So what would I keep in this list? What would I add?
My current understanding is that there are six key areas to fight chronic pain, chronic fatigue and fibromyalgia:
Knowledge and taking control for ourselves
Central nervous system
Fatigue and pacing
What works for me right now?
Find the video here
Sleep is the biggest component of my journey. I will discuss this more under Low Dose Naltrexone, below, but it is HUGE. See also my giant insomnia post for more.
Aside from sleep and physiotherapy I do a lot of stretching, self-trigger point work, yoga, meditation, essential oils, heat and more. I am employing more natural remedies than medicinal.
Low Dose Naltrexone– is now number one on my list. This one covers sleep and pain management . It helps me sleep in more than one hour blocks, which has been the biggest part of my puzzle. Now, when I sleep only six or seven hours (due to the baby) but a few hours in a row, I feel infinitely better than I ever did on my eight or nine broken hours. As a result I experience less pain, less anxiety, less brain fog. More health and a much better quality of life.
Physiotherapy – this is still crucial, more specifically the insertion of dry needles into trigger points and left for 15 minutes to rest to encourage blood flow and relaxation followed by stretching and mobilizations. I only have to go every three weeks at the moment, which is a big win as I pay privately for every treatment. Learn more about myofascial pain syndrome and trigger points here.
A combination of reduced work hours and reduced activity levels. Both are key. Reduced work hours is the first thing that jump started my journey to wellness and is still part of managing my energy envelope.
Perpetuating Factors/Normal Human Needs
For me, this means managing the myofascial pain syndrome and the fibromyalgia. Most of my six key ways hit multiple symptoms. Aside from managing my posture, avoiding triggers and sleeping as best as I can, these two are important:
Nourishment – I am learning about the importance of nutrition right now. I haven’t yet finalised my template for eating going forward but all of my research seems to suggest the number one thing we can do is prioritize vegetables and fruits. Then I am prioritizing healthy fats (olive oil, coconut oil etc) and good quality protein. This leads to a lower consumption of grains. As an offshoot, supplementation, is key. I am using magnesium and 5HTP to sleep (after finally getting off amitriptyline after years which precluded 5HTP). I also supplement with MSM as our soils are generally deficient in sulphur and this seems to help me. I am preferring whole foods over supplements – I am taking moringa powder or hemp powder for naturally occuring vitamins and minerals.
Gentle exercise – this is still key but I am able to do more than I was previously. I can now do 30 minute walks without pain hangovers. My exercise of choice includes yoga, walking and Pilates.
Central nervous system
Meditation– this has only become more integral to my daily life. I have meditated daily for more than five years now. I use it for rest (I can’t nap), for pain relief (or a break from it when it is bad) and stress relief. The benefits I have reaped since my initial post are so many that I am a mindfulness and meditation cheerleader. You can sign up for my free workshop Mindfulness for the Chronic Life here.
So these are the key things that are working for me now.
I know it is complex. It has taken me years and a lot of research and personal trial and error to figure out. I have provided many links in this post to help you in your research.
Do you miss learning? Or want to up-skill but don’t have any spoons leftover after life to go to class? Online learning options might be the way to go.
I have found online learning options to be excellent for filling that gap as a mama with chronic illness. I’m not expected anywhere at any specific time. I can access lectures while wearing the fussy baby in the wrap. And while I am tired from the baby waking regularly in the night, since I have experienced the improvement in my symptoms from low dose naltrexone, I can’t bear not to indulge my love of learning.
Affiliate notice: Some of my links are affiliate links, if you make a purchase using my link I will make a small commission at no extra cost to you.
Benefits of online learning for those with chronic illness
You can lie or sit however you need (in bed with your heat pack?)
You don’t have to leave the house at a specified time
You don’t have to do the work at a specified time
You can do as little or as much as you can fit in (around energy, children, etc)
You can use your phone, laptop, tablet or computer – whatever works best for you
Keep your brain active
Up-skill yourself no matter your current employment status
You can learn a hobby you have been curious about
Online courses are the most useful when you do the work and can demonstrate what you’ve learned. So if you want to put it on your CV, be prepared to talk about how it helped you and relate it to your work.
How to get the most out of online learning
Complete all of the work offered, the reading, the quizzes, the videos, the extras
Ensure you understand it all
Participate in forums provided
Practice what you have learnt
Ensure you understand what you have learnt and how it can help you in your career (if you intend to use it on your CV)
Below I share some learning platforms I have come used.
When I was off work while pregnant due to severe pelvis issues last year I did a course on SEO (search engine optimisation) through Lynda.com. I had free access to this as my public library has a bulk membership which was awesome. The app was easy to use and there is a great selection of both longer and shorter courses. As a bonus it shows the certificate of completion on LinkedIn. There were no assignments but I practiced everything on my blog.
Earlier this year I completed a life coach certification through Udemy. I paid just $11.99 USD (down from $200!) for my course in the January sale and it is a fairly comprehensive one. After this one I moved on to mindfulness certification and group coaching. Once I had completed my courses I received my certificate. I also joined the networking group associated with my course provider (The Transformation Academy) to learn even more. I also practiced my new skills as I went. I have loved every minute of the training, the practicing and then using my skills in this blog. It will also be useful when I go back to part time work. The beauty and tricky part of Udemy is that the courses are run by different people and are not necessarily vetted by Udemy. I highly recommend the Transformation Academy though.
Their About page says, “We believe that free education, more than anything, has the power to break through boundaries and transform lives.” And living with chronic illness is definitely a barrier to further learning.
I have just found Alison and have my eye on a few of their free courses for some future up-skilling. With options for 2-3 hour certificates or pathways for diplomas there is a lot to search through. Subjects range from touch typing to French to graphic design to project management.
You can choose the premium (paid) option and gain access to all courses for as long as you need, or you can enroll in courses and complete them within a designated time frame without paying (but you won’t receive a completion certificate). You can choose short courses up to online degrees.
Subject ideas you may like to explore as a start
pretty much anything you like!
Have you embarked upon any online learning? Do you have one you recommend?
If you are curious about up-skilling yourself for your fight to be well you might like to look into my learning options. To learn from the comfort of your bed, couch, or comfortable chair with your phone, tablet or computer. Take my shortcut – all my years of research, personal learning, trial and error to make your plans.
This is another interview with a fellow fibro mama, this time we are learning about how one mama uses essential oils to manage chronic pain, fibromyalgia. Since this interview was conducted Kara welcomed her gorgeous baby.
Could you introduce yourself in a few sentences for us?
My name is Kara Carril, I’m 28, and soon-to-be first time mom! I live in Arizona with my husband and our two dogs, Diesel and Rain!
How did you get into essential oils for fibromyalgia?
My mom is a distributor for Young Living Essential Oils here in the US. After she had breast cancer 10 years ago, she got into living a more chemical-free lifestyle. She did a lot of research on essential oils and the potential help they could give to autoimmune diseases. She has fibromyalgia as well as ankylosing spondylitis amongst other health issues. The oils helped her pain management dramatically, so she eventually introduced them to me, and I was hooked!
What are your favourite ones and what do they help with?
The ones I use most often are lavender, frankincense, copaiba, PanAway (a blend), Valor (a blend), cedarwood, and eucalyptus/peppermint. I use lavender and cedarwood mixed with distilled water for a pillow spray before bed. It helps calm and relax to be able to go into a deeper sleep. I use lavender/cedarwood in mascara to help strengthen lashes (I know it’s not fibro related but a cool trick!-just a drop of each).
I use lavender/frankincense in homemade face soap with coconut oil and baking soda. PanAway I use on my back spasms. Valor and copaiba I also use on my back spasms. Valor is often referred to as a “chiropractor in a bottle” and copaiba is compared to “morphine in a bottle” and often enhances whatever other oils you use in conjunction with it. I use eucalyptus/peppermint on my sinuses and throat when I feel I’m getting sick, and I also use either with lavender and epsom salts in baths when I’m having a bad flare up.
I will stop using peppermint when I’m breastfeeding though because it is said to drastically reduce your milk supply (good for when you’re trying to stop producing though!).
“The ones I use most often are lavender, frankincense, copaiba, PanAway (a blend), Valor (a blend), cedarwood, and eucalyptus/peppermint.”
Do you have any blends you make yourself?
Lavender/Cedarwood for sleep/relaxation- 5-10 drops of each in a 3oz spray bottle filled with distilled water. Make the strength based on your scent preferences. I also spray it on the bottoms of my feet before bed or will use straight lavender drops when my feet are really sore. I also use this combo in my diffuser at night next to my bed.
I make a ton of diffuser blends based on what my needs are. Lemon/peppermint combo is really good for getting rid of stinky smells, lavender/cedarwood is great for relaxing/sleep. Orange and lemon or any citrus combination is great for morning and energy! Ginger, peppermint, and lemon is good for tummy aches too!
For more research into using essential oils in your journey you may like
As we know, fibromyalgia is a painful condition that many suffer from. In fact, it’s believed that in the United States alone, over 10 million people have some form of it. While medications might help calm symptoms, they don’t always have the best side effects or lasting results. Because of this, many often look for other methods they can use to help ease their symptoms.
This is a guest post from Dr. Brent Wells, a chiropractor who founded Alaska-based Better Health Chiropractic & Physical Rehab. There is more detail about his work below.
Surprisingly, one of the best ways to help with fibromyalgia pain is to stretch. This is because it will reduce inflammation in the body and help to keep it active. Because of this, it will keep the body calm which can significantly reduce the symptoms of this medical issue. Below you’ll find more about why stretching is so important for those with fibromyalgia and some stretching options you can use to help with it.
Benefits of Stretching for Those Who Suffer From Fibromyalgia
There are many benefits that come with stretching if you have fibromyalgia. Below are some you’ll find if you do.
It Increases Serotonin and Endorphins in the Body
When you suffer from fibromyalgia, it can decrease the levels of serotonin and endorphins in your body. Serotonin and endorphins are neurotransmitters in the brain that help with emotions. When they have low levels, they cause the body to feel drowsy and irritable which can affect your mood and physical wellbeing. Stretching can help by boosting the levels of these two chemicals in the body. It will help to improve your overall mood which can lower the side effects of fibromyalgia, like anxiety and stress.
It Can Help with Muscle and Joint Movement
Stretching works to help increase muscle and joint movements in your body. This can prevent nerve pain as you will keep these areas active. It also helps you to be more flexible.
It Works to Improve the Heart
You might be surprised to learn that stretching can actually help to improve the heart. This is because it will expand the surrounding arteries and keep them open and pliable. It also reduces any fat around the heart and can help you to maintain healthy cholesterol levels.
It Can Improve Your Sleep
Stretching can improve your sleep because it reduces tension in the body. It also helps to release endorphins which can make you feel better both mentally and physically. This will encourage your body to stay calm which can help you to get a better night’s sleep.
Stretching Options for Those with Fibromyalgia
If you suffer from fibromyalgia, you’ll find there are a few simple yet extremely beneficial stretching options you can consider trying out.
Make Circular Motions with Your Joints
One simple stretching option for those with fibromyalgia is to make gentle circular motions with your joints. For instance, move your ankles around in circular motions and then counterclockwise ones. This will help to awaken your muscles and joints in the area but do so in a simple and pain-free way.
Do Calf Stretches
Calf stretches are very important as it helps to relieve tension in the Achilles tendon. To do a calf stretch, place your hands on a flat surface, ideally a wall. After doing so, press and bend one leg forward while keeping one leg back. Lean gently against the leg that is forward and then switch it with your other leg. You can continue this stretch for a few minutes.
Try Aerobic Stretching
Aerobic stretching can be very simple and helps to keep your heart healthy. There are a few different types of aerobic stretching you can consider:
Circular arm motions: stand straight and hold your hands out sideways. Then, move them in circular motions forward and then backward.
Jogging in place: you can stand in one place and start doing a gentle mini jog. This doesn’t have to be intense, just a few minutes of you slowly running in place.
Do Pool Exercises
Stretching in a pool can help you to move around more freely because the water doesn’t mix with gravity. This can make it feel as if you’re floating and give you more mobility. There are plenty of pool exercises to consider doing that are very easy to do. Some include:
Sidestepping: hold on to the pool’s wall and then take about 20 steps to one side while holding on to the wall. You can then reverse the direction.
Knee lift: hold on to the pool’s wall and carefully lift one knee up to your chest. Hold this position for about five seconds and then switch to the next leg.
Hip kicks: stand with your body sideways to the pool’s wall while holding on to it. Then, lift one leg up in the water as if you are kicking something and then switch to your other leg. Continue this motion with both legs for a few minutes.
Keep in mind though that if you feel any pain when doing stretches, stop immediately. This could not only worsen your fibromyalgia pain, but cause muscle strains and injuries. Fibromyalgia doesn’t have to overtake your life. By doing simple stretches, you can work to naturally relieve many of its symptoms. Better yet, most of them are very easy to do so everyone can try them out no matter what stage of fibromyalgia you might have. Because of this, stretching is ideal to implement into your lifestyle to help give you relief.
About Dr. Brent Wells
Dr. Wells is a chiropractor who founded Alaska-based Better Health Chiropractic & Physical Rehab. This practice offers numerous services to help those with everything from mild to severe pain and is designed to provide great care to those on the search for top Anchorage chiropractors in AK 99515.
Insomnia is a serious and often ignored problem, especially for people with chronic conditions like fibromyalgia.
I would like to suggest that we need to take this more seriously.
This is a long post. You may want to grab a cuppa and get comfortable! If you have fibromyalgia and brain fog is an issue, there is a handy (free) PDF document below for you to download!
The video: Insomnia and Fibromyalgia
Key facts about insomnia and fibromyalgia
A key problem for people with fibromyalgia and many other chronic illnesses
Debilitating and makes other already incapacitating symptoms worse
A recipe for a shorter, less fulfilled life
Pain inducing – even for those without chronic pain conditions
A money drain – in health care costs from those who suffer the side effects, in absenteeism from inability to work, in lost income, if you could place a value on a fully functioning human being able to participate fully in life then multiply that by the 10 million people estimated in the US alone (and 3-6% of the world’s population) it would be a massive number.
Sleep helps pretty much every symptom of fibromyalgia
Sleep improves our quality of life and our emotional state
We can improve sleep! It might be multi factorial and a doctor needs to help in many cases, but we can improve sleep.
Shall we take a look into the literature that supports my statements?
Does insomnia lead to death?
Laboratory animals subjected to extreme sleep deprivation can die relatively swiftly of unknown causes — exactly what goes wrong is not clear, but their body temperatures start to drop and then they suffer rapid and widespread physiological failure. 
Does insomnia cause pain?
“According to the majority of the studies, sleep deprivation produces hyperalgesic changes.” (That means yes!)
What side effects does insomnia cause? A summary based upon all of the research I have ever done and experienced after more than a decade living with it:
Anxiety and/or depression
Sleep as a treatment for pain
“More broadly, our findings highlight sleep as a novel therapeutic target for pain management within and outside the clinic, including circumstances where sleep is frequently short yet pain is abundant (e.g. the hospital setting).”
Why is sleep a novel (or innovative) treatment for pain??
So we have found that research supports insomnia as life threatening, costing money, leading to pain (and sleep is a treatment for pain) what is the insomnia problem specifically relating to fibromyalgia?
What is insomnia, exactly?
Trouble falling asleep
Difficulty staying asleep
Waking too early
Not achieving good quality sleep
What’s happening for people with fibromyalgia and sleep?
Dr Ginevra Liptan, MD, writes about sleep in her book The Fibro Manual (2016):
“Sleep studies show that Fibromyalgia subjects show abnormal ‘awake-type’ brain waves all night long, with reduced and interrupted deep sleep and frequent ‘mini-awakenings’ (Brandi 1994; Kooh 2003). This deep-sleep deprivation leads to pain, fatigue, and poor brain function (Lerma 2011; Moldofsky 2008; Harding 1998). Treatment focused on increasing deep sleep is the key to improving all these symptoms.”
In plain terms, people with Fibromyalgia don’t tend to reach stage four of the sleep cycle (the deep, restorative stage), and therefore, they suffer from chronic, deep sleep deprivation, which causes all sorts of issues with the body: pain, fatigue, fog, anxiety, etc.
Insomnia—along with poor sleep in general—is believed to make fibromyalgia symptoms more severe, which means treating your sleep problems may have the secondary effect of improving pain, fibro fog, and more.
Let’s just repeat that – treating sleep should help with pain, fatigue and fibro fog.
How have I experienced insomnia?
Every single night for more than a decade (including my entire twenties), despite researching and using a lot of sleep hygiene tips and natural sleep aids, having trouble falling asleep, not staying asleep for more than one hour at a time, spending time awake in the night too exhausted to get up but too sore to remain lying still and waking feeling more tired than I went to bed.
This was while on the only option the doctor every offered me – amitriptyline.
Finally in 2017 I began taking low dose naltrexone and it helped me to start sleeping in blocks of up to a few hours. This made such a difference on my quality of life. But I still struggle with insomnia every single day.
I can’t imagine how much more I could achieve if I could sleep well. Or what it might have been like if my doctors had been willing to work with me to help me achieve more sleep. Even utilizing low doses of medicines for a short amount of time to achieve some rest, like two prominent physicians who have fibromyalgia and treat patients with it suggest (Dr Teitelbaum From Fatigued to Fantastic and Dr Liptan The Fibro Manual – thank you so much to these two doctors who have done so much for our community).
I was miserable and missed out on the usual things one does in their twenties. I couldn’t do my OE, I could hardly make it through the day let alone travel long distances.
Now, with the amount of sleep I’ve been able to reclaim I am managing day to day, but I still experience severe costs. I cannot stay up late, it is difficult to manage my children myself, I cannot work and when I do work I can only manage part-time work (so a cost of 30,000-80,000 per year lost there). Add the costs of things I need to manage such as the low dose naltrexone prescription, doctors’ visits, supplements, physiotherapy, and the many, many things I have tried to help myself. Add in the impact on my quality of life of dealing with chronic pain all day every day. I don’t know what a pain free day might look like!
And there are people who are worse off than me.
What do other people with fibromyalgia and insomnia say?
“Fibromyalgia insomnia is a very real issue for me. I am currently breastfeeding a six month old. She wakes for one feed a night and resettles quickly back to sleep. It then takes me two to three hours to get myself back to sleep. I am exhausted. I have not had a good night sleep in years.” – Amanda
“Where do I start? It’s a vicious cycle in so many ways. If it’s not the pain keeping me up, it’s restless leg syndrome or another of the plethora of symptoms and comorbid disorders that come with fibro. Otherwise, it’s pure anxiety from having night terrors brought on by my medication and the trauma that landed me with fibro in the first instance. The more I get into a terrible sleeping pattern, the worse my pain and other symptoms get, the worse my mental health gets, the worse my relationships get because I just cannot function or am not physically able or awake to conduct a “normal” life. And of course all of these things contribute to not being able to sleep or sleep well. Which perpetuates the issue.
While I was at uni my insomnia was seriously affecting my studies but I got flat out told by several doctors that they refused all students sleeping meds because they were so highly abused. I cried in Drs appointments, I cried as I lay awake at night in pain, I cried when I was forced to ask for extensions on my coursework, I cried when I got sub-standard grades because I knew it wasn’t a reflection on my ability but my circumstance. It’s such an underestimated burden that so many are forced to “put up with” because “everyone’s stressed” or “everyone’s tired” for one reason or another. I wish it was taken as seriously as my pain, which has had all manner of meds thrown at it. I’m sure it hurts me just as much.” – Rebekah
So for them, and for me, I want to beg doctors to take the sleep problem much more seriously. I want to beg researchers to look into how we can fix this (ideally without long term drug use).
If you are suffering from insomnia and fibromyalgia what can you do?
Step four discusses using the breath as an energy source, “Pranayama can increase your fitness and energy levels – without getting out of bed!”
Step five is the actual yoga! Kuran provides a more active routine, a gentle restorative routine and discusses yoga Nidra.
“Like other forms of meditation, yoga Nidra helps release serotonin and decrease cortisol which lowers your stress response.” I adore yoga Nidra and it’s a vital part of my coping when I’m tired, especially when I have tiny babies and am not sleeping much at night – so I always enjoy learning more about it.
I loved the suggestion that even in a flare up we can do yoga. Practicing yoga doesn’t mean a big routine or even physical movement – Kuran points out that even visualizing yourself doing yoga poses can be useful. A breathing practice while lying in bed is sufficient. This makes yoga such a useful tool for those fighting chronic fatigue – its adaptability.
If you enact the action points suggested at the end of each step you will be a long way toward a holistic healing process.
I highly recommend this book and yoga if you struggle with chronic fatigue.
Get your reading on
Purchase your copy from Amazon here. (Affiliate link: Please note that if you make a purchase using my link, I will make a small commission at no extra cost to you).
If you love reading like me try Amazon Kindle Unlimited Membership – you can try your first month free and access unlimited reading or listening on any device! They now have magazines too! It’s also available for those of us who use Amazon.com.au *squee*.
If audio books are more your speed, as they are for me with three little ones, you know you can get a free trial of Audible on Amazon here. I’ve recently started reading a lot more audio books as the hands free option is far easier to access with the wee ones. You will get access to two audio books, plus two Audible Originals, and other cool membership options for 30 days. Cancel anytime if you don’t want the full subscription.
Copaiba essential oil is relatively new in the chronic pain relief discussion however has been widely used in traditional health practices since the 16th century.
What is copaiba essential oil?
The essential oil is distilled from a resin that comes from tapping the Copaiba tree.
What it does
It works in the endocannibinoid system- much like low dose naltrexone, cannabis and CBD oil. Copaiba is thought to directly effect receptors that deal in the nervous system with effects in inflammation, endocrine system, pain, cardiovascular system and more. The nervous system is a part we would like to positively influence in fibromyalgia.
I have found success with low dose naltrexone and write about that here. So when I found out that CBD oil can work synergistically with LDN, I put it on my mental wishlist.
Unfortunately CBD oil is classified the same as cannabis under the law in New Zealand. Meaning it will be a long time before I can try it. People with certain conditions can receive a prescription for it but if they do get one, the CBD oil is very expensive.
Topically is the most often recommended way to utilise essential oils. You can also diffuse or inhale. Some companies say you can ingest their oils if they are food grade. Do check with a qualified professional about this as some oils can be dangerous if ingested.
Also remember that essential oils are like super charged herbal teas – they are way more concentrated so a little goes a long way. Please check with a medical professional before using essential oils to ensure safety of their use and any potential drug interactions.
My experience with copaiba
It was suggested that I try either one drop sublingually (under the tongue) or a drop with some coconut oil topically where the pain occurs.
I found it difficult to administer the sublingual drop but found you can take a drop in water or juice.
On the first night, after being unable to get a drop under my tongue I wiped the dropper saw some oil in my finger and wiped that under my tongue. I did seem to be able to fall asleep faster than I had been.
The next day I tried a drop in coconut oil and placed it directly on my neck and shoulders – my trigger points had been playing up since a car accident a few weeks prior and those muscles became more tight and sore again. It really seemed to help. The effect was probably amplified as I lay down to do a 30 minute meditation too.
It became my go to for increased muscle pain and tightness in my shoulders and neck. It was especially useful as my trigger points were flared up due to a car accident and being unable to take a muscle relaxant while breastfeeding.
I am super excited for this addition to my pain plan!
Where to get your own to try?
Eden’s Garden is voted the number one non MLM essential oil company and has copaiba – not all companies do. You can get that here. (Affiliate link, I will receive a small commission if you purchase using this link at no extra cost to you).
I was so frustrated that they had woken the baby again that I yelled. I yelled so loudly I am sure the neighbour was sorry the baby was awake. My heart rate rose, my headache was exacerbated and I felt terrible. The boys didn’t mind because they were used to periodically top blowing. This was not mindful parenting.
And then it clicked for me.
I am a Fibromyalgia and Mindfulness Coach. I have learnt and teach others to utilise mindfulness and meditation in their fight against chronic pain, chronic fatigue, insomnia, anxiety and overwhelm. But what about utilising this knowledge in my daily life? What about using it to help not only myself but my kids?
I dug into the research. As I do.
I found this article, “Analyses showed that parents who reported more mindful parenting engaged in more positive and less negative parenting behavior, which was then linked to more positive behavior in their kids—meaning less anxiety, depression, and acting out.”
I have seen these pain relief apps and been curious for a while. The basis of science and the mind-body connection as a way to help treat chronic pain resonates strongly with me.
When I was offered the opportunity to review the Pathways Pain Relief App, I jumped! I am beginning a one year trial now in exchange for my honest review. I will keep you updated.
A bit about Pathways Pain Relief App:
It is designed for those of us with chronic pain – pain that has lasted more than three months, for which little helps. It provides an interactive journey through educational sessions in pain science, meditation and mindfulness and more.
What can Pathways help with?
According to their website any pain of a chronic nature (lasting three months). This includes fibromyalgia.
What can you expect from the app?
“We take patients on an interactive journey that starts with pain science education. Understanding that pain is much more complex (and interesting!) than a signal from damaged tissues, is an important step towards turning down the volume on pain.
We then move onto breaking any behaviours that could be keeping your pain system in high-alert. We also cover physical therapy, guided imagery, visulization and mindfulness exercises, hundreds of meditations and more.
Our sessions are audio based and between 2 and 20 minutes long.”
My take at the beginning of my journey with it
As a busy mama of three children five and under I don’t have the time for full on programme. I do have time for 2-20 minute audio sessions to be completed on my own schedule. In addition there really is nothing to lose, this is all natural and is bound to have relaxation benefits if nothing else. And we can all benefit from relaxing more.
The first thing I went through was the collection of meditations, there is a great selection for pain, relaxation, sleep and more. So that is a great resource.
I am looking forward to reporting back on my progress.
Please note: I never make things look like a cure all – there is no such thing. This could be one part of your fibromyalgia puzzle.
If you want to download it and have a look at the free content before purchasing, you can find more information here.
Have you tried the Pathways app? Or one similar? I’d love to hear your experience.
One of the things the You vs Fibromyalgia free micro course will take you through is pain relief. Sign up to my newsletter and receive access to this and more free resources.
I am a big fan of coffee. Huge. If my gut could stand it, I would rival Lorelai and Rory. If you don’t get this reference, I feel for you. Please go to Netflix and remedy this with all the episodes ever of Gilmore Girls.
I thought I would share the coffee I have been preparing to get around tummy issues, in case you suffer too.
Affiliate notice: Some of my links are affiliate links, if you make a purchase using my link, I may make a commission at no extra cost to you.
For my birthday last year, my husband bought me this Nespresso machine. Why? Because it has a tiny footprint (read: doesn’t take up too much space in our tiny kitchen), I can operate it one-handed (while holding a fussy baby), and a mama with three children under five needs coffee.
The aeroccino machine is an amazing bonus. I previously had a Nespresso machine with the built in milk frother and it was nothing compared to this. In the mornings I can whip up some frothy milk for my son’s hot chocolate (it’s how we get milk into him) in a jiffy.
As I was playing with my new machine and coffee recipes, I noticed something awesome. Coconut oil makes the coffee more tummy friendly.
When my symptoms are higher, so is my tummy sensitivity. But now I don’t have to forego coffee when my tummy is mad, yay.
The below recipe has been my go to ever since.
While the coffee is pouring, I add 1/2-1 teaspoon of coconut oil, a healthy sprinkle of cinnamon and a teaspoon of maple syrup.
Stir it all up and froth the milk.
Pour the warm, creamy milk in and enjoy!
I have been so happy since I learnt I could tolerate lactose free milk. I just dislike all milk alternatives in my coffee. But you can easily have a go at using soy milk, almond milk etc. Here is a lovely home made almond milk coffee creamer recipe.
If you don’t have an aeroccino machine and Nespresso machine then you can make coffee (plunger, mocka pot, filter, instant in a cup – if you must). You can warm the milk in a saucepan on the oven to pre-boiling (as in, don’t let it boil) and then use a handheld frother or whisk.