Member Comments are provided by individuals and reflect their personal opinions only. Under NO circumstances should you act on any advice or opinion posted in this forum. ALWAYS check with your personal physician before taking any action regarding your health! MedHelp International and our partners, sponsors and affiliates have no obligation to monitor any comments posted on this site, or the content and/or accuracy of such exchanges. MedHelp International does not endorse the views of any user.
I wanted to post this and share it with everyone. My daughter who has the chiari went to see the neurosurgeon yesterday. I thought that we would be talking about surgery. She had vestibularAcoustic neuroma testing done and everything came back normalNormal saline flush. I assumed that that meant that her dizziness and vertigoBenign positional vertigo Dizziness Vertigo Vertigo-associated disorders was coming from the chiari malformationImperforate anus Imperforate anus repair Pulmonary arteriovenous fistula. he explained that "usually" not always something would have come back abnormal if it was from the chiari. This is her main problem. Anyway he is sending us to another pediatric neruologist. He wants her to be checked by this man because he said that there are certain kinds of migraines that do not cause pain but the person can experience dizzinress and vertigoBenign positional vertigo Dizziness Vertigo Vertigo-associated disorders. I was not aware of this. When i think of migraines i think of pain. Sure enough I was doing some research myself and found this out. Some other symptoms were tingling and things like that.
I know many people here experience the same things so I wanted to pass this onfo on.
I really like this surgeon that we have. He wants to be sure before we start talking about surgery that he has ruled other possiblities out. He feels that if he is going to do the surgery he wants to have a good result. If the dizziness is not helped by this other doctor than we will discuss the surgery. I am so pleased that he is not rushing but trying things before we just say OK lets do the surgery and hope for the best.
I hope that some of this info we found out may be helpful to someone looking for some answers.
Hope everyone has a happy, healthy new year.
Chadry
I'm not very familiar with Chiari Malformation but I am quite familiar with migraines. I have been having migraines since I was 8, which is about 30 years. I have experienced migraines where I thought that I would never make it til the next day as the pressure in my head was so extreme that I thought my veins would explode. I also get a lot of "optical" migraines which range from the blindness,tunnel vision, streamers, stars, distortion, imbalance, etc. all without pain. These optical migraines started after I had my child. I still get the painful full blown migraines but the optical migraines are more common with me. From what my doctor told me, the migraines are not true migraines because they are related/symptom of the Chiari. I was told for years that "they were all in my head". At least they had part of it correct.
I am glad to hear u found a dr u r comfortable with and like his plan of action as well!!
This info is appreciated as I am sure not all r aware of the different types of migraines.
"selma"
I am glad u found us, but for the resons u sought us out.
We all seem to have the same story...drs that don't listen and the "it's all in ur head" is the only thing most of them get right!
I hope u cand find out more on ur condition here and find the support these warm people have shared with me.
Do u know if u have a CSF blockage?....or how long ur herniation is?
Please start a new thread of ne questions u may have.
Godspeed
"selma"