- Link
- Pin it
- SubscribeUnsubscribe
- Embed
Esha Vogel hasn't added a story.
Hello, my name is Esha and I am 17 years old.
I developed trichotillomania, an impulse
control disorder that causes one to pull their own hair (previously
thought to be a form of OCD), when I was only five years old. Over the
years I have suffered from this disorder, I have gone from having
eyelashes to having spotty eyelashes or no eyelashes at all, from
having hair on the crown of my head to absolutely none at all. The
changes I can go through in a matter of days can be quite drastic, or
barely noticeable, thanks to different methods of hiding bald patches
I've acquired over the years.
The featured image is a photo of my eye from 2011. I recently
made a massive breakthrough in my painstakingly slow recovery from
this disorder by completely regrowing my eyelashes.
It took me a very long time and a lot of tears, will power and
moral suppport to be able to achieve this feat. It may seem like
something so small to someone who doesn't understand this disorder,
but to me it's huge. I'm no longer the girl people in middle
school would go up to and ask, "What happened to your
eyelashes?". I no longer have to hide behind heavy layers of
eyeliner and try to handle wearing false eyelashes that irritated my
sensitive eyes, and I can actually take a shower without having to
constantly wipe my face with a washcloth because water would run into
my eyes.
But my eyelashes aren't the point. For years, I have
struggled with, stressed over, and tried desperately to hide the
growing bald spot that still covers most of the crown of my head. This
is one place I haven't been able to control, no matter how hard I try.
And trust me, I have tried. I've tried medications that other people
who suffer from the same disorder swear by, I've tried therapy, I've
tried wearing bandanas all of the time (I now resort to hats simply
because I'm too worried not to wear one), playing with play dough,
putting tape on my fingers, having super long fingernails, sitting on
my hands.. This list could go on. This causes me a lot of grief,
extreme low self esteem and self worth, and self hatred. These
feelings only cause me to want to pull my hair, which in turn, if I do
it, and most often I do, causes these feelings to intensify. It's a
seemingly endless cycle that I can't escape.
Sadly, not much is actually known about the disorder itself and
there is no real 'cure', but you can find most information on
trichotillomania here.
Due to trich, I can't go outdoors on a windy day without
carrying a hat or wearing a hat, I can't go swimming, I can't go
running, I can't go out when it's raining without a hat, and car rides
are a living hell for me if the windows are down. I can't even do
things normally at home. I can't shower normally, due to the expensive
stuff I have to apply on a daily basis to 'paint' my scalp the same
color as my hair so it's less noticable when I comb my hair over. I'm
limited to what I can and cannot do, because of this disorder.
No, it's not the end of the world, and it's not the worst thing
that could possibly happen to anyone, or cause anyone to need a wig.
It's just hard. Actually putting this out there for the world to see
is embarrassing and scary, but this is something I need to do for
myself. I will not post a picture of my worst bald spot.
This fundraiser, if successful, would allow me to get a high quality
wig so I
can feel normal and worry free when I go out. I
have gone through wigs when I was younger, but they were always cheap
(under $60), shiny, hot and itchy things that didn't look like my real
head of hair. They just looked like, well, a wig.
A wig of higher quality would allow me to do things that I
currently can't even think of doing without fear and stress.
I'll be able to enjoy a day out without a hat as a constant companion,
brush my 'hair', save myself and my parents tons of money on special
hair care products I require to live a normal looking life, and feel
better in my own skin. It won't take away this disorder, but it will
make it easier to live with.
My family and I can't afford to buy myself a wig of this quality
without help, which is why I'm setting up this fundraiser.
Please think about making a donation. It would honestly mean
the world to me.
- Esha
Highlights
See all activity7Activity
Delete media item?
Delete this item from the media gallery? It will also be deleted from any related story update.
Set as ?
The campaign video will appear in social media and email.
The campaign cover picture will appear in social media and email.
The will appear at the top of your campaign page and in social media and email.
Reset ?
It will be removed from the top of your campaign and won't be used as default in social media and email. The will remain in the media gallery.
Embed
Share a link
Delete update
Delete this story update?
Any pictures or videos will remain in the campaign's media gallery.
Report campaign
Report submitted
Thank you. We take reports like yours very seriously. Our goal is to keep the community safe.
Please know that we may contact you for more information, but that we won't notify you personally of our decision. If the campaign remains available within a few days, it's likely that we determined it not to be in violation of our policies.
Thank you. We've already received your previous report. If the campaign remains available within a few days, it's likely that we determined it not to be in violation of our policies.
Tell us about the problem. Please fill in both fields below.
Record a video
Upload a video
Nothing grabs attention for your cause like a personal video. Take a minute or two to record one now. Record a short video message of support. Or upload one from your device. You can preview or redo your video before you post it.
Nothing grabs attention for your cause like a personal video. Upload a short video message of support. Upload a short video message of support. Or record one right now.
- Most effective video length: about a minute.
- Maximum length: 5 min.
- You can preview or redo your video before you post it.
Heads up! The existing video will be replaced.
Email your friends
Join our team
Your endorsement banner
Use your endorsement banner to tell why our cause matters to you. Such personal endorsements are proven to increase campaign contributions. When enabled, your endorsement banner appears at the top of the campaign for everyone who visits a link you shared.
You can always adjust your endorsement from the campaign Share page—even if it's been disabled.
Your message
Tell people why our cause matters to you. Your personal message will encourage others to help. Easy, effective, optional.
Say it in video
Short personal videos by supporters like you are incredibly powerful. Record one right now and you'll help us raise more money. Easy, optional, effective.
Add a personal goal
Set a personal fundraising goal. You'll encourage more contributions if you do. And rest easy. There's no obligation to achieve your goal or bad consequences if you don't. Easy, optional, effective.
We have a video!
Video thumbnail
We'd love to show you our campaign video. Want to take a look?
, you're already on the team.