Over the years it is true to say that on the days I have felt my worst I am invariably greeted with the words by somebody or another “you look really well”.
I have always kind of smiled at this, even joked about how crap I feel yet people think I look amazing. However, this week it really got to me and set me thinking about the realities of living with what is effectively an invisible illness. I remember once a doctor saying to me that I would probably be better off having a leg missing at least then people would know I was suffering – I am of course not suggesting that we all go out to have legs amputated but I kind of see his point.
I am guessing that for many of us suffering from Fibromyalgia, we look pretty normal, nothing really to distinguish us from the next person. Standing at the train station this morning, I am sure nobody looked at me and thought “Poor girl, look at the pain she is in”. However, in reality, my current flare-up is so bad I could cry.
I work, I socialize, I run home and I exercise (albeit slowly and gently with yoga), hey maybe I am luckier than most but the reality is the effects of Fibromyalgia are never far away. Sitting chatting yesterday, without thinking I tapped the biro onto my thigh and there it was, the familiar painful nudge reminding me of Fibros presence. On the outside looking in, nobody noticed, and had I have yelped out or grimaced who would have believed that a tap from a pen could evoke such a painful response. At best, I may have been labeled a wimp, at worst a hypochondriac.
In the early days before my diagnosis, my doctor had given the suggestion that I was maybe imagining it and would investigate this further. She concluded that I must have had some mental stress that could manifest as “imaginary pain”.
I knew that my pain and fatigue were very real but after being written off so many times, even I began to wonder.
I can imagine that for friends and family, it is as equally confusing when their husband, wife, mother, father, son, or daughter are tired and lethargic all the time, they are in constant pain, and yet there is nothing to show for it and they are tested by the doctors only for the tests to come back normal. What are they to think? It doesn’t take a genius to figure out the frustrations and conflicting emotions on both sides.
Due to the nature of our condition, we are often left feeling lonely and vulnerable. Unless we have a very sympathetic doctor, then we may feel that we have no place to turn, nobody who can fully understand how it feels to look Warrior and yet feel wretched. Nobody can understand, no matter how well-intentioned or how much a person loves you, they will never grasp the reality of Fibromyalgia. That is why the Fibro community is so important.
So, the next time somebody tells you that you look great and so well, hold your head up and be proud.
Fibromyalgia is horrible and robs us of so much, but it can’t take our life or our will. We have to work hard to function as normally as we can and that takes strength and guts to get up every day and face the world in so much pain particularly knowing that nobody will probably even notice.
We love hearing stories about people who have gone into Fibromyalgia remission. So here at But You Look So Healthy, we have decided to seek out those people! Most doctors give little to no hope or guidance on how to feel better. Who better than to ask about feeling better than the experts themselves? No, not the doctors, but the people who have managed to figure it out themselves and live it!
Today we talk to Dawn from New York about her Fibromyalgia journey and how she stays healthy after living in pain for years.
DAWN: I had injured my back playing with my kids a few years prior, but never got a diagnosis on that until 2006 when a sedentary job caused everything to flare back up. I believe it was a cross between this injury that caused herniated discs and getting the flu that was truly brought on by fibromyalgia.
BYLSH: How long did it take for you to get diagnosed and what kind of doctor diagnosed you?
DAWN: I struggled with the pain and ended up on disability for over a year before seeing a pain management specialist. He was the only Dr, other than my chiropractor, who believed me and diagnosed me. I dealt with the pain and various medications over the years.
BYLSH: What was your rock bottom when you decided you needed to change in order to heal? What changes did you make in your life to feel better?
DAWN: In October 2019, I decided to try a keto lifestyle to lose weight. I was convinced that I would always be in pain. I can’t recall exactly in my weight loss journey when it happened, maybe a few months in, but I realized that I was no longer in pain! My inflammation was gone. I no longer needed my pain meds! I feel that by cutting out potatoes, rice, pasta, sugar, grains, and gluten, I was relieved of the inflammation, which I believe has put my fibromyalgia into remission.
BYLSH: Looking back in time is there anything you would have done differently to not get fibromyalgia?
DAWN: I am not sure of the causes of fibro, or if I could have avoided getting it, but I wholeheartedly believe that we can change our outcome with diet and exercise!
BYLSH: What do you want other fibro people to know they need to do in order to go into remission?
DAWN: I highly suggest changing your diet by ridding yourself of processed foods and eating meats, vegetables, eggs, and healthy fats.
BYLSH: For you, what is the number one thing to stay in remission, AKA your secret sauce or holy grail? It is the number one thing you have to do to stay in remission.
DAWN: I realize that we are all different in our journey but start by taking control of your diet and exercise! I will continue to eat a low-carb/keto lifestyle because this is what has worked for me! I hope that you, too, can find relief in your journey to better health!
Cryotherapy is a treatment that uses freezing or near-freezing temperatures to attain specific results, namely pain reduction. The most popular thing right now is whole-body cryotherapy (WBC). WBC involves standing in a chamber called a cryo-chamber for anywhere from two to five minutes. While you are standing in this chamber, the temperature is taken down to a range between negative 100 and negative 140 degrees. You are virtually naked while you stand in a cryotherapy chamber.
Usually, the facility where the cryotherapy is performed will give you a pair of clean, thick socks (a nice alpaca blend) to wear, as well as thick slippers and thick industrial-strength winter gloves. For women, they can either wear underwear and a bra or they can stand in there completely naked. It is highly encouraged for men to keep their underwear on while cryotherapy is performed. For men, it is not recommended to stand in the buff unless they want their “bits” to get a little bit extra chilly (frostbit). A nice furry, fluffy robe is provided for you so you can get from the dressing room to the cryotherapy chamber.
You step up into this cryo chamber that has a door on the front that hinges open and close. Once you’re inside the chamber, the operator will close the door tight and only your head will stick out of the top. It doesn’t matter if you’re short or tall, just about everybody fits in a cryotherapy chamber. There are little mini foam platforms that are placed on the bottom for you to stand on. This makes the height completely adjustable so almost everybody fits.
Once you are inside you will notice that it is a little bit chilly. Surprisingly, it’s a different kind of cold than what you think it would be. You’ll then be locked into the chamber and the doors closed so you can take off your robe and toss it over the side to the staff member who is monitoring the controls.
The temperature when you enter the cryotherapy chamber is usually around 32 degrees Fahrenheit. Depending on whether there was already someone in there prior to you, the temperature can be colder than that. So now that your robe is off, hold on tight because your three-minute journey is about to start. If you have any “bits” that you don’t feel like you want to have icicles grow from, I suggest holding on to them tight, because that is exactly what will happen if you don’t.
Now that you are officially ready to go, the cryotherapy practitioner will set the time and the temperature on the cryo–chamber. Generally, when you’re new to cryotherapy the operator will start you at a temperature around negative 120 degrees Fahrenheit. Once that is set, it triggers the nitrogen to release its gas that cools off the inside of the chamber. Cold, smoky steam will start billowing out of the top where your head sticks through and will make it hard to see. You can feel the cold air coming from the jets that are positioned in several different places throughout the inside of the chamber. After about a minute or so you can see icicles forming where your fine body hair “used to be” on your arm and other places of your body.
While cryotherapy is cold, it is not the kind of cold that you would think about not being able to tolerate. I live in the snow belt of Ohio and I have lived here my entire life, so I know cold. In the winter of 1996, we had five feet of snowfall in less than a week and the National Guard had to come to my hometown and dig us out. In the Cleveland area, we are used to having winters where, when the wind chill is factored in, it will easily be negative 40 degrees outside. Let me tell you, it is the most unbearable thing you could ever possibly imagine. It does not matter how layered up you are, or the quality of your “thermal underwear,” it’s dang cold and there’s no way to get around it.
I don’t know how the designers did it, but cryotherapy is different. There is absolutely no way in hell that you would ever catch me standing outside in the middle of January in the snow belt of Ohio butt naked for three minutes and be able to tolerate it. It doesn’t matter what lifetime, it’s not happening! Somehow the geniuses that came up with the cryotherapy chamber have made it just cold enough for you to be able to stand there butt naked and not pray for death. Don’t get me wrong, it’s miserable. It’s very, very miserable. I counted in my head the seconds until the nitrogen would be turned off and I could find some relief from the cold. It still wasn’t January snowbelt cold miserable.
Even while you’re standing there freezing off your cha-chas, you start to get a sense of invigoration and energy that you hadn’t had before. It is amazing the energy you feel from doing a whole-body cryotherapy session. The theory behind this and why this happens is because the air becomes so cold that in order to protect itself, your body concentrates all of its blood to your main internal organs, away from your extremities.
This affects both your brain and the pain receptors in your body. Your body starts releasing anti-inflammatory molecules and endorphins to protect itself from the extreme cold. Cryotherapy increases white blood cells, anti-inflammatory cytokines, and beta-endorphins. Once you are done with the cryotherapy and your body starts to return to normal temperature the blood that was protecting your major organs moves back to your extremities. Immunostimulation due to noradrenaline responds to cold which causes a reduction of pain through the alteration of nerve conduction. This causes oxygen-rich blood to be returned to the extremities, which in turn helps with decreasing pain and inflammation in your muscles and joints.
To have the best results for Fibromyalgia, it is suggested that you perform three to five consecutive whole-body cryotherapy sessions in a row. After that, it is suggested that you follow a maintenance schedule of two to three times a week to maintain the benefits.
Cryotherapy is being used for many different conditions. Some of them are Fibromyalgia and chronic pain, sprains, different types of arthritis, pain, and swelling after surgery, tendonitis, sports injuries, low back pain, broken bones, and more.
You may be wondering how effective cryotherapy is for Fibromyalgia. That is a very good question. According to one study, whole body cryotherapy worked for 83% of Fibromyalgia patients during the three weeks while they were undergoing treatment. Results may last for up to a week after the last treatment. Long-term effects were not measured in this particular study.
My personal experience with cryotherapy was that it wasn’t worth the monetary cost to continue. I spent hundreds of dollars and felt minimal relief that only lasted for an hour or so after my treatments. On the other hand, when I did localized cryotherapy on my neck where I have spinal stenosis, I had an incredible amount of relief. I also highly suggest a cryotherapy facial. It is so relaxing and amazing and refreshing. You walk away with a glow and tightness you could never imagine.
To see the full benefits of cryotherapy, it is suggested that you have continuous treatments. Unfortunately, the pain relief results aren’t permanent. On the other hand, when you are in the throws of pain and agony, cryotherapy could be the answer to alleviating some of your symptoms.
In past posts, I’ve written about feeling ill-equipped to handle the role of spouse, the (still ongoing) process of learning that I can’t fix everything, and just being there for my loved one. Those are all key components of becoming the best you can be as a partner, spouse, relative, or friend of a loved one who suffers from a chronic illness such as Fibromyalgia.
However, some days are just tough…
tough to watch your loved one suffer a Fibro flare
tough to watch your loved one have a good Fibro day but is sick with a cold, the flu, etc.
tough to watch your loved one deal with a separate health issue unrelated to Fibro (i.e. back and/or neck problems, migraines, etc.)
If my loved one has managed to avoid a Fibro flare by doing everything “just right” I feel it is a tragedy if she gets socked with another health issue that sours an otherwise good day. THOSE ARE THE DAYS THAT REALLY FRUSTRATE ME!!
This is a time to put worry and anxiety to bed. One thing I need to remember in these instances, and I encourage you to do so as well, is that worry is essentially pointless. I am a HUGE worrier, so this is something that I struggle with on a minute-to-minute basis.
Worry is trying to control the uncontrollable. Fibromyalgia, chronic pain, and other conditions that afflict our loved ones are often, if not always, out of our control. As caregivers and helpers, we need to only tackle the things within our control that can be beneficial for our loved ones.
What are some of the things that are in our control?
Cooking (meals that are conducive to our loved one’s dietary needs, not ours; that means using ingredients that will NOT cause a flair)
Reassuring and supporting
Sacrificing (putting many things second to our loved one)
We’re all human. I know that changing our way of thinking, our way of eating, our way of living life…for the benefit of someone else…is very difficult!
No matter how hard it seems, after all, some days are just tough, we have to remember that we’re called to love one another, and the well-being of our most special lovedone(s) should be a concern that rivals none other.
Cannabis for fibromyalgia patients can be life-changing. At least it was for me! As a neuroscientist diagnosed with fibromyalgia, I tried all the traditional treatments, but nothing worked and the side effects were awful. Cannabis and CBD are helpful for fibro patients because they treat some of the root causes of fibromyalgia instead of just covering up symptoms.
Fibromyalgia is characterized by widespread musculoskeletal pain accompanied by fatigue, sleep, memory, and mood issues. It is often diagnosed by pressing on tender points throughout the body that results in pain upon light touching. Fibromyalgia flares occur when symptoms rapidly increase in severity or number; these flares may last for days or weeks and are often dependent on stress levels or triggers like a poor diet.
Approximately 10 million patients in the United States have fibromyalgia, and 75-90% are women. While the cause of fibromyalgia is unknown, infections, physical or emotional trauma, and genetics appear to play a role in onset. Patients with lupus, osteoarthritis, and or rheumatoid arthritis are at higher risk of developing fibromyalgia.
In Canada, 30% of patients with fibromyalgia are on disability, whereas in the United States, the percentage is unclear because disability, as well as a fibromyalgia diagnosis, is harder for patients to obtain. In a survey conducted by the National Fibromyalgia Association in 2003, 99% of the respondents who were currently disabled because of fibromyalgia said that they would return to work immediately if they could find some relief for their pain.
Symptoms of fibromyalgia include muscle pain and tenderness, muscle spasms, joint pain, bone pain, neurological pain, pelvic pain, fatigue, sleep disturbances, headaches, anxiety or depression, gastrointestinal issues, and cognitive issues including memory problems.
Common treatments of fibromyalgia include anti-inflammatories such as Aleve (naproxen), Advil or Motrin (ibuprofen), aspirin, and meloxicam, pain relievers Tylenol (acetaminophen), morphine (MScontin), and Percocet (oxycodone), and anti-anxiety medications including Valium (diazepam), Klonopin (clonazepam), Ativan (lorazepam) and Xanax (alprazolam). Anti-depressants include selective serotonin reuptake inhibitors (SSRIs) like Prozac (fluoxetine) and Zoloft (sertraline), selective norepinephrine inhibitors (SNRIs) like Cymbalta (duloxetine) and Savella (milnacipran), and tricyclic antidepressants like amitriptyline are also used.
Anti-seizure drug Lyrica (pregabalin) is most well-known for fibromyalgia because of the constant commercials played in the United States; Neurontin (gabapentin) is another anticonvulsant used to treat fibromyalgia. Finally, alternative therapies such as acupuncture, myofascial therapy, massage therapy, yoga, meditation, and cognitive therapy are also used to treat fibromyalgia.
Cannabis helps fibromyalgia by reducing neuropathic pain, pelvic pain, and other forms of pain. It reduces spasms, headaches, inflammation, anxiety, and stress that may trigger or worsen flares. It can improve mood and depression that often comes with having a painful chronic disease with no cure. Finally, cannabis may improve serotonin or other neurotransmitter imbalances in fibromyalgia.
No genetic causes of fibromyalgia have been found yet, and a blood test for diagnosis was only recently developed and is not widely used or covered by most health insurance plans. It is possible that mutations in genes that regulate the endocannabinoid system could be involved in its development, but no study has looked at that.
There is limited clinical research on cannabis and fibromyalgia because of its Schedule 1 nature in the United States and limited funding on the medical benefits of cannabis. However, a survey by the National Pain Report found cannabis was more effective than standard treatments for fibromyalgia including Cymbalta, Lyrica, and Savella, and fibromyalgia patients prefer it. No research has suggested harm from using cannabis in fibromyalgia patients.
Patients are already using cannabis, partly due to tightening restrictions on opioid use in the United States. The National Fibromyalgia and Chronic Pain Association completed a survey on the impact on patients of changing hydrocodone from Schedule 3 to Schedule 2. The survey found 17% of fibromyalgia patients who were no longer able to fill their hydrocodone prescription shifted to medical marijuana, and 13% moved to alcohol to treat pain, a much less desirable outcome. Another study published in 2012 found 13% of fibromyalgia patients used cannabis, with 80% using smoked marijuana and 24% using prescription cannabinoids.
In a pilot study of nine patients, THC in doses of 2.5-15 mg per day for three months significantly reduced subjective pain in the four patients that completed the study. In a study of 40 patients with fibromyalgia, four weeks of 1 mg of nabilone, a synthetic THC-like drug that binds strongly to the CB1 receptor improved insomnia but has little impact on pain, mood, or quality of life.
Twenty-eight fibromyalgia patients using cannabis had significantly reduced pain and stiffness and increased feelings of well-being, relaxation, and sleepiness two hours after use in another study. Finally, a survey of fibromyalgia patients in Israel found 50% of patients stopped using all prescriptions medications for fibromyalgia when they began using cannabis, and there were significant improvements in all quality of life and symptom scores on the Revised Fibromyalgia Impact Questionnaire (FIQR).
It’s been 5 years since I was diagnosed with fibromyalgia and 12 years since I got my Ph.D. in Neuroscience in the Department of Molecular Psychiatry.
To be honest, I’ve never met another neuroscientist who has fibromyalgia. And maybe that’s why my approach to treating fibromyalgia is so different than most clinicians.
When it came to treating my fibromyalgia, I let the professionals take the reins at first. I went through the typical medications like opioids, Lyrica, muscle relaxers, antidepressants, and hormone pills.
When all I got was dependence on opioids, and side effects like weight gain, nausea, and more pain, the scientist in me said there has to be a better way.
As a neuroscientist, I understand the brain, how both emotional and physical pain is processed, how pharmaceutical drugs impact brain chemistry, and how disease harms it.
I also know how to research solutions to complex problems, compare weak versus strong evidence, test hypotheses, communicate my findings, and teach students.
Fibromyalgia is a complex disease that requires a personalized medicine approach and no two cases are the same. It’s a disease that is worsened by stress, and the mind-body connection must be respected.
I did my research. Part reading the clinical research, part talking to alternative medicine experts and caregivers, and part playing guinea pig on myself and other patients.
I have a unique protocol that uses cannabis, kratom, and magic mushrooms to rewire the brain and heal the emotional and physical pain underlying fibromyalgia.
I’m sharing my secret sauce to how I ditched all my pills, got out of my walker, back to work, got my executive MBA, and wrote multiple books, all when my fibromyalgia doctor told me my best case scenario was to accept my illness and collect disability checks.
10 million patients in the United States with fibromyalgia, 75-90% are women. While the cause of fibromyalgia is unknown, infections, physical or emotional trauma, and genetics appear to play a role in onset. Patients with lupus, osteoarthritis, and or rheumatoid arthritis are at higher risk of developing fibromyalgia. Symptoms of fibromyalgia include muscle pain and tenderness, muscle spasms, joint pain, bone pain, neurological pain, fatigue, sleep disturbances, headaches, anxiety or depression, gastrointestinal issues, and cognitive issues including issues with memory.
Common prescription or OTC treatments for fibromyalgia include anti-inflammatories and pain relievers, antidepressants, and anti-seizure drugs including gabapentin (Neurontin) and pregabalin (Lyrica), the first drug to be FDA approved for fibromyalgia. Massage, physical therapy, acupuncture, meditation, yoga, diet change from going gluten-free, and cognitive therapy have also provided relief for patients but are not widely adopted nor covered by health insurance.
In Canada, 30% of patients with fibromyalgia are on disability, whereas in the United States, the percentage is unclear because disability as a well as a fibromyalgia diagnosis is harder for patients to obtain. In a survey conducted by the National Fibromyalgia Association in 2003, 99 % of the respondents who were currently disabled because of fibromyalgia said that they would return to work immediately if they could find some relief for their pain.
There has been a lot of clinical research on cannabis for fibromyalgia in the last 10 years. We’ve transitioned from fibromyalgia being a medical condition linked to endocannabinoid deficiency based on Dr. Ethan Russo’s research, to anecdotal evidence that over 90% of fibromyalgia patients benefit from cannabis, to clear clinical trials showing evidence that cannabis works.
The holiday season is fast approaching. Traveling when able-bodied has its fair share of challenges but, if you suffer from complex regional pain syndrome (CRPS), it can seem like a passport to problems.
The Government recently announced new proposals for disabled flyers but the implications of these will not be known until early 2019. So, in this blog, we offer some useful tips on how to make traveling with CRPS less daunting now. Read on to find out more.
You might be planning on taking a holiday but unfortunately, CRPS will not be taking a break from you. The likelihood is, you will be in pain but, if you prepare and plan well in advance, the trip you are looking forward to should not turn into one you end up regretting.
First and foremost, ensure you pack your pain relief medication. If you are traveling abroad, you should not encounter any problems if you approach this in the right way.
Some medicines such as Tramadol, Morphine, and Oxycodone are referred to as controlled drugs and subject to stricter controls to prevent potential misuse.
For all prescription medication, but particularly for controlled drugs, ask your GP for a letter outlining why you need the medication, the daily dosage, and the amount you need to travel with. Keep this close to hand for inspection by sea or airport staff and officials and make sure it includes your full name – as it appears on your passport – address, date of birth, and dates of travel.
Check the requirements and regulations of the destination you are traveling to in case there are any restrictions. You can usually do this on the country’s Embassy website, which tends to be very informative and helpful. Keep your medication in your hand luggage but, if it is in fluid form, check with the airline or provider you are traveling with about whether 100ml restrictions apply and, if necessary, ask your pharmacist to dispense accordingly.
Inform your air or cruise line well in advance of your condition and any assistance you may require. Read the special requirements page on your travel provider’s website for more information about procedures.
You should be able to ask for and receive assistance from when you arrive at the airport through customs and security to your boarding gate. Once on board, you should expect help stowing cabin luggage in the overhead locker.
At your destination, you should be assisted off the plane, to the point where you leave the airport, including retrieving your luggage and any mobility equipment you may have. However, it is advisable never to presume this will happen but to double-check with the individual provider you have chosen to travel with.
Be aware – cabin pressure on an aircraft can exacerbate CRPS. Not everyone is affected and some only mildly, but others experience a significant increase in pain and swelling during a flight.
It may be helpful to carry an inflatable pillow to ease discomfort and perhaps a lightweight blanket or shawl, as planes are notoriously chilly.
Whatever mode of transport you are using on your journey, factor in time to take comfort breaks and to stretch your legs. If sitting for a long period of time, try to extend your arms, legs, and neck, and wriggle your ankles and wrists on a regular basis to encourage blood circulation.
Rest as often as you can. Even a five-minute cat nap can do wonders for positive mental health and well-being and stop you from becoming anxious about the travel time remaining.
The raft of new measures proposed by the Government will dramatically improve travel for the less-able bodied if given the go-ahead. They include limiting the time passengers must wait for help with boarding and disembarking and ensuring they get their own wheelchairs back quickly by creating priority storage for wheelchairs.
Ministers are also looking at whether airlines should be made to remove seats to allow wheelchairs in the cabin – a measure long campaigned for.
Having CRPS and having a great holiday are not mutually exclusive. Managing your trip as well as your condition will hopefully leave you with a sense of well-being as well as many happy memories.
Fibromyalgia is a chronic pain disorder that is difficult to diagnose and harder to treat. As a neuroscientist and health coach with fibromyalgia, Dr. Ross has combined modern science with ancient plant wisdom to not only stop the pain but also heal emotional and physical trauma from the disorder.
Approximately 10 million patients in the United States have fibromyalgia, and 75-90% are women. While the cause of fibromyalgia is unknown, infections, physical or emotional trauma, and genetics appear to play a role in onset. Patients with lupus, osteoarthritis, and or rheumatoid arthritis are at higher risk of developing fibromyalgia.
Cannabis helps fibromyalgia by reducing neuropathic pain, pelvic pain, and other forms of pain. It reduces spasms, headaches, inflammation, anxiety, and stress that may trigger or worsen flares. It can improve mood and depression that often comes with having a painful chronic disease with no cure. Finally, cannabis may improve serotonin or other neurotransmitter imbalances in fibromyalgia.
There are 1000s of cannabis strains and CBD products that can improve the quality of life with fibromyalgia. If cannabis isn’t right for you, some people prefer microdosing magic mushrooms, while others prefer calming strains of kratom. Your plant medicine guide will go over the pros and cons of each plant medicine and help you decide which one is right for you.
The plant-based health revolution is here! I’m your guide to understanding cannabis, mushrooms, and other healing plants so you live a life free of pain.
My name is Dr. Michele Ross and my mission is to empower patients with the knowledge and use of plant-based medicine so they can live their healthiest and happiest lives.
“Dr. Ross is so knowledgeable about the hottest topic right, CBD, and her passion for using it to heal people is amazing. Her energy, humor, and relatability are refreshing and inviting. The type of wisdom and warmth that you’d want if your health journey should include CBD.”
“Dr. Ross will open your mind to so many new ideas about holistic health. WHY are we not taking care of ourselves as our instincts direct us? Well, the law has not been on the side of cannabis users for most of history. Now, things are changing and it’s up to us to reclaim our health.”
This is something I have been working on for a long time.
As a neuroscientist with fibromyalgia, I’ve worked for years to test the available treatments and debunk fibro myths.
I’ve come up with a protocol that has helped me cure my fibromyalgia naturally (putting it into recovery mode) and has helped so many of my patients.
And I want to share it with you.
Here’s what Ashley R. says about my work:
“Dr. Ross is so knowledgeable about the hottest topic right now, CBD, and her passion for using it to heal people is amazing. Her energy, humor, and relatability are refreshing and inviting. The type of wisdom and warmth that you’d want if your health journey should include CBD.”
Many of you know me from my turn as the first scientist to star in a reality TV series, Big Brother 11 on CBS, where I was a beast at winning competitions and almost won the whole game. There’s another part to my story, one that includes the struggle of getting a fibromyalgiadiagnosis.
Several years ago I used a cane and even a walker to move around. I had no energy, had permanent brain fog, and barely could sit up to work on my laptop at home for an hour or two before having to take a nap. I was prescribed Lyrica, morphine, and a laundry list of other prescriptions to manage severe pain, spasms, and depression. And I wanted to die.
I got off all my prescriptions using cannabis, and today, I’m healthy enough that I work full time and travel all over the world teaching doctors and patients about cannabis medicine.
Fibromyalgia isn’t stopping me from living my best life anymore. Now it’s your turn.
I created the Fibro University Membership to help patients design a life that supports their progress to cure fibromyalgia naturally – so you can feel connected, supported, and motivated every day.
Each month I deliver you brand-new content that’s easy to access on your computer, phone or tablet.
But this deal will not last forever. In fact, the lifetime membership disappears Saturday, July 25th, 2020 & the price goes up for an annual membership.
Are you ready to invest in your health today, for less than 10 cents a day?
