Low dose naltrexone Archives - Melissa vs Fibromyalgia

It’s a Wrap 2019: What Were You Looking For? Plus grab your free You vs Fibromyalgia course invite

Posted on December 28, 2019March 14, 2020 by melissanreynolds

It is a wrap 2019! It is that time of year! Time to recap 2019 and look ahead for 2020. A new decade and a new year at the same time. It is full of promise.

Here I share the top posts of 2019 so that you can recap the key things we have been looking at in our journey fighting chronic pain and fatigue.

Ways to make money with fibromyalgia.

ways to make money online with fibromyalgia

In this post I shared genuine, micro business ideas. Not get rich quick ideas. These are ways that you can look to make an income from home on your schedule.

Post Exertion Wipe Out

This is a surprising one, this is a post from the very beginning when I was writing diary-like entries to share my journey while pregnant with no knowledge or resources available.

6 Practices for calming the central nervous system

In this post I share six very helpful ways to calm down after a stressful situation. I used these when a car drove into the back of us when me and my tiny baby were in the car!

My daily log, why I track fibromyalgia symptoms

In this post, I shared why and how I track my symptoms. It has been really helpful and I suggest finding a way that suits you to track patterns.

What works for me now 2019

In this post I updated the first post I wrote about what works for me – hint: it is mostly the same but I provide more detail. This is my protocol!

My low dose naltrexone one year experiment

My life has irrevocably changed thanks to this off-label, low-side effect medicine. I am so grateful for the past two years. This post shares the five ways it has helped me so much.

Inexpensive items I use to fight fibromyalgia

In this post I shared 9 inexpensive items I use to fight fibromyalgia. The first I use almost every day!

So there you have it, the key posts people were searching for this year. I hope they help you as you consider what you will tackle in 2020 for your journey toward thriving with chronic pain and fatigue.

Free live talks

In 2020 I have big plans to keep supporting you with this blog, the Facebook group, more live trainings and of course, adding to Yoga and Meditation for the Chronic Life virtual mindful movement studio.

Do join us for the free training on the Facebook page “My Top 5 Self-Care for 2020” on the 5th February.

For more information:

Hello friend, are you new here? I’m Melissa and I am on a mission to see that everyone receives resources and encouragement to thrive with fibromyalgia. Please come and join my free You vs Fibromyalgia micro course by signing up to my newsletter. You will receive access to a free resources page too! If you are curious about me and my journey you can have a search through the archives. Check out the What I Offer Page for all of the resources here.

Fibromyalgia Framework Series Part Six – Pain Management for Fibromyalgia and Chronic Pain

Posted on March 17, 2019October 12, 2020 by melissanreynolds

Welcome to part six of the Fibromyalgia Framework series – pain management for fibromyalgia and chronic pain fighters!

The fibromyalgia framework series has been presenting my (evolving) view of managing fibromyalgia. In 2018 some of my strongly held theories were proven true by experience and research.

We have discussed:

The Fibromyalgia Framework
Diagnosis, Misdiagnosis and Fibro Books
Tracking Your Progress
Sleep
Central Nervous System

PAIN MANAGEMENT FOR FIBROMYALGIA/CHRONIC PAIN

We could spend a long time going through pain management options in depth, but that is outside the scope of this series. I will give you a brief introduction to the multiple options and give you extra reading you can follow up on. As you will recall from my fibromyalgia puzzle, low dose naltrexone and physiotherapy are key pain management options for me. Yours might be entirely different.

LIFESTYLE FOCUSED PAIN MANAGEMENT

Sleep
Gentle movement
Rest
Seeing food as fuel
Observing your work/life balance

SPECIFIC FOR PAIN – WHAT I DO:

Affiliate notice: Please note that some of my links are affiliate links, if you make a purchase using this link I may make a small commission at no extra cost to you.

Heat pack. This is my first line of defense, I use it on my neck first thing, whenever I can during the day, in the evening and at bedtime.
Essential oils – lavender is my all time favourite for sleep, pain and relaxation.
Deep Heat, a non-medicated heat producing rub that eases muscle pain, especially when combined with a good massage.
Specific stretches – like those I share in the free Yoga for Fibromyalgia: Five Minutes a Day for Five Days Challenge.
Biofreeze – a cooling pain reliever, especially good for during warmer weather.
A hot bath is my best treat and the first thing I want when the pain increases.
I see the physiotherapist every three weeks and they do neck tractions and place acupuncture needles in trigger points in my neck and shoulders. This is the only thing that keeps the neck free and keeps the severe headaches, dizziness and nausea that accompanies the severe neck pain away.
A Theracane trigger point massager for self-trigger point release. You can use your fingers, but mine get too sore for this now, you do have to push rather hard.
Magnesium oil on my back and shoulders at bedtime.
Low dose naltrexone. Over a period of 12 months, it has decreased my neck pain levels more than anything ever has. It is not a miracle drug – if I don’t take it, the fatigue skyrockets, and if I overdo it, my neck pain increases. It is not a standalone treatment. But I am super thankful for it!
It helps me get to sleep where nothing else has ever worked. I do have to combine it with a heap of sleep hygiene routines, but it’s the base of the plan. In addition to helping me sleep (and thereby, reducing pain), it reduced the wider spread pain and near constant headaches.
MSM (Methylsulfonylmethane) for muscle and joint pain. It helps with the pain in my index fingers as well as a little difference in my neck.
Slow release, high dose ibuprofen for period pain, for about four days – it’s pretty severe.
Ibuprofen or paracetamol (Acetaminophen) for headaches or low level pain that breaks through.
A muscle relaxant for spasms in the neck or back – the frequency of these has decreased since I began LDN.

OTHER PAIN RELIEF OPTIONS:

TENS machine
Foam roller
Essential oils
- Lavender
- Chamomile
- Peppermint
Herbs
- Thyme
- Devil’s Claw
- Jamaican Dogwood
- Cayenne
- White Willow Bark
- Corydalis
Supplements
- Curcumin – specifically the Curamin blend.
- MSM
- Malic acid
- Magnesium
CBD oil

For medicinal pain relief, please discuss these options with your doctor and do your own research. Do always check for interactions between herbs/supplements and medicines that you are on.

LOW DOSE NALTREXONE

I haven’t been quiet about the benefits of low dose naltrexone (LDN). Since beginning it in 2017 I have experienced the best improvement of any single thing I have ever tried. I believe it is all down to sleeping better. The offshoots of this have been many. I have decreased pain levels, increased stamina, decreased fatigue, dramatically improved quality of life.

Find my Low Dose Naltrexone One Year Experiment post here. It includes a full write up of how it is changing my life with some links to further information.

For an overview of LDN see this website.

Low Dose Naltrexone (LDN) for Fibromyalgia Survey

Posted on October 18, 2018 by melissanreynolds

Since I have written up my one year experiment conclusion about low dose naltrexone (LDN) and Fibromyalgia, I have developed a bit of an itch to share my knowledge. I want others with chronic pain, chronic fatigue, Fibromyalgia to hear about this potential treatment option.

To this end, I am creating an eBook about LDN for Fibromyalgia.

I believe that patient-evidence (this term, which I love, was coined by Julia Schopick in her book Honest Medicine) is very important – that’s your voice, not the researcher’s voice (though, I will include research too).

If you are on LDN could you please take some time to fill in this survey for me? Please do send it on to anyone you know taking LDN for Fibromyalgia. It is my hope that we receive a wide number of audience responses to really show the breadth of experience with this medicine.

For my previous posts on Low Dose Naltrexone see:

Low Dose Naltrexone: An Experiment

Low Dose Naltrexone: Update 16 Weeks

Low Dose Naltrexone (LDN), Fibromyalgia & Me

My Low Dose Naltrexone (LDN) for Fibromyalgia One Year Experiment

I also reference LDN in both of my books, more so in the Melissa vs Fibromyalgia: My Journey Fighting Chronic Pain, Chronic Fatigue and Insomnia book – because it is a big part of why I was able to write this book.

Affiliate note: Please note that the link to my book is an affiliate link, if you make a purchase I will make a small commission at no extra cost to you.

If you have any questions, please do use the contact page and send me an email. Or come along and join the Melissa (you) vs Fibromyalgia Facebook page and ask me there.

Here is the survey link.

For more information and to stay up to date:

My Top Three Treatments to Fight Fibromyalgia

Posted on August 16, 2018February 22, 2020 by melissanreynolds

There are a lot of treatment options for fibromyalgia, but no sure fire fixes. So what are my top three treatments to fight fibroyalgia? Let’s delve in!

If you’ve been fighting fibromyalgia for any amount of time, you likely know there’s a multitude of therapies to try and that there’s rarely one magic bullet.

Fibromyalgia is an illness of unknown origin or cure and there are debates as to whether it will eventually be classed as autoimmune and/or progressive.

3-6% of the world’s population is has a vested interest in finding a cure. Until then we can only try to wade through the treatment options to try.

My posts about other treatment options

Essential Oils for Pain Relief and a Pain Cream I am Loving

What Works for me: 9 Things to Fight Fibromyalgia

Amitriptyline – Off and On Again
MSM Supplement: A Review

Today I’m sharing my top three treatments to fight Fibromyalgia- as a person who’s been fighting it for more than a decade, who’s been researching for several years and who wrote a book about all I do to thrive despite this illness.

affiliate notice: Some of my links are affiliate links, if you make a purchase using one of these links I will make a small commission at no extra cost to you. Every bit helps me provide these resources.

1. Low Dose Naltrexone (LDN)

This was something I found back in 2015 and followed the research for some time before I asked my doctor to try it. As I documented in the posts linked below, I began in April 2017. It took nine months for effect and now I can’t be without it.LDN, Fibromyalgia and Me

My One Year Low Dose Naltrexone for Fibromyalgia Experiment

It is not a magic fix for me but the results are astounding. You see, for more than 10 years I hadn’t slept well (read: in one hour blocks with great difficulty, every night was a fight) and the LDN actually helped me to sleep in two, three or four hour blocks. This is miraculous for me and I believe the sleep is what helped the rest. Read the above posts for the full experiment and outcome. What I love most about this medicine is that it is not a typical medicine and does not have any of the nasty side effects that most medicines prescribed for Fibromyalgia have. The worst I experienced was vivid dreams when I was titrating up to find my ideal dose. It essentially tricks the body into producing more endorphins, there is research theorizing that people with Fibromyalgia suffer from endocannabinoid deficiency. I believe it took nine months for me to see effect because my body was slowly healing from a deep sleep deprivation behind the scenes. This leads me to believe that LDN may be the only way to address an insufficiency that currently has no other satisfactory treatment option. I certainly prefer it to pain killers that have many negative effects and few positive ones.

2. Heat

If I had to choose one heat treatment, it’d be my heat pack. I use it first thing in the morning to get going, a couple of times during the day, in the evening and when I get into bed. It’s my go-to treatment. I use it mostly for my neck, but I also use it for the symphysis pubis disorder I experience in pregnancy. I also use:

This electric heating pad is on my wishlist! To complement my trusty heat pack.
Hot baths
Hot showers
Deep heat rub

Heat is one of my top five listed natural treatment options.

3. Yoga/Meditation

Meditation is part of yoga, so it may be cheating to name both, if you really want one it’d be a hard call, but yoga would win and only because LDN helps me to sleep at night.

Yoga is a multi-use tool. I adore the ability to mold it to what I need: one pertinent stretch or pose (cat and cow all the time), a few poses to hit one issue (cat and cow, forward bend and eagle for the back) or a full flowing sequence (sun salutations). It’s stretching, strengthening and calming for the central nervous system. Meditation has been a lifesaver since I realised I could experience deep rest to help counteract the lack of sleep. The effects have been profound and I share that in my post about meditation. I am so passionate about it that I incorporate mindfulness and meditation into my coaching programmes and offer one off sessions to teach meditation.

Come and join the free Yoga for Chronic Pain and Fatigue challenge here.

So here are my top three plus ways to fight Fibromyalgia

Low Dose Naltrexone
Heat
1. Heatpack
2. Electric blanket
3. Hot bath
4. Hot shower
5. Deep Heat rub
Yoga/Meditation

What are yours?

Do you enjoy this work? Want to help me ensure people with fibromyalgia receive the tools, encouragement and hope that they deserve? When you join the team to support my work in the pay what you can (starting at just $5 per month) Melissa vs Fibromyalgia membership you will immediately access an exclusive members library of resources and tools.

I’d like to support

My Low Dose Naltrexone (LDN) for Fibromyalgia One Year Experiment

Posted on April 19, 2018December 22, 2019 by melissanreynolds

It’s been a year since my giant experiment with low dose naltrexone (LDN) for fibromyalgia and chronic pain/chronic fatigue/insomnia. What a year it has been. Spoiler: It has been life changing!

See my post LDN, Fibromyalgia and Me for my last update. Also see Low Dose Naltrexone: An Experiment my first post introducing the experiment.

Affiliate notice: Please note that some of my links may be affiliate links. If you make a purchase, I may make a small commission at no extra cost to you.

How Low Dose Naltrexone works in a nutshell

It works in the endocannabinoid system – it temporarily blocks the receptors encouraging the body to make more endorphins. There’s research and explanations in my introductory post here and in the chapter about LDN in my book Melissa vs Fibromyalgia. I also created a printable of the LDN chapter from my book with research list so that you can do some research and take it to your doctor in my Etsy shop here.

What I love most about this medicine is that it is not a typical medicine and does not have any of the nasty side effects that most medicines prescribed for Fibromyalgia have. The worst I experienced was vivid dreams when I was titrating up to find my ideal dose. It essentially tricks the body into producing more endorphins, there is research theorizing that people with Fibromyalgia suffer from endocannabinoid deficiency. I believe it took nine months for me to see effect because my body was slowly healing from a deep sleep deprivation behind the scenes. This leads me to believe that LDN may be the only way to address an insufficiency that currently has no other satisfactory treatment option. I certainly prefer it to pain killers that have many negative effects and few positive ones.

There is also plenty of research and patient evidence available – groups on Facebook about LDN and the LDN research trust have a wealth of knowledge.

So here are the five benefits I have noted from LDN:

Benefit One Sleep

What it’s helped me with – first and foremost is sleep. For the ten years or so prior to LDN I had not slept in more than one hour blocks, that’s rarely completing a whole sleep cycle, therefore my body was in chronic deep sleep deprivation. Since LDN, I can sleep in two, three, four or even five hour blocks! I am so grateful for this, I can’t even tell you. I believe this is what has created the other benefits.

Please do note that I still have to take amitriptyline to get to sleep and enact my sleep hygiene list daily.

Benefit Two Pain

Since about nine months into treatment I have noticed a reduction in neck pain. Neck pain has been a 24/7 issue for over 10 years. In 2017, while starting LDN, I learnt that my neck issue is actually myofascial pain syndrome. After throwing the severe, recurring “muscle knots” (trigger points) into the fibro basket, I finally had an answer. The physiotherapist has been helping me to work on these trigger points through intramuscular needling (gently inserting a tiny needle into the trigger point and letting it relax a little) and neck mobilisations. This and the sleep (potentially reducing the fibromyalgia worsening the issue) has helped. My pain levels were 6-8/10 with severe headaches (with dizziness and nausea) daily back in 2010 before I started this journey. Just prior to LDN they were approximately 4-6/10 with occasional severe headaches. In early 2018, after one year on LDN, the average is 3-4/10 with the occasional spike to 5/6 with a bad headache and it’s usually when I’ve overdone it.

I wrote the LDN mini eBook with the research summary, my experience, notes on pregnancy with a handy list of research you can take to your doctor if you’re considering trying low dose naltrexone.

Benefit Three Emotional

If you haven’t lived with pain that interrupts sleep, interferes with daily life all day, every day for over a decade or been unable to sleep for more than an hour at a time for about the same length of time – it’ll be hard to convey the depth of impact on my emotional well-being.

Not fighting to sleep at 3am, not swapping pillows, getting my heat pack, applying pain cream and basically not sleeping due to unrelenting pain is huge for me.

My quality if life is so much better. I never let myself lose hope, but it was dwindling. This was a necessary win.

Benefit Four Stamina

Slowly my stamina increased. Activities that used to wipe me out can be tolerated for longer. I can exercise slightly more. I can do slightly more.

Having had a baby with reflux, I feel I coped exceptionally well and that is down to LDN. The demands on a mama of two is much higher than a mama with one! It’s been a busy year.

Benefit Five Fatigue

Fatigue is the second of my two worst symptoms (neck pain being the first). Yes, that’s “is” not “was”. It’s improved but I still have a limited energy envelope. I can get through the day on a 15 minute meditation and a brief sit down with the heat pack. I still can’t physically stay up past 9pm and that’s a fair trade off to me.

A Note on Pregnancy

I did some research around the use of LDN in pregnancy for my book and found a fertility doctor who has been using it for years and it’s had benefits for mama and baby.

There isn’t a lot of literature around medicine use in pregnancy, but I took what I had and presented my choice to stay on it to my doctor. We decided for my context it was worth continuing. But that is individual and you need to take the research to your doctor if you are considering taking it during pregnancy – know your stuff in case your doctor doesn’t, they’ll hopefully appreciate the information.

Conclusion

LDN is not a miracle medicine nor standalone treatment option for me, but it is changing my life and I’m so thankful.

2017 – Melissa vs Fibromyalgia in Review

Posted on December 21, 2017 by melissanreynolds

What a year! My second baby has been in this first year, learning to roll, crawl and, now, trying to walk. My first has been in this third year, learning and growing so fast.

I’m in a period of healing, that phase where you feel like things could get better. The low dose naltrexone (LDN) seems to be helping with stamina, pain and fatigue. I’m not sure how far it will go, but I am grateful for a renewed sense of hope.

Despite extended sleep deprivation due to the baby with reflux, I have coped excessively well. I’ve also had a separate health issue that drained on me for more than two months and I managed to cope and keep going forward despite it.

New Medicine

I began low dose naltrexone in April. After nine months and many dose varieties, I am holding at 4mg with improved stamina, slightly reduced fatigue and a slight difference in pain levels. I look forward to further improvements.

Supplements

MSM supplement has been a useful addition to my arsenal. It is supposed to help with muscle, tendon and ligament pain in addition to healing the gut.

Magnesium oil right before bed around my neck and shoulders. I’ve taken magnesium for a long time, and it’s nice to not have to take it in tablet form.

Moringa powder provides 18/20 amino acids in addition to being a good source of iron and other nutrients. I am not very good at remembering to take it as it’s best taken with juice or in a smoothie – I dislike juice and I usually share smoothies within my three year old.

Exercise

After dealing with symphisis pubis disorder for several months after having Wyatt last December, I am pleased to be walking 20-30 minutes a few times a week (it’s a time thing with two small children, I’d love to do it more). I’m also back to my sun salutation sequence whenever I can.

Work

I’m looking at going back to work and am trying to find something that won’t demand too many hours, too much energy. I am looking forward to it.

A life goal

I accomplished a life goal when I published my book Fibro Mama: Pregnancy and Fibromyalgia. Since I was a young teenager, I have loved writing. When I wrote my life goal list up in my early twenties (doesn’t everyone do this, write it up physically?), publishing a book was on there. As I researched and shared my journey with pregnancy for the past four years, my mission became to help even one person not feel so alone in this vulnerable time. Now that I’ve felt some concrete results of the past several of real work on my health – I’ve compiled a large list of things I do to manage my illness, and I will be writing about this in a book due out early next year, Melissa vs Fibromyalgia: My Journey Fighting Chronic Pain, Chronic Fatigue & Insomnia

It’s very exciting, I’m so glad to be able to share this journey with you.

I hope you have a restful and lovely Christmas holiday period and a happy New Year.

To stay up to date and receive access to my free resource page – sign up here.

Some of my links are affiliate links, I receive compensation at no extra cost to you if you purchase using these links. I never promote anything I don’t 100% support myself.

Low Dose Naltrexone (LDN), Fibromyalgia & Me

Posted on November 12, 2017 by melissanreynolds

Low dose naltrexone came on my radar last year and after consuming all of the research and anecdotal evidence about its impact on Fibromyalgia, I earmarked it for my major experiment post-baby (I had baby W last December).

Donna Gregory Birch, a well-known Fibromyalgia writer who explains how LDN works: “in low doses (typically 1-4.5 mg), naltrexone enhances the body’s immune system by boosting the production of endorphins, which in turn promotes healing and lessens inflammation.

Research has been showing promising results. Dr Jared Younger started with a tiny study and found positive results, approximately 65% of patients experienced clinically significant results. He’s doing a bigger study this year.

As a member of an active group about what works for Fibromyalgia and two groups about low dose naltrexone on Facebook, I have seen many testimonies from people with Fibromyalgia experiencing changes due to LDN ranging from mildly beneficial to miraculous. There are also those for whom it does not work or they do not try it for long enough – this is not a quick fix for most.

Further information on how LDN works is well explained in this article, which includes many links to research.

If I could experience a 30% (this is considered clinically significant and therefore as success) decrease in pain and fatigue, my life would change! I could be a mama, a wife, do my work and have some form of a life outside that and not pay with such significant levels of pain, fatigue and other side effects of the Fibromyalgia.

I can only share research and what works or doesn’t work for me. We are all unique and react differently. If you’re interested in LDN then read the research/information and then discuss it with your doctor.

My updates

Low Dose Naltrexone: An Experiment
Low Dose Naltrexone: Update 16 Weeks

Now

I have been reluctant to post this update, I was waiting for something solidly quantifiable but in lieu of that I’ll give you my anecdotal evidence that it is working.

Around 8 months ago I began taking low dose naltrexone and have slowly titrated up to a dose of 4 milligrams. It took me about six months to get to 4 milligrams as previously my body couldn’t cope with that level, I experienced vivid dreams and flare ups of ulcers and cold sores each time I tried to titrate up too fast. I may try 4.5 milligrams later on.

For now the effects that I have noticed are:

slightly more stamina
slightly better sleep
slightly less fatigue and
slightly less neck pain – from an average (which changes over a day as well as the week) of 4-7/10 down to about 3-5/10

Anyone who has been following my blog for a while would know that my neck is the area I struggle with the most. With that a little more in check, the fatigue is a close second.

I don’t think my functionality has increased however the quality of my life while performing all that I do has increased. When I do overdo it or have a bad night’s sleep the pain will increase. The heatpack is still my best friend, the computer is still my neck’s nemesis and I can’t hold it for too long in one position – but it’s better than before.

I still have hope that as we edge toward the one year anniversary that I’ll experience more miraculous effects. For now it is definitely worth the $30 a month I pay for the perscription.

This combined with meditation and gentle exercise, paying attention to what I eat and trying to limit stress have been the best things I could do. I hope that when I start working I will be able to maintain half-time hours and not return too much closer to the previous pain levels.

I’d love to hear your experiences with LDN. I’ll write an update when we get closer to a year.

For more information

Low Dose Naltrexone is one of many ways that I manage pain. This printable contains the chapter of the same name from my book along with some templates for making your own plans. I created this series for those of us who are not able to consume an entire book right now, or who want to work on one thing at a time.

MSM Supplement for Fibromyalgia: A Review

Posted on September 16, 2017March 26, 2020 by melissanreynolds

MSM (methylsulfonylmethane) is a useful supplement to consider for fibromyalgia, chronic pain, chronic fatigue. It has a wealth of support behind it and I have personally found benefit from it. I share all of this below.

Some of the links are affiliate links, I may make a small commission at no extra cost to you. I only recommend what I believe in.

MSM is an organic sulfur-containing compound that is meant to help with pain in the tendons, ligaments and muscles. It is also said to help with energy, post-exertion malaise, and for cellular energy (to support mitochondria). In New Zealand it is one of those nutrients the soil is now depleted of.

The benefits of MSM

Dr Axe outlines six benefits of taking MSM, including joint pain, digestive problems and muscle pain and spasms (a biggie for me):

“Research suggests that MSM can act like a natural analgesic, helping prevent and treat muscle aches and pains, throbbing and swelling while improving range of motion and mobility.”

The article goes on to state that, “MSM also restores the flexibility and permeability of cell walls within muscles, which means nutrients can pass through the tissues more easily, facilitating repair work faster and removing lactic acid, which causes that “burning feeling” following exercise.”

This is great for people with Fibromyalgia, who often feel greater post-exercise pain – I often get severe pain in my lower body for up to three days post exercise, if I have overdone it.

An article on the Shawn Stevenson Health Show website includes detoxification and increasing energy as other benefits of MSM:

“Digestion is the biggest energy requirement of the body (Approximately 70-80% of your energy is spent on digestion each day). MSM increases the absorption of nutrients so that the energy expenditure on digestion is vastly reduced.”

This is good news for a person like me who doesn’t tend to take the nutrients from food efficiently, using iron as an example, despite a healthy level of iron rich foods I cannot keep my iron levels up without regular injections. Also, any efficiency in energy is a bonus for people with limited energy levels.

MSM and mitochondria

This article on Prohealth.com states a couple of extra benefits:

“Preventing and reducing symptoms of autoimmune diseases by supporting reduction of chronic inflammation.” and supporting “Your body’s electron transport system, as part of iron/sulfur proteins in mitochondria, the energy factories of your cells.”

This is important as there is a lot of noise about supporting our mitochondria. Ari Whitten believes mitochondria are the key to overcoming chronic fatigue. He has a fantastic free masterclass that I highly recommend signing up for. It is a little information-dense so take your time with it. While COq10, D-ribose, PQQ and many other energy enhancing supplements are usually recommended (and are not cheap) – MSM is often left out.

Below I share how MSM helps me.

MSM and me

I began taking MSM (this is what I used) in July 2017 as this was when I began to suspect the pain in my neck was actually Myofacial Pain Syndrome – painful, severe trigger points that recur no matter the treatment. Trigger points are usually considered separate to Fibromyalgia but there are some doctors who believe them to be part of it (like Dr Liptan).

See my giant introductory post about Myofascial Pain Syndrome here.

After a Google search for potential side effects, potential benefits and checking any interactions with my current medicines (amitriptyline and low dose naltrexone) – I decided to try it.

It took about six weeks to build up in my system. At this point I noticed a slight reduction in pain, perhaps one pain point on average in my neck, which is actually a big deal for me. This helped reduce the number of severe headaches and I didn’t have any other pain relief for several weeks.

I began with tablets, they were big! I had to take one tablet two times a day, and it was difficult swallowing them. So when I finished the bottle, I ordered a powdered version. During the wait the symptoms returned. It took another few weeks to feel the benefit of the powder. It is much less of a burden to take the powder, half a teaspoon dissolved in a cup of water (which I skull) is really easy for me.

A minor medical event, separate to the Fibromyalgia occurred in August which set me back. I am going to keep the low dose naltrexone and MSM going for the year’s experiment and I have just added moringa powder (which I will report on later) – moringa is a good source of protein and amino acids, as well as iron and magnesium which is said to work well with the MSM.

2019 Update

After finding the mitochondria research trail again as my third baby began nursing less and less (making me feel more comfortable adding in some natural supplements) I began taking MSM again. It makes sense to me to help support the many mitochondria with my energy crisis. I will let you know how it goes after several weeks.

I’d love to hear your experience with MSM, please share in the comments.

Grab your MSM powder here (do always check for interactions with your medicines and supplements and check with your doctor if you are pregnant or nursing):

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4 Lessons I have Learnt While Living With Fibromyalgia

Posted on July 23, 2017 by melissanreynolds

After more than a decade fighting Fibromyalgia, I couldn’t imagine that the last two years could bring as much learning as it has.

I have stepped up the fight. I am trying Low-Dose Naltrexone and an MSM supplement at the moment. I am using yoga as therapy (targeted poses to keep my body moving). I am devouring research and books and articles about fighting the symptoms and the illness. And as I have gone through the research, I couldn’t help formulating a list of lessons.

Lesson one: Don’t be surprised, or discouraged if one avenue of potential healing doesn’t produce results.

A large school of thought in the cause of Fibromyalgia, is that it is caused by underlying issues that need to be resolved. For example thyroid issues, Candida, viral infections, allergies etc.

Many Fibromyalgia bloggers/writers/doctors blame Candida overload for Fibromyalgia problems. They recommend cutting dairy and sugar and gluten and taking varying supplements. There are entire articles devoted to clearing Candida. Well, I have zero Candida in my system at the moment and my neck has been worse and the fatigue has been higher.

I also have “optimal” results in the usual blood tests (thyroid, iron, antibodies etc). All worth checking and noting that “normal” does not always mean “optimal”.

I don’t give up, I store this in my “don’t worry about it” column and move on.

Lesson two: Fibromyalgia is a massive undertaking of trial and error, which feeds into lesson three: you have to do the work yourself.

I have had precisely one doctor who is willing to listen to me, work with me and trial things with me in the 15 plus years I’ve been dealing with chronic pain. That Dr still doesn’t have a lot of avenues to offer me, but he is willing to let me trial things I research.

I turned up with research papers prepared to be persuasive about a trial of Low -Dose Naltrexone, he agreed immediately.

I have tried a multitude of things to fight Fibromyalgia. Physical therapies like osteopathy, chiropractic, massage and physiotherapy (neck traction and acupuncture needles in trigger points help me). Supplements like MSM, magnesium, multivitamins, iron, olive leaf extract, probiotics and a truckload more I can’t remember! (A helpful note here, using powders dissolved in water seems to absorb better than tablets for me).

Yoga, walking, stretching and swimming are helpful exercises that I enjoy. I have to modify for my neck and knees though. There’s also a clearly defined line that I must keep to, 25 mins of walking is enough, less causes pain in the lower body and more causes pain also!

Avoiding allergenic foods specific to me (bananas and dairy are occasional foods, corn and wheat are once per day foods according to my test). This was the one good thing that came out of hundreds of dollars spent on a naturopath. I trialed gluten-free eating a couple of years ago and found no effects while off or adding them back in. However, I do prefer non-glutenous grains like quinoa and millet as they have extra nutrients too.

There is a mind-body component. Meditation simultaneously helps me rest (I cannot nap) and teaches my central nervous system to calm down. Gratitude practice keeps me looking for the silver lining. Prayer helps sustain my hope (and hope is crucial, without that I’m done for). Colouring is calming and enjoyable. Reading is my favourite hobby and doesn’t require physical activity. You need hobbies and you have a right to enjoy these even with a limited energy envelope.

Almost every time I read a book written by a Fibromyalgia doctor, I have found that I have made my way to an approximation of their protocols myself.

This is all by time consuming, expensive, roller coaster of emotions, trial and error.

Lesson four is that you can do All The Things and still have Fibromyalgia.

Clearly I do a lot to manage my health as best as I can. I have learnt a lot and do a lot, daily. But I still struggle everyday with these symptoms. Mostly my neck and sleep. However, until a doctor helps me with my neck, my quality of life and my sleep will not improve. (Ps. My Low Dose Naltrexone (LDN) for Fibromyalgia One Year Experiment has helped with this a little!)

I have come a long way since I was struggling through the day, so sore I wondered how my body was functioning, so exhausted I was nauseas most of the day and only managed by holding on to the glimmer of hope that getting enough work experience would mean I could earn enough per hour to reduce my work hours. But there is more to go until I am healed and I fight on.

Hopefully these lessons and everything I write about in my blog, book and courses helps you.

This blog post is featured as a chapter in my book, this is everything I have researched and do to fight Fibromyalgia

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