Today I am going to present you with a spring cleaning idea that you may not have thought of……. sprucing up your view!
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.
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.
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.
Instead of waiting until 2020 to set and reach health goals, I am doing it now with the help of a Pack Health coach!
It is time to apply some good old fashioned spring cleaning to our social media accounts.
Whether it is one single tear rolling down my cheek or many pouring out of my eyes, they still represent the kind of pain you secretly wish upon the wickedest of people.
Here is a rundown of this week’s articles! Read what you missed and share what you liked! *Disclosure: This post includes affiliate links. Meaning that at no additional cost to you, I receive a commission […]
I know that there are times when you don’t feel tough. I also know that there are days when you truly lack physical strength, but that doesn’t mean that you aren’t tough.
Today I want to tell you that it is okay to not be okay with traveling during the holiday season! And here is why!
You might think you are comparing apples to apples when you compare your abilities with someone who has the same chronic illness, but it’s not that simple……
Do you or someone you love live with a mental illness? Do you struggle to communicate with your friends and family? You are NOT alone!
Are you ready to embrace 2018 as your healthiest and most vital year yet? Here’s the first gift to help you make this resolution a reality!
When I found out I was accepted into 23andme’s depression/bipolar study, I was excited! Not only would I get to be part of a study that could have a huge positive impact for generations of people with those conditions, but I also would get
If you’ve experienced emotional abuse, the following post could be potentially triggering……Growing up in an emotionally dysfunctional family, I didn’t learn healthy skills for coping, communication, or relationships. What was modeled for me (and done to me) was ….
Do you feel unworthy of having fun or enjoying life because of the time your chronic illnesses force you to spend in bed? In my latest vlog I share why you need to stop punishing yourself for the crimes your chronic illnesses have made and instead start rewarding yourself