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07-07-2008, 03:11 PM | #1 | ||
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New Member
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Hello!
My son is 5 and he was diagnosed with a large arachnoid cyst on the left temporal lobe last week. We are currently waiting to hear if the neurosurgeon wants to operate on it, or wait and see. I had never even heard of this condition until last week, so am looking for information from other people who have experience of this. The doctor said it is the size of a small apple. He doesn't seem to be experiencing symptoms thankfully, other than the head bulging which is what led us to see the doctor in the first place. Look forward to hearing from other people thanks Cathy |
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07-07-2008, 03:17 PM | #2 | |||
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Grand Magnate
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I'm sure one of our Mods with chime in to say welcome and give you a helping hand...here is a hug...at least that helps sometimes...
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My best friends live in my computer.... . Suffered with back problems since birth...7 back surgeries to date, the last one being on 5/13/2015. Fibromyalgia, PTSD, Chronic Pain “Being my sweethearts full-time care partner, I have to remind myself, when some well-meaning friend or relative questions my methods or motives, that I know more than they do because I Live this life 24/7, and they only come for short visits.” Tamiloo . Gotta love my Olhipie! Dx'd RRMS 1986, SPMS 2004 . Watch my Olhipie Skiing.... . |
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07-07-2008, 08:13 PM | #3 | |||
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Legendary
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Hello Cathy and welcome to NeuroTalk.
I'm so sorry to hear that you're going through this with your son. It's ever so scary when loved ones go thorough something like this, let alone one of our children. Us mother's would always take these conditions onboard and have the operations ourselves, if only we could spare our children. What a shame it doesn't work like that. I've given you a couple of links here where I hope you'll get advice and the support that you will obviously need. Here's the link to our Hyrocephalic Forum : http://neurotalk.psychcentral.com/forum14.html This one is to our Rare Disorders Forum: http://neurotalk.psychcentral.com/forum2.html Try those, but let us know if we can help in any other way. Hugs to your little man.....
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"Thanks for this!" says: | weegot5kiz (08-01-2008) |
07-07-2008, 08:20 PM | #4 | |||
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Wisest Elder Ever
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Hi Cathy and welcome to NeuroTalk! I'm so sorry your little one is having to experience this. There are lots of very caring and helpful people here and I'm sure you'll find lots of support and information on the forums that Koala provided you with. Glad you're here!
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These forums are for mutual support and information sharing only. The forums are not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. Always consult your doctor before trying anything you read here. |
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07-08-2008, 11:01 AM | #5 | |||
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Wise Elder
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Hi, Cathy! Welcome to NeuroTalk!
Poor little guy, tell him that I'll be praying for him.
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—Cindy For every day I choose to play, I set aside a day to pay. —AMN "Sometimes plastic wrap just won't cling, no matter how much money you put in the meter." —From the Book of True Wizdom |
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07-08-2008, 01:06 PM | #6 | |||
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Legendary
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Hello Cathy and Welcome to NeuroTalk. Sorry to hear of your son's problems and hope that you can find some comfort of info here that will be helpful. Really glad you found us.
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08-01-2008, 01:52 PM | #7 | ||
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Junior Member
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Hello, I am sorry about your son, I have an arachnoid cyst in the poster fossa (back of the brain) I know what it is like to live with this condition and it is not fun, so my heart goes out to you and your son.
There is this great place that is called the skullbaseinstitute.org If I spelled it correctly. the acctual place is in LA, CA. their is a wonderful doctor that opporates on this and other conditions. there is a program called Davids foundation and he is a 12 year old boy that is the ambassodor for the program there. He was featured on the ellen show. if you have the time go to the web site and check it out. it has information about arachnoid cyst's and how they are opporated on. they also have information about conseltaions. They will fly you out and rent a hotel room and if you don't have the money for the surgery they will pay for it. Good luck to you and your son. Maile Quote:
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