Your donations will help us to grow. We are a foundation run by other AC sufferers. Every buck counts! Please help us and Donate this season.

NAME
(years diagnosed)

THE BABES

Ema(2)

Ruben(2)

Daniel(2)

Katie(3)

Mom(11)

Justin(3)

Jessica(1)

Meg

Hobie(4)

Tanner(3)

Jacob(3)

Chance(3)

Hunter(2)

Sara(2)

Jacob(2)

Anon

Logan (4)

Mandy(4)

Mandi(7)
heridetary...
her brother has one too.
Tracey


THE ADULTS

SPINE

Kathi (2)

Marvin(1)

Loretta(2)

Anabel(4)

Carrie

MIDDLE

Kate(5)

Catherine(me) &
Journal

Mare(3)

Yvonne(5)

Jason(11)

Angie(1)

Pam(10)

Nate(7)

Kevin(23)

Sally(1)

Theresa

Cin(2)

LeslieU. (1)

Meagan (3)

Lavona(2)
*hereditary

Royalyn(2)

Rita(5)

Justin(7)

Jill (1)

Barry

Linda

Jen D

RIGHT TEMPORAL

Telisha(1)

Darren(5)

Andrew(4)

Sheri(4)

RIGHT
TEMPORAL & PARTERIAL

Katie D (6)

                        100+ other people know it's not "all in your head" Please join me in keeping it real.

Want more information? Because I hit a gold mine recently but... Donate to our cause. If I can take the time to put the information together for you on this site of what is really going on and we can provide a forum on arachnoidcyst.net as well as blogs and forums of real people then don't you think we deserve just a little kickback?

Can you afford just $20? Keep me off the streets begging for bucks now that I am disabled and living on nothing that way I can spend more time putting together information for YOUR EDUCATION if you can help me out some too. Are we not more entertaining than most sites out there?

Wait until you see what we've found. There is a lot more going on your doctor is not telling you about. It's all new as of August 2005. This site has been updated to include the latest information and you are not going to like what you have to read.

Catherine answers calls and e-mail from people to offer emotional support, goes over doctor reports and explain to you what's really going on. If I do not answer the phone or e-mail please re-e-mail or call me, I is brain damaged too and there are more of you than me and wow are you growing! We are not medical professionals but simply patients that have taken getting medical care into our own hands and figuring out how to get and what to ask for.

Catherine New mommy and disabled by Syringomyelia and Multiple sclerosis which are diseases that have nothing to do with her arachniod cyst, cough cough.

There is an entire community of AC sufferers. Please get hooked into us as we all keep one another amused, smile, watch after one another during surgeries, listen when our spouses don't understand and just follow one another lives. It's worth it to follow one another because we need it.

BLOG
YOUR
"FEELINGS"

MARK YOUR
TERRITORY
Join us at arachnoidcyst.net so others can feel your pain and we can get "them" to listent to us~

PINEAL

Deborah(4)

POSTERIOR
FOSSA

Bev(6)

Dawn(2)

Christi (6)

Rebecca

Karen(2)

Angelea (7)

Owen(2)

Amy(3)

Amy(5)

Dana

VENTRICLES

Jan(1)

Steven(7)

RIGHT POSTERIER

Laureen(7)

Dani(1)

Shauna(2)

POSTERIOR FORAMEN

Jessica (5)

RIGHT
PARIATAL

Marge(2)

Babs &
Journal

CEREBELLUM
Michelle(3)

Bill L. (2)

Tom B (15)

Adrianne

Jo-Lin(16)

Lisa

Amy

BRAIN STEM

Robin

CORPUS
CALLOSUM

Jennifer (2)

OCCIPITAL
LOBE

Rashad(3)

LEFT
TEMPORAL
(MOST COMMON)

Leslie(11)

Vicki(16)

Chris(2)

Warren(2)

Courtney(7)

Robert(3)

A Husband's
Plea(2)

Don(5)

Melody(1)

Debbie(2)

Henry(13)

Sand(2)

Mat(4)

Alex(7)

Bill(3)

Olene(21)

Deb(2)

Stéphane(2)

Karen(3)

Lance(2)

Lisa(4)

Christine(7)

Richard (3)

LEFT OCCIPITAL

Francine

MIXED STORIES

Some people just send snippets so I put them all together here.

You can help the most by adding your story to arachnoidcyst.net