GRIFFIN AND HRONN (GRIFFIN'S MOM)
  • Toronto
  • Canada
Share on Facebook MySpace
  • Blog Posts
  • Photos
  • Photo Albums
  • Videos

GRIFFIN AND HRONN (GRIFFIN'S MOM)'s Friends

  • Karen( Mom)
  • Carol
  • Cindy

Gifts Received

Gift

GRIFFIN AND HRONN (GRIFFIN'S MOM) has not received any gifts yet

Give a Gift

 

GRIFFIN AND HRONN (GRIFFIN'S MOM)'s Page

Profile Information

Relationship Status
Married
About Me
I am the mother of 8-year old Griffin who has alopecia. He has lost several large patches of hair on his head and is starting to lose his eyebrows. Tough kid...handles it well...but as any parent we wish we could get their hair back for them.

Griffin is a great kid....very social ...his friends call him the 'funny guy'. He loves to play sports like hockey, baseball and soccer. He has been very brave and has not been shy to show his `patches'. When he was a baby his nickname was `BEAR"....when he got alopecia one day he stood in the middle of the room and recited `Fuzzy wuzzy was a bear.....(then he rubbed his head) and continued....`Fuzzy wuzzy had no hair'. Gotta love him. I have 5 kids and he is the middle one and out of all of them he has the best personality to cope with this. I really admire him for it.
Do you have alopecia? (Choose appropriately)
Parent or guardian of child with alopecia
Are you age 18 or older?
Yes

Comment Wall (8 comments)

You need to be a member of Alopecia World to add comments!

Join Alopecia World

At 5:15pm on June 14, 2009, Elyse and Laura(mom) Armstrong said…
Hello Griffin and Hronn, my 8yr yr old daugther Elyse also has a great attitude in dealing with her alopecia. She also loves playing soccer and the piano. She recently started going out in public (sometimes when she feel like it ) without a bandana and I am very proud of her. Sometimes at school she takes off her bandana, yes there are some mean comments but they don't always bother her. Maybe they can get together sometime this summer?
At 4:17pm on January 16, 2009, Cherylnz said…
Hi Griffon and Hronn
Welcome to Alopecia World
At 9:51am on January 14, 2009, Karen( Mom) said…
Hi and welcome, my daughter is 8 also and was just diagnosed. This site has been great for support. We are in Edmonton and don't have any local support groups that I know of so this site has been the only way to find info. I am glad that he is coping well with it.
Karen
At 9:05am on January 14, 2009, Roger said…
Welcome.

Roger.
At 8:53am on January 14, 2009, Cindy said…
Meant to ask how your son is coping with it all?
At 8:52am on January 14, 2009, Cindy said…
Hi Giffin's Mom, my name is Cindy and my 7 yr old daughter has been living with Alopecia for a year and half now..It is very hard for us moms, but the resilience our kids have is amazing. My daughter is on a regrowth cycle with treatment right now. We just need to love and support our kids and surround them with people that have positive influences over them and encourage them to do and try anything they want. My daughter does not let having no hair stop her being who she wants to be or do the things she loves. You will find some wonderful support and advice on this board. I find a lot comfort coming to this board, especially on the days I am feeling sad. I look forward to chatting with you..Cindy
At 12:33am on January 14, 2009, Cheryl, Co-founder said…
Hi Mom & Griffin, 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 3:32pm on January 13, 2009, rj, Co-founder said…
Hi, Griffin. Welcome to Alopecia World! This is a great place for great people, so be sure to make your positive presence known. :-) - rj, Co-founder
 
 
 

Disclaimer

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.

© 2025   Created by Alopecia World.   Powered by

Badges  |  Report an Issue  |  Terms of Service