A joy to be alive

I can’t believe its the last day of Diabetes Awareness Month. When I set myself the task of writing a post a day it felt daunting. How was I going to come up with something to say every single day about diabetes? Turns out it’s not that hard. When you live with diabetes 24/7 there’s always something to say!

That’s the thing about the passage of time, it’s a human construct. We’ve decided based on a calendar we’ve created as to what time, day and month it is. Have you ever wondered what time it is on the sun? Timeless.

Living with diabetes is like that. It never ends. I’d like to think there’s a cure around the corner, but I’m realistic. For now the management tools we have available are enough. I’ve added yoga, ayurveda and a primarily plant based whole food, organic diet. I use every peer support group available and do my best to give back to the community. That’s the cool thing about living with type 1 diabetes I’m not alone. In every country around the world I know people just like me thriving.

At diagnosis I isolated myself and lived with guilt and shame until it became imperative that I educate myself about my condition. I still can’t believe it took me six years to do that. It shows how much the internet and knowledge around the condition have shifted in the last decade. A very good sign.

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With such positive changes in the way the general public and the diabetes community perceive diabetes I can only hope and pray that the situation around insulin pricing also changes for the better. No one should have to pay for their life.

Living with diabetes certainly isn’t boring, it’s a never ending kaleidoscope of unpredictability that put’s me on the razors edge. But I’m up for the task. It’s given me a strength I never knew I had, a conviction to make a difference and a willingness to let go of my ideas of how I think things should be.

Living with a chronic illness is more than just rising above a condition. It’s about living life to the fullest without preconceived notions, other people’s standards or idealised projections.

It’s a joy to be alive.

With great respect…

rachel

My best diabetes hack

One thing I love to do is scour the Diabetes Online Community for diabetes hacks. The best way to deal with all the little and big things that happen when you live with diabetes.  Best place to inject, how to dose for pizza, top CGM insertion points, ideal hypo snacks and that’s just a small glimpse into the vast ocean of support that can be gleaned from others who’ve been riding the tiger. At first, a newbie on the scene, I didn’t have any tips or tricks to share. Eleven years on there are definitely some hacks I swear by. If I had to distill my diabetes management into the ‘best diabetes hack ever’ it would be ‘routine’.

Having a consistent routine in place from the moment I wake up means I can relax. I know that I’m going to have my morning long acting insulin at 6 am, my breakfast at 7 am, I’ll be practicing yoga around 8 am, lunch at 1 pm , walk at 4 pm, long acting shot at 6 pm and dinner at 7.30 pm. I think of this set routine as a framework. Anything that happens in between these times is spontaneous, creative and fluid. Having a non negotiable routine creates stability in my blood sugars, a sense of trust that things are taken care of.

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Living with diabetes can feel out of control. Having a routine puts me back in the drivers seat. I may not be able to tame the factors that affect blood sugar  but I can manage my time impeccably. Routine may be boring for some, for me it’s a balm.

Routine is not just about the timing of shots it’s about consistency of meals, same kinds of foods at each meal. Exercise, a twice daily yoga practice and afternoon walk. Rest, heading to bed before 10 pm and waking at sunrise. These routines are part of in Ayurveda what’s called Dinacharya and are the staples that each Ayurvedic constitution relies on to stay balanced.

As we head into the holiday season it can be daunting to maintain our routines. For me a routine takes the stress out. I’d rather spend my time enjoying special times with family and friends, than try to fit in. It’s taken me a while to get to this. I still need to explain to family and friends why I’ve eaten before the 3 pm Thanksgiving meal, or 11 am Christmas brunch.  Knowing that I’m going to stay in range keeps me sane. After over a decade with diabetes it can be so frustrating to have days and days of insulin resistance after eating and dosing at a time that doesn’t suit. Call me boring, fixed…whatever I don’t mind!

Routine is also what’s enabled me to write everyday here for Diabetes Awareness Month. At first it was quite a task and I wasn’t sure I could keep it up. Consistency has been the key. Sitting down everyday to share my inner world with diabetes has been both healing and cathartic.  Thank you to everyone who has stayed the course with me. Tomorrow is the last day so make sure to check out the final wrap up for what’s been an amazing month of connection, sharing, awareness and community.

See you tomorrow #NDAM #DiabetesAwarenessMonth

with great respect…

rachel

Sick with Diabetes

Usually I can fly 30,000 miles without a hitch but not this time. I’ve been hit by some sort of bug. Could be an allergy, could be my body trying to eliminate all the toxicity from breathing in smoke from the Australian bushfires or could be I actually picked up a bug. One thing I’ve consistently noticed about myself since diagnosis is that I hardly ever get sick. I know others have mentioned this too. It’s like diabetes gives us some sort of immune super power, where we are chronically ill but never sick. Weird!

I try to avoid exposure to bugs as much as I can. It can make me antisocial.  I won’t go to hangout with someone when they have the flu. Getting sick can wreak havoc on blood sugars. Fighting off a bug can raise levels, and having to take extra herbs or medications can lower levels. Even something supportive like Vitamin C can affect the accuracy of the readings on a continuous glucose monitor. Basically a cold or flu is a minefield I’d rather avoid.

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When I travel I wear a mask. It’s not pretty and I’m often the only one on the plane who wears one, but it seems to help. If nothing else it gives me a feeling of security.  Insecurity rears its ugly head when I am tired, sick and feeling irrational. Same as one of those out of control hypo moments. Brain offline, body shaking, must get glucose now kind of stuff.

Obviously this time the mask was no match for the super bug. Now I’m in that lovely cycle of watching and waiting. Watching how it progresses from excruciating pain at back of nose, to yellow phlegm, to sore throat, waking up every hour during the night, to loss of  voice. Where to next? No idea… Such fun!

Meanwhile my blood sugar seems to be staying in range for once. Go figureIMG_7258

And it’s a beautiful day in Africa! Nature is in full force in spite of my gluggy head. A little bird is building its nest in the rafters, the lion down the road is roaring, the natural bush around us is filled with cheeps and chirps and there is a presence and stillness in the surrounding forest and mountain scape that can’t really be described.

Yep, it’s definitely annoying to get sick when you live with diabetes, but it’s also a good opportunity to rest, reflect and appreciate one’s health.

Happy Thanksgiving!

See you tomorrow #NDAM #DiabetesAwarenessMonth

with great respect…

rachel

The fear is real

My whole life I’ve been dealing with fear. When I got into yoga and especially Ayurveda I found out that fear is a constitutional characteristic of vata dosha, the combination of the air and space elements. Having vata in my constitution has inspired my creative pursuits and enabled me to be adaptable and free spirited. It’s also been one of my biggest challenges. With the tendency to get carried away with thoughts and anxieties I’ve found it hard to land and ground. Little things can trigger the deep seated traumas.

Like anyone caught in a shocking situation, one does the best to cope. My coping mechanism for past traumas was to numb out, quash the grief and keep going. Keeping on keeping on has served me well for the most part. It has driven me to teach, share and now write. But just because I look like I’m happy and settled doesn’t mean I have been able to go beyond my fear.  Like I said, when I least expect it it creeps up on me.

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Last night and most nights when the lights go out and I’m nearly asleep I have this terrifying moment. I think I’ve forgotten my evening shot. Before I can catch myself and calmly go through my evening routine, my heart is leaping out of my chest. In that moment the fear is real. A few moments later I realise I’m being irrational and I start to relax. This kind of automatic response bugs me. I should have it all together.

But that’s crazy. They say that someone living with diabetes makes about 182 decisions per day. What to eat, how much to eat, how much insulin to take, how much insulin to correct, how many carbs to treat when low, how much and how long to exercise. What to carry just in case. OMG and that’s just a small glimpse. I think fear is natural amidst a pile of unpredictable factors. Besides my diabetes decisions, I have to keep my life going like everyone else. Bills to pay, work to do. You get the gist.

What I have learnt about fear is that it’s one of the supportive mechanisms of the nervous system. Fear gives us the capacity to move away from danger. It’s protective. I know a lot of people have used this anachronism of F.E.A.R, false-evidence- appearing- real.

Can we stop right there.  Yes we can overreact to our thoughts and yes we can project onto a situation, and yes it’s good to overcome our fears.

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HOWEVER…

As someone living with diabetes my fears are not a false projection. My life is in danger if I don’t get my medication dosage right. I can suffer from a host of complications, without the appropriate technology  to measure my levels I could go into a coma and if I don’t have access to medication, I die. These are real and tangible things that would make anyone afraid. Terrified actually.

So whats the solution? Quash the fear? Push onward and upward?

The simple answer is acknowledgement. When I acknowledge the reality that diabetes sucks and its not easy to manage. I feel more capable. When that bolt hits me at bedtime and I’m in its grip I remind myself, I am here and alive.

“Sometimes the best coaching advice you can get is simple acknowledgement that there’s nothing else you could have done.” Hannah Kearney- American Athlete

See you tomorrow #NDAM #DiabetesAwarenessMonth

with great respect….

rachel

The Good News

I’m not one to write about the latest news on diabetes. It’s not because there aren’t amazing new technologies, cures and treatment protocols on the horizon. It’s just that I’d rather focus on what’s tangible and practical in my personal day to day management. When someone sends me a message with the latest ‘cinnamon’ cure I find myself ranting about the differences between type 1 and type 2 diabetes and how there is no cure for type 1. There are only useful management protocols that may or may not consistently work. A lot of my friends who were diagnosed years ago were told not to worry because a cure was coming in five years.  More than five years have come and gone and we are all still waiting.

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One of the biggest and scariest moments for me was realising that I had a life threatening, incurable disease. I was on the yoga mat in a pose when it dawned on me. I cannot adequately describe that moment. It was a mixture of shock, disbelief, denial and confusion. Coming to terms with that feeling and finding acceptance has been the core of my practice since.  I guess anyone when faced with any kind of diagnosis, or crisis goes through this. That’s why community and support are so needed.

What I am excited about in the diabetes space is how we can thrive with diabetes. There are some really cool organisations out there to tap into. As a regular contributor to Beyond Type 1 I am inspired by how they raised awareness through brilliant community building campaigns. It isn’t just about finding a cure, it’s about networking, inspiration and collaboration. Another powerful resource is Diabetes Daily. Daily updates and articles on all types of diabetes, recipes and research and a thriving community, I feel blessed to have so much information and support on tap.

In fact, today I received an email from the team at Diabetes Daily about a large study that identifies the habits of successful diabetes management. Compiled by the thrivable insights research panel the study looked at what habits those with optimal glycemic have in common? They surveyed 1,938 people and I’m pretty sure I was one of them.

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The survey analysis data demonstrated that those with type 1 and type 2 diabetes who have optimal glycemic control are significantly more likely to:

  • utilize low-carbohydrate diets
  • use insulin pumps
  • exercise regularly

Moreover, patients with type 1 diabetes were significantly more likely to:

  • use a continuous glucose monitor (CGM)
  • eat consistent meals daily
  • incorporate the protein content of their meal in calculating their insulin doses

The comprehensive data report was published on October 16, 2019 and can be found here: Habits of a Great A1c Survey Data Report. The lead researcher, Maria Muccioli, Ph.D, is also available for interviews about the findings. 

To me the best way to control my diabetes is a no brainer. I have heard many people in the diabetes space talk about diabetes as carb intolerance. It’s not that we shouldn’t include carbs its just how much. I find that about 100 carbs per day is my maximum. In my last blog on diet I talked about eating at the same time and roughly the same thing every day. I have also emphasised how important it is to have some way of seeing blood glucose data in real time. The more I know what foods do what, the easier it is to manage my levels . And you know how much I love exercise. Yoga for diabetes is the bomb!

That’s why I get all nerdy about these kind of studies. The more evidence we have of what enables us to live well with this condition, the more health care providers will come onboard. Believe it or not up until a year or two ago my doctor was still giving me a hard time for my dietary choices. Luckily education around this is shifting.

When I personally reflect on how I feel about diabetes management and the resources we have available I feel lucky. When my great grandfather had diabetes, there was no insulin and no education around diabetes. He died of diabetes complications. Ironically my birthday falls on the month and day of his passing. A powerful reminder of how grateful I am to have the education, choices and support to live a long, healthy and happy life with diabetes. Thats the good news!

See you tomorrow #NDAM #DiabetesAwarenessMonth

with great respect…

rachel

Catching a relax

Today the whole of our shire is blanketed in a smokey haze. The smoke is everywhere. It’s awful and there doesn’t seem to be much respite on the way. Meanwhile life seems to continue as normal…or does it? It’s pretty hard to ignore what’s happening not just on a local but global scale. The word that comes to mind is chaos.

When I think of managing diabetes I also think of the word chaos. Not because I can’t manage it, because overall I do that really well. Rather its the unpredictable nature of diabetes that keeps tripping me up. One day I’m struggling to stay above 4 mmol and the next I can’t get under 9 mmol (in range numbers are between 4-8 mmol). There is no X=Y with diabetes. The pancreas is a strange and elusive animal which doesn’t like stress. And how many times have I been stressed without even knowing I’m stressed? A lot.

The opposite of stress and what the pancreas loves is relaxation. Recently I’ve been catching those moments when I’m relaxed. Noticing a nice deep relaxed breath, a feeling of calm, soft tingles through the body, mind slow and centred. Every time I feel a ‘relax’ coming on I remind myself with a verbal prompt. This is me relaxed, this is what it feels like. Simply acknowledging these moments has helped me to sleep better, digest better, even think better. In fact, Relaxing makes everything better.

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This morning I went to a yoga class with my teacher and friend Louisa Sear. Her classes are hard. Not because there are complicated postures or sequences, more because she asks you to be in the pose with every fibre of your being. She instructs the class to hold the pose, fix the gaze and still the mind. Every pose is taught like this so that by the end of the class there is a sense of being cleansed from the inside out.

The ultimate agitation is our habitual need to identify with the moving miasma of the mind. Thoughts will always be there, including thoughts about diabetes, its up to each one of us as to whether we uptake that thought or not. Thoughts don’t have power. You do!

Understanding the triggers for relaxation and  fixing the gaze on that is a profound way to deal with the constant stress of living with diabetes. Instead of focusing on the tension you’re experiencing, mentally, emotionally or physically try and find somewhere in your body that is at ease. It could even just be your big toe. As soon as your mind goes there all the awareness and focus goes there too. When I do this, within seconds I’ve forgotten what the problem was.

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As I write this I’ve decided to take my own advice. There’s not much I can do about the external factors such as the choking smoke or annoyance with erratic levels. What I can do is take a full breath, be kind to myself and catch a relax.

See you tomorrow #NDAM #DiabetesAwarenessMonth

with great respect…

rachel

The number of tests?

“How many times do you test per day?” this was the question put to me this morning by the Accuchek Guide rep while I was trying to replace my meter. “About twenty,” I replied adding that my blood sugar can tend to be volatile. The rep murmured a sympathetic sound. But I wondered what she really thought.

I know what my Endo thinks. He’s mentioned to me on more than one occasion that I am obsessed with checking.  Do I really need to wake up throughout the night to check? Ummm…YES!  It’s not like I set an alarm or anything, I seem to naturally wake up between 1-3 times per night anyway so why not check?

Overnight lows are the worst. In the days before I had the whole diet thing mastered I’d wake up and have to eat at 2 am. Nothing worse than sitting by myself in the kitchen watching the clock tick over while I wait for my blood sugar to rise.

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And what about in the day? Do I really need to check every hour? I actually don’t check every hour, it depends on whether I’m insulin resistant or have had some sort of injection blunder. Most mornings I can go from breakfast to lunch without even checking. I know my liver is doing its thing, dumping some extra glycogen into my system so it’s rare for me to drop. It’s usually between 12-5 pm that I like to be vigilant. I can never seem to get my lunchtime bolus right, and then there might be some extra exercise thrown in the mix around 4 pm.

Checking vigilantly when you live with Type 1 Diabetes is a make or break situation. Especially if you can’t tell when your low. Its called hypo unawareness, it happens when you have too many lows and the body stops recognising the feeling of being low. Like my horrible hypo two weeks ago, before I knew it I’d dropped to 3.2 mmol. Scary!

It was also after that horrible hypo and sharing it here that some friends encouraged me to use a CGM (continuous glucose monitor). This is something I would love to have but sadly here in Australia there is no subsidy for someone like me. To be eligible for the Dexcom or Medtronic CGM you have to be hypo unaware and admitted to hospital more than once or under the age of 21.

The Freestyle libre flash glucose system is also on offer here, but this has no subsidy at all. I have written before on the blog about how much I love this product. Sleek, discreet and accurate using it has increased my peace of mind and saved my finger tips. I’ve attended  product launches and #dx2Melbourne and can honestly share the company, its ethos and care are palpable. I’ve even lobbied the government to make access affordable for people like me and had a small feature in the Noosa News. In spite of my passion and efforts, I still can’t justify spending $100 every fortnight.

But wait ho… my wonderful parents, after reading my blog, gave me the best early christmas gift ever! A 6 months supply of the freestyle libre. I am touched and grateful.

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Here I am ready to launch. So excited to have some time off from the drudgery of test strips and the ability to see whats actually happening minute by minute with the food I am eating, the insulin I am taking and the sleep I’m sleeping. I’ll probably put one in starting next week so stay tuned…

See you tomorrow #NDAM #DiabetesAwarenessMonth

with great respect…

rachel

7 Things or thereabouts

There are a lot of things that influence blood sugar.  42 to be exact, according to Adam Brown from diatribe.org . If you’re keen to know what those are you can check out his handy chart here.

In the spirit of Diabetes Awareness Month and to share more about what its like to live with diabetes, I’ve put together my own short list based on personal trial and error. For those who don’t have diabetes and are just coming along for the ride, your blood sugar levels might also be influenced by these ‘things’ the only difference between you and someone with diabetes is. When your blood sugar rises your pancreas produces insulin to lower your blood sugar level, mine doesn’t. So unless I inject insulin or do something else to lower my level like exercise, I can’t just kick back and let my body do the work. When blood sugar levels go low in a non-diabetic , the liver kicks in with a drip feed of glycogen, to bring them back to homeostasis. My liver kicks in too, but as there is no insulin to meet the liver dump my blood sugar goes up again, hence the need for more insulin and round and round I go. Fun, fun fun…NOT!

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So here’s my list in no particular order.

  1. The Sun. Every time I lie in the sun for more than 20 minutes, I have higher levels for 24-48 hours afterwards. Apparently its the oxidative stress. It’s a double edged sword because if I avoid the sun I don’t get enough Vitamin D. I’ve worked out that if I limit exposure to 15-20 min and only sunbathe every two days I stay in range.
  2. High Fat Foods. I absolutely love my avocados and olive oil. I also love Haloumi and Feta cheese. My blood sugar however is very fussy when it comes to what I eat when. I’ve learned to avoid fatty dairy products before bed because I go high over  night and for 24 hours after. Avocados are a little more friendly, they actually help me keep my blood sugar from tanking while I sleep. So I load up on a hefty avocado with my dinner. But sometimes it backfires and I am still high when I wake up. I’m still trying to work out how to dose for fat. I feel like if I could figure it out I’d eat pizza again.
  3. Not enough sleep affects everything. Sleeping less than 7 hours a night for me definitely messes with my levels. I wake up about 1-2 times a night too so not sure what would happen to my levels if I was able to sleep through the night. I’d probably have lower levels in general.
  4.  A Daily Walk can either reduce my blood sugar level, which can be a bonus when I’m high, or raise my blood sugar level which is not ideal. When I walk, for how long and at what pace is also a factor. Walking directly uses the thigh muscles which burn glucose for fuel. It’s suggested that when levels are higher, or you’ve had a carb heavy meal, a walk will help insulin to work more effectively and reduce blood sugar. In my case a long walk (over an hour) on flat terrain  raises my blood sugar whereas a short 20 minutes hike up and down hills reduces my levels.
  5. Cleaning definitely drops my blood sugar in spades. All I have to do is look at the vacuum and I’m low. No joke!
  6. Travel. This is also very specific to the type of travel. When we travel by car anywhere over long distances I have lows. When we fly I usually have lows and then struggle with a stubborn high when we land. Jet lag is included in travel and wreaks havoc.
  7. Any kind of stressor like unexpected news, seeing a snake on the path, (that  happened yesterday) a loud noise, change in routine, fears, emotions, frustrations. So that covers the gamut right? All of this always gives me higher levels. Especially emotional outbursts.

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The one thing that doesn’t affect my levels is my yoga practice. That includes postural yoga, breathing and meditation as well as adhering to an ayurvedic daily regime. No matter how often, or how intense the practice my levels stay steady. In fact they flat line. That’s why I personally use yoga as my goto when I’m getting stressed out about my blood sugar levels. It’s like pushing the reset button.

It may not lower a stubborn high or fix a scary low, but it will calm me down enough to handle it.

See you tomorrow

with great respect…

rachel

I have diabetes, so what

Today ‘diabetes’ was the big topic of conversation amongst everyone I spent time with. I love how friends are curious about how I manage my daily life with this condition. I enjoy clarifying the differences between type 1 and type 2 diabetes, why we take insulin or sugar and the ins and outs of daily management. There are many diabetes myths out there, like people with diabetes can’t have sugar, or we take insulin for every situation, whether low or high, or that our diets caused our diabetes.

Diabetes is so much more complex and mysterious than that. It’s a bit like trying to put a square peg in a round hole. What I deal with in my iteration of diabetes is different to every other person with diabetes. That’s what makes it both frustrating and predictable. Living with diabetes means you can rely on its uncertainty.

And don’t get me started on how each person living with diabetes relates to their condition emotionally and mentally. In a recent conversation, a friend with type 2 diabetes stressed how exhausting it felt having to stay so vigilant with daily blood tests and visits to the doctor. In the end her way of dealing with it was to say, “I have diabetes, so what.”

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Listening to her take on diabetes made me reflect on my own approach. I could completely understand her position. Taking anything so seriously that it restricts your life can make you more unwell.

This is where I segway into my personal approach to management. It’s definitely the serious approach, where fear of complications such as loss of vision, amputation, kidney damage,and neuropathy give me the discipline and impetus for strict control. I’ve used my body my whole life to express myself through dance and yoga. The body being my joy meter. I remember thinking as a teenager that if I couldn’t walk, or dance I didn’t know how I’d cope. I feel the same way now as an avid yoga practitioner. I see the body as a powerful tool for health and wellbeing. If you can open, stretch and strengthen the body you can directly affect how you deal with any physical , mental or emotional stressor.

Luckily the daily discipline required of a dancer and yogi has its benefits, I utilise it  to be comfortable with eating the same kinds of foods at every meal, taking approximately the same amount of insulin, walking at a specific time each day, checking my blood sugar often and using yoga and meditation to mange my mindset. When I veer from my daily routine it takes days to catch up. It’s hard for me to experiment and try new approaches even when I know those changes would benefit me. I don’t want to beat myself up about my approach though… I’m fine with it. As one of my diabuddy’s once said,  “You do diabetes your way and if it ain’t broke, don’t fix it.”

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Walking with my friend today we talked about how it feels when I see a positive number on my glucometer or I know I’m doing good time in range. ” Do you feel like you can take a moment to soak in the tone of that feeling? In other words stop and feel how good it feels to know your managing well? ” I absolutely loved the way she put this. If I can acknowledge the good feelings, really soak them in then perhaps those more challenging moments i.e low or high blood sugar freakouts, will be less stressful. I like the idea that even something as stressful as diabetes gives me the opportunity to embrace those feel good vibes and to heal my nervous system.

A nice way to acknowledge that even though I have diabetes, so what.

See you tomorrow

with great respect…

rachel

It’s not up to me

Setting myself the task to write something every day for 30 days about diabetes to spread diabetes awareness is definitely daunting. I live with diabetes for 365 days a year and deal with it 24/7 so it should be easy to articulate that right? In reality the way I deal with diabetes is deeply private.

After spending 6 years ignoring it and then spending 4 years shouting about it via writing a book and being a fierce advocate through social media, it’s been interesting to spend this past year taking a break from the need to externalise my experience.

In 2019 I set a goal to lower my Hba1c, heal some of my underlying digestion issues and be brave when it comes to taking Insulin. I started 2019 using the Diabetic Health Journal, created by yogi and  diabetes health coach Lauren Bongiorno, with incredible results. Writing down daily goals, things I was grateful for and staying accountable made a big difference. My Hba1c went from 6% to 5.6 % in 6 months. If you’re not sure what that means it’s like dropping your cholesterol levels or blood pressure. Moving it from a pass to a win.

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I also went into hyper drive with my digestion, adding different supplements, bone broth and more variety into my daily meals. I worked on stored trauma with network spinal analysis and neuroimmunology sessions. Finally I made sure to keep up a daily walk and my twice daily yoga practice.

Making a concerted effort to shift some deep seated patterns has been an interesting process. I didn’t necessarily make great strides or have major revelations, instead I settled more into accepting what is.

“What is” might not be what I want but if I can accept it that’s a pretty good place to be. It’s how I dealt with diagnosis after fighting it for so long and pretty much how I manage my finicky digestion and volatile blood sugars and everything else that comes my way.

My latest go to phrase for everything is, ” It’s not up to me” That’s not about not doing everything I can to stay balanced. It’s about understanding that I don’t know the recipe of creation.  Letting go of needing to know, enjoying the gifts I’ve been given and trusting that whatever comes is perfect, goes a long way in helping me manage my condition.

I never expected to be diagnosed with diabetes but now that I have been I can honestly share it’s a blessing in disguise.

More on that tomorrow  #NDAM #DiabetesAwarenessMonth

With great respect…

rachel

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