Fibro Warrior Creates Exercise Program Just For Us!

Fibro Warrior Creates Exercise Program Just For Us!

By Donna Gregory Burch.

Exercise is a sore subject (literally!) in the fibromyalgia community. That’s why I’ve avoided writing about it for so long. I know a lot of fibro warriors will agree with me when I say I’m sick of hearing doctors and researchers tell me that I’ll feel better if I just exercise. But I also know, based on the current research, they’re probably right.

Donna Gregory Burch

The problem is when we’re struggling to get the basics done each day, like showering and prepping meals, the idea of taking a power walk around the neighborhood is just ludicrous. Even 10 minutes of yoga is enough to send most of us into a days-long flare.

As someone who used to do 5Ks, I really WANT to exercise, but when I’ve attempted it in the past, it just made my pain and fatigue so much worse. (There’s actually a name for this: post-exertional malaise, and it’s a real thing, despite the fact that most doctors have never heard of it.) I learned very quickly that standard exercise programs just don’t work for me. They’re too strenuous and stressful for my body.

Over the years, I’ve wished there was an exercise program designed just for people with fibromyalgia and similar conditions, and now I’ve found one! Andrea Wool developed Autoimmune Strong after becoming ill with fibromyalgia, Hashimoto’s thyroiditis and celiac following the birth of her second son. Like many of us, she couldn’t find solutions for her health issues within the paradigm of conventional medicine and decided to see if lifestyle changes might improve her symptoms, but that only led to yet another challenge: Most exercise programs are designed for (at least semi-) healthy people and don’t address the physical limitations of living with a debilitating chronic illness. Normal exercise would cause her to crash.

Eventually, Andrea decided to devise her own exercise program to heal her body and is now sharing it with others. I’ve watched the first few videos of Autoimmune Strong, and I immediately knew I wanted to share it with my readers. Andrea’s approach is so slow and gentle that I think her program may help those of us who want to begin an exercise routine, but don’t have the stamina for traditional workouts.

So today, I’m sharing a Q & A with Andrea where we discuss her health struggles, how those inspired the creation of Autoimmune Strong and how her program answers the need for gentle movement within the fibromyalgia community. I hope you enjoy our interview.

You’ve had a number of health challenges, including fibromyalgia, Hashimoto’s thyroiditis and celiac disease. Can you share your story of chronic illness?

Almost 6 years ago, I was very sick. I had just given birth to my second son, and I just knew something was really wrong with my body. I was exhausted with mind-numbing fatigue. I was rapidly gaining weight, and I had constant, fiery and intense pain all over my body at all times.

Andrea Wool

I was on maternity leave with a newborn and a 3 year old at home, and I was completely unable to care for my babies, my household or myself. I needed constant support from my mom and my husband just to make it through each day. Simple everyday things like playing on the floor with my son, or carrying my infant up the stairs, or going to the grocery store would be impossible, debilitating. I spent the days in tears, in incredible pain all over. The exhaustion was intense and overwhelming.

I saw many medical doctors, most of whom told me that I was fine. But obviously, I was NOT fine. I was so sick I had to quit my job. I was desperate for anything that could help me get better. I started to look at the things I could control – what I ate and how I moved my body. Over time, I pieced together a food-based healing protocol I thought could work. I started by eliminating gluten, then sugar, dairy, alcohol, and caffeine. I started eliminating processed foods and buying only organic produce and meat.

Having been an athlete all my life, I knew movement needed to be a part of the healing as well. I hired a personal trainer and started to move again, but it was really tough. I was too weak to do any of the things I used to do, and the workouts we were doing were causing intense flare-ups in my body. I would feel great for a week, and then crushed for two weeks with exhaustion and fatigue. After a few months of this self-designed protocol, I was starting to feel better, and I realized that I was on the right path. But I was by no means back to “normal,” and I needed to know how to get there. I wanted to know what I was missing. So I made a big decision – I decided to go back to school. I became a nutritional therapy practitioner and a certified personal trainer so I could learn more and go deeper into my own healing.

Two years into this process, I finally was diagnosed with Hashimotos [thyroiditis], celiac and fibromyalgia, and my doctors continue to be amazed at my personal healing journey using only food and movement. I now hope to inspire others, that they too can create their own healing journey and that they don’t have to suffer in pain forever.

How are you feeling these days?

Actually, I am feeling great these days. I can’t even believe, looking back at this story, that I am the same person. It has been a slow recovery, and it’s not finished yet. But 6 years later, I am now capable of doing things I didn’t think was possible. I have been able to return to the active lifestyle I used to enjoy. I run, I do yoga and I have recently started to learn how to powerlift. I can deadlift 185 pounds! Not only am I healthy enough to hold down a job, but I am capable of running my own business.

But most importantly for me, I can keep up with my boys. They love to run around, and I am totally capable of running around with them. I go rock climbing with them, I can carry them on my shoulders, I play tag, I can tackle them and rough-house, and my body can manage it. They have no memory of a “sick” mom. They only know me as I am today. And for that, I am eternally grateful.

I think all of us with fibromyalgia have been told that we should exercise to reduce our symptoms, but it’s so hard – especially in the beginning because exercise tends to cause even more pain and fatigue. How did you get started and stay motivated to continue?

Yes, I have found that with fibromyalgia, as well as other chronic pain issues, exercise is a double-edged sword. Movement is essential, but too much movement can stimulate a flare of the worst kind. It took me a long time to figure out where the balance needed to be. As I shared above, I hired a personal trainer, but she did not understand my body at all. I have found that with most personal trainers and fitness professionals out there, they want you to push your body so you can get stronger faster. “No pain, no gain,” right? Well, I tried that, and it did NOT work for me. Instead, it made me sicker. But as a former athlete, it was hard to wrap my brain around the concept that I needed to SLOW DOWN. Pacing is the most important part of a fitness regime for people with fibromyalgia. Slow, steady and consistent over time is what I believe works the best.

I stay motivated because now that I exercise in the right way for my body, it actually does make me feel better! I find that when I feel a flare coming on, exercise can help rather than harm. For me, exercise is now my medicine. It’s not something I do to get “skinny” or work off my last meal. It’s something I do to further my own healing process.

Why is it important for those of us with fibromyalgia and similar conditions to stay physically active?

If done properly, exercise can help us manage our symptoms and flare-ups. Chronic pain conditions are exacerbated by inflammation, and, if done properly, exercise can help to reduce inflammation. Additionally, the right exercises can teach our bodies to adapt to a pain response, which can help us get through the pain and exhaustion of our daily activities. Our bodies need to learn to be comfortable being uncomfortable.

What is Autoimmune Strong and what led you to develop it?

Autoimmune Strong is an online fitness program designed specifically for people struggling with chronic pain conditions like fibromyalgia, autoimmune disorders and Lyme disease.

I developed it because I was so frustrated that nobody in the fitness community knew how to handle my body. I spent a ton of time trying to find someone who could help me exercise without a flare-up, and I couldn’t find anyone who even knew what I was talking about. I created this program for myself, and it felt good. So I started using it with my one-on-one personal training clients, and they felt good, too.

Based on these great results, I was inspired to create a program that was accessible to everyone, easy to do at home, that helped people with chronic pain conditions like myself start getting stronger and feeling better. Autoimmune Strong was born!

For those who are interested in starting an exercise program, how is Autoimmune Strong different than other programs on the market and what can participants expect?

Autoimmune Strong is the only strength-training fitness program specifically designed for people struggling with chronic pain. The thing that sets Autoimmune Strong apart most is the program design. First, Autoimmune Strong is designed to target specific postural muscles without doing big movements. These movements are effective in building strength, but they don’t trigger stress and inflammation on the body.

Second, the pacing of the program sets it apart. Most exercise programs push you to your max. Autoimmune Strong starts off very slow, so that your body can adapt properly to the movements, so you can progress through the movements without a flare. And finally, Autoimmune Strong has a community component, where members can chat with each other in a private Facebook group so we can share our goals, our successes and our struggles. Chronic pain is an invisible disease, and it’s hard for the people around us to understand what we live with. The more we can support each other, the better we will be!

Where can people learn more about Autoimmune Strong?

Go to Autoimmune Strongfor more info! There is a 7-day free trial so you can check the program out in its entirety for 7 days and see if it’s right for you. And you can always email me at andrea@getautoimmunestrong.com. I would love to hear your stories of struggle and healing so please share with me. (And of course, you can find me on Facebook,too!)

Donna Gregory Burch was diagnosed with fibromyalgia in 2014 after several years of unexplained pain, fatigue and other symptoms. She was later diagnosed with chronic Lyme disease. Donna covers news, treatments, research and practical tips for living better with fibromyalgia and Lyme on her blog, FedUpwithFatigue.com. You can also find her on Facebook and Twitter. Donna is an award-winning journalist whose work has appeared online and in newspapers and magazines throughout Virginia, Delaware and Pennsylvania. She lives in Delaware with her husband and their many fur babies.

Subscribe to our blog via email

Enter your email address to subscribe to this blog and receive notifications of new posts by email.

Authored by: Donna Gregory Burch

There are 7 comments for this article
  1. Maureen at 9:47 pm

    Hi Jean, thank you! I sent you an email a couple of days ago and look forward to hearing from you. Maureen

  2. Jean Price at 10:42 am

    Maureen…it’s amazing to me how many “soul mates in pain” we see commenting on various sites! I have some situations in common with you…and find even simple stretches add significantly to my pain! My RA adds to all my past and current spinal issues and definitely impacts my abilty to exercise…and also the fatigue of RA can be down right painful, too….like I imagine you deal with from fibromyalgia, also. And like you said here, I also think it’s good to be aware of others’ trials and successes, as we work out what’s best for us…and differentiate what we’re even capable of doing! It goes back to the individuality of us all, I think. We each must find our own personal best therapies, especially these days with pain medication being all but taboo! Something’s will be helpful…some not so much!

    If you’d ever like to connect, my email is jeankprice@hotmail.com. I also have thought about the cbd oil lately…and oddly my doctor and a couple of the nurses at the pain management place I go to had never even heard of it!! I thought this was sort of sad, really… especially since I think they are fairly good at what they do, and also because I was offered both a trial of methadone and a spinal stimulator for some increased lower leg pain I’d been having! (Neither of which would I consider for myself!). I’m glad you posted about the information on Donna’s website! I always enjoy her articles and I’ll check it out! Thanks!

  3. Sandra Stedinger at 11:13 pm

    This patient apparently has no medical or exercise physiology or relevant training. I am happy that the program she put together for herself has worked so well. But it is anecdotal, at best. There is no reason to generalize her program to other people who have quite differing medical problems, especially without running it past their own doctors. Go find a certified PT or trainer who is experienced in your particular diseases. Don’t take advice from a random person who may only be guessing about what they tell you.

  4. Maureen at 8:58 pm

    Donna, i thank you,always, for your awesome efforts on our behalf! Your journey has been an incredible and interesting one.
    I checked out the autoimmune strong site and watched most of Andrea’s video. Been there done that. Big Kudos to her though for finding what works for her and making a business out it.
    With 4 failed spine surgeries, fusions, hardware, FM etc I simply cannot exercise (even some core strenghtening, although I already do some of what she shows)
    anymore aside from keeping busy at home and an occ. walk on a rare good day. I’m currently in BIG TIME FM flares due to the increase heat/humidity in Florida and will remain this way through the hotter months now.
    It’s amazing how it poorly effects my body. Everything I do hurts so much more and my mornings are even more horrid than usual.
    Keep up the good work in informing us on what is out there! Thank you! Maureen

    Regardless, I finally checked out your website and signed on. I love reading the info you’ve posted about CBD oil etc since I’ve been look into researching it and possibly trying it. The CBD vape somewhat relaxes me but seems to make me feel tired therefor I gave up on that. I didn’t try it long enough to see if it helped my pain.

  5. Jean Price at 8:33 pm

    I’m curious if you had anything to help for the pain while you were starting this program of yours? That’s what I find so hard about even minimal exercise…the added pain makes consistency difficult at best…impossible more times than not! And obviously pacing is important, yet when extreme additional pain makes pacing impractical…that’s when some pain medication can get us through. Now though…there isn’t a good understanding of this, from what I’ve seen. And although diet and exercise can be one of the answers, some multiple conditions, like with failed spinal surgeries, also require medication to fulfill any kind of regime,

  6. Bobbie Hudson Penick at 4:09 pm

    Many of us just can’t afford this. I think it’s a wonderful thing and you have my support in spirit! I’m sure you know many live on very limited incomes.

  7. MichaelL at 8:27 am

    As with every treatment known to man, every patients has a different response. Some people cannot tolerate an exercise program. It does not matter who develops it. It is just not tolerated in many fibromyalgia patients. If some get improvement, that is great! I think every patient, who is new to their fibromyalgia, should try it out. Just don’t feel like a failure when you don’t meet the expectations. This person, with good results, is trying to push on EVERYONE with fibromyalgia. When everyone but medical professionals is giving medical advice, we should be very careful in who we listen to. I suffered with it. It was very helpful when treating patients. They thought that I was a genius, when I hit every tender “trigger point” on their physical exams. Most had seen several doctors trying to get a diagnosis, by the time they made it to my office.

Leave a Reply

Your email address will not be published. Required fields are marked *