Hello,
I am 48 years old.
I lived in total naivety of my condition until
I had a sinus cat scan about 8 years ago to diagnose recurrent "sinus" infections. As I'm sure you all know, it was not sinus infection, but severe hydrocephalus. When the doc called to tell me this, I said, "hydro what?"
I was born 3 months prematurely and have always had a much larger than avg head. I graduated in the top 7% of my h.s. Class and went on to graduate college with a computer science/math degree and work in optics at a prominent research lab.
All I have to say, is if the technology to detect hydrocephalus when I was born in the 1960s or even in the 1970s, I believe it would have been pigeon holed into special ed with no hope for advancing my education or career.
I have had memory issues for a long time and have relied heavily on notes.
About 6months ago I started having very severe headaches. I had an ETV this January. Won't realize all the benefits of surgery for another 4 months or so but I do believe, I have a new lease on life!
Tectal glioma will be followed with regular scans. My follow up care is now with an oncologist.
Smurf
Best wishes to all of you dealing with this disease!
My son was diagnosed with a tectal glioma at age 5. And had a VP shunt placed at that age. He is now 15. He started with MRI's every 3 months and then gradually decreased the frequency until we were at annual scans. At 11, he started have some small tumor growth and some internal changes with the tumor. Still no treatment required, only back to every 3 month scans. Then he needed a shunt revision. He had about one revision a year until last year when he had multiple revisions and a shunt infection. He has recovered almost fully from those surgeries and the infection. His tumor size is stable. Frankly, his biggest issue has not been with the tumor per se, but rather with the shunt. He is not a candidate for a third ventriculostomy, unfortunately.
Hi,
I have a daughter and she is 14 years old and has a tectal plate glioma, also an ETV was done due the hydrocephalus. The tumor was discover July 2013.
We go back to Duke hospital every 6 months now. She has headaches every day and is taking Elavil daily (that helps) the headaches are not so severe.
I hope your daughter is doing better now.
Hi my wife has been diagnosed with a tectal glioma and she's 38. I have tried to join this group many times in the last few months and keep getting knocked back. We have had countless tests, neurosurgeons/neurologists and nobody can agree on what to do or what she has. She hasn't got hydrocephalus yet and only seems to have had vertigo as her main symptom. She had her hearing tested the other month and we got the results to say that they have picked up issues with her and that it is commonly from a lesion in the brain stem. We are desperate to talk to others with this same problem. Thanks..cliff
My son was diagnosed in May of 2014. I too would like to join your group.
Hy maike,
am 32 years old with tectal glioma diagnosed 2 years back mistakenly. The best doctors and neurosurgeon I have seen they told me not to worry and it will regress with time. Please try to think positive, don't be negative.
Even this go worst, which should not, there is gamma knife which can treat the glioma. Google it. If you have any more info about how to treat this kind of glioma if grows please share it here.
Thanks, keep up, be positive. Don't panic yr daughter and keep yearly MRI