Katie Dennis
Katie Dennis
  • Female
  • Port Huron, MI
  • United States
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  • Photos (19)
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Katie Dennis's Friends

  • Alison Hobbs
  • Tatum Miller
  • Doll
  • Mackenzie
  • elena f.
  • Isabelle O'Donnell
  • Erin
  • Susan - Jon's Mum
  • Tracy and Amanda
  • Carol Solis
  • Cheryl, Co-founder

Katie Dennis's Groups

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Katie Dennis's Page

Latest Activity

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Cheryl, Co-founder left a comment for Katie Dennis
Hey Katie, Alopecians in Michigan will celebrate International Alopecia Day (August 6th, 2011) with a late lunch at T.G.I Fridays in Livonia. We will be meeting at 3 PM. Come for lunch, come for dinner, come for an appetizer or just come for…
Jul 29, 2011
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Katie Dennis is now friends with Cheryl, Co-founder and Alison Hobbs Jan 1, 2011
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Cheryl, Co-founder left a comment for Katie Dennis
Here is the link: http://www.alopeciaworld.com/events/michigan-international
Jul 13, 2010
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Cheryl, Co-founder left a comment for Katie Dennis
Hi Katie, Did you see our event for International Alopecia Day, really hope you can make it. Let me know.
Jul 13, 2010
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JeffreySF left a comment for Katie Dennis
Hi Katie, Ran across your page tonight. Hope you're going to the NAAF Conf in Indy and have a great time! Jeffrey
Jun 23, 2010
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Losing hair again:(
Status posted by Katie Dennis Jun 22, 2010
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Katie Dennis commented on Carmen Dayhoff's group 'Alopecians of Indiana'
hi everybody. im new to this area and im so glad to be part of this ongoing alopecia community!
Jun 22, 2010
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Alopecians of Indiana

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This group is especially open to those in Indiana.I would like for us to Get To Know One Another Better!
Katie Dennis joined Carmen Dayhoff's group Jun 22, 2010
9 Comments
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Katie Dennis is now friends with Tatum Miller and Carol Solis Jun 22, 2010
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Alyce Martin left a comment for Katie Dennis
Hey Katie! I love your photos! I am so glad I can go swimming, go down water slides, ride a roller coaster and wash my hair WITH IT ON ME. I wear a vacuum piece and I LOVE it. I only wish I would have had it when I was a teenager. Those years were…
May 20, 2010
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Katie Dennis is now friends with Tracy and Amanda and Erin Mar 4, 2010
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Mackenzie and Katie Dennis are now friends Feb 22, 2010
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lovin' life
Status posted by Katie Dennis Feb 22, 2010
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Susan - Jon's Mum left a comment for Katie Dennis
Thanks Katie, Good on you. I am so glad that you are doing fabulous. Hope you enjoy your weekend with your sister. I am very close to my sister. My two daughters are very close too. It is a nice thing to have- a good relationship with your…
Feb 13, 2010
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Katie Dennis left a comment for Susan - Jon's Mum
Hey susan, I am doing fabulous! Im going to new york this weekend to visit my sister. She is so supportive of me and so is my whole family. I think thats important in any situation. Im glad Jon has such a wonderful supportive mother like you and i…
Feb 12, 2010
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Susan - Jon's Mum left a comment for Katie Dennis
Hi Katie Welcome to Alopecia World. I read your comment on Teenagers with Alopecia. Glad to hear that you are coping well with AA. You have a good attitude towards it. I love your photos - looks like you have some very supportive friends. My son…
Feb 9, 2010

Profile Information

Relationship Status:
Single
About Me:
I have had alopecia for about a year now and im in high school. I found my first blad spot on the first day of 9th grade. Which was pretty horrifying but i keep it cool now
Do you have alopecia?
Alopecia areata
Are you age 18 or older?
No - I am not 18 or older

Katie Dennis's Photos

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Comment Wall (6 comments)

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At 2:19am on July 29, 2011, Cheryl, Co-founderCheryl, Co-founder said…
Hey Katie,

Alopecians in Michigan will celebrate International Alopecia Day (August 6th, 2011) with a late lunch at T.G.I Fridays in Livonia. We will be meeting at 3 PM.

Come for lunch, come for dinner, come for an appetizer or just come for coffee and dessert!

We want to meet you!

T.G.I Fridays
20120 Haggerty Road
Livonia, MI 48152-1087
(734) 464-8443

Please RSVP on the Events page:

http://www.alopeciaworld.com/events/international-alopecia-day-det
so that we can make reservations if needed.

Thanks and we really look forward to meeting you!

TGI Fridays has been kind enough to offer our group a 10% discount on the meals.

PS: Please note that this is a dutch treat and everyone is responsible for their own bill!

Cheryl
At 12:27am on June 23, 2010, JeffreySFJeffreySF said…
Hi Katie,

Ran across your page tonight. Hope you're going to the NAAF Conf in Indy and have a great time!

Jeffrey
At 6:14pm on May 20, 2010, Alyce MartinAlyce Martin said…
Hey Katie!

I love your photos! I am so glad I can go swimming, go down water slides, ride a roller coaster and wash my hair WITH IT ON ME. I wear a vacuum piece and I LOVE it. I only wish I would have had it when I was a teenager. Those years were very hard for me.

I have worn my vacuum piece since 1989.

I will be in Michigan next month!!

Alyce
At 1:06am on February 13, 2010, Susan - Jon's MumSusan - Jon's Mum said…
Thanks Katie,
Good on you. I am so glad that you are doing fabulous. Hope you enjoy your weekend with your sister. I am very close to my sister. My two daughters are very close too. It is a nice thing to have- a good relationship with your sister.
Yes high school is only a short time of your life. If people can't accept you for who you are then they are not worth your time. It is amazing how different people deal with things in different ways and how some of us can accept situations and change easily and some of us find it very hard and have a hard time of it. So you should be very proud of yourself. You have learnt the secret to being happy in yourself. Even people that don't have a condition like alopecia haven't learnt what you obviously have. People who don't treat you right or don't accept you for who you are- they don't matter!
So feel good about yourself. You are one smart cookie.
I hope Jon learns that lesson as well.
Take care now
Susan
At 6:20pm on February 9, 2010, Susan - Jon's MumSusan - Jon's Mum said…
Hi Katie
Welcome to Alopecia World. I read your comment on Teenagers with Alopecia. Glad to hear that you are coping well with AA. You have a good attitude towards it.
I love your photos - looks like you have some very supportive friends.
My son Jon, 13, has had Alopecia since he was 6. He has just started developing Universalis. He had a hard time accepting the onset of Universalis but I think he is beginning to get used to it now.
How are you at the moment?
At 12:39am on January 28, 2010, LeslieAnn ButlerLeslieAnn Butler said…
Hello and welcome, Katie!
How are you doing?
LeslieAnn
 
 
 
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