Wow- you really spelled it out in words! Your poem should be distributed to all doctors, your feelings was mine 4years ago.
And a fantastic tatoo, if its yours :)
That was a beautiful poem you wrote!!! Absolutley beautiful!!!!
I don't know if you remember me, but we had met on another Alopecia support group.....I've lost the link, because I got a new computer after mine crashed & I lost everything!!! But it's the one that maude had......
Nice to see you are doing well!!
I love your story. My mother use to tell me that she had eyes in the back of her head too. lol! I haven't got my tattoo or tattoos yet, but I am sure the pain would not hurt as much as watching my hair fall out too. Thank you for helping me look at getting a scalp/head tattoo from a different perspective. I always thought about getting it, but I actually never seen anyone with one. It is good to know that someone else has one, especially a fellow Alopecian. Thank you for sharing your story with me and when I do get my tattoo, I will think of you and your story. Thanks again :)
I was actually thinking about getting one tattoo on my head/scalp area. I was wondering how painful it was getting yours, if you don't mind sharing it with me?
Hey girl.. loved to see that you were on here too.. I can not for the life of me get back onto MSN.. its very frustrating.. can you send me an invite for that site by chance? I miss everyone... PLUS oh yes.. my yahoo is gone. I do not know my password so please send me an email so I can get in touch.. please let everyone on MSN I say Hello my alopecian friends and especially Joanne...Hugs to you from the UP :-)
Hi Dotty,
I think I have seen you on the MSN site many times. I check in on the message boards quite frequently. I have had alopecia areata for the past 6 years. It is comforting to come to these sites and meet so many people that have alopecia. Sometimes I feel like I am the only one! You are an inspiration.
I think that you wishing that you could snap your fingers to make alopecia understood by eeveryone, instead of snapping to make your alopecia disappear shows me that it is possible that Della and I can one day accept it. I personnaly think she may accept it a little more than I do. She thinks your head is beautiful, by the way. But I don't condone that yet, she's only going to be 5!
Thanks! I love havin a mohawk, i feel like a bad ass. hahaha. I can see how the tattoos are a good way to open up conversations about alopecia. Very cool. I love it. Are you going to conference this year?
Dotty, I saw in someones comments that you may not make it to the coference...I will put together a "Dotty Fund" lol...This will be my 1st coference and I have to meet you. I'm sure I eventually will though...
Hiys how have you been. I miss eveyone too. I have a couple new friends that might be coming to the conference withme this year. I hope you can come. You would be missed if you dont go.
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And a fantastic tatoo, if its yours :)
I don't know if you remember me, but we had met on another Alopecia support group.....I've lost the link, because I got a new computer after mine crashed & I lost everything!!! But it's the one that maude had......
Nice to see you are doing well!!
Your are an inspiration !
Wonderful to see you here my friend. Hope you and Brett are both well.
I only joined here today so will be updating my profile with more info very soon.
Love (n) Hugs
Sarah x
I think I have seen you on the MSN site many times. I check in on the message boards quite frequently. I have had alopecia areata for the past 6 years. It is comforting to come to these sites and meet so many people that have alopecia. Sometimes I feel like I am the only one! You are an inspiration.
Hope all is well with you and yours...Take care
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Any mention of products and services on Alopecia World is for informational purposes only; it does not imply a recommendation or endorsement by Alopecia World. Nor should any statement or representation on this site be construed as professional, medical or expert advice, or as pre-screened or endorsed by Alopecia World. Alopecia World is not responsible or liable for any of the views, opinions or conduct, online or offline, of any user or member of Alopecia World.