Tasha Dingler
  • Female
  • Grand Ledge, mi
  • United States Minor Outlying Islands
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  • Tracy Hild.
  • Misty Boggs
  • MiNAH
  • Tracy and Amanda
  • Ohio
  • suzanne
  • Natalie
  • Tammy -mom of Ramsey
  • Cherylnz
  • Cindy
  • Roger
  • Steve

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Relationship Status:
In a Relationship
About Me:
I am 23 year old mother of two. My daughter Sierra Sue 5 was diagnosted with alopecia areata a year ago. She has 50-75% hairloss currently. My youngest Jersie Lee-Ann jsut turned 3. It makes it really nice Jersie not being the dazzle dazzle kind of girl that likes her hair curled n pinned up so sierra doesnt have to feel left out. Because Sierra is so into fashion.
Do you have alopecia?
Parent or guardian of child with alopecia
Are you age 18 or older?
Yes - I am 18 or older

Tasha Dingler's Blog

To an alopecia artist

Posted on August 10, 2009 at 10:40am 3 Comments

Hi my name is Tasha im 24 year old mother of two. my eldest daughter Sierra5 have alopecia areata. I am looking to create a newletter to be sent some with all the children in her school. instead of putting a picture of an actual person with alopecia or a picture of her, I thought it would be nice to have an animated drawing of some children playing happily. I think it will catch more eyes and interest to create better awareness. Unfortanatly i stuggle with stick figures. Drawing doesnt come… Continue

"THAT MAN HAS ALOPECIA TOO MAMA" She yells

Posted on May 6, 2009 at 1:26pm 3 Comments

So when we moved into our appartment there was carpet in the kitchen....yeah not really feezable with two kids right. So we got it replaced with lanolium, well the men were finishing yup doing it and headed down to their van. (were second floor) She runs to the belconey and says mama he has alopecia too!!! All excited! Then I explained to her that men lots of time loose their hair with age. It was so cute!

all the children in her class wear bandannas

Posted on April 28, 2009 at 6:19pm 2 Comments

Hi, My name is Tasha and I am new to this whole alopecia world, as of yesterday! My daughter Sierra Sue is 5 1/2 and has had alopecia for over a year. What a journey it has been. Ive done so much research about alopecia. When she was 1st seen by the family doctor for her quarter sized bald spot, she said it probably got rapped around a toy and pulled out. I refused to excet that as an answer and ended up researching. Alopecia is what I came up with, never hearing of the issue before I was… Continue

Comment Wall (10 comments)

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At 11:20am on September 19, 2011, Sarah Eisenhardt said…
http://www.alopeciaworld.com/events/apple-orchard-with-children-s-alopecia-project-of-michigan
At 2:32am on July 29, 2011, Cheryl, Co-founder said…
Hi Tasha, 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 8:53am on August 17, 2009, Tracy Hild. said…
We could meet up this Sat. if that works for you.
At 10:12am on August 11, 2009, Tracy Hild. said…
I would love to meet for a play date. When is a good time for you?
At 12:14pm on May 3, 2009, Melanie said…
thank you ♥
At 2:41pm on May 1, 2009, LeslieAnn Butler said…
Hello and welcome, Tasha!
How are you and Sierra doing today?
LeslieAnn
At 5:58pm on April 29, 2009, Cindy said…
Hi Tasha, Welcome to AW! Your daughter is beautiful and it sounds like she has a great support system to help her through this. How did you daughter feel to see all of her friends where bandannas? And, how are you doing?
At 10:37pm on April 28, 2009, Cherylnz said…
Hi Tasha,
Its a great site and I joined about the middle of last year (I think AW started in March last year).
I wish these groups were available when I first got Alopecia. Unfortunately computers were not available then either :)
Cheryl
At 8:33pm on April 28, 2009, Natalie said…
Hi Tasha! Welcome to Alopecia World! I read your blog about your daughter and her class wearing bandanas, and that is such a wonderful idea! You sound like a really involved, supportive mother to your daughters- that is terrific :) Just out of curiosity, does anyone else in your family have alopecia, like an aunt or brother? Because no one in my family has it, and I can't seem to figure out where this came from. I suppose my "innovative" genes got the best of me and decided to start a new trend haha. And I'm also wondering if my children will have it, too......sorry, I am rambling! Anyways, please feel free to chat anytime or ask me any questions.
Cheers,
Natalie
At 3:51pm on April 28, 2009, Cherylnz said…
Hi Tasha,

Welcome to Alopecia World :)

Cheryl
 
 
 

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