Sam G
  • Female
  • Devon
  • United Kingdom
Share on Facebook MySpace

Sam G's Friends

  • thinlizzyfairy
  • velvet
  • Gemma G
  • hannah sophia holland
  • lucey smith
  • lee willsmer
  • Nicola Jones
  • Gale Moorman
  • Gail
  • Goran jovanovic
  • Diana Hastings
  • Barbara A Helnore
  • Lucy Rogers
  • lynne
  • margaret watson

Sam G's Discussions

UK Teenagers/Parents with Alopecia

Started this discussion. Last reply by Heather Nov 11, 2010. 1 Reply

Hi GuysI have Alopecia Areata and my daughter was diagnosed with it 8 months ago. She is 15 and is finding it very difficult to accept, crying whenever a new bald patch appears and worrying about the…Continue

Where did it start?

Started this discussion. Last reply by Franchesca N, Sanchez Jul 12, 2010. 13 Replies

Just looking through the photos I notice several people showing their alopecia began at the back of the head above the neck. This was the case for me and now for my daughter who has it. Is this the…Continue

What will the reaction be?

Started this discussion. Last reply by Rebecca Benjafield Apr 5, 2010. 6 Replies

Hi Guys, I have alopecia areata, I shave my hair with clippers to take control and more comfort wearing a wig. If I was bald I would go out uncovered, however, with very dark thick hair where it…Continue

Gifts Received

Gift

Sam G has not received any gifts yet

Give a Gift

 

Sam G's Page

Profile Information

Relationship Status:
Married
About Me:
Married, 2 children, recent illness resulted in auto immune diseases including alopecia.
Do you have alopecia?
Alopecia areata
Are you age 18 or older?
Yes - I am 18 or older

Sam G's Photos

  • Add Photos
  • View All

Sam G's Blog

Bring it on!

Posted on October 19, 2010 at 3:55pm 2 Comments

Hair fell out, shaved rest off. Started to grow, now falling out again. People say "oh no what a shame" but seriously, I'm not bothered. I have accepted my hair will grow, fall out etc probably forever and that's ok. I will keep it short when it does grow and not worry about bald patches showing. If I have to shave again thats fine - I can stay in bed longer in the morning cos it takes less time to get ready! I control my life not alopecia. Bring it on!!!

I'm not that old!

Posted on April 20, 2010 at 1:13pm 3 Comments

So,taking into account Thea's baby steps programme(trademark?) I took my daughters shopping with no wig or scarf! A little girl saw me and said "Look Mum it's Jade Goody's Mum". For those that don't know Jade was a British Z list celebrity who died last year of cancer and lost all her hair from treatment. Now I don't mind the bald reference but I am NOT old enough to be her mum!!!!!!! The little girl must have forgotten her glasses that day? :)

Anniversary - gonna do it!

Posted on March 14, 2010 at 8:30am 9 Comments

It's the year anniversary of my accident that started the alopecia. Empowered by everyone's comments I am going for lunch with no head covering. Will let you know how I get on. At the very least I should get extra portions cos they feel sorry for me!!!!!!!

Maybe cruel but very very funny!

Posted on March 8, 2010 at 4:35pm 10 Comments

I work in a secondary school and wear 3 wigs and headscarves according to my mood. Some year 7's stopped me and asked if I had a twin who worked at the school as there is someone who looks like me but with different hair. I laughed and said I wear wigs. They wouldn't believe it and a particularly cheeky one said prove it then, take it off. So I did! Their faces were a picture, chin's hitting the floor doesn't cover it. I said was that ok and they said yes miss and sheepishly walked off. It was… Continue

Comment Wall (10 comments)

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

Join Alopecia World

At 4:54pm on August 30, 2011, margaret watson said…
Hi there! I am holding an unformal meeting at my house on thursday 15th September at 7.30pm. I do hope you will come along and meet 1 or 2 other people who also have various forms and stages of alopecia. We have a good chat and a laugh and just take it from there. Please let me know either way but I hope, very much, that you will attend.

My address is :

Westcroft,
Town Lane.
Woodbury
Exeter
EX5 1NH
Tel 01395 233620 or 07734102776 (bad signal in house though)

Margaret Watson
At 12:27pm on March 28, 2011, Rose said…
Hi Sam, where did you get your wig in your profile pic, it looks a good density thanx
Rose
At 4:46am on August 23, 2010, Gemma G said…
Thanks Mum xxx
At 7:08pm on August 8, 2010, Gail said…
Hey Sam G! Not a marathon (I wish!), but a mere 10K. I may run a half-marathon in the Fall though.
At 5:40pm on March 17, 2010, Jessica said…
hi sam,

love the brown bob wig who's it by... can you send me back a msg w/ the info.? thanks
jess
At 8:49pm on March 15, 2010, Gale Moorman said…
Hey, thanks a lot Sam G. You have a nice face so going without any head covering is bound to look cute. You are a brave soul. Good for you!
At 3:13pm on February 3, 2010, Sam G said…
Thanks Margaret, if you have another get together would love to join you. Excellent that you have a boat in Torquay, I'm rubbish at sea, can't even do a pedalo without feeling sick!!!! Samxx
At 1:47pm on January 26, 2010, margaret watson said…
Sorry for some reason my web page wouldn;t open to alopeciaworld for the past couple of months, but tonight it seems back to normal.
So hello to you. I really wanted to be in touch. I live in woodbury,exeter and often pop down to Torquay as we have a boat down there. I met up with 2 new alopecia sufferers last week. We had a fab time just chatting and knowing what we were saying was really being heard - such a relief! I do believe noone understands what we feel and how we cope on a dily bases. It is so important to be with each other and chat like this.
Margaret x
At 2:48pm on January 19, 2010, Beverley said…
ps nice wig
At 2:48pm on January 19, 2010, Beverley said…
Thanks. I am not sure about the local meetups etc. sorry. :-)
 
 
 

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.

© 2024   Created by Alopecia World.   Powered by

Badges  |  Report an Issue  |  Terms of Service