health · Uncategorized

Fibro Friday – Anger, In Retrospect

When it comes to chronic illness, it’s very easy to get so lost in symptom management that you lose sight of your emotional life. Figuring out your new lifestyle is a massive undertaking and doesn’t give you a lot of space to think, and act, and feel, simultaneously. You often have to forgo examining your feelings in order to figure out how to get the pain under control, and you put those difficult emotions on the shelf while you do the work of figuring out what’s happening with your body. Many times, those hard-to-describe emotions . . . are anger. Anger over the excellent health you may never enjoy again, anger over the misdiagnoses, dismissive attitudes within the medical profession, anger over the people who simply don’t understand what you’re going through.

So you do the doctor visits, buy the medicine and supplements, try adjusting your routine. You do a few things, figure out what’s working, then revise as needed. You do this for weeks and months, and hope that you’ll finally figure out a recipe for wellness that you can sustain over the long term. And while you do all of that . . . the anger sits.

And trust, that’s all the anger does. It sits, and it doesn’t budge an inch. It waits for you while you run around and try to put out the fires with your health condition. It doesn’t go anywhere until it’s processed. So, it stands by as you try to do everything you need to get your health back on track.

When you finally get things under control, or when you just accept what your life will be with your chronic condition, then the anger bubbles up. The lucky ones of us have a few times where the anger explodes, gets processed quickly, and it’s on to the next thing. But for some of us. . . it doesn’t happen like that. It may not feel like white-hot rage initially. It may feel like discomfort, being a little less patient with yourself and others, a repressed or otherwise forgotten memory reappearing and knocking the wind out of you. It doesn’t always look or sound like anger, that is, until you start peeling back the layers.

After you inquire within yourself, “Is this sadness? Disappointment? Frustration? Fear?” and find that none of those emotions fit, then (if you’re honest with yourself) it’ll hit you. You’re mad. Furious, even. Mad at your body for not responding to your medication, improved diet or modified routine. Enraged at the many doctor visits that didn’t get you an answer despite you always telling them your laundry list of symptoms. Fury over how little your family, friends, or acquaintances believe or understand your discomfort. And yes, white hot rage over the insurance systems, employers and government frameworks that make it more advantageous for you to suffer and expire than to get real help on your path.

Your anger may not appear at the beginning of your journey. It may appear in retrospect, like mine did. And it’s still just as holy, justified, and worth acknowledging as it was when you first felt it but didn’t realize what it was.

Give your anger space, and give yourself grace for feeling it. It is part of your journey, and it deserves space. And then, when the rage has cooled down, care for yourself, and press forward. Your improved health is on the other side of your process.

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Fibro Fridays – The Latest on My Health Journey

Happy Fibro Friday, friends! I hope you all have had a great, pain-free week. And, if you experienced any pain at all, I hope you were able to get relief quickly.

I’m taking another (mini) break from reviewing the various fibromyalgia protocols (the last one I reviewed was Dr. Wylde’s protocol) to talk about a different fibro topic; namely, I’ll be discussing what’s been happening with me and my health journey.

For starters, I’ve been feeling pretty good overall. I tend to experience a lot less pain during the warmer months, and that’s due to the temperature (I am more uncomfortable in cooler temps), the increased vitamin D (since I spend a lot more time in the sunshine), or some combination of the two. I’ve been taking advantage of those low-pain days and getting as much done as I can.

I have also been making changes to my diet and medication. I’m incorporating a lot more raw fruits and vegetables into my meals, usually opting for whole fruits for breakfast as opposed to eating a lot of grain or processed foods, salads for lunch, and protein and veggies for dinner. I have been tapering my medication in the hopes that I’ll be able to eventually fully transition off of them. So far, so good: I haven’t had any major pain or flares since I started the tapering process.

Another thing that has been helping with my health is doing yoga more frequently. I do it for the fitness aspect but one of the bonuses of yoga is being mindful of my breathing. I often forget to take deeper breaths, so it’s nice to have a reminder. Yoga is amazing for fibromyalgia, since it gently stretches the muscles while simultaneously encouraging the release of stress. It’s one of the most frequently recommended exercises for people dealing with fibro.

Part of the plan over the next few months involves experimenting with some plant-based eating plans, progress in my yoga practice, and find more natural pain relief options. I’ve been working on some products and supplements to help with fibro pain but it’s still early in my experimentation. Here’s hoping I’ll be able to create something amazing that I’ll be able to share with you all soon!

That’s my brief rundown of how I’ve been feeling lately, as well as where I am in my health journey. I’m looking forward to hearing from you all in the comments. Take care, and have a great weekend!

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Fibro Fridays – My Current Vitamin and Supplement Regimen

Happy Friday, friends! I’m looking forward to this weekend: I will be getting lots of sleep and doing some additional writing. Here’s hoping I can get a good chunk of writing done!

Since I’ve never shared many details about the medication, vitamins and supplements I take, I thought that would be a good think to discuss on Fibro Friday. I believe wholeheartedly that filling in nutritional gaps can improve fibromyalgia symptoms. It doesn’t mean that fibro is a nutritional condition, but having a properly nourished body can do wonders for us and our pain levels.

Let’s start with medication first. Though these aren’t particularly nourishing, these help with pain management and other symptoms. I currently take 900 mg of gapapentin daily: 300 mg in the morning, and 600 mg in the evening. I also take 10 mg of escitalopram in the morning, and 10 mg of amitriptyline at night. These help with my serotonin levels and the nerve pain and discomfort I feel. When my pain is too intense, I may reach for 10 mg of cyclobenzaprine (a muscle relaxer).

Now, onto vitamins! I take organic prenatal gummies from Smarty Pants. These taste really good and cover a lot of my nutritional needs. I also take a vitamin D3 supplement (I purchase one through Melaleuca’a Vitality brand). I also take chelated magnesium from Country Life, calcium with vitamin D3 from Nature’s Measure, as well as the Super B Complex by Nature’s Measure.

Lastly, I also take supplements. I use the Koala Pals protein shake by Melaleuca company. I also like taking Good Zymes (a digestive enzyme supplement) available through Melaleuca. Also, I really enjoy Pacifica’s beauty powders. After sharing information about my two favorite powders, I realized that Pacifica no longer sells them. However, I did find a seller on Amazon for the Slay All Day powder. I also really like Sambucol Elderberry gummies for immune support.

I also made a video about this, if you prefer to hear about the products as opposed to reading about it:

(This post contains affiliate links)

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Fibro Fridays: Why It’s Difficult to Treat Fibromyalgia

Happy Friday, friends! Today’s post is one that I’ve been eager to write, because I feel that explaining this (from the perspective of someone living with fibromyalgia) may give a little clarity to others that are struggling with their diagnosis, or may help people that are unfamiliar with the condition to better understand why there is no easy “fix” for fibro.

Whenever you try to learn about fibromyalgia online or directly from a medical professional, there is generally a lack of consensus on the causes of the condition. The condition is treated as a bit of a “catch-all” category for a set of uncomfortable (to the point of painful) symptoms. This “catch-all” designation is one reason why there are still some medical professionals that continue to deny the existence of fibro (I already wrote a post touching on this topic).

In any case, the overall lack of understanding behind the WHY of fibro leaves a lot of questions regarding the HOW of treatment. Different root causes call for different treatment protocol. However, fibromyalgia can be linked to muscular, nervous and even digestive malfunctions, so most treatment is, at best, akin to a game of darts. Medical professionals will try to hit the “bullseye”, and many treatments can offer a level of relief, but it seems that no one has hit the “bullseye” of fibromyalgia – YET.

Prescription medication is one treatment option for fibromyalgia

There are many researchers that are getting closer to an agreed-upon definition of fibromyalgia, including its root causes. However, until consensus is achieved, we have an assortment of treatments that can be explored and that may have varying levels of effectiveness. Many of the most popular treatments include physical therapy, aquatic therapy, acupuncture, prescribed medication, nutritional supplements, lifestyle overhaul and lots of intentional self care (which is, by far, usually the most effective treatment [maybe I’ll write more about this in the future]), chiropractic care, etc.,. The trick to managing the symptoms is finding the perfect cocktail of treatments, along with having an excellent support system and medical team in your corner.

Well friends, that’s it for this Fibro Friday! I hope you all have a great weekend, and I’ll talk to you on Monday. Take care!