Today I am going to present you with a spring cleaning idea that you may not have thought of……. sprucing up your view!
Fibromyalgia stress flares debilitate our mind and body plus disrupt our daily lives. Here’s how to cope with them and reduce occurrences.
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Within a few months of seeing me for psoriatic arthritis and fibromyalgia, my rheumatologist could see how much I was struggling to walk any distance. In fact, it was he who suggested that I get a parking placard for my car and handed me a form with his signature to get one asap. What was strange is that he never discussed use of a mobility aid.
There two forms of self-care. There’s the fun kind that everybody likes and the not so fun kind that feels more like work than a good time. Today I am sharing the importance of both and why they should be discussed with newly diagnosed patients.
I can’t imagine anyone likes asking for help. I know I don’t. But as the pain and fatigue from fibromyalgia and psoriatic arthritis increased, I had no choice but to give in. I often wonder if it would have been such a painful process had I been warned at the time of my diagnosis. My guess is that….
I was caught off guard by the changes that took place in regards to my relationships with others. As a stay-at-home mother and wife my role was to care for everyone. But that all changed after my body was hijacked by fibromyalgia and psoriatic arthritis.
To expect millions of people who are as different from each other as the sun and moon are to find relief from one, two, or even three options is absolutely ridiculous! What we need are pain management plans that address us individually, not as group.
The problem is
For doctors and patients to have a better understanding of how the disease progressing, what could be triggering symptoms/pain, and the impact it is having on the patient’s life they both need to see the full story, not just one day or week of the patient’s life.
Let’s talk about sex!
Chronic pain from fibromyalgia and psoriatic arthritis will destroy your sex life unless you are willing to accept and make changes.
What needs to change?
Things that may need reevaluating are:
Our prescribed treatments aren’t going to help if we are struggling with our mental health. Reasons why therapy is important after receiving a chronic illness diagnosis.
Receiving a diagnosis of an autoimmune disease is overwhelming. There is so much to take in, especially if you have no knowledge about your diagnosed disease and weren’t expecting it.
My favorite site for natural remedies has just released some amazing new products and a discount code to save big!
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You’d think that after living with multiple chronic illnesses for as long as I have that I would have this waiting game down pat. I’m improving, but boy is it tough!
When chronic pain made going to the movies difficult my first inclination was to stop going. Later, I found ways to make going to the cinema enjoyable and today I am sharing those tips with you!
Tears poured down my face as he outlined a diet plan and told me to return if the pain became worse. When he asked if there was anything else, I said yes, find what is wrong with me.
In last week’s blog post Why I fear hospitals, doctors, and test results I shared some of the ways that the medical profession has failed me and in some cases almost cost me my life. Who knew when I scheduled that post that I would once again be mistreated and misdiagnosed just a few days later.
I know my body well. In fact, I know better than any test or doctor. Not to sound conceited, but not one test or scan has ever shown the destruction that has been taking place in my abdomen since 2003. NOT ONE!! However, my theories have been validated in surgery and each surgery was proved necessary.