Rebecca Rae
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  • Scotland
  • United Kingdom
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About me...
Well i don't really know what to say!
Every since i have developed AA, i feel less confident about my self, i always feel if i'm out people can see my bald patches and stare.
I supose everyone is different.
Do you have alopecia?
Alopecia areata
Are you age 18 or older?
No - I am not 18 or older

Rebecca Rae's Blog

Can anyone help?

Posted on May 21, 2009 at 1:53pm 2 Comments

I have noticed an incress of my hair loss and the growing size of my patches. But i used to regulary dye my hair, but ever since i have had AA i have been more aware of the risks it may cause. I supose that nothing may happen or something extreme could.I would just like some help on how to go about this, i would really be thankful to anyone how can offer me support or share there stories with me. Thankyou.

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At 3:26pm on July 3, 2009, Karina said…
What type of wig do you wear? Is it comfortable?
At 11:49pm on June 16, 2009, Rachael Louise Salmond said…
Hi Rebecca, My names Rachael and I have AA as well and I too dyed my hair all the time (My dad told me when I was 16 that all that shit I put on my hair would make it fall out) I reminded him of that, and I tell you there is nothing more fun than having your parent feel dreadful and guilt ridden. Its amazing what they will do for you!!! But all jokes aside dying you hair didn't do this! Its just one of those F@#ked up thing that happen. My hair fell out within 6months just over 2.5 years ago, and I have tried every dr know to man, Ive taken chinesse meds, minerals, vitamins, had needles stuck into me, stuck magnets in stupid places on my body, painted lotions on my head turning it red itchy and blistery (now that was an attractive look)
Ive even had my eyes, nails and poo ( have a laugh at this - walking in to a dr rooms with a jar of poo - I did that) to have looked at - and for me nothing has worked - UNTILL NOW - I went to a Physican of Immunology and Allergy . I once only had 5% of hair on my head - I now have 70 - 75% of it back and still going strong - that was 6 months ago. DO NOT GIVE UP - TRY EVERTHING!!! its hard. I had times when I thought I can not do this any longer - But you do - YOU ARE MORE THAT YOUR HAIR. - And in 8 weeks time I am going to be married, to a scotsman!!! (YES YOU ARE THINKING I MUST BE A NUTTER) And of all the races on earth they are the harshes!!! We got engaged when I was bald (like baby bottom bald) and now 2 years on we are getting married. I thought no one would want me - but being bald for me has made me stronger, It has weeded out people in my life and I have been left with the best friend any girl could ever want!!! and met a better type of people in the process - I am getting a freedom wig - there is one based in glasgow have you looked them up???? they are expensive but if it makes you feel better then i say f@%k it - just get one (also revert back to making mum and dad feel bad) My dad's buying mine!!!! They look great and you wouldn't know its not your hair - my girlfriends were amazed when they saw 2 ladys I know that have them - they all thought that it was there real hair.
I am going to be in Scotland in 6 weeks in Hawick and in Skye, Are you near any of these places?? - If I can help you in any way let me know - It can and will get better even if it doesn't look like it now - Love Rach xoxo
At 1:21pm on June 6, 2009, Somaaya said…
Hi how you doing hope your keeping ok how yae gettin on with yae alopecia?

Sam xx
At 11:01am on June 6, 2009, Lizzie said…
Hi Rebecca :)
I'm doing fine thanks, hope you are too?
Never feel alone sweetheart, I'm 18, but I've had Alopecia since I was 6, and I know that there's a lot more young people out there with AA too. Keep your head high, and keep going!
Ever want to talk, or just vent, you can always come to me, leave a comment or send me a message I really don't mind :)

Keep smilin' :)

Liz x
At 6:51pm on May 31, 2009, Lizzie said…
Hi Rebecca :)
Hope your doing well :)

I just thought I would say, that You look beautiful :)
seriously honey, you go for it girl.

Ever wan to talk you know where I am :)

Liz x
At 6:33am on May 27, 2009, Kayleigh George said…
Yes i was the same when my hair first started falling out only my close family and 2 of my friends new, until i got diagnosed then all my close friends people i see everyday new so they didnt get the "shock" when they see me. They are all brilliant and really help me, we all have a giggle about things but never in a spitefull manner. I found my mum found it harder than me. I guess its because you know there is nothing you can do.
Iv had people ask me if i have cancer, and people stare and now i just stare back at them to make them feel uncomfortable!
That is good when you go into a wig shop and it feels comfortable cos it is such a bit step.
My profile picture that wig is a plum colour but that wig isnt mine but i would like to get one that colour!
x
At 6:20am on May 27, 2009, Kayleigh George said…
sorry about online chat it wont let me type... Im not ignoring you!
At 6:19am on May 27, 2009, Kayleigh George said…
Im ok thankyou... Thankyou for compliments! Um. i went to a wig specialist and tried on a few, the long one just looks like my natural hair so was so happy to find that one and the shirt hair is for work. I found it harder to find a short hair one i liked as i was so used to having long hair i didnt want to think that i has to have short hair, if you know what i mean.
is your wig like your natural hair or is it different?
x
At 6:09am on May 27, 2009, Kayleigh George said…
Yes it always good to be prepared, i hope you dont loose all your hair. I was angry more than upset, but now i look at it as it only hair and could be worse. I do get upset though and i miss simple things like washing my hair or just tying it up!
Hope your well x
At 1:00pm on May 25, 2009, Kayleigh George said…
Yes completely! I found it quite hard to go out when my hair first started falling out. But im not too bad. I wear wigs now as my hair fell out from front to back.
 
 
 

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