Hello Ursula
Thank you for beeing my friend. I come from a little country in the middle of Europe named Slovakia, former Czechoslovakia. I am at the same age as you are, married for 12 years. I have got 6 children, 3 boys and 3 girls. The yongest girl 15 months old has got congenital alopecia aerata due to hemolyza after rh-inkompatibility during pregnancy. Simply she was born with it. Alopecia aerata at all is very rare in our country maybe becouse we have got only 5 000 000 inhabitants and our dermatologists are not very experienced with it. My child began regrowth in december after her first haircut, fortunately. I like your children , they are so cute! Especially your youngest one. How old is he now? In our country women used to stay with children at home until they are 3 years old, to have a babysiter is very expensive. Do you work? What do you do? I am florist and gardener.
Looking forward for hearing from you soon. Dana .
I also live in rural BC - though not as rural as you I think! - in Nelson. Just wanted to let you know that I have a friend in Prince Rupert who is a teacher in a school there... she has told me that she works with another woman who has alopecia universalis, just in case you want to perhaps speak to someone in person who has been through it all. I believe this woman wears wigs and so may be able to give you some info if you are interested in going that route. I think you are fairly close to Prince Rupert? In any case I wish you all the best. I am near the same age as you and lost my hair last year. It does get easier.
I just read your most recent Blog Post and I was really touched.
I hope you are having a good day today. I pray you will get stronger each day no matter what happens.
You have a wonderful support system Love them and let them love you.
Hi ursula, some one once sent a saying to me that really help me deal with different types of relationships- Friends are in your life for 3 reasons.
some for a season
some for a reason
and some for a lifetime.
Remain blessed,God is faithful and He is a friend that sticks closer than a brother. Looking forward to talking with you!
Danach'ea Ursula! I'm a proud ALopecian First Nation Irishman currently in Calgary cisiting and working - brrr it's chilly here! Welcome to AlopeciaWorld! Cheryl's a groovy friend of mine - we met years ago through an MSN support group. I love the photos you posted! Cheers from Alberta!
Hi Ursula, Glad to see you here! 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
Hello and welcome, Ursula!
I know how hard it can be. I have had alopecia for about 30 years. After I became the spokesperson for the National Alopecia Areata Foundation, a lot of women were needing my help and support, so I wrote a book called, "If Your Hair Falls Out, Keep Dancing!" It might make you feel better. You can find out more on my page -- and let me know if there's anything else I can do!
LeslieAnn
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Thank you for beeing my friend. I come from a little country in the middle of Europe named Slovakia, former Czechoslovakia. I am at the same age as you are, married for 12 years. I have got 6 children, 3 boys and 3 girls. The yongest girl 15 months old has got congenital alopecia aerata due to hemolyza after rh-inkompatibility during pregnancy. Simply she was born with it. Alopecia aerata at all is very rare in our country maybe becouse we have got only 5 000 000 inhabitants and our dermatologists are not very experienced with it. My child began regrowth in december after her first haircut, fortunately. I like your children , they are so cute! Especially your youngest one. How old is he now? In our country women used to stay with children at home until they are 3 years old, to have a babysiter is very expensive. Do you work? What do you do? I am florist and gardener.
Looking forward for hearing from you soon. Dana .
I also live in rural BC - though not as rural as you I think! - in Nelson. Just wanted to let you know that I have a friend in Prince Rupert who is a teacher in a school there... she has told me that she works with another woman who has alopecia universalis, just in case you want to perhaps speak to someone in person who has been through it all. I believe this woman wears wigs and so may be able to give you some info if you are interested in going that route. I think you are fairly close to Prince Rupert? In any case I wish you all the best. I am near the same age as you and lost my hair last year. It does get easier.
I just read your most recent Blog Post and I was really touched.
I hope you are having a good day today. I pray you will get stronger each day no matter what happens.
You have a wonderful support system Love them and let them love you.
Hugz,
Jeff
some for a season
some for a reason
and some for a lifetime.
Remain blessed,God is faithful and He is a friend that sticks closer than a brother. Looking forward to talking with you!
Welcome to Alopecia World
I know how hard it can be. I have had alopecia for about 30 years. After I became the spokesperson for the National Alopecia Areata Foundation, a lot of women were needing my help and support, so I wrote a book called, "If Your Hair Falls Out, Keep Dancing!" It might make you feel better. You can find out more on my page -- and let me know if there's anything else I can do!
LeslieAnn
They have two in BC. One in Vancouver and one in Victoria area.
I have some numbers and names if you need it.
Roger.
Roger.
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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.