WOW!! What a blessing! My first meeting was today, and it was amazing! I got to meet lots of new friends, and there were Alopecians there from children to adults. Our guest speaker was Tracey Casey-Arnold, an Alopecian for 36 years, since the age of 6, who has her own business called Whatever It Takes. She recommended a book to us called 3 seconds, and spoke of how it takes 3 seconds to fuel your passion. We need to all find what our great passion is, and to embrace it! We can all change our mindset, in only 3 seconds.
She is one of the most beautiful women I have ever met. Of course, there were tears (mostly mine), and a heartfelt warmth, of sharing with others that all can relate to each other on one level or the other. I was so anxious about my first meeting, I could hardly go to sleep last night, and then, by 5 am, I was awake this morning, and again, I couldn't sleep. The youngest of our group today was two young boys, ages 7 & 8, both living their lives, happy, energetic boys, and they were both precious! As with our journeys, where every story is different, it was obvious to me, the same holds true with how we cope with AA, and our choices that we make with it. For some, a wig; others, a scarf. Some choose the steroid injections, while others, opt not to have treatments at all. Some were so thankful to have a support group to go to, having grown up without the much needed support. I feel lucky. The support has been there for me the day I was diagnosed. Educating myself was also a big help to me. When I was diagnosed, I had never heard of Alopecia Areata.."I have what?" I was the newest Alopecian there today.
Alopecia ....do we ever get used to it? "Emotional roller coaster" I heard from many. How true! With no predictability, no cure, and no guarantees that the treatments will even help, that's only the beginning: THAT I have figured out.
By the time we get "used to" where we are with our Alopecia, then it hits us with something else.
Examples: Ok, I am used to my hair falling out now..and then it stops. I am used to being bald, then my hair is now growing in. I am used to now having hair again, then, woops...it's falling out again. Always wondering, "what's next?". There are no black and white answers for any of us. Everyone's story is different. Some cope well. Others, not so well. Where am I?? I am only just beginning to find out. I feel like I must be strong. It will be easier on my family if I am.
At first I thought it would be easy. I went to the store the other night with my baseball cap on. Not being a hat person, I was so self-conscious that ppl were looking at me. Who am I kidding to think I won't be self-conscious with a scarf, or wig, or bald?
When I fould out my insurance would not pay for my treatments, I was so floored. I felt they took that choice away from me. That power. But there are LOTS of other choices I have that I CAN make! I guess the bottom line after today for me is this: I have Alopecia: it does NOT have me!
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