attended a live forum in the US to discuss mental health and social media. The other panelists were there in person, while I was present via video call, on a big screen off to one side of the stage. To mark the launch of our book, Fran and I had an online party with friends and followers from all over the world. We also organised a live event at a music venue to raise funds for a local mental health non-profit. Again, I attended via a big screen placed next to Fran on the stage!

Ultimately, distance, whether measured in miles or minutes, needn’t prevent people connecting and supporting each other. It can even be beneficial. As we like to say, “no one is too far away to be cared for or to care.”

3. What has been the most rewarding aspect of running Gum on My Shoe for the past ten years?

As I mentioned, our initial aim with the blog was to provide a platform for us to share and publicise our book and our wider interests in the mental health arena. It remains focused on mental health and supportive friendships, drawing extensively on our experience as friends. It’s not about awards or recognition as such but I was very proud to be included in a 2020 article at Health Central that showcased seven people who have changed how we view bipolar disorder.

Initially my contributions were mainly written from the perspective of the “well one” — the supportive friend of Fran and others who live with mental health issues. That’s still very much our focus, but over the ten years we’ve been running the blog, other themes have developed. These include my own mental and physical health, friendship and relationships in general, and blogging itself. Writing for the blog each week has shifted from being something I do, to being an important part of who I am. Writing has always been important to me. I’ve kept a daily journal since I was fourteen, and at different periods in my life have written poetry, short stories, and creative non-fiction. I still write my journal each day, but my weekly blog posts give me an additional opportunity to explore ideas and topics that are important to me.

I must mention guest posts here. I love showcasing the work of other writers, whether that’s someone already established in their own right, or someone who’s maybe never shared their thoughts, ideas, and experience publically before. If you’re reading this and would like to contribute, check out the contact page of our blog. I’d love to hear from you!

Blogging also contributes a great deal to my friendships. Many of my posts are inspired by conversations I’ve had with friends, and they help me develop my ideas around whatever I’m currently working on. That’s especially true of one of my closest friends Aimee Wilson who has her own immensely successful blog, I’m NOT Disordered. The fact that we’re both so committed to blogging is something we both value immensely because not everyone understands how much goes on behind the scenes. There have been a few times when I’ve wondered why I continue to blog and considered either stopping or reducing the frequency of the posts we publish. Having Aimee there as a support and encouragement is a major reason that Gum on My Shoe is still up and running.

4. In your experience, what are some common misconceptions about bipolar disorder, and how does your blog work to dispel them?

A while ago I was stuck for something to blog about and asked Fran if she had any ideas. She replied, “Write about how you help me with my relationships. Bipolar is a relationship disease.” It reminded me of something I came across when we were researching our book. It was an account online of a man whose girlfriend had been diagnosed with bipolar disorder. She broke up with him because her therapist told her she could never have a deep relationship with anyone. She was twenty-eight years old.

That kind of misconception — especially from a professional who ought to know better — is so damaging. It’s one of the key messages we hope to share through our book and blog. Because while Fran has experienced difficulties with relationships in the past, and to some degree still does, many of these can be attributed to ignorance and stigma around what it means to live with mental health issues in general, and bipolar in particular. Mania can be particularly difficult, because its very intensity tends to push people away. We have a highly successful, close, long-term friendship, and we want people to know it’s possible for people living with mental health issues to have and maintain good relationships, and to have — and be — great friends.

It’s worth saying that it’s not all one way. I’ve learned as much about friendship and relationships from and with Fran as she has. In particular, I’ve learned not to slam the door shut on relationships if they appear to have run into difficulties, but hold open the possibility of them resuming in the future.

Another misconception is that a mental health diagnosis is a life-time sentence with no hope of change, recovery, or remission. There’s no cure for bipolar disorder, and it can be very difficult to manage. That’s true for the person living with bipolar and their friends and loved ones. But it’s categorically not true that a diagnosis condemns you to a life that is in any way hopeless, less than, or devoid of potential. Fran and I both hope that our book and blog contribute to countering those unhelpful stereotypes around bipolar disorder in particular, and mental illness in general.

5. Could you describe a particularly memorable moment or story that has come from your interactions with readers of Gum on My Shoe?

If it‘s okay, I’ll widen the question to include readers of our book and our followers on social media, because it’s not always clear how someone first came across us online. I’ve met a great many wonderful people through over the years, including several that have gone on to become good friends. It’s no exaggeration to say that all my closest friends over the past decade or so have happened through my friendship with Fran and our online presence, in one way or another. Several friends have written guest posts for our blog, and a few times I’ve written joint pieces with friends, which is especially meaningful. I’ve already mentioned my friend Aimee. We met through the former mental health anti-stigma campaign Time to Change rather than online, but I’d never have thought of volunteering with TTC if it wasn’t for my friendship with Fran and our other mental health work.

It’s not only friends, though. There have been many occasions when someone I don’t know has come across our blog or book and contacted me to share something they’re going through or to ask for advice. That kind of direct personal connection is the most rewarding aspect of what Fran and I do. It reminds me why I began on this journey, and why I continue to write and share as I do.

6. What advice would you give to someone who wants to support a friend or loved one living with bipolar disorder?

In our book, Fran and I are explicit about not providing specific advice that will be applicable to everyone in a similar situation. Fran actually describes High Tide, Low Tide as a kind of menu, like in a restaurant, where you might choose this idea, or that approach, whatever feels right to you. Being there for a friend or loved one who lives with a mental health condition doesn’t mean you have to be an expert in that condition, to have special skills, or always know the right thing to say. Educating yourself about their diagnosis and what it means for them to live with it is certainly valuable, and I recommend taking advantage of the many resources you can find online to do that. But the most important things aren’t actually related to mental health at all, they are true of any supportive friendship or relationship. My friendship with Fran works because we trust and respect each other, because we’re open and honest, and because we’re committed to keeping the channels of communication open between us, no matter what’s going on in our lives.

7. How do you balance the personal nature of your experiences with mental health with the need to maintain boundaries and privacy?

For me, the key thing is to sharing honestly but appropriately. Not everything is to be shared with everyone, and even close friends may not always be available or able to handle what we want to share. That’s where having a support network is so valuable, whether that’s friends, professionals, or a mix of both. Fran and I are each blessed in that regard. If one person isn’t around for any reason, there will be someone else who is.

When it comes to blogging and social media, I’m reminded of something our friend, bipolar expert and bestselling author Julie A Fast once said. That is, never share publically about mental illness or other personal issues while in the middle of that situation. I think it’s wise advice. I keep it in mind when inspired to write about my friendship with Fran, my personal situation, or that of other friends. Waiting until we’ve passed through whatever was going on provides valuable distance and perspective. On top of that, they are some topics I’d never discuss publically, for reasons of privacy.

8. What role do you think technology and online communities play in promoting mental health awareness and support?

This is something Fran and I talk about a lot in our book, because it’s central to our own long-distance, mutually supportive friendship. You asked earlier about how distance affects us. It’s certain that we couldn’t have grown and maintained our friendship without the technology that means we can stay in more or less constant touch. Over those years we’ve used just about every channel open to us, including e-mail, text (SMS), instant messaging (chat), social media, and voice and video calls. It’s equally true for my connection with other friends, whether they live on the other side of the world, as Fran does, or more locally. Being able to reach out to someone easily, no matter the time of day, provides that baseline of support that says, “If you need me, I’m here.”

Technology plays a wider role than that, though. I’ve mentioned the courses and other information available online on all kinds of mental health topics, including suicide awareness and prevention. Most of this information is available free or at very low cost. That includes blogs and podcasts such as Gum on My Shoe, and others by people I know and respect enormously, including my friend Aimee Wilson, Julie A Fast, and another friend of ours, Gabe Howard. You’re also never more than a few clicks away from the information, resources, and support offered by official organisations, crisis lines, and respected peer support communities.

That’s not to say there aren’t risks associated with social media and online communities. The dangers and pitfalls are real and need to be taken seriously. But on balance I feel technology is massively beneficial in enabling people to keep in touch with one another and access the information, help, and support they need, as and when they need it.

9. Have you faced any challenges or pushback in your advocacy work, and if so, how have you navigated them?

Another really good question! My first thought was, no, not really. Family, other friends, and colleagues have all been immensely supportive of my friendship with Fran, our book and blog, and everything else we do in the mental health space. My interest in mental health was very much encouraged where I work. For a time I was part of a small team working to improve mental health awareness throughout the organisation. I later joined the community of workplace Mental Health First Aiders.

All that said, there have been a few obstacles along the way. One time, a friend invited me to attend the local recovery college, where she was both a student and a tutor. I loved the supportive atmosphere and went along several times, attending very helpful classes on self-harm and WRAP (Wellness Recovery Action Plans). Later, however, I learned that some of the other students didn’t understand why I was there when I didn’t have a mental health diagnosis and had no experience of being a service user. It’s was a totally valid concern on their part. The recovery college is run for, and by, people with that kind of experience, and I ought to have realised that or at least checked that it was okay for me to be there. It nevertheless hit me hard at the time. It took a while to get past those feelings of not being “mental enough” to be helpful or effective in the mental health arena. It’s all part of the learning process, though, and I’m grateful for the lesson. It’s something I’d definitely take into consideration in future.

10. Looking ahead, what are your hopes and aspirations for the future of Gum on My Shoe and the broader conversation around mental health?

Fran and I fully intend to continue with our blog on its current weekly publishing schedule. We’ve held true to our original themes of mental health and supportive friendships, inspired by and based on our respective roles as “well one” (me) and “ill one” (Fran). Those are as important to us today as they were when we started out, not least because we feel the role of supportive friends isn’t something that’s discussed widely. That’s really why we wrote our book High Tide, Low Tide: The Caring Friend’s Guide to Bipolar Disorder.

As I mentioned earlier, we’ve broadened the scope of our blog quite a bit over the years. We’ve been keen to invite guest bloggers on a wide range of topics, and that’s something I’m eager to continue, perhaps with one or two regular guest contributors. I’ve also written more about my own health and mental health, rather than focusing solely on my role as a supportive friend to Fran and others. I’ve explored my experience of anxiety, imposter syndrome, my lack of a sense of belonging, and alexithymia. I’ve also written about aspects of my physical health, men’s health and mental health in general. These are all things I’m keen to develop further, as is the role of philosophy in helping us deal with whatever’s going on in our lives. Albert Camus’ ideas of absurdism have been very helpful to me personally.

I’m also interested in exploring ageing, death and bereavement, and personal legacy. Those topics might sound somewhat morbid but they are things that affect us all. I’m also keen to learn more about psychosis. I have no personal experience of it, but it’s something that affects several of my friends and I’d like to understand how I might support them better. I’m thinking about revamping the blog’s look and feel, so that’s something our readers can look forward to. Finally — you didn’t ask but I thought you might so I came prepared with an answer — Fran and I don’t have any plans for another book. Then again, never say never!

 

Thank you, Martin, for sharing your insights and experiences with us today. Your dedication to fostering understanding, empathy, and support in the realm of mental health advocacy is inspiring. We wish you and Fran continued success with your book and blog and look forward to seeing the positive impact of your work in the years to come.

You can find Martin and Fran’s blog at www.gumonmyshoe.com. Their book High Tide, Low Tide: The Caring Friend’s Guide to Bipolar Disorder is available on Amazon (print and Kindle) and in print via all good booksellers.

 

Disclaimer

This interview was generated by the artificial intelligence app ChatGPT in response to the following prompt.

With my best friend Fran who lives with bipolar disorder, I run a blog called “Gum on My Shoe” which is focused on mental health and mutually supportive friendships. We started the blog ten years ago, and also published a book in 2016 called “High Tide, Low Tide: The Caring Friend’s Guide to Bipolar Disorder” based on our experience as friends. Fran lives in the US. I live 3000 miles away in the UK. We met online in 2011. Write a ten question interview that I can answer, as though you are interested in these topics. Give the interview a title and include short opening and closing paragraphs.

I edited the opening and closing paragraphs a little for clarity and added book contact details. The questions are unedited. I hope it's obvious that the answers are all mine.

— Marty

 

Photo by Michal Czyz at Unsplash.

 

Saturday, 9 September 2023

Free Books for World Suicide Prevention Day

To mark World Suicide Prevention Day 2023 Fran and I are offering our book HIGH TIDE LOW TIDE for FREE on Kindle for five days between Sunday September 10 and Thursday September 14, inclusive. Once the offer is over the prices will return to normal.

In High Tide, Low Tide: The Caring Friend’s Guide to Bipolar Disorder we share what we’ve learned about growing a supportive, mutually rewarding friendship between a “well one” and an “ill one.” With no-nonsense advice from the caring friend’s point of view, original approaches, and practical tips, our book is illustrated with real-life conversations and examples.

Buy it here.

World Suicide Prevention Day (WSPD) was established in 2003 by the International Association for Suicide Prevention in conjunction with the World Health Organisation. This year’s theme is Creating Hope Through Action.

Creating Hope Through Action serves as a powerful call to action and reminder that there is an alternative to suicide and that through our actions we can encourage hope and strengthen prevention.

This is a topic very close to our hearts and never far from our thoughts. Suicidal thinking has been part of my friendship with Fran since we met twelve years ago, and we devote one chapter of our book to dealing with how to support a friend who is feeling suicidal.

For more information check out the following links.

 

Wednesday, 21 September 2022

A Few Thoughts on Taking My Own Advice

This post was inspired by a recent conversation with my friend Brynn. I was talking about the piece I was working on at the time; a collection of articles on self-care. She asked, “Do you take your own advice?” I paused before answering. “Sometimes! You know, that’s such a great question. No one has ever asked me that before.” I knew it deserved more than a fleeting response, and resolved to explore it further. This article is my reply to Brynn, and anyone else who’s ever wondered if people who share their wisdom publically ever take their own advice.

What Kind of Advice Are We Talking About?

I’ll start by saying I don’t consider myself in the advice business. I’m wary of offering advice to anyone unless it’s been specifically asked for. For the purpose of this article I’m going to use the term as a shorthand for “ideas, suggestions, wisdom, and guidance.” I’ll focus on the contents of our book High Tide, Low Tide: The Caring Friend’s Guide to Bipolar Disorder and this blog, because that’s the context in which Brynn asked her question. First published in 2016, High Tide, Low Tide is not a how-to book. Its approach is descriptive rather than prescriptive. Fran and I wrote it hoping the lessons we’d learned and the insights we’d gained would help other people; specifically people wanting to support a friend living with mental illness. As we state in the introduction:

We hope our book will inform and inspire you. There are no steps you have to follow, or things that are guaranteed to work under all circumstances. Illness, especially mental illness, does not work that way. What works is having a framework of trust and commitment, and a menu of approaches, suggestions, and options you and your friend can explore together.

Our blog is an extension of that endeavour, albeit broader in scope and more responsive to events and new ideas. What we share, we believe in. It’s also truthful. I touched on this in a Q&A article titled Write without Fear, Edit without Mercy: Eight Questions for the Honest Blogger. Question five asked “Do You Always Tell the Truth in Your Blogging?”

I choose what I want to blog about, and what I want to share or say on that topic. There may be — and indeed are — things I choose not to write about or include, but if I write it, it’s true.

So, that’s the “advice” I’m taking about. The question remains. Do I take that advice myself? The answer I gave Brynn is still the most honest and accurate: sometimes. There’s a great deal in our book and on our blog which I refer back to and use; some rarely, others much more frequently. There are also things I hardly, if ever, use anymore. There are a few reasons, but the most fundamental is relevance. Everything we’ve shared was true and valid at the time, but situations and people change. We learn new solutions to old problems, and face challenges we’ve not previously faced.

Advice That’s No Longer Relevant

High Tide, Low Tide is based on the first four years of my friendship with Fran. For much of that time she was living through extremes of mania or depression, with suicidal thinking never far below the surface. Distance notwithstanding, I was at her side through it all, supporting her on a day-by-day, often hour-by-hour, basis. I didn’t always get things right, and neither did Fran, but we remained committed to each other and to making our friendship work. Our book was written to share what we learned in our journey together through those times.

Depression and suicidality still raise their heads from time to time, and we remain vigilant for red flag changes in symptoms or behaviour that might herald a return to more serious episodes, but Fran’s health is far more balanced these days. In particular, she’s been free of mania for some time. This was devastatingly traumatic in the early part of our friendship. These are wholly welcome and healthy changes, but they’ve inevitably led to shifts in the balance of our mutually supportive friendship. We no longer meditate together, for example, or read to each other as often as we used to. We still connect every day, but Fran is much less likely to need me outside our regular call times.

The net result is that much of the advice — the ideas and strategies — I learned and used on a regular basis are less relevant than they used to be. The advice itself remains valid, though, and I wouldn’t hesitate to turn to it again should the situation arise.

Bad Advice

The mention of valid advice invites me to consider its opposite: invalid or bad advice. I don’t believe any advice can be completely correct or universally applicable, and it’s certainly possible to employ sound advice inappropriately or out of context. Other people may disagree with my advice, opinions, or suggestions, but I can’t think of anything Fran or I have written that I’d disavow or refute.

I remain open to revising or clarifying what I’ve previously written. Someone recently questioned something I wrote a few years ago in an open letter to my father. I was grateful for the challenge, which led to a new article exploring emotional vulnerability and weakness, but I decided not to withdraw or change the original content.

There have certainly been times when I’ve ignored my own advice or followed it in ways that were clumsy or ineffective. It was important to me and Fran that we included examples of us “getting it wrong” in our book. The last thing we wanted was to give the impression we always knew what to do or say. I’ve shared several such examples on our blog, covering topics such as honesty and openness, codependency, and anger. These “bad examples” can be useful in themselves, reminding me what not to do in the future.

Advice I Still Refer to and Use

Having talked about the advice I no longer use, let’s look at what’s still relevant and useful. The principles of healthy relationships are valid no matter what’s going on for me or the people in my life, and I turn to chapter one of our book (“The Caring Friendship: Key Skills and Attitudes”) to remind myself of the basics. These include trust, openness, honesty, and a commitment to keep the channels of connection open. We’ve added new insights over the years, finding new ways to enhance our friendship, such as spending quiet time together. Everything we’ve learned about growing and maintaining a successful long-distance friendship also remains relevant; not only to me and Fran but also my other friendships.

Our book includes little about my needs beyond my role as a supportive friend. This imbalance initially carried across into our blog, but I’ve begun exploring my wellbeing and mental health in such posts as THIS BOY GETS SAD TOO, Return to Down: How My Baseline Mood Has Slipped from Positive to Low, Flatness and Disinclination, and How International Men’s Day Inspired My First Doctor’s Appointment in 30 Years. I return to them when I’m low, flat, or depressed. They help me gauge where I am compared to where I was when I wrote those articles. I turn to the range of self-care posts I’ve written to remind me of strategies that have helped me in the past.

I’ve recently begun a series of articles collecting posts on themes including self-care, open letters, and pieces written to mark mental health awareness days and events. I wanted to make it easier for people to find related content. They also make it easier for me to locate content I want to refer back to and use in my own life.

As I’ve grown in experience and confidence as a blogger, I’ve begun sharing content for other bloggers, especially those working in the mental health space. I’ve shared blog prompts, image prompts, my blogging workflow, and how to handle blogging setbacks. I refer to these myself when I’m stuck with my writing.

I mentioned changes in my friendships have made some advice less relevant than it used to be. I haven’t always found these transitions easy but I’ve taken the opportunity to explore how I handle them. Some of the articles I’ve written about that remain very relevant to me. I return to such posts as What My Mantra Means to Me: Healthy Boundaries, Supportive Disengagement: How to Be There for Your Friend When They Need Space, Spokesfriends and Insular Groups: What Kind of Support Network Do You Have?, and Too Small for Comfort: When Life Closes In On You from time to time, especially when I’m feeling disconnected or adrift.

(As Yet) Unpublished Advice

I’ve focused on our book and blog, but that’s not the sum total of my “personal wisdom.” I often turn to things I’ve discussed in chat messages, written in my personal diary, or jotted down in private notes on my phone. Some or these are too personal or raw to share publically. Others fall under the category of things I’m unlikely to blog about, as I’ve described previously.

I’m wary of writing if I have little or no experience of the subject under discussion, unless I’m presenting the insights, opinions, and accounts of others who do. [...] I mostly discuss mental illness from the perspective of a supportive friend, although in the past couple of years I’ve begun sharing aspects of my mental health.

There are topics I’d like to write about but haven’t yet found a way to approach them as I’d wish to. These include my perspective as a caring friend when someone I know has taken an overdose or harmed themself. I can’t imagine ever writing about abuse, addiction, rape, or trauma. Those are too far beyond my lived experience for me to do them justice.

I may share some of this currently unpublished content in the future. Likely candidates include more on healthy boundaries, expectations, acceptance, and letting go.

Bringing It All Together

High Tide, Low Tide represents our collected wisdom at a particular point in our friendship. It remains valid, honest, and useful — to us and to others — but it no longer fully reflects our situation, or the totality of my experience as a supportive friend. Our blog enables us to share new insights and as we grow as friends and as individuals. Where past advice and ideas fail to meet my needs, I’m open to returning to basics and allowing the present moment to inform my decisions and approach.

Do I take my own advice? Yes, definitely, and often! I’m careful in selecting which advice is most relevant to my present situation, however. In that I follow Fran’s suggestion in the Epilogue to our book.

How do I help my friend? What should I try? What works? So many choices. So many possibilities. To me this book is less of a memoir than a menu. You would never order and eat everything on the menu if you went for a meal. You would choose. Something familiar, perhaps. Or something new. Use our book like that. Choose something. A bit of this. A bit of that. And let that something ease another’s pain.

I’ll close with a quotation that came my way whilst writing this article. It’s a perfect reminder that advice — however loosely defined — is not always what we need. Sometimes we need to be in the moment, listening to ourselves and one another, open to what’s actually going on.

The best way to help someone is not to give them advice, but to listen to them. (Jordan B. Peterson)

That sounds like pretty good advice to me!

Over to You

In this article I’ve explored my relationship to the advice Fran and I have published in our book and on our blog. What are your thoughts on this topic? Do you take your own advice? Do you find it easier to give advice than to take it? Whose advice do you trust? What’s the best piece of advice you’ve ever given or received?

We’d love to hear from you, either in the comments below or via our contact page.

 

Photo by Christopher Jolly at Unsplash.

 

Wednesday, 13 April 2022

I Want to Write: How Our Book HIGH TIDE LOW TIDE Came to Be Written

This is the story of how our first book High Tide, Low Tide: The Caring Friend’s Guide to Bipolar Disorder came to be written, taken from the book’s Preface. It’s available from all good booksellers; check our book page for details.


Preface

Writing has always been an important part of my life. I remember the teacher who encouraged me by providing a notebook for my extracurricular stories. I remember being snubbed by my classmates for asking if I could submit a poem in place of the expected essay: our teacher thought it such a good idea he set poetry for the entire class. I remember volunteering as assistant editor on the school magazine because I had a crush on the teacher. I remember the yellowing copy of Ezra Pound’s poetry I borrowed from the library and neglected to return. I wrote poetry through sixth form (my final two years at school) and university; later essays, articles, and short stories. I have kept a personal diary for over forty years.

A keen science student, I studied pharmacy at the University of Bradford, Yorkshire. I graduated in 1983 and took up a postgraduate position at the Department of Neurology, Institute of Psychiatry and King’s College Hospital Medical School in London. In 1987, I moved north to work in the biomedical sciences laboratory at Newcastle’s Royal Victoria Infirmary. I met my wife Pam that same year. I later retrained in business computing and have worked in the information technology services industry ever since.

I met Fran Houston online in May 2011. Fran lives with bipolar disorder, chronic fatigue syndrome, and fibromyalgia, and we joke that when she discovered I was a pharmacy graduate with three years’ research experience in neuroscience she thought all her worries were over. Here at last was someone to sort her life out for her! In fact, little I had learned in the lecture theatre or laboratory prepared me to help someone living with chronic, debilitating illness. Education is extremely valuable — I have completed a number of courses and workshops since meeting Fran which help me support her more effectively — but ultimately caring is not about how much you know, it is about who you are and what you do.

This book was conceived in October 2012. During a phone call with Fran I mentioned that I felt inspired to do something creative. Without hesitation, she suggested I write a book about befriending someone who lives with illness. The idea made a great deal of sense. Despite living three thousand miles apart, we had forged a relationship that was strong, caring, and mutually rewarding. I saw immediately that my experience could be of value to others. But if the suggestion was inspired, it was also scary. My first thought was that I had never looked on her as “someone living with illness.” I saw her as my friend.

That is the point, Marty! It is how you are with me. People do not usually treat me that way once they know I have illness. It is a powerful thing. It has helped me see that I am not just my illnesses. I have value and gifts to give.

In the weeks that followed, we discussed possible approaches, formats, and the likely audience for such a book. I researched similar titles, made notes, and sketched outlines. The further I pursued the idea the more it eluded me. I could see the book only as an autobiographical account of our friendship, and while that could be a tale worth telling, it wasn’t what Fran had envisaged. I began to lose heart. Our conversations turned to other topics and the idea of the book lapsed.

One night in late November, Fran telephoned me. It was four o’clock in the morning here in the UK. She was very excited. She had been to dinner with someone who wanted advice on how to support a friend diagnosed with bipolar disorder. Fran offered suggestions from her own experience, and mentioned she knew someone in England who was writing a book on that very subject. Her friend thought it was a great idea and wanted to know when the book would be published. My heart sank. Too sleepy to be anything but honest, I told Fran what I had come to realise, but had not until that moment shared with her. Our book was never going to happen. Fran didn’t press me for details or explanations. She said goodnight and let me get back to sleep.

I went to work next day as usual, and avoided thinking about our conversation until I was walking to catch the train home. It was a shame nothing would come of Fran’s idea. My thoughts turned to a book on depression I had recently finished reading. Written by a clinical psychologist, it had an easy style and was illustrated with snippets of conversation. It was nothing like the book Fran and I had talked about, but could a similar approach work for us? Something clicked. I messaged Fran from the train.

Thank you for mentioning our book to your friend last night, for telling me about her reaction to the idea, and for the response it stirred in me. It was the jolt I needed. Just now, in the very act of repeating to myself how our book will never come into being, I caught a glimpse of how it might. I want to rededicate myself to the project. I want to start making notes, drafting ideas. I want to write.

It was a breakthrough moment, and one utterly in keeping with the central message of the book you are holding. No matter what happens or what you are struggling with — be that some practical or creative project, your relationship with others, your own health or that of a loved one — the important thing is to set aside preconceived notions of how things should be, or whether you are up to the task. Instead, be honest with yourself about what is happening. Acknowledge your limitations, but refuse to be bound by them. Trust in your ability to grow to meet the challenge. Recognise joyfully the potential of each moment. Be who you are. Do what you can. Embrace the journey.

Martin Baker
Newcastle upon Tyne, UK

 

Photo by Thought Catalog on Unsplash.

 

Wednesday, 23 March 2022

No Pedestals

No Pedestals

No relationship can flourish if there is a perceived difference in stature or status. It is important to remember that we are all human, all fallible, all flawed. As Fran puts it so well, “We are all perfectly imperfect.” Despite recognising the dangers, we have each been guilty on occasion of putting the other on a pedestal. I am a great support to Fran, and offer a degree of commitment she has rarely known. It was easy in the early days of our friendship for her to see me as some sort of hero or saviour figure.

Fran: you are my world.. you are.. my life.. the reason.. of it.. all.. how how how.. do i deserve you..?

Martin: Don’t make me into more than I am, Frannie.

Fran: ok ok.. for you no pedestal.. you are an oak.. rooted.. grounded..

Fran’s spirit, courage, and resilience have occasionally led me to put her on a pedestal of her own, a situation complicated by her inclination to compare herself unfavourably to other people in terms of health, relationship status, financial security, and social standing. I counter her sense of unworthiness and inferiority, but I have sometimes overcompensated, boosting her mood and self-image unrealistically.

At such times, “No pedestals!” reminds us we are in unhealthy territory. It is worth highlighting that there is a difference between putting people on pedestals and the distinction of client–therapist or patient–clinician roles in professional relationships. But I am neither Fran’s therapist nor her doctor. I am her friend. We work best when we stand side by side, feet planted firmly on the same ground.

 

Excerpted from our book High Tide, Low Tide: The Caring Friend’s Guide to Bipolar Disorder.

Photo by Levi Meir Clancy at Unsplash.

 

Wednesday, 3 February 2021

High Tide, Low Tide: The Caring Friend's Guide to Bipolar Disorder (Revised edition)

A few weeks ago, Fran and I reported our new creative partnership with Kingston Park Publishing. Today we are delighted and proud to announce the publication by KPP of a new revised edition of our book High Tide, Low Tide: The Caring Friend’s Guide to Bipolar Disorder.

When we launched the first edition back in 2016, I commented that “writing a book — a book like ours at least — isn’t about the book itself. Not really. It’s about connections.”

Throughout its four year journey from inception to realisation, our book has brought me and Fran into contact — into connection — with folk we simply would not otherwise have met. Some call it networking. Some call it platform building. It is both these things, and much more. It is what happens when you find your feet on the right road (what Spock described to Kirk as one’s “first, best destiny”) and open yourself to what the journey may bring.

Those words are no less true today, a further four years down the road. Our book has met with considerable success, led to important new friendships, and opened the door for us in many ways. A major highlight was a feature article by Bob Keyes in the Maine Sunday Telegram. We are particularly proud that Bipolar UK lists High Tide Low Tide amongst its top books on bipolar disorder.

More important than success or kudos, though, is knowing our book has helped people. That’s why Fran and I wrote it in the first place, and why we’re excited to release this new edition. The book’s content itself is unchanged but we’ve corrected a few inconsistencies and brought the references and resources up to date. The Kindle version has also been updated to improve readability. With a new publisher and price point, we hope this revised edition will carry our message of hope to an even wider audience.

Published by Kingston Park Publishing, High Tide, Low Tide: The Caring Friend’s Guide to Bipolar Disorder (Revised edition) is available for Kindle, and in print from Amazon and other booksellers.

Amazon COM: Print | Kindle
Amazon UK: Print | Kindle

For further details and sellers see our books page.

Copies of the first edition (Nordland Publishing, 2016) may still be available from Amazon and other sellers for a time.