Psoriatic arthritis resources for the newly diagnosed, those looking to improve life with PsA, or someone just wanting a better understanding of it.
Psoriatic arthritis Twitter chat is taking place this Wednesday! Get all the details here and find out how you can help spread awareness!
🧐 1 in 3 people with psoriasis may develop psoriatic arthritis. Learn more about it here!
Chronic pain is misunderstood by our family, friends, doctors, and even ourselves. If not careful those misunderstandings could lead to more pain.
No need to leave home! Shop these Black Friday and Cyber Monday deals from home. Everything from pain relief to products that will make life more comfortable and easier!
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.
Whether you have a chronic illness like fibromyalgia, autoimmune arthritis, or any other condition that has caused you to struggle with balance, these canes will have you looking sharp while remaining on your feet!
This month we are scaring up healthy habits! No tricks just a bag full of treats for your body and mind.
Has anyone attempted to comfort you by saying “At least you don’t have…”? Have you comforted yourself with the same thought? he thing is, no matter how you end this phrase, it is never okay to say, not even to yourself! And here is why!
I don’t know about you, but when I find a pain relief medication/product/treatment that works, I make sure to use it every single day. When that same thing continues to provide relief month after month and year after year, I have to tell everyone I know because I want them to experience the same relief that I have.
It wasn’t until I was diagnosed with fibromyalgia, psoriatic arthritis, psoriasis, endometriosis, degenerative disc disease, and coccydynia that I learned to value and appreciate a comfortable bed.