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Can someone with digestive tract paralysis eat? Yes, most of us are perfectly capable of putting food into our mouths, c...
09/03/2020

Can someone with digestive tract paralysis eat? Yes, most of us are perfectly capable of putting food into our mouths, chewing, and then swallowing the delectable morsel of our choosing.⁣

SHOULD an individual with severe gastroparesis and/or chronic intestinal pseudo obstruction eat? Maybe not. Or at least nothing significant. Every patient varies in their ability (or lack there of) to eat. Still, it’s important to keep introducing food to the gastrointestinal tract. The stomach is a muscle. If you don’t use it, you lose it. ⁣

So, how do I handle not eating anything substantial? The long periods of being NPO? That’s a loaded question. The answer is—I don’t. ⁣

Those with digestive tract paralysis have a strange relationship with food. For me, I do attempt to eat here and there when not in a massive flare, but what I do eat is vented out of my PEG tube attached to my stomach. Essentially, it’s like puking without it coming out of my mouth. Gross. However, venting is not fool proof. Inevitably, minimal amounts of food escape past the tube creating the potential for illness (bowel obstruction, nausea, vomiting, etc). ⁣

While trialing bites of food on occasion is important, I’m fully aware that my “pleasure eating” will result in illness comparable to food poisoning or a stomach flu. Yet, I do it anyway. Why? ⁣

Food is such a basic component of life. Celebrations stem around food. Families bond over meals. I like to feel included. So, it’s difficult to consider the consequences in the moment. ⁣

I may have acquired the skill of being hungry and nauseous simultaneously (I bet you didn’t know that was possible!!), but finding balance between eating enough to preserve bowel motility and not making myself emergently ill is a skill I’m unsure if I will ever successfully master. ⁣

As I shove a bite of cupcake into my mouth, nauseating dry heaves overtake my body. I curse my stupidity—claiming “I’m never eating again.” That is, until next time. Because when nausea no longer swirls in the bit of my stomach and the pain relents, I always do it again...eventually. ⁣

Some would say that’s the definition of insanity, but I call it hope.

Cre: hospitalprncss

😅😅😅 Sounds about right!The world is a hot mess right now, bed for a few months sounds is more appropriate. Follow:     ...
09/03/2020

😅😅😅 Sounds about right!

The world is a hot mess right now, bed for a few months sounds is more appropriate.

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😴😅😅 A huge cost, that's what! Follow:
09/02/2020

😴😅😅 A huge cost, that's what!

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Check out all our new productsGet link in our profile ⤵️         👕 If you want this   please check the link in my bio (p...
09/02/2020

Check out all our new products

Get link in our profile ⤵️
👕 If you want this please check the link in my bio (profile)
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👕 If you want this please check the link in my bio (profile)
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IPhone cases and Samsung cases➡️GET YOURS FROM THE BIO LINK!!➡️Choose your favourite colour and style!➡️Made in the USA🌏...
08/29/2020

IPhone cases and Samsung cases
➡️GET YOURS FROM THE BIO LINK!!
➡️Choose your favourite colour and style!
➡️Made in the USA
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Each year on May 12, millions of people observe National Fibromyalgia Awareness Day.Perfect Shoes for Fibromyalgia Aware...
08/15/2020

Each year on May 12, millions of people observe National Fibromyalgia Awareness Day.

Perfect Shoes for Fibromyalgia Awareness😍
Get yours from here ⤵️ (link on bio)

Tag someone who need this.
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Autoimmune brain and mom brain both cause brain fog due to sleep deprivation. An autoimmune brain is working exponential...
08/13/2020

Autoimmune brain and mom brain both cause brain fog due to sleep deprivation. An autoimmune brain is working exponentially harder than a normal brain does simply to function. Misfired synapses takes a lot of brain power to correct. Mom brain is the combination of sleep deprivation and extreme multitasking. An autoimmune mom brain means I rarely know what I’m doing.
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I want to introduce you to a dear friend,  , and share with you her story of life with Fibromyalgia.We were placed in th...
08/13/2020

I want to introduce you to a dear friend, , and share with you her story of life with Fibromyalgia.
We were placed in the same lab group, and I instantly knew she was someone I would be inspired by. She recently started chronicling her journey with Fibromyalgia and as part of Fibromyalgia Awareness Month I knew I had to help spread her story.
The facts are staggering; one in three will battle Fibromyalgia or Chronic Pain, and it significantly affects women greater. It is a complex chronic pain disorder that causes widespread pain and tenderness in the body with no cure currently. I encourage you to follow her and learn more about this disorder that has physical, mental and social implications.
“We have two options, medically and emotionally: give up or fight like hell”

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Here’s some facts about us  . Read every single one of these, and that’s us! I’m sure we have all thought these things, ...
08/12/2020

Here’s some facts about us . Read every single one of these, and that’s us! I’m sure we have all thought these things, or been told them. But what we thought/were told is not true. This is our truth!

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Check out all our new productsPerfect Sticker for Fibromyalgia Awareness😍Get yours from here ⤵️ (link on bio)Tag someone...
08/12/2020

Check out all our new products

Perfect Sticker for Fibromyalgia Awareness😍
Get yours from here ⤵️ (link on bio)

Tag someone who need this.
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✔️ Free returns & 100% cash back.
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I'm never not in pain 🤕I am always in some level of pain, 24/7. I think this is hard for people to fully understand if t...
08/12/2020

I'm never not in pain 🤕
I am always in some level of pain, 24/7. I think this is hard for people to fully understand if they only get pain once in a while and don't live with chronic pain
Those of us with chronic pain have had to learn ways to live with it and to cope with the pain. That doesn't mean it's any easier, it definitely isn't. It also doesn't mean that we don't have days where we can't do anything at all or very little... We do!
There is definitely a greater need for chronic pain management and for chronic pain to be taken seriously. Our pain deserves to be treated, even if it only takes the edge of off it sometimes!
What are some misconceptions you've heard about chronic pain? 💕

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