Posted in Autobiography, coping with chronic illness, coping with life threatening illness, Empowerment, Living with Illness, Storytelling

Advice from an Acting Teacher

I watch a lot of interviews because I believe they give a behind the scenes look at people’s lives and circumstances.  It’s similar to what Andy Andrews shares about autobiographies, no one ever wrote an autobiography who didn’t succeed.  The same can be true for interviews, only those who overcome challenges (I’m not referring to celebrities, it’s all walks of life) get interviewed.

Jake Gyllenhaal’s new movie “Stronger” about Jeff Bauman who survived the Boston Marathon bombing was the focus of the interview.  When asked about his process he shared advice from an acting teacher, “The target draws forth the arrow”.  What do you think about when you read that statement?  It shouldn’t be a surprise that when I heard the quote I jumped for a pad and paper because these words of wisdom will make you think about how you take on life’s challenges.

When faced with a life challenge, especially a chronic or life-threatening illness there is a primary target…wellness!  It’s similar to the saying Keep Your Eye on the Prize!  When we have a target to focus on, we are given something to aim our physical, emotional, and spiritual energies.

The doctor gives us the target.  The moment you hear the words “I’m sorry to tell you but…” you become an arrow.  You are summoned to take aim and make conscious decisions.  It will take the momentum you absorb from friends, family, medication, and faith to propel yourself toward the target.

Champion 24-Inch Bullseye Archery Target (2-pack)

There is something empowering about picturing yourself as an arrow, moving with force and speed toward a desired outcome.  My ongoing reminder is, you may not get well, but you can always get better.  Remember a target has rings with the bulls-eye in the center.  What do the outer rings mean to you?  What if you don’t hit a bulls-eye the first time or ever?  What level of comfort do you have focusing on other aspects of your life if wellness isn’t in the cards?

I hope when picturing yourself as the arrow, you equate it with being a real-life superhero.  Your journey is unique to you!  The outcomes may or may not be within your control, but where do you have control?  You have control over your determination, perseverance, and attitude.  You have the right to create a relationship with your doctor that is both respectful and honest.

We will all have targets that arise in our lives because challenge is part of the human experience.  The arrow you become shapes your narrative.  Your narrative is the force behind your momentum…keep it going!

Posted in coping with chronic illness, coping with life threatening illness, Emotional Health, Empowerment

The Constants In Our Lives

Do you remember taking algebra and having the constant in the equation?  Constants are important because they create stability.  When we have constants in our lives we have a sense of safety and security.  They say, “The devil you know is better than the devil you don’t know.”  I started thinking about what’s constant in my life because I work all over the country and it feels like things are constantly changing.  Knowing someone at home loves me even if I’m not there is critical to continuing my work away from home.  Experiencing support in the form of life updates keeps me in the loop even when I step out of the circle physically (but never emotionally or spiritually).

I was listening to an interview with Buddhist nun, Pema Chodron where she shared, “The sun is always there-sometime clouds are disguising it, but it never leaves.”  That’s the simplest way to describe object constancy, knowing something still exists even if we can’t see it.  How is that possible?  We experience the world through multiple senses and on top of that we have our innate sense of intuition.  When we pair all these sensory and experiential aspects we build a spiritual nest where in our hearts we know we’re protected.

I’m not sure why, but many equate constant with boredom.  You here things like same s**t different day.  If we’re coming up against the same challenges repeatedly and you think that’s a constant there’s a problem.  Incurring the same obstacles over and over is insanity.  It’s in that moment that changing your strategy is critical to moving forward.  The constant experiences in your life should be the things that support you, encourage you, provide you with a sense of security and allow you to take some risks to hopefully improve your pilgrimage to health and healing.

Remember, the sun really is there even if you can’t see it and so your humanity!  The world needs you!

Posted in after the diagnosis, overcoming adversity

We Need To Change How We Interact In This World

Valentine ’s Day is right around the corner and stores are displaying merchandise and cards for the occasion.  I started thinking about the messages sent by some of the big companies like Ma Bell and Hallmark and what’s been lost with the invention of Facebook and other social media.  Ma Bell wanted us to “Reach Out and Touch Someone”, and Hallmark told us buying cards, “When You Want to Send the Best”.  These two company taglines spoke more, to me, than just about commercialism, but how we interact in the world.

I’ve watched the number of birthday cards dwindle significantly over the past four years.  I used to have a mantle full of cards, and now it’s down to a select few.  Don’t get me wrong, I get plenty of Happy Birthday messages on Facebook, but it’s different.  We no longer have to plan on how we interact.  We are now able to wake-up in the morning and see who we need to send a birthday wish, congratulate for an achievement, or commiserate about a dilemma.  What happened to sentiment?  Have we lost the ability to connect more than electronically?

I sent out a bunch of cards today because there are people who I haven’t spoken to in a while that I wanted to send a special message.  I want to appreciate certain people who have supported me, kept me in the loop of their lives while I’ve been traveling the country.  It gave me an opportunity to say I took the time to spend a few minutes devoted to connecting with you.  I know I may be a bit over the edge, but social media has left too many people connected to others with only a dotted line, and they’re still lonely.

When going through difficult times we need to make those phone calls, send those calls, and show that we’re making an effort and that this person matters to you more than just a count on your Facebook page.  Illness, divorce, death, financial struggle to name a few are life events that require deeper connections to emerge with a sense of peace and to have the ability to continue on life’s pilgrimage!

Posted in Community, Empowerment

Your Tribe Will Get You Through the Unknown

If you follow my blog you know that I travel around the country for work, months at a time. I work long hours and in return my time off is really off. I’ve had the good fortune to visit some great cities and in each one I make sure and find my tribe. My tribe is anyone who engages in artistic endeavors, no matter the genre. In addition, I always make it a point to visit the local attractions such as museums and botanic gardens not to mention quilt shops and knitting shops.

My current work assignment is in Baltimore. My other blog www.manofthecloth.wordpress.com is where I focus on stitching as meditation. I was looking for a particular yarn and found that a local art supply store happened to carry this gorgeous 100% wool yarn. I made it over to the shop, found the yarn, but they didn’t have enough for my project. Little did I know, until I got up to the register, that they have back stock that isn’t on the floor. I found five more skeins of yarn and proceeded to check out.

The staff inquired if I was affiliated with the Art Institute as a student or faculty member, to receive the discount. I explained that I’m visiting from out-of-state for a work contract. Once I divulged where I lived, the two employees proceeded to tell me about all the art spots that I had to see while in town. First they were focused on fiber art, since that’s my medium, but I explained I’m open to anything art related. They gave me a list of locations, exhibitions, and venues to visit before I leave town. They made me feel very welcomed and over the next few weeks will give me things to see and do while I’m far away from home.

So who is your tribe? What makes a tribe? I find that it’s about common passions. It doesn’t matter what you’re passionate about, these folks exist all around you. Another way that tribes are formed is by common experience. I’ve worked in outpatient drug and alcohol programs and the bonds that are formed are very strong. When I worked at The Wellness Community, serving cancer patients and their families, they created a tribe. The tribe can tell you the things you need to do, see, look for, and experience, as well as where the land mines are to avoid.

I was fortunate to attend a graduate school that had the ancient Wisdom Traditions as the foundation of the curriculum. I met amazing people who were on the same pilgrimage as me. We took classes together, worked on our dissertations together, and fortunately graduated together. The experience of traveling with other seekers was amazing. It eased much of the anxiety of the process and increased my level of devotion to the work. My tribe supported and nurtured me throughout my journey.

Where we got the notion that it’s better to go it alone I’m not sure. What I do know from personal and professional experience is that having a tribe makes me feel a part of something larger than me. It gives me the sense of expansion and possibility that exists beyond what I can see in my world today.

Who makes up your tribe? How have they created a safe haven on your personal journey? How have you benefited from being part of a tribe? Be conscious of these questions and I think you’ll be amazed at the connections that are all around you!

Posted in coping with chronic illness, coping with life threatening illness, Emotional Health, living with chronic illness

Have A Good Life: Lessons from Vacation Part 1

Recently I took a Trans-Atlantic cruise from Barcelona to Fort Lauderdale. After stopping at a few ports it was time to cross the Atlantic Ocean, a journey that would be seven days across the sea. The trip was fourteen days so there was plenty of time to interact with other passengers along the way. It’s not uncommon to become friendly with people you see over and over throughout the trip. On the last day when everyone is getting ready for departure we say our goodbyes. One person shook my hand and said, “Have a good life”. I walked away and began to think about this interaction. It left me wondering about the people we meet every day and the impact they have on our lives.

Unless you meet someone and make plans to cross paths in the future it’s likely you’ll never interact with those you meet along your life path. I found it interesting to exist in a microcosm of the world.   Twenty-eight hundred passengers and about fourteen hundred crewmembers created a city on the sea. The people I gravitated to I met at activities such as lectures and other scheduled meetups. Two weeks gives you plenty of time to maintain ongoing discussions in an attempt to get to know the others on the ship.

It’s not as if you become friends with everyone you meet, but you do have an affinity for certain people. You seek these people out because they become your onboard social network. It makes the trip more enjoyable, and in some cases friendships do develop.

It was the statement, “Have a good life” that made me consider who enters and exits my life over time. There are people who I have spent a lot of time with and over time when the group disbands the associations remain in tact through Facebook and other social media, but the day-to-day interaction seems to dissipate. How do we measure the impact and the lessons learned from those who enter and exit our lives? What is it that these people we gravitate to are sent to teach us on our journey of life? How can we make the most of the interactions we experience and develop a deeper understanding of our social nature and its impact on health and healing?

I’m grateful for the people I met, the stories I heard, and the experience of sharing the gift of travel with wonderful people. I was happy to deepen friendships with those I have traveled with before and extend my social circle with those I met who I know I’ll see again. I’m grateful for the life lessons I learned through anecdotes and activities. It’s important to know that all we want for each other is to “Have a good life”, but to hear it is reassuring!

Looking to further your journey of health and healing?  Visit http://www.survivingstrong.com

Want to explore how to have a good life through creativity?  Visit http://www.timetolivecreatively.com

Follow me on Twitter: @GregKatz2

Posted in after the diagnosis, coping with chronic illness, coping with life threatening illness, Emotional Health, Illness Narrative, living with chronic illness, Living with Illness

We Walk This World As Pilgrims

We’re familiar with the pilgrims of the Middle Ages struggling to make it to the Holy Land. They overcame many obstacles, fought wars, and hopefully in the end found peace. There are many who make pilgrimages for personal reasons; physical challenges and healing of health issues, emotional freedom, or attaining spiritual enlightenment. The truth is that we walk this world as pilgrims because we’re all in search of something, even if you’re not aware of what it is in this moment.

Last night I facilitated a call for students working on their doctoral dissertations. I believe these students are on their own personal pilgrimage. They are expanding their personal and professional boundaries. They are taking on a pursuit that will change their lives forever. They are creating a soapbox on which they will stand for the rest of their lives. As someone who has completed this process I am honored and privileged to serve as their Sherpa, carrying the heavy load when necessary giving each pilgrim the space to move forward on their journey.

Richard R. Niebuhr, noted scholar from the Harvard Divinity School, stated “Pilgrims are person in motion, passing through territories not their own-seeking something we might call completion, or perhaps the word clarity will do us well, a goal to which the spirit’s compass points the way.” When we set out on a pilgrimage we have a nagging question that keeps showing up in our lives and is demanding attention. Many believe that the “good” life is one where we have a sense of completion. We have tackled the challenges set forth by that whisper in our ear nudging us to take action in our lives.

Roger Housden in Sacred Journeys in a Modern World writes, “Whatever its destination, what sets a sacred journey apart from an every day walk, or a tourist trip, is the spirit in which it is undertaken. It is sacred if it sensitizes the individual to the deeper realities of his or her own being, and those of the world in which we live.” Our pilgrimages are sacred because it’s part of our narrative. It is a catalyst for change. As Pilgrims we are making conscious what has been seeking a voice, an answer, or possibly leading us to new questions.

I’ve sat in many counseling rooms with those facing life-threatening illness and each person’s pilgrimage had similarities, seeking hope, some sense of control over their lives, and empowerment. Since not everyone who is diagnosed with an illness recovers, some individual’s pilgrimage is seeking a good death and making sure they do not have an unlived life.

Whatever your pilgrimage I hope you make each step a conscious one. Your pilgrimage will keep you consciously engaged in your life opening your body, mind, and spirit to new heights. Set out on a pilgrimage and experience the wonder this journey to the depths of soul will reveal!

Facing a chronic or life-threatening illness and looking for education, support, and inspiration?  Visit http://www.survivingstrong.com

Want to take an Art and Healing pilgrimage?  Visit http://www.timetolivecreatively.com

Follow me on Twitter: @GregKatz2

Posted in after the diagnosis, coping with chronic illness, coping with life threatening illness, Emotional Health, living with chronic illness

The Anxiety Fugue

Yesterday I talked about taking my black lab, Tashi, to the vet because of her trouble walking. I wrote about needing cue cards because the questions I should have asked escaped my consciousness in the midst of the exam. What caused my lapse in consciousness? What is it that prevented me from following my own protocols that I’ve set in place for my own healthcare when it came to Tashi? Anxiety!

Anxiety can be an overwhelming tidal wave of angst. It causes panic attacks and evokes a stance of fear. I don’t find myself to be an anxious person, but when anxiety does strike it strikes hard. It’s not invited. It’s a party crasher to our lives. I’ll give you an example.

I’ve got asthma. It’s under control with the use of a couple of inhalers. I am under a doctor’s care and have had numerous pulmonary and cardiac tests to insure that I’m getting the right care. I don’t know if you’ve ever had trouble breathing, but the anxiety of not being able to breathe, for me, is worse than not being sufficiently oxygenated. There is an anxiety of doom and potential death.

Prior to taking Tashi to the vet she was having trouble walking. She was agitated and would move around the house quickly and without purpose. Her back was hunched like one of those black cat pictures you see at Halloween. You could look in her eyes and see the angst she was feeling.

Watching Tashi struggle evoked my anxiety. Instead of waiting for the exam I was already struggling with her impending euthanasia. For me, in that moment, there was only one ending to the story and that put me in a tailspin. By the time I got to the vet I had forgotten my own medical exam process. I didn’t have enough clarity of mind to ask the questions I knew in my heart needed to be asked. It wasn’t until I got home that the fog cleared and the questions surfaced.

When anxiety strikes it can be debilitating. This is why when facing a chronic or life-threatening illness it’s important to either record your doctor’s visit or bring a family member or friend as a witness. There are too many of us who miss vital information when the anxiety fugue hits and when it comes to our health and healing we don’t want to miss anything!!

Experiencing Anxiety?  Facing a chronic or life-threatening illness?  Visit http://www.survivingstrong.com

Want to alleviate anxiety through art?  Visit http://www.timetolivecreatively.com

Follow me on Twitter: @GregKatz2

Posted in after the diagnosis, coping with chronic illness, coping with life threatening illness, Doctor's Visits, living with chronic illness

I Need Cue Cards When Visiting the Vet

The saga of my black lab Tashi continues. At the beginning of last week I noticed that she was having some trouble walking and would drag her behind on the ground. Noticing the symptoms I took her to the vet and had her anal glands expressed. Unfortunately, that didn’t seem to do the trick and over the course of the next twenty-four hours her walking continued to be problematic.

I decided to take her to the vet and see what else may be going on. The vet, a new doctor to the practice, examined her making his observations. After checking for a bowel blockage, he determined that the problems with her legs buckling were neurological in nature. He prescribed a medication that would take about a week to build up in her system. The question I kept asking the doctor is, “Why would something like this have a sudden onset? And “If it wasn’t neurological what else could it be?”

Twenty-four hours goes by and she’s still in a lot of discomfort. I was rubbing her hind legs and thought I noticed a hemorrhoid and then realized it wasn’t her rectum; it was gynecological. Of course, as many of you know who have pets, they only present symptoms or get hurt once the vet closes. It was 8:03 and the vet closes at 8pm.

The next morning I took Tashi to the vet without an appointment. I figured I’ve paid for the building at this point; the least they could do is see her without an appointment. The staff is terrific and took her right in for an exam. She was prescribed a host of medications. Once again I asked the doctor if he still thought the problems with her legs was neurological and he feel that is still an issue.

I need cue cards because I’ve read Dr. Jerome Groopman’s book How Doctors Think and I didn’t follow most of his recommendations. I didn’t ask at the initial consult what else it could be if it wasn’t neurological. I’m better at the human health issues, but when it comes to veterinary medicine I’m at a loss. As you know, our anatomy and physiology is not the same (well maybe if you have a pet chimp/gorilla it may be close).

I’m following the treatment strategy we’ve outlined at the last visit. Her walking is greatly improved and not sure if it’s because we’re treating the gynecological issues or if the steroids have made all the difference. Perhaps it’s a bit of both which only leaves me more confused. I think I’m going to skim Groopman’s book again because I still have my doubts and I want to go in with a clear head. It shouldn’t be a surprise that when we’re with someone or a loved pet who is sick, our emotions take over and all rational thinking goes out the window.

I would love to have a set of cue cards with the questions I need to ask; that would be ideal. Instead, I’ll put some questions together and be prepared for her follow-up visit to determine her progress. She’s feeling better and that’s most important. I do want to make sure going forward that I’m better prepared!

Facing doctor’s appointments and lab work?  Want to be prepared for your doctor’s visits?  Visit http://www.survivingstrong.com

Want to explore health and healing through creative outlets?  Visit http://www.timetolivecreatively.com

Follow me on Twitter: @GregKatz2

Posted in after the diagnosis, coping with chronic illness, coping with life threatening illness, Having a Voice in Healthcare, living with chronic illness, overcoming adversity

I Wish My Vet Saw People

If you follow me on Twitter (@GregKatz2), Facebook, or on these posts you know I have a black lab named Tashi that was diagnosed with MRSA (Methicillin-resistant Staphylococcus aureus) about seven years ago. Half her life has been spent visiting doctors, taking a host of medications, and having numerous tests where she’s been poked and prodded to get cultures. Throughout this process she has endured pain and discomfort, never giving up her loving nature.

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After fighting her most recent infection for the better part of a year, I’ve had the chance to be grateful for her doctor (Dr. B). He’s dedicated to her well-being. He took her case and as a result changed the infection control policies at the Veterinary Hospital. Most of all, I’ve watched him spend time with Tashi, never giving up on her and always trying to make her as comfortable as possible. What could he teach medical students who will eventually be treating us in doctor’s offices and hospitals?

Meet the patient where they are. I’m fortunate because I feel as if I’ve become partners with my medical providers. I always ask questions and I’m aware of the latest research on my own conditions. There is no power play in the exam room. Our vet is very sensitive to the power dynamic and when he examines Tashi he sits on the floor so he can see her eye-to-eye. He will often bow his head so that she knows that he doesn’t have to be dominant, in theory. He’s also the keeper of the treats, always a way to endear himself to her.

Follow-up is very important to the health and healing process. I feel like I’ve attracted patient positive doctors. They’ve been concerned and their follow-up has been extraordinary. One of my doctors had ordered some lab work and I didn’t do it within a timely manner. I received a phone call from him saying he hadn’t seen the results come across his desk and wanted to make sure I had gone for the lab tests. I felt like he was definitely looking out for me. Dr. B goes above and beyond the call of duty. After Tashi has an office visit, the phone rings about 8pm a couple of days later (after the vet office closes), the doctor checking to see if she’s making progress. Wouldn’t you like a follow-up call from your doctor to see if you’re making progress?

Dr. B always dialogues about side-effects and outcome strategies. He’s clear about what I’m willing and unwilling to do for treatment. Some of the medications Tashi has been on have had such horrible side-effects that they have been removed from the repertoire of possible treatment strategies. Minimizing suffering while seeking treatments that work is paramount to us working as a team. Dr. B doesn’t make it a “my way or the highway” session.

What can you take away from my experience with a vet that treats Tashi as if she were a person? Never allow your doctor to talk down to you. Be clear that you may not have gone to medical school, but it’s your body, your health, and your journey. Let the doctor know what’s important to you regarding the relationship. I always share with the doctor my professional background in healthcare so he knows from the start I’m going to be very involved (sometimes too involved when I begin to self-diagnosis. Read my post on anchor bias).

Select a doctor that makes you feel like you’re a priority. Unfortunately I spent five months taking Tashi to the vet a minimum of three times a week for treatment so I had a lot of time to ask questions and discuss her progress. Stay in contact with your doctor so he has up-to-date knowledge of how you’re doing. Many healthcare systems have email for their staff; use it! Don’t be afraid to ask questions in between appointments.

Lastly, find a doctor who has a strong commitment to compassion. Dr. B has always treated Tashi as if she were his own. He has done amazing amounts of research on her condition and is always looking for the latest and greatest treatments for her condition. I wish he saw humans because I’d be his first patient!

Looking to explore how to select a physician that is willing to partner with you?  Looking for education, support, and inspiration when facing a health challenge?  Visit http://www.survivingstrong.com

Want to explore how art improves healing?  Visit http://www.timetolivecreatively.com

Follow me on Twitter: @GregKatz2

Posted in Caregiving, coping with chronic illness, coping with life threatening illness, living with chronic illness, Living with Illness, overcoming adversity

The Unified Person

One of the things I had to break myself from doing when I spoke was splitting parts of myself. I can look back and see how I had confused indecision with no commitment. If you’re wondering what I’m talking about let me give you an example. I would be discussing an issue and would find myself saying, “A part of me….” How is that possible? Did I really think that only the cells in my right pinky believed a particular thing and the rest of body was in revolt? I’ve spoke with many people over the years that try and exile a part of the body that is causing them trouble but that never seemed to work. Unifying the body, mind, and spirit is the only path to health and healing.

If we divide ourselves in physical, emotional, and spiritual beings it’s like having three people fighting for limited resources. When we unify our forces we create an incubator for healing. It’s that incubator that provides a safe place to nurture a strategy for growth, renewal, and peace. It takes some work, but it reaps huge rewards.

Dr. Jeff Miller shared, “Body and soul cannot be separated for purposes of treatment. For they are one, and indivisible. Sick minds must be healed as well as sick bodies.” Having had the privilege of spending thousands of hours with individuals facing chronic and life-threatening illness I understand the importance of a unified front. You can’t play the game we did as kids, if mom says no ask dad, because we diminish the odds for health and healing.

We have to remember that when we’re facing emotionally draining situations our bodies defenses are compromised. The ideal situation is that when one of the three components that makes us whole is feeling compromised the other two can step in and bolster the compromised part of our being. If you’re emotionally drained your faith may take over, sending in reinforcements helping until you’re emotionally restored. (I’m not talking about mental illness, that often requires the help of a mental health or medical professional)

We all have to remember that all three parts of our being won’t be firing on all engines all the time. There is a dance that happens between the three and understanding that our being is always in a fluid state will make the ebb and flow more natural and not so scary!

Experiencing the ebb and flow of the physical, emotional, and spiritual parts of your life?  Visit http://www.survivingstrong.com

Want to explore how to create a natural state of balance with body, mind, and spirit?  Visit http://www.timetolivecreatively.com

Follow me on Twitter: @GregKatz2