In honor of Alopecia Awareness Month, you can add this twibbon to your Twitter avatar. Please check the site out now and help support Alopecia Awareness!
Welcome to my random ramblings and deep thoughts...
I hope you enjoy reading my blog -- and if you're newly diagnosed with alopecia areata, totalis, or universalis, I personally want you to know that you're not alone.
I've lived with alopecia for 27 years -- and each day has its ups and downs; joys and sorrows; successes and failures; and yet, getting through the day knowing I am loved and that I made it is its own reward. If you have a question, please leave a comment and ask me, and I'll answer it as best I can.
If you're the loved one (spouse, significant other, family member, or friend) of someone with alopecia, I want you to know that acceptance and understanding comes one day at a time, and that your love and support are the most crucial parts of living with this condition. From all us alopecians out there, thank you -- we can't make it without you!!!
For more information about alopecia areata, visit the National Alopecia Areata Foundation website at www.naaf.org. To meet other alopecians and their loved ones, please visit the Internet's fastest growing social network for alopecians, their friends and families at Alopecia World (http://www.alopeciaworld.com)
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