I wonder if you will remember me. My name is Linda Krusmark. My husband is Lee Krusmark who is deaf. I have been diagnosed with frontal fibrosing alopecia and lichen planopilaris. I joined this group and saw your picture. How are you?
Hi Scott,
Nice to meet I was looking saw your pictures.
And thought I would say hi.
Just wanted to ask your a question or ask your wife.
How does she feel about you having alopecia?
Look like from your pictures that she is a very caring person.
I have Alopecia Universalis too, and I have a great husband that accepts me the way I am.
He said he didn't marry me for my hair.
Isn't it great to have someone who really cares for us. For us .
I still have hard time with me excepting it. I know that its for a reason.
And I am taking one day at a time.
Just wanted to say hi.
Take care:)
I was living in Western Washington state when the job was offered to me. I no longer work there I now work in the Milton Freewater school system. I work with elementary kids who have behavior disorders. I love them a lot and it's been great teaching them ASL.
You sound like such a wonderful and diverse person. Tell me about Krav Maga. I have heard it is one of the best things to do to stay in shape. I have got to find ways to get fitness back into my life. My goal, run 3 miles.
Hi Scott, I wanted to welcome you to Alopecia World. I can honestly say that we are a great community here and I hope you enjoy the time you spend with us. Cheryl, co-founder
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Scott,
I wonder if you will remember me. My name is Linda Krusmark. My husband is Lee Krusmark who is deaf. I have been diagnosed with frontal fibrosing alopecia and lichen planopilaris. I joined this group and saw your picture. How are you?
Jeffrey
Jeffrey
Nice to meet I was looking saw your pictures.
And thought I would say hi.
Just wanted to ask your a question or ask your wife.
How does she feel about you having alopecia?
Look like from your pictures that she is a very caring person.
I have Alopecia Universalis too, and I have a great husband that accepts me the way I am.
He said he didn't marry me for my hair.
Isn't it great to have someone who really cares for us. For us .
I still have hard time with me excepting it. I know that its for a reason.
And I am taking one day at a time.
Just wanted to say hi.
Take care:)
Stopped in to say hello.
Hope your holidays are going well.
Jeff
take care and thanks for the note.
Eileen
Welcom to the site.
I love the trumpet!!!
Jeff
Yes, its a great site to meet people with alopecia.
I notice that you live in Portland. It really looks like a nice city.
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.