T, you crack me up. Love what you said on your page. I love, love the wig in the pic with you holding the coffee cup. That looks just like my "old" hair. What is the brand, if you don't mind? The baby is toooooo cute BTW.
I love what you wrote on ur page, that is soooooooooo true. I love ur pictures and ur eyelashes, I am trying to find out where to get them and how to wear them. Please help.
I seem to have the same approach to my alopecia as you! I wear a wig or scarf when I go out but am generally bald around the house, I have a 9 month old nephew and I often wonder if he thinks he has 3 aunty jo's!!
Love all the pics and your baby is sooo cute. I have a little baby also his name is Aiden he is 11 months. When i can I will add pic's of him soon. I also have 2 girls Grace 7 and Ava 3
Gosh! I'm such a nerd...Sorry new friends that I did not accept for WEEKS!! I just now figured out how to accept new requests *lol* I'm so awesome...love it!
Hallo.
I don't know whether that will prove well tell.Your words are very wise.They may much people here assist in better manage its baldness.Say why. 28 ys backward I fell ill serious neurological illness movement.Mine doctor me said, that the longest behind 10 ys I'll on disabled armchair.It was shock and I mentally was on that very badly.
One elderly gentleman same illness me but learn heaven this infliction of like illness,but as a something due back to me.
Thanks that I have got though big severity,but always go.Therefore I think, that the most incurable illness or infliction of puts manage.Only man
mustn't it treat as ill and be sorry for oneself.So won't help.Get, that the female be bald,is very heavy,unpleasant and stressful.Alone I don't know how would it managed be woman.Right its baldness is for me always quite heavy namely am man.
My alopecia scar began within days on May 2007.Was it for me very heavy,but came to be it slowly manage.Came but January 2008 and to us unexpectedly obiit son.Mentally am again was on that very badly.Doesn't know am what shell I do and began be looking for on Internet cafe,different help.Found am Alopecia world.For the first time am here found out,that also women and little children are bald.Was I shocked and was me of all very sorrow.
Began be read various sections and examine photo and slowly find out how strong and primely personalities are.I said to myself,that when this female heavy thing know how to manage further prove assist in and second.So it I have to manage so did I.I wanted also somehow assist in.It but I don't know.Place Alopecia world and largely instance you brave and wise women on the contrary me much assisting manage its baldness and even mitigate pain above death child.Also me turns view of eye - appeal women.Not to be angry if it say badly,but for me bald woman has only other kind hairstyle and be like each other beautiful like if has hair.
Therefore again I say ,yes your words are very wise !Also ; access to baldness,as well as of several of other members and founders hereof seats is for us other instance.
Thank you and other.My English is very bad so I hope, that the me do you understand.Unless,please about erasure mine benefit.
Keep lovely day.as
Can I add a comment to my own page?!?! If it's here...I guess that's a yes, right?
Thank you guys for responding!! So far I have absolutely loved this site. I want to clarify that I am not saying in anyway that I look down on being depressed about alopecia, or being discouraged or being scared....The comments I've received before were down right pitiful....no one was going to help these people through life....they were bitter and blaming life for what 'happened' to them.
I don't like that....not having hair is nothing compared to what I could suffer from!! I'm healthy, I'm happy, I have a wonderful attractive husband and a beautiful baby boy, a house a great job and my health!! And....during my lifetime I'm sure I will have more crap to live through and cope with....so I will.
Being angry doesn't help fix anything!! And there is no use crying over spilled milk!! So we don't have hair....wear a wig and keep on keepin' on!! Be the coolest person with no hair anyone's ever met....and chances are you'll be the only one they have ever met ;) No one likes a complainer...but people will recognize you for your strength in character!! My mom always says I am her hero. From the time I started to lose my hair through today....I've never been bitter. I never let hair keep me from doing everything and anything I wanted to do. I cried when I was picked on, but I got over it and jumped back on my feet. I just think we should be thankful that we don't have hair and we are perfectly healthy and normal!! That's a blessing!! And please don't ever deny someone who questions your condition, the opportunity to learn and be educated about it. It will allow more people to understand our disorder and allow for it to maybe someday become more commonly accepted.
My mom used to get really angry when people would stare at me as a child....and I didn't even notice that they were (still wouldn't, I tend to live in my own world most of the time....and I'm always thinking about something so I may walk around looking snotty, or so I've been told, when really I am deep in thought about what I need to do when I get off work :)
And then one day she realized that....she was fighting the world, and possibly making me think I had a reason to be self conscious when I wasn't. She started me in a wig during fifth grade school pictures....I hated wearing a wig...I usually wore a cap if anything to prevent sunburn when playing outside.
Every picture of me as a child with stringy hair, clumps falling out in my brush and no one knew why....I was always smiling!!
I'm not a hero....I guess I just always knew that I had two choices. Live. Or, spend my life miserable and whine and complain and cry and blame and have a horrible time, not because I had no hair....but cause I chose to be miserable!!
I've had a great life! I have a lot of plans and goals for my future. And if my son turns out to have alopecia (I have some concerns...his toenails don't grow and he's got very light hair...small amount....I could be wrong, I hope I am), I will do my best to raise him to believe that he is special! And that he is normal. And that he can do anyyything anyone else can do! I will help him to be secure and have self esteem.....something I worked on until I was 18....when I got my first peggy knight hair piece, my whole world changed!! (All of a sudden I was Taylor....not the girl that wears a wig, cause no one can ever tell!! Unless it's because maybe they notice that my eye brows are tattooed and/or if they know someone else with alopecia....this has happened!! I love it now when someone says...Can I ask you a question?
Ummmm.....you sure can...wait, bet I can answer it before you ask! (People don't say that unless it's going to be something personal...right?) But I welcome it!! That way they get to learn about us. They get to know that we have a disorder....not a disease! They get to hear in my tone of voice that I'm confident in who I am and I'm proud to be an example in life.
If you are a Christian you'll know that God tests his children and uses us in special ways that we may not be aware of! With alopecia I can honestly say I have always passed his test and I know he will never give me more than I can handle.
My mom is my hero. Along with people I meet all the time, with much more on their plate than hair loss....that are the best damn leaders in this life I've ever known!! The ones who face significant loss, health issues, hardships...etc. and have the best attitude and strongest character! I am lucky to meet them! People touch others everyday! They may never know it. You all probably inspired someone in someway by coping with alopecia....it's awesome to think about it on a greater scale!!
It is embarrassing for someone to feel sorry for you because we don't have hair. Makes me feel really really low, like there's something I should be ashamed of. But, I also know that those people probably don't know how to react and they don't want to seem cold and unsympathetic. It's not their fault. I just stop them really quick and say...'No no, don't be sorry!! I'm not!! I haven't had hair for twenty years and I don't even remember what it was like to have hair!! So while this is new for you, it's far from new for me....it's a huge part of who I am and played a huge part in the making of who I have become! And, today, I can say in all honesty!! I do not want my hair back!! I like being me, just the way I am!! I love having a good head massage!!! (It's fantastic!!) I love the fact that my family and friends know I can take a joke and rub my head for good luck....or tug on my random scraggly hairs on my scalp to see if I can feel it *lol* (My husband loves that game!!) I'm a good sport and I get through a lot with humor!! I will never turn down the opportunity to make someone laugh, especially if it's at my own expense!! And once they know I can take it, and they crack jokes about me later....I love that just as much!!
I'm rambling, and I hope ya'll read this...it's so hard to respond to everyone, although I want to, when I work so much and have a seven month old...ROTTEN ROTTEN boy!! *lol* He is down right spoiled!! (He's so darn cute, it's hard not to....I mean it....I'm biased and I'm his mother....but seriously, he's a beautiful baby!!)
Take care guys!!
Get a good head rub for me!!
Please keep commenting, I love to read your profiles and I really do try to get back to everyone...just takes me a while sometimes :)
Goodnight
Hey T, I like your intro to yourself..pretty cool. Ya I cant say that I am anyway affected by this whole hair loss thing... I hate it when I tell people and they are like awwwww you poor thing...I find it quite embarrasing!! Anyway welcome to Alopecia world!!
Hi T,
The pictures on my page are the only ones of me without nothing on my head... they were taken either by my daughters or my husband, telling me that ours kids have the right to have picture of their mother..... what to say to such arguments?
Diane
Aww thanks Taylor. :) Actually the biggest advice I'm looking for right now is wig advice. I want to start looking, but find that I have no idea what I'm doing!! I started a forum discussion on it if you want to see the feedback I've gotten so far, or else I'd just appreciate any info at all. Hope you are having a good day today!
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T's Comments
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I love what you wrote on ur page, that is soooooooooo true. I love ur pictures and ur eyelashes, I am trying to find out where to get them and how to wear them. Please help.
Thanks,
Nini
I seem to have the same approach to my alopecia as you! I wear a wig or scarf when I go out but am generally bald around the house, I have a 9 month old nephew and I often wonder if he thinks he has 3 aunty jo's!!
Love the hair who is it by can you give me some info.
Jessica
Love all the pics and your baby is sooo cute. I have a little baby also his name is Aiden he is 11 months. When i can I will add pic's of him soon. I also have 2 girls Grace 7 and Ava 3
Roger.
Have a nice Thursday tomorrow ;)
I don't know whether that will prove well tell.Your words are very wise.They may much people here assist in better manage its baldness.Say why. 28 ys backward I fell ill serious neurological illness movement.Mine doctor me said, that the longest behind 10 ys I'll on disabled armchair.It was shock and I mentally was on that very badly.
One elderly gentleman same illness me but learn heaven this infliction of like illness,but as a something due back to me.
Thanks that I have got though big severity,but always go.Therefore I think, that the most incurable illness or infliction of puts manage.Only man
mustn't it treat as ill and be sorry for oneself.So won't help.Get, that the female be bald,is very heavy,unpleasant and stressful.Alone I don't know how would it managed be woman.Right its baldness is for me always quite heavy namely am man.
My alopecia scar began within days on May 2007.Was it for me very heavy,but came to be it slowly manage.Came but January 2008 and to us unexpectedly obiit son.Mentally am again was on that very badly.Doesn't know am what shell I do and began be looking for on Internet cafe,different help.Found am Alopecia world.For the first time am here found out,that also women and little children are bald.Was I shocked and was me of all very sorrow.
Began be read various sections and examine photo and slowly find out how strong and primely personalities are.I said to myself,that when this female heavy thing know how to manage further prove assist in and second.So it I have to manage so did I.I wanted also somehow assist in.It but I don't know.Place Alopecia world and largely instance you brave and wise women on the contrary me much assisting manage its baldness and even mitigate pain above death child.Also me turns view of eye - appeal women.Not to be angry if it say badly,but for me bald woman has only other kind hairstyle and be like each other beautiful like if has hair.
Therefore again I say ,yes your words are very wise !Also ; access to baldness,as well as of several of other members and founders hereof seats is for us other instance.
Thank you and other.My English is very bad so I hope, that the me do you understand.Unless,please about erasure mine benefit.
Keep lovely day.as
Roger.
are fabulous and beautiful woman.Thank you for your wise words. as
I love your energy and outlook on life, I agree being bald is not an handicap it's only a big deal if you make it one.
Thank you guys for responding!! So far I have absolutely loved this site. I want to clarify that I am not saying in anyway that I look down on being depressed about alopecia, or being discouraged or being scared....The comments I've received before were down right pitiful....no one was going to help these people through life....they were bitter and blaming life for what 'happened' to them.
I don't like that....not having hair is nothing compared to what I could suffer from!! I'm healthy, I'm happy, I have a wonderful attractive husband and a beautiful baby boy, a house a great job and my health!! And....during my lifetime I'm sure I will have more crap to live through and cope with....so I will.
Being angry doesn't help fix anything!! And there is no use crying over spilled milk!! So we don't have hair....wear a wig and keep on keepin' on!! Be the coolest person with no hair anyone's ever met....and chances are you'll be the only one they have ever met ;) No one likes a complainer...but people will recognize you for your strength in character!! My mom always says I am her hero. From the time I started to lose my hair through today....I've never been bitter. I never let hair keep me from doing everything and anything I wanted to do. I cried when I was picked on, but I got over it and jumped back on my feet. I just think we should be thankful that we don't have hair and we are perfectly healthy and normal!! That's a blessing!! And please don't ever deny someone who questions your condition, the opportunity to learn and be educated about it. It will allow more people to understand our disorder and allow for it to maybe someday become more commonly accepted.
My mom used to get really angry when people would stare at me as a child....and I didn't even notice that they were (still wouldn't, I tend to live in my own world most of the time....and I'm always thinking about something so I may walk around looking snotty, or so I've been told, when really I am deep in thought about what I need to do when I get off work :)
And then one day she realized that....she was fighting the world, and possibly making me think I had a reason to be self conscious when I wasn't. She started me in a wig during fifth grade school pictures....I hated wearing a wig...I usually wore a cap if anything to prevent sunburn when playing outside.
Every picture of me as a child with stringy hair, clumps falling out in my brush and no one knew why....I was always smiling!!
I'm not a hero....I guess I just always knew that I had two choices. Live. Or, spend my life miserable and whine and complain and cry and blame and have a horrible time, not because I had no hair....but cause I chose to be miserable!!
I've had a great life! I have a lot of plans and goals for my future. And if my son turns out to have alopecia (I have some concerns...his toenails don't grow and he's got very light hair...small amount....I could be wrong, I hope I am), I will do my best to raise him to believe that he is special! And that he is normal. And that he can do anyyything anyone else can do! I will help him to be secure and have self esteem.....something I worked on until I was 18....when I got my first peggy knight hair piece, my whole world changed!! (All of a sudden I was Taylor....not the girl that wears a wig, cause no one can ever tell!! Unless it's because maybe they notice that my eye brows are tattooed and/or if they know someone else with alopecia....this has happened!! I love it now when someone says...Can I ask you a question?
Ummmm.....you sure can...wait, bet I can answer it before you ask! (People don't say that unless it's going to be something personal...right?) But I welcome it!! That way they get to learn about us. They get to know that we have a disorder....not a disease! They get to hear in my tone of voice that I'm confident in who I am and I'm proud to be an example in life.
If you are a Christian you'll know that God tests his children and uses us in special ways that we may not be aware of! With alopecia I can honestly say I have always passed his test and I know he will never give me more than I can handle.
My mom is my hero. Along with people I meet all the time, with much more on their plate than hair loss....that are the best damn leaders in this life I've ever known!! The ones who face significant loss, health issues, hardships...etc. and have the best attitude and strongest character! I am lucky to meet them! People touch others everyday! They may never know it. You all probably inspired someone in someway by coping with alopecia....it's awesome to think about it on a greater scale!!
It is embarrassing for someone to feel sorry for you because we don't have hair. Makes me feel really really low, like there's something I should be ashamed of. But, I also know that those people probably don't know how to react and they don't want to seem cold and unsympathetic. It's not their fault. I just stop them really quick and say...'No no, don't be sorry!! I'm not!! I haven't had hair for twenty years and I don't even remember what it was like to have hair!! So while this is new for you, it's far from new for me....it's a huge part of who I am and played a huge part in the making of who I have become! And, today, I can say in all honesty!! I do not want my hair back!! I like being me, just the way I am!! I love having a good head massage!!! (It's fantastic!!) I love the fact that my family and friends know I can take a joke and rub my head for good luck....or tug on my random scraggly hairs on my scalp to see if I can feel it *lol* (My husband loves that game!!) I'm a good sport and I get through a lot with humor!! I will never turn down the opportunity to make someone laugh, especially if it's at my own expense!! And once they know I can take it, and they crack jokes about me later....I love that just as much!!
I'm rambling, and I hope ya'll read this...it's so hard to respond to everyone, although I want to, when I work so much and have a seven month old...ROTTEN ROTTEN boy!! *lol* He is down right spoiled!! (He's so darn cute, it's hard not to....I mean it....I'm biased and I'm his mother....but seriously, he's a beautiful baby!!)
Take care guys!!
Get a good head rub for me!!
Please keep commenting, I love to read your profiles and I really do try to get back to everyone...just takes me a while sometimes :)
Goodnight
Zoey~
The pictures on my page are the only ones of me without nothing on my head... they were taken either by my daughters or my husband, telling me that ours kids have the right to have picture of their mother..... what to say to such arguments?
Diane
Welcome to the group. I think you will enjoy it.
Jeff
Hugs,
Mandy
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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.