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Debbie
(years diagnosed)

THE BABES

Ema(2)

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Katie(3)

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Meg

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


THE ADULTS


SPINE

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Carrie

MIDDLE

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Journal

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*hereditary

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Barry


Linda

Jen D

RIGHT TEMPORAL

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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.

Hi, my name is Debbie and I am 45 years old. Let me start by saying that my entire life I have struggled with headaches and always being extremely tired. I have been to so many doctors and have had every test run on me possible.

Last year I was diagnosed with breast cancer and had surgery and radiation therapy to conquer that. Just recently I went to yet another doctor to see if there was anything that could be done about my headaches and tiredness. I have been told that the tiredness is because of the radiation and that it will go away over time.

The doctor sent me for an MRI to check my brain basically to rule out any type of brain tumor because of my cancer history. The MRI results were mailed to me and said that my brain appeared normal with no signs of malignancy (cancer). At the bottom of the result page was a sentence that said however, a small 15 m arachnoid cyst is present on the left side of my brain. The radiologist also wrote a not on the results saying "no worrysome findings". I personally find this rather worrysome!

I phoned my doctor's office the next day and the doctor didn't even speak to me. The nurse came on the phone and simply said, "there is nothing to be concerned about". I continue to have headaches, on a daily basis, and I am extremely tired all the time. I work a full time job and there are days that I simply can't hold my eyes open and I am unable to work. I have all but given up on getting any type of relief from doctors and have made up my mind that this is the way I am going to feel the rest of my life. I am discouraged about the uncaring attitude of the medical staff and their inability to understand their patients feelings and well being.

I hope this letter is of some help to others who live and feel the way I do on a daily basis to know that you are definately not alone. Good luck in your endeavors and god bless. Take life one day at a time and live your life to the fullest.


Sincerely,
Debra E.
Belleville, Michigan

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YOUR
"FEELINGS"

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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)

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RIGHT POSTERIER

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Shauna(2)

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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

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LEFT
TEMPORAL
(MOST COMMON)


Leslie(11)

Vicki(16)

Chris(2)

Warren(2)

Courtney(7)


Robert(3)

A Husband's
Plea(2)

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Alex(7)

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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

The Arachnoid Cyst Foundation
c/o Catherine Clay
PO Box 66820
Los Angeles, Ca 90066
1-(800)-493-5022
11am-10pm PST Weekdays

PLEASE REALIZE THE TIME DIFFERENCE
Please read through this site before calling as your answers very well could be here already.
No we do not have printed materials, you will have to print out this site.
Amy and Catherine are giving telephone suppport at this time. Amy for emotional support and Catherine for MRIs.
If you didn't find the info you need on this site or arachonidcyst.net please do call.
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This site was designed and is maintained by Miss Catherine Clay She has recently had a child and is not the best communicator at this time. Please be patient and call or e-mail back!