Apeople. Life After Diagnosis The diagnosis hit me hard. I was years old and I didnt know what life was going to be like from then on. I did a lot of Googling on my condition and read a lot of information on it. I was depressed for a while after my diagnosis and life felt like a blur. I dont remember much from those days. Luckily as time went on and life got a little bit easier the diagnosis didnt feel so bad. I started to realize that it wasnt a beall endall situation.
Instagram and what I was going through
I would be OK and I just needed to learn how to adapt to my new lifestyle. How Ive Connected With Myself and My Body Once I was diagnosed I decided to make a blog. I began writing about my experiences and what it was like to live with this condition. I found my love for writing and advocacy. I also started posting about my life on . The community Ive found Cayman Islands Mobile Number List from telling my story has been amazing. Ive talked to people all over the world people with ankylosing spondylitis and with other conditions as well. resonates with people and most of all I love helping others. This is something I never would have found had I not been diagnosed with ankylosing spondylitis.
I can tell when a flare is coming I know how
Life Over the Years Now that Ive had ankylosing spondylitis for years Ive learned a lot. Ive learned more about my body and how it operates. to deal Germany phone number list with them for the most part bad flares can be hard to handle and I know what helps with the pain and what doesnt. What Helps I usually find that heat helps me the most during a flare. I use a heating pad or a microwavable hot pack. When flares are particularly.