Diayogi Dialogue Karo Sharma Bonus Episode 1

Diayogi Dialogue with Karo Sharma

Welcome to our first bonus episode with Karo Sharma. Karo is someone you have to meet. She’s trained teachers all over the world and walks her talk. In our interview she shares how yoga helped her turn a negative into positive, fear into certainty.  For her diabetes is just a part of the story. Find out how she deals with the stress of a full time yoga teaching schedule and travel in countries like India and Bali with diabetes and how embracing the spirit of serving others has impacted her life on and off the mat. Take it away Karo

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Karo has been practicing Yoga for 18 years. She is a Yoga Alliance Registered Senior Yoga Teacher and Prenatal Yoga Teacher and Trainer and the cofounder of Trimurti Yoga.

For the past 20 years Karolina has been living with Type 1 diabetes, therefore her main focus in practicing yoga was, and always is health. “Living with diagnosis like this is a life sentence. Everyday you are in a trap of self-control, 24 hours, no break, no holidays…counting carbs, injecting insulin, waiting for complications. Everybody wants you to be afraid, to make diabetes your enemy. The words I heard from doctors – I am ashamed to repeat. But Yoga helped me to get rid of fear and to find my space, my freedom, my unwounded spot. I am not my body, I am so much more…

Where you can find Karo on Social:

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Diayogi Dialogue with Karen Rose Tank Episode 9

Diayogi Dialogue with Karen Rose Tank

Wow! We are up to Episode 9 which was supposed to be the last vlog in the series but instead, I have two more bonus episodes with yoginis Karo Sharma and Synne Roisland. The summit will occupy the blog until October 31. After that I’ll head into a new flavour for November’s Diabetes Awareness Month.

Karen Rose Tank, our next diayogi is an absolute force of nature. Loved by so many for her enthusiasm for all things health and wellbeing our interview crosses a range of topics from yoga to nutrition. If you are someone who is sitting on the fence about trying yoga because of a physical limitation Karen’s words will revolutionise the way you see yourself and your practice. Her yoga snack is accessible and so much fun and full of healthy benefits. Take it away Karen!

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Karen Rose Tank, MS, CHC is a Certified Integrative Nutrition Health & Diabetes Coach with Rose Health Coaching based in Princeton, NJ. She specializes in working with people with diabetes, obesity and other chronic conditions informed by her own 22 years of experience with type 1 diabetes, Hashimoto’s Hypothyroidism, Menopause and weight challenges. 

Karen is passionate about yoga for physical as well as mental benefits and has completed several yoga teacher trainings including 200 hours in Yoga and Wellness and 180 hours in Therapeutic Yoga Teacher Training. Along with her low carb eating approach, Karen is a fan of exercise, walking, biking, skipping, weight training, yoga, meditation and just plain breathing as a way to manage weight, blood sugars and stress.

Where you can find Karen on Social:

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DIayogi Dialogue Sarah Tomlinson Episode 7

Diayogi Dialogue with Sarah Tomlinson

Sarah Tomlinson our next diayogi is generous, wise and lives her yoga. Our conversation is not just about the benefits of yoga its about the intangible and subtle aspects of yoga and how life with diabetes can be transformed through the power of tools like yantra and mantra. If you are curious to know what those words mean, all will be revealed in our in depth conversation. I left our discussion feeling more determined than ever to relax and trust in something greater. I hope you will too. Take it away Sarah.

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Sarah Tomlinson is an internationally acclaimed Yantrika (Yantra teacher and practitioner), yoga teacher and artist, with renowned fans across the globe including Elena Brower and Sharon Gannon, co-founder of Jivamukti Yoga. Sarah worked extensively with her mentor Harish Johari in India, he initiated her into the spiritual practice of painting Yantras. Sarah is the author of the informative coloring book: Coloring Yantras, the creator of the Yantra Bliss Oracle Deck and the author of the Planetary Yantra Workbook “Nine Designs For Inner Peace”.  She leads retreats and Yantra workshops around the world and enjoys lots of time by the ocean with her husband and two young boys.

Where you can find Sarah on Social:

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I’m Possible

What I love most about the Diabetes Online Community is the beauty that flourishes through sharing our stories. Today I wanted to share a guest post by Doris Hobbs the founder of Rich in Love. Doris reached out to me just after my crowdfunding campaign and shared her story with me. Type 1 diabetes runs in her close family. Her courage in accepting her eventual diagnosis and how she met it with glamour and determination is the subject of her blog. In her guest post, she shares how attitude and mindset help her to manage her disease with grace. Take it away Doris!

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I was diagnosed with diabetes at 33, I would have never imagined that just 3 years later I’d see this auto-immune disease as a gift rather than a curse.

10 months before my diagnosis I lived in uncrated fear, unwilling to admit I could be a diabetic. With each passing month, my life slipped from underneath me. I began to lose weight rapidly, a feeling of fatigue followed each action, endless thirst and blurred vision with momentary blindness; I was fighting to stay alive and ironically knew the solution and chose to ignore it.

The night I was hospitalized I was near death later discovering my A1C was 11.2%. If I hadn’t sought medical attention I would have eventually slipped into a coma during the night. While the doctor shared my laboratory results, I clearly remember staring at the cold white walls of the emergency room, a number of IV’s stationary in my veins and saying to myself with determination, “I will find a cure, this is not my ending”. From that moment, I’ve gone on an empowering life journey as a type 1 diabetic seeking a cure.  For what others say is impossible I see as possible as I know I’m possible.

Diabetes has allowed me to view the world I want to create, not the world I currently live in.

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I am proud to share I currently have an A1C of 5.9% pre-diabetic, with the goal of 5.6% in the next year ahead (approx. 6/2018). How did I reach this astonishing result? Through the daily practice of leading a health-conscious mindset that is fed by a BE-DO-HAVE Paradigm Shift, in addition to clean eating, the knowledge of our bodies biochemistry and a daily fitness routine.

When I was diagnosed I didn’t want to wear a pump or go on an impractical diet plan, instead, my desire was to create a new lifestyle, something of substance which in return would only enrich my life positively.

Have you ever wondered what was on the other side of life for you? It’s quite simple to know because, what you want, wants you. We forget that our actions, daily behavior, and spoken words carry enormous weight in creating our reality.

“Death and life are in the power of the tongue,” King Solomon once said. Whether we realize it or not, we are shaping our future by the words we use every day.

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Change is inevitable. Nothing stays still. Life is in constant motion shifting you through positivity and setbacks, but if you take a closer look at those hardships you’ll find a hint of glamour, I did with the mindset to not allow my diagnosis to define my existence.  Now, with a footing in what my true purpose in life is I awake each morning with gratitude for another day to inspire others with glamour, a story, authenticity, and an unbinding courage to never give up despite what my day or diabetes may bring.

Try and remember that each day; you become what you think of most. Rather than registering difficult thoughts, look around you and make note of what you appreciate most in life. There is hidden treasure filled with fortune if you do.

Since my diagnosis I’ve brought a message of positivity through worldwide media exposure for several prestigious diabetes organizations: Beyond Type 1, JDRF, American Diabetes Association, Diabetes Alive, and T1D Exposed. I’ve also been featured on Hawaii News Now, 101.7 KKIQ, 92.1 KKDV, Healtheo360, Diabetes Connections, East Bay Times, Diabetes Power show, T1D Exposed Nude Calendar Advocacy Project, Bay Area Focus, and Diabetes Late Nite for my advocate efforts.

At the end, exploring your health and evaluating the areas that are in need of change will enable you to develop constructive behavior. By being proactive you are bringing freedom and new meaning to not only your life but to those who cross your path.

Live in love, find your inner peace and abundance will follow.

KKDV Beyond Type 1 PSA

A San Francisco based Luxury Liaison, Doris Hobbs bridges the world of MEDIA with unmistakable elegance through both written Storytelling & Visual Imagery. Known as the Creative Visionary of Rich in Love, an accomplished Media Maven and Fashion Doyenne she has partnered with some of today’s Leading Publications and Television Networks. Named by Diablo Magazine as “Best of the East Bay”, featured in the San Francisco Chronicle, InStyle Magazine, Hawaii News Now, CBS13/CW31 and KPIX-TV CBS television networks. Doris continues to breathe new life into her sought-after glamour persona & profitable branding campaigns while maintaining a voice as a Diabetes Awareness Advocate.

Twitter: doris_hobbs
IG: richinlovefashion
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Web: richinlovefashion.com

When I go Low, I reach Higher

I can remember having a conversation with my doctor early on about my condition. I kept telling him I was afraid of going low because I’d read about it online. He kept telling me not to worry. “You can’t go low because your problem is high blood sugar. You’re not on insulin so we don’t need to even go there.”  

Now that I’ve been properly diagnosed as a Type 1 LADA and on insulin things are different. I’ve learned that balancing your blood sugar is like playing Russian roulette and that a low blood sugar happens because I’ve either miscalculated the amount of insulin I need to match the number of carbs in a meal, or I’ve exercised and injected too much insulin, or my basal insulin ( long-acting insulin) is set too high.  

Luckily I’m not hypo unaware (a condition that occurs when your body can no longer sense a low blood sugar due to repeated hypoglycemic events) but that doesn’t mean I don’t have anxiety around a low.

Being hypo unaware is probably the single biggest issue anyone has living with type 1. To remedy this we prick our fingers and check our meter’s incessantly, use CGM’s, have something called Glucagon (a shot which has to be mixed and prepared on the spot by someone else to get glucose into the blood stream fast) or have special diabetes alert dogs who can smell the change in our blood sugar levels, to remind us through barks and nudges to check that we are going low.Parents of young kids who live with diabetes set their alarms throughout the night to finger prick their kids, or check their CGM’s making sure they are in range. Imagine a young mum waking through the night year after year hoping their little one is still alive.

I don’t want to paint a horrific picture but it IS horrific.

So what happens when we are conscious enough to treat a low? Well often the fear and impatience of having to wait 20 minutes to see if your levels rise means 2 sips of juice turn into eating the entire contents of the fridge (no joke) By then, your blood sugar is screaming high and you have to inject again to bring it back down.Because I still produce that little bit of insulin and because I eat such a low carb diet my levels are very stable.

I’ve only gone below 3.9 a few times and have experimented enough to know exactly what will raise my levels. But I have had a few fridge binge moments that I’m not proud of. Like the time my meter said I was below 3.9 and I actually wasn’t and by the time I checked again it was too late!

For me having a steady yoga practice to help me deal with the stresses associated with the complexity of this disease has absolutely saved me.

It’s the number one reason why I jump on my mat, work with my breath and explore all aspects of this beautiful and ancient discipline. When I go low I reach higher inside myself to be grateful and accepting of whatever comes along. And sometimes a little thing like a flower on my afternoon walks makes all the difference.

 

Dancing with Diabetes

This last month has been all about my obsession with Ballet. It started when I was in the airport on my way back to Australia and Misty Copeland’s, Life in Motion miraculously leaped off the shelf and into my hands for the long flight ahead. Reading about her incredible talent and rise to stardom amidst a very unstable home life and her detailed descriptions of a life in Ballet, brought back vivid memories of what it was like to live and study dance in New York City during the early 80’s.

Back then I was an aspiring Ballerina and spent every spare minute either attending dance classes or watching the greats in American Ballet Theatre and New York City Ballet. My own career in dance lasted well into my 30’s. I never made it to a big company, ( I danced with a regional dance in education company in Tasmania), but I did get to taste what it’s like to perform day in and day out.

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Don’t let anyone tell you that dancing is glamorous. It takes grit, hard work, and guts to do all that graceful stuff and nerves of steel…not only to face external criticism but one’s own nagging self-doubt, fear of failure and much more.

Initially, when I was diagnosed with diabetes, I tried to dance down my blood sugar levels. I’d wake up, head to my yoga room, blast out music and thrash about for 20 minutes hoping for the best.  It worked quite well in the beginning stages when I was still producing quite a bit of insulin but later, not so much. After a while, any kind of exercise raised my levels and depleted my adrenals and sadly I stopped dancing.

Reading Misty’s book made me wonder. Are there other dancers out there who live with Type 1 Diabetes?

Enter, Zippora Karz, a former ballerina with the New York City Ballet who was diagnosed with Type 1 diabetes just as her career was taking off within the company. Lucky for me she is also a writer so to continue my passion for all things Ballet I couldn’t help devouring her book, The Sugarless Plum. It’s such a great read and perfect for anyone living with type 1 diabetes who also loves all the intrigue of the Ballet. I soared along with Zippora as she realised her dream of joining the company, and then crashed when she was diagnosed, misdiagnosed and re-diagnosed again. Her journey to health and wellbeing is remarkable, her courage unshakable and her persistence in living her dream in spite of the many challenges and unknowns awe inspiring. Can you tell I love this book!

So after a month of watching videos of Ballet, reading about Ballet and thinking seriously about attending an Adult Ballet class, I decided it was time to digress from my usual yoga for diabetes topic and share with you a short interpretive dance about what it feels like sometimes to live with diabetes.

I’d love to know how you find creative ways to manage the many emotions that arise in a life with diabetes so feel free to comment below…

With great respect…

Rachel

The worst visit ever

I’m sitting here in the airport in Johannesburg after 10 hours of non-stop flying. With a couple of hours before my next flight, I have time to share my 3rd post for Diabetes Blog Week 

Having diabetes often makes a visit to the doctor a dreaded experience, as there is invariably bad news of one kind or another.  And sometimes the way the doctor talks to you can leave you feeling like you’re at fault.  Or maybe you have a fantastic healthcare team, but have experienced blame and judgment from someone else in your life – friend, loved one, complete stranger.  Think about a particularly bad instance, how that person talked to you, the words they used and the conversation you had.  Now, the game part.  Let’s turn this around.  If you could turn that person into a puppet, what would you have them say that would leave you feeling empowered and good about yourself?   Let’s help teach people how to support us, rather than blame us!

My GP had always been a cool guy. Into alternative things, he swam with dolphins, played the didgeridoo and always recommended herbs before meds. I’d been seeing him on and off since my son was born and we had a nice friendship outside of the doctor’s office.

The day of my diagnosis was just like any other day.  I’d been feeling fatigued, dizzy when I ate sweet things and my ex-husband had suggested we both get some blood tests. He’d gone to see the doctor first and was told that he had high blood pressure, but the news about me was way worse. The doctor wanted to see me straight away. “What do you think it could be?” I asked him. “Well I know it’s not Cancer but it is something to do with your blood.”

Sitting in the waiting room that day I was jittery. It seemed odd that I was that unwell. I’d always managed everything holistically with my health, hence seeing that sort of doctor.

As soon as I entered his office he told me to sit down. He swiveled back on forth on his chair and tapped his pencil on my blood test result form. I don’t know how to tell you this…but the news isn’t good.

And then he just blurted it out. You have diabetes!

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I can’t begin to tell you how I felt, my heart rate went through the roof, the bottom dropped out of my world. Diabetes is everywhere in my family, especially on my mother’s side. In fact, my great grandfather died from diabetes ( he was diagnosed before there was Insulin) Ironically, My birth date is the date he died.

It was hard to keep track of what the doctor said next. He told me that he had seen that my blood sugar levels were elevated so he checked my A1c. Sure enough, that was elevated too. “It’s a long journey to reverse this, you’ll have to find your own cure. I’m not quite sure how you got this…”

Next, he’s started telling me that I had to change my diet and exercise more while shoving pamphlets in direction. Then as a parting gift, he told me to Google diabetes.

As I drove home I just couldn’t believe what he was saying. It couldn’t be diabetes.

I think things could have gone really differently that day and if they had I might not have gone on to deny my diagnosis. It took almost 6 years to have actual diabetes symptoms so it was easy to shove his diagnosis under the rug.

If he had sat me down and explained to me that the beta cells in my pancreas were attacking themselves and that it couldn’t possibly be my fault. If he had asked me if there had been some really stressful event that may have triggered the onset.  If he’d told me that there were resources and tools to help me manage this and a worldwide community for support. That I could live a full happy healthy life. That there were people just like me that I could connect with, who could mentor me through the little things. Even just a few words of support and encouragement could have made all the difference.

Luckily in spite of that god awful doctor,  I survived!  In a way, diabetes has grown on me. I no longer blame myself for getting sick.

After nine years of living with diabetes, a lot of yoga and study of traditional yoga teachings, I’ve realized that there is no ‘ rhyme or reason’  for anything. Rather the whole of life, whatever happens, whether we call it good or bad… is a reminder to enjoy everything exactly as it is.

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If you’d like to find out more about how yoga can help you manage your diabetes each and every day check out the rest of my blog and if you’d like to get the first chapter of my book for free go here

With great respect…Rachel

What can I do to make a difference

Today is Day 2 of Diabetes Blog Week and already it’s been amazing to read and share with our thriving #DOC. I feel completely inspired and in awe of the writing talent out there and if you are reading this, you guys are my diabetes heroes! Even though I was diagnosed 9 years ago I still feel like the new kid on the block when it comes to managing this disease. After yesterday’s topic,  I feel armed with a whole new arsenal of tools to manage my diabetes. Thank you!

Here’s today’s prompt…

 So today, let’s discuss how cost impacts our diabetes care.  Do you have advice to share?  For those outside the US, is cost a concern?  Are there other factors such as accessibility or education that cause barriers to your diabetes care?

I feel like I am one of the lucky ones. I was born in Holland, grew up in the U.S and moved to Australia when I was 18. I can still remember the day I received my medicare card and my shock at how anything related to doctors and medical tests was free. While my siblings and parents complained about the costs of doctors and insurance in the States and worried about my health care, I told them not to worry. Australia isn’t called the lucky country for nothing.

That was when I was 18… things are definitely more costly now, but as my friend, Frank from Type 1 writes  just shared on his blog,

” If I have to have diabetes, then there’s no place I’d rather have it than in Australia.”

Living in Australia with Diabetes has been affordable and it’s one of the reasons I feel grateful to call it my home. But I do live and travel often to other countries and have come to realize that Insulin, test strips, needles and diabetes devices aren’t always on tap and don’t come gift-wrapped.

Recently I’ve been living in South Africa. It’s a land of contradictions with a huge disparity between the people who have and the people who have not. I’m basically a tourist here so not really part of the medical system but recently the harsh reality of what it’s like for the people here hit home.

A friend came for a visit and with her was Abongile.  Somehow it came up in conversation that I had type 1 diabetes. Abongile just happened to be a dietician in a clinic in Johannesburg for about 30 kids with type 1 diabetes. I was showing her my freestyle libre flash glucose monitor and how it worked. She was astonished. The kids she cares for and their parents can’t even afford the insulin they need to survive. Not only that, because there is no awareness of type 1 in the school system, the kids can’t take the risk of being on more than two shots a day. Apparently, hypos are a no go because the teachers don’t have the skills to respond appropriately. So all the kids in the clinic are on mixed insulin and do something called ‘carb blocking.’ They are allowed a certain number of carbs per day, based on the types of foods they eat. A packet of sweets is one block, a bag of potato chips another.

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As a nutritionist, Abongile works hard to educate parents about the types of foods that are good to help the kids manage their levels. But some parents can’t even afford healthy fruits and vegetables. When I asked her if there was any money from the government to help the kids she laughed and shook her head. The one thing they have been able to achieve is to give each child a glucometer.

After speaking with Abongile I was completely floored and felt ashamed. How could I even consider complaining about the fact that the freestyle libre was $90 out of pocket, or that my favourite brand of test strips was on back order, or that I have to pay very little for a years supply of Insulin when these kids don’t even get to take the Insulin they need.

It immediately made me want to help. Before Abongile left I made sure I had her contact details I told her about an organization called Type 1 International which helps people get access to Insulin and medical supplies. I wrote a letter to one of the founders about the clinic and my meeting with Abongile. It felt good to put them in contact with each other and that somehow I could make a difference.

Abongile wrote back to me a few days later…

“Thank you very much for your quick connection with the T1 international on my hospital’s behalf. I am very grateful for your keeping to your word as well :). I will keep you updated with any/all positive developments for the clinic from the T1 foundation. “

Something I learned from my exchange with Abongile was that whatever we can do to help others have access to Insulin and diabetes-related supplies we must do. Whether it’s helping someone with less access, lobbying our governments, writing about it or networking to spread awareness.

Even the smallest action helps.

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If you’d like to find out more about how yoga can help you manage your diabetes each and every day check out the rest of my blog and if you’d like to get the first chapter of my book for free go here

With great respect…Rachel

The wonder and magic of a life with diabetes

Woohoo! It’s here! Diabetes Blog Week!

For the next 5 days I’ll be writing on a specific topic along with other diabetes bloggers, sharing how I navigate the world of diabetes. Below is the first topic and my corresponding thoughts.

Tell us about some good things diabetes has brought into your life that you never could have expected?

The nervous system is a delicate thing, tiny fibers that crisscross the body and send signals from your brain to different key areas, telling it to move, breath, digest, feel etc. For some reason nine years ago, mine started to go haywire. Being a long time yogi I consulted my yoga books to see what the problem might be. After months of research, I reached my conclusion.

I was in the middle of a spiritual crisis.

Thinking that I was on the fast track to enlightenment wasn’t necessarily the best approach. For starters, it kept me from questioning my physical symptoms or seeking medical answers. If I had known that diabetes isn’t something you get from poor diet and lifestyle, or that it doesn’t just affect children, I would have dug deeper.

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Back then there wasn’t much awareness about the signs and symptoms of diabetes.  Even now when I tell people I have Latent Autoimmune Diabetes in Adults ( LADA) they scratch their heads and look at me funny.

Finding out that there was a reason for the strange jittery sensations, erratic digestion, food sensitivities, a constant sugary taste on my tongue and the feelings of exhaustion was a total relief. It’s not that I was happy to have diabetes, it’s just that my search for answers caused so much internal havoc, that having an actual diagnosis released the pressure valve.

I cried a lot those first few weeks after diagnosis. It felt so good to let go.

It’s been quite a journey since then and aside from those initial feelings of relief, I spent years trying everything I could to conquer the beast. What I’ve learned though is that you can’t ‘conquer’ diabetes. It’s not a country you can invade and call home.

Am I the proud owner of a life with diabetes? hmmm….it’s hard to put that answer into words…

What I can say is that diabetes has changed me for the better. It’s made me raw, honest and put my feet on the ground.  It’s also motivated me to open up and share through my writing more about what it means to live with chronic illness and spread awareness about the disease.

Diabetes has also inspired me to be deeply grateful. I used to take life for granted. I’d wake up every morning, dive into the day and never stop and think. Wow! I’m alive.

Now, I make a concerted effort to stop, look around me, drink in the beauty of this life and remember…

Life is precious. It’s not a given.

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If you’d like to find out more about how yoga can help you manage your diabetes each and every day check out the rest of my blog and if you’d like to get the first chapter of my book for free go here

With great respect…Rachel

Why I dropped the ball

Hey there, it’s been a while! Firstly I want to apologise for the long break between blogs. I’ve been plowing through a few ‘moments’ in my life that have garnered my full attention.

Things like:

organising my book tour in the US

getting published in Elephant Journal

creating vlogs for Yoga for Fertility and Yoga for Adrenal support

hosting my parents first visit to South Africa

did I mention, marrying the man of my dreams?

and finally getting a printed advance readers copy of my book on Yoga for Diabetes, How to Manage your Health with Yoga and Ayurveda 

Here’s a little photo collage to put you in the picture….

Meanwhile, diabetes has been kicking my but!

I’ve been splitting my basal dose, upping ratios, wrestling with unexpected highs and lows and doubling down on my yoga practice to manage the associated stress.

Amidst all the celebrations, I’ve been dealing with a ton of fear. So much so that I found myself writing about it for Beyond Type 1, my favourite online yoga charity and community.

Here’s a little exerpt

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“Meeting my fear has never been easy. But slowly over time I’m getting better at taming the beast, especially now that I live with Type 1 diabetes.

My initial response to my diagnosis was to deny that I had diabetes. The theory being: what doesn’t exist can’t hurt me. It took time and courage to realize that the only thing standing in the way of me accepting my condition was fear.

Fear of hypoglycemia, fear of ketoacidosis. Fear of insulin. Fear of forgetting to take insulin. Fear of food, fear of what other people think about what I eat. Fear of getting fat or losing too much weight. Fear of complications. Fear of losing my livelihood. Fear of losing my relationships. And the biggest fear? Fear of dying. We all grapple with that one, diabetes or not…” read more here

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So… it’s been a crazy few months and I can’t wait for some sense of normalcy to return so I can keep sharing with you really great ways to use yoga to help you manage your diabetes.

….And I’d love to hear from you what kind of things you’d like to see more of on the blog.

Wishing you an absolutely beautiful day wherever you are!

with great respect

Rachel