Tag Archives: pain relief

The Disabled Diva Blog Weekend Recap April 1-5, 2019

the disabled diva blog recap april 1 vacation, cannabis review, arnica salve, pain relief, mobility aids, choosing the right one

 

 

 

 

 

 

 

The Disabled Diva Blog Weekend Recap April 1-5, 2019

  1. White Widow Marijuana Strain Review: Cannabis posts are now password protected.  Click here to learn how to access them.  
  2. How to plan the best summer vacation despite your chronic illness
  3. Arnica Salve Review
  4. Choosing a Mobility Aid That Fits Your Needs and Lifestyle  
  5. Looking for new slippers? Click here for a selection that is fun and comfy!

  New Deals!

*Disclosure: This post includes affiliate links. Meaning that at no additional cost to you, I receive a commission when you make a purchase through my links. The proceeds earned fund the giveaways I host in my Facebook groups.

 

 

 

 

 

 

 

 

 

 

 

 

 

Arnica Salve Review

Arnica salve review

 

 

 

 

 

 

Earthley Arnica Salve Review

Back in 2018 the state of California legalized marijuana for recreational purposes.  At the same time Disneyland banned all forms of cannabis, including CBD products from their parks.  Don’t waste your time telling me that CBD and THC aren’t the same thing… I know, you know, but as a business it is their right to allow or restrict what they want on their property. However, as someone who relied on topical CBD lotions and oils to relieve muscle tension and pain while spending time with her family in the parks, this did not sit well with me.  Thankfully I found a solution!!!

Earthley Arnica Salve to the rescue!

When I first became an affiliate with Earthley ( Disclosure: This post includes affiliate links. Meaning that at no additional cost to you, I receive a commission when you make a purchase through my links. The proceeds earned fund the giveaways I host in my Facebook groups) I purchased a bunch of different products to see which ones lived up to their promise and which ones didn’t.  Included in my shopping spree was their arnica salve travel stick.

Oh what a relief!

Before I share the basic mumbo jumbo about the product, I have to tell you why I love it so much.

These statements have not been evaluated by the FDA, and this product is not intended to diagnose, treat, or cure any disease.

After having nothing to relax my muscles or to address muscle pain while at Disneyland for an entire year, I was floored when I discovered that this simple and inexpensive stick worked just as well as the CBD oils that I used to bring with me.

When I feel tension in my neck, I just rub a little arnica salve on it and voila, tension and pain is GONE.

I have even been rubbing it on my belly when I experience pain from tearing and swelling of my abdominal muscles.  It also reduces the amount and severity of my muscle contractions.

I use this stick everywhere!  My neck, temples, wrists, shoulders, elbows, hips, belly, sacrum, knees, ankles, and feet!  Is it a cure all? Not at all, but it makes it possible to spend the day at Disneyland without worrying about arriving home with a stiff neck or with a level of pain that would normally take days to recover from.

This wonderful natural pain relief stick also makes it possible for me to focus my PEMF treatments on the areas of my body that need them the most throughout the day, instead of constantly having to move my device around.

 

 

 

 

 

 

 

 

 

 

Why you should love it

If the fact that this fabulous stick actually relieves minor pains and pain caught soon after it begins isn’t enough, here are a few other reasons you should be falling head over heals for this product:

  • It is affordable! Seriously, it is only $4.99 per stick!!!!
  • It contains NO harmful chemicals: Ingredients>Organic arnica flowers, organic extra-virgin olive oil, and candelilla wax.
  • No need to worry about the legality of the arnica flower, so you can take and use it anywhere!

Those who have been following my blog for any amount of time know that I never recommend a product unless I think it will enhance, benefit, or improve your chronic life.  If you are new to my blog, I welcome you to join my product picks or alternative pain fighting group on Facebook where you can talk to others who have benefitted from my recommendations.

This products gets TWO thumbs up!!

Click here to order today!

 

Other Earthley reviews:

Good Night Lotion

Soothing Skin Balm

Charcoal Soap

 

 

How Charlie’s Angels Prepared Me to Live with a Chronic Illness

Pictured Charlie's Angels. Title: How charlie's angels prepared me to live with a chronic illness

 

 

 

 

 

 

 

How Charlie’s Angels Prepared Me to Live with a Chronic Illness

I may have been born in the late 60’s, but I am a child of the 70’s!

One of my favorite television shows of the seventies was Charlie’s Angels.  Not only did I never miss an episode, the following day I would make my friends act them out with me! For those of you who are not familiar with this show, Charlie had a private detective agency and he hired three sexy women that he called angels.  The original angels were Farrah Fawcett as Jill Munroe, Kate Jackson as Sabrina Duncan, and Jaclyn Smith as Kelly Garrett.  They were badass women kicking butt and uncovering mysteries.

I wanted to be an Angel, Jill in particular because, well, hello that hair!!!!!

Little did I know that a show about beautiful, strong, and intelligent women would also give me the “know how” I would need to surviving life with not just one, but multiple chronic illnesses!

*Disclosure: This post includes affiliate links. Meaning that at no additional cost to you, I receive a commission when you make a purchase through my links. The proceeds earned fund the giveaways I host in my Facebook groups.

Look for clues

When I was diagnosed with fibromyalgia, psoriatic arthritis, psoriasis, degenerative disc disease, coccydynia, and endometriosis, I had no clue that each chronic illness would lead to a life of searching….

Searching for what you ask? What not would be easier to answer, but whether you have one chronic illness or a slew of them, the life of the chronically ill is spent searching for ways to relieve pain, new symptoms, reoccurrence of old symptoms, side-effects, and treatments. The chronically ill spend a lot of time investigating their bodies, the fluids that come out of them, their mental status, abilities and disabilities.

Thankfully Charlie’s Angels taught me to never give up and that there is always an explanation.  My doctors may have given up, but I will never give up searching for the source of my chronic illnesses.

Trust my instincts

Like any good detective, I have learned to trust my instincts.  I received my first chronic illness diagnosis in 2001 and since then I have had countless tests come back and show nothing wrong when I went in with a complaint of pain.  Thanks to my Angel training I knew not to accept that answer and kept pushing the issue and presenting new clues to my doctors.  In several cases, tests showed absolutely nothing wrong with me, but surgeries revealed the truth.  The findings of each surgery proved and validated my complaints by being something that no test could have ever revealed.

Trusting my instincts has saved my life countless times and will until I am no longer able to speak for myself.  I can never stress enough how important it is to be your own advocate!

Know when to fight

Like a well trained private eye, I know how to protect myself.  While I may not be punching or handcuffing my enemies, I have to fight to receive the care I deserve and need.  I have learned when fighting a doctor about a diagnosis or test is worth my time or not.  Sometimes my energy is better spent finding a new physician.

I have also learned to listen to my body.  It will let me know if the situation is urgent or if it can wait a little longer.  This instinct also helps me get through life.  I have learned what levels of pain and exhaustion can be pushed through and what cannot.

Teamwork works

Living alone, void of any assistance from others when you have a chronic illness is possible, but it’s not realistic.  Whether you are married or not, it is best to have a team.

First you need a medical team that is working together and not against each other.  They and you, need to be on the same page about treatment of the disease and pain.

Then you need your personal team.  You need someone that you can confide in, because trust me there are going to be days when you just need to vent your fears without terrifying your spouse/partner.  My husband is a fantastic team member that I don’t ever want to be without.  He has witnessed the horrific treatment from surgeons and has been there for me at the absolute worst moments of my illnesses.  Other teammates that are beneficial are folks to help with transportation, provide an occasional meal, or to tidy up your home when you are at your worst.   No matter what, you need someone in your life to make you laugh, because without laughter we are only left with sorrow.

Be sure to train one or more of your team to be your patient advocate.  You may not always be alert enough to express your requests or needs.  Having someone who can speak for you when you are unable is invaluable!!!

Thanks to the skills I learned from Charlie’s Angels, I continue to fight pain, solve symptom mysteries, and refuse to give up!

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

The Disabled Diva’s Blog Weekend Recap March 4, 2019

 

 

 

 

 

 

 

 

 

The Disabled Diva’s Blog Weekend Recap!

March 4-8, 2019

Tears: I hold them back, until pain pushes them out

Spring Clean Your Chronic Life

Mobility Aids: Everybody uses them

What I have learned from using PEMF daily for two years!

*Disclosure: This post includes affiliate links. Meaning that at no additional cost to you, I receive a commission when you make a purchase through my links. The proceeds earned fund the giveaways I host in my Facebook groups.

Hey psoriatic arthritis buddies or caregivers!!!

Could you please spare a few minutes to take a survey that will help create beneficial programs for the psoriatic disease community?
Click here to take survey
Thank you!

 

 

 

Spring Clean Your Chronic Life

 

 

 

 

 

 

 

Think spring cleaning only involves giving your home a good cleaning?

Think again!

Disinfect Your Diet

Clean up your personal care products

Spruce up your view!

Spring Cleaning doesn’t have to be painful

Sanitize your social circle

Five ways to make your home chronically safe and friendly

Scrub away negative thoughts

Spring Clean your social media feed

Cleanse your calendar!

 

 

The Disabled Diva’s Blog Weekend Recap Feb 25 – March 1, 2019

 

 

 

 

 

 

 

 

The Disabled Diva’s Blog Weekend Recap!

Feb 25 – March 1, 2019

March Madness Fitness Challenge

Packing for your chronic illnesses

What Happens When I Live My Old Life

Fibro Farts

Telling me that it could be worse won’t make me feel better

One PEMF Device, Two Years, Tons of Pain Relief!

 

*Disclosure: This post includes affiliate links. Meaning that at no additional cost to you, I receive a commission when you make a purchase through my links. The proceeds earned fund the giveaways I host in my Facebook groups.

 

 

 

 

 

 

 

 

 

 

 

What Happens When I Live My Old Life

 

 

 

 

 

 

 

 

What happens when I live my old life

I received my cluster of diagnoses during the early 2000’s.  During that time not one doctor urged, nudged, or hinted to me that I needed to make changes to how I lived my life.  Not ONE!!!

Instead of issuing warnings or advice to improve the quality of my life, my doctors insisted that they would be able to find the right pill(s) to offset my symptoms and pain.  Of course everything they tried failed.  Click here if you would like to take a peek at the pain management plan that finally helped reduce the pain I experience from fibromyalgia, psoriatic arthritis, psoriasis, degenerative disc disease, coccydynia, and abdominal adhesions from endometriosis and surgical scarring.

Between the false hope my doctors were issuing and the pressure from friends and family to get better, making changes to how I lived never crossed my mind.  But it should have and here is why:

When I live my old life:

  • I ignore the needs of my body/chronic illnesses
  • I injure myself more often
  • I spend more time in bed than actually living my life
  • My family loses precious time with me
  • I spend more time and money seeing doctors and visiting emergency rooms
  • I took no responsibility towards reducing my pain.  I trusted and followed everything my doctors said.

*Disclosure: This post includes affiliate links. Meaning that at no additional cost to you, I receive a commission when you make a purchase through my links. The proceeds earned fund the giveaways I host in my Facebook groups.

Why changes had to be made

  • The longer I ignored the needs of my body/illnesses, the sicker I became and more damage was done to my body
  • Refusing to accept the need to use a mobility aid created more opportunities to fall, which I did often.  Each fall resulted with either a broken bone or blood clot.
  • I was killing myself
  • My family needed me
  • I would rather take my family to Disneyland, then to spend money and time in the emergency room over an injury that could have been prevented had I listened to my body, done things differently, or utilized a mobility aid.
  • I had to take responsibility and to accept that my doctor may never be able to help me.

 

Changes that literally changed my chronic life

  • I made friends with my diseases.  I got to know them and my body so well that I after awhile I could feel the beginning stages of a flare coming on.  In the past, I just pushed until I collapsed.
  • Using mobility aids may have been hard to accept on an emotional level, but when I look back and see how little I have fallen since I began using them, I know I made the right decision.
  • By recognizing and addressing signs of a flare or physical distress I am able to avoid complications like my body mimicking a stroke or muscles freezing to the point of feeling rock hard for months on end.
  • Spending the amount of time that I do in caring for my body, doing things differently, accepting what I can’t do, and letting go of unrealistic expectations has gifted me with less time in bed and more out making memories with my family.
  • I took responsibility and charge over my care.  I researched and tried alternative treatments. While I may spend more money on those treatments than any pill that my insurance would cover, I save by not having to visit my doctor for a refill every month and not visiting the emergency room throughout the year. Click here to read about my pain management plan.

All of these changes, plus others that you can read about in my eBook Make Pain Your Bitch: How to Dominate Your Chronic Life, has restored my independence.  Going grocery shopping no longer makes me anxious, because I can finally do it without needing a day or two to recuperate.  I can drive and clean my house again.

Now I am not saying that everyone who reads my book and follows my pain management plan will have the same results.  The changes you need to make may differ, but no matter what, any change that involves listening to and respecting your body/disease is going to improve your life.

Don’t make the mistake I did by waiting 12 years before even accepting that there was no way I could go on living like I used to.

Living our old lives doesn’t make us strong, instead it makes us weaker.

Living our old lives does more than increase our physical pain, it hurts us and our loved ones emotionally too.

Are you still living your old life? 

Whether you are or not, I challenge you to examine your day to day life and pick one area/task that could be done differently, in a way that won’t increase your pain level.  Then make that change.  You don’t have to change every aspect of your life immediately, take your time and make your changes one step at a time.

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

%d bloggers like this: