Per Kjellqvist
  • Male
  • Full time sailor
  • Sweden
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  • Catharina
  • JeffreySF
  • Roger

Per Kjellqvist's Discussions

Hairdressers

Started this discussion. Last reply by Leah Turlo Apr 11, 2010. 10 Replies

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Profile Information

Relationship Status:
Married
About Me:
Hi,
I first noticed I had AA when I was 23, it was a small spot which grew back quite quickly. Had spots coming and going for almost 20 years, but they never stayed for long, and I grew my hair long with a pony tail to be able to hide them. Then at 42 my hair started thinning out real fast (over 4-5 months) so I decided to shave it all off. At 45 it became AU, grew back a year later, but is now again AU since a year.
My mother has autoimmune thyroid disease, but I don't know anyone else in our family with any related autoimmune disease.
I am really happy to see that the knowledge and awareness about Alopecia is expanding rapidly now, and would like to share my experiences with anyone who is curious.
I don't wear any hairpiece, am always in the sun (check out my website) and am waiting for someone to invent a baseball cap that looks cool on a bald head :-)
Do you have alopecia?
Alopecia universalis
Are you age 18 or older?
Yes
Your Website (Leave blank if you don't have one):
http://www.kjellqvist.ch

Comment Wall (12 comments)

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At 4:40pm on February 8, 2009, JeffreySF said…
Hi Per,
Stopped in to say hello. How is everything with you?

Jeff
At 12:17am on January 27, 2009, Cheryl, Co-founder said…
Hi Per, I am going to send your question to rj and we will get back to you. Thanks, Cheryl
At 5:11pm on January 24, 2009, Eileen Simpson said…
You bet

Take it easy

Eileen
At 4:32pm on January 24, 2009, Catharina said…
Hej och tack för Ditt svar.Härligt liv Du har! Vi får hålla kontakt.Önskar
att det kom en nyhet ang.forskn.av Alopecia snart.Saknar verkligen hår!
HälsnCatharina
At 10:25am on January 24, 2009, Catharina said…
Hej Per! Roligt att bli vän med Dig! Var bor Du? Är Du medl.i Alopeciförb.?
Jag är ledamot i Riksf. Vore kul att räffas! Finns så mkt.att göra för oss alla drabbade.När man ser hur det är i USA. Tittade på segl.!Intressant! Kanske!!
Ha det.. Hälsn.Catharina
At 2:10pm on January 21, 2009, Cherylnz said…
Hi Per
Welcome to Alopecia World
At 8:50am on January 21, 2009, Cheryl, Co-founder said…
Hi, I wanted to take this opportunity to welcome you to Alopecia World. I have been living with Alopecia Areata since 1991 and know full well the struggle it can be. I look forward to getting to know you. Cheryl, Co-founder
At 12:03am on January 21, 2009, Eileen Simpson said…
Hi and welcome to Alopecia World.

Eileen
At 7:59pm on January 19, 2009, JeffreySF said…
Hello Per,

Welcome to Alopecia World.

Jeff
At 6:55pm on January 19, 2009, Roger said…
Hej.

Var inne och kollade din hemsida. Trevlig.

Roger.
 
 
 

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