dizziness and headaches from wearing hats
This forum is for questions and support regarding neurology issues such as:
Alzheimer's Disease,
ALS,
Autism, Brain Cancer,
Cerebral Palsy, Chronic Pain,
Epilepsy,
Fibromyalgia, Headaches, MS, Neuralgia, Neuropathy, Parkinson's Disease, RSD, Sleep Disorders,
Stroke, Traumatic Brain Injury

Please be advised that my response to you is not professional, is not medical advice, is educational, and that I am not a representative of MEDHELP.
Of course you are "for real" because you are posting here. And, your question is legit.
I assume that you do not wear a helmet at home, after work, and that you are paying close attention to have linked the hat/helmet and the symptoms together.
Do you like your profession, your job? If not, you may want to consider that this is psychosomatic. Not that the symptoms do not occur but that their cause is from stress or anxiety. In this case, you would see a psychotherapist and this specialist would send you to a neuropsychologist to differentiate and to make sure that there is not an organic cause. You need to be safe and sure.
How are your sinuses? Your sleeping regimens? Your vision?
JCmcc.
From personal experience, wearing a close-fitting riding helment (I use to train and show jumpers)almost always gave me a headache. Tight hats had the same effect. Loose fitting hats or helmets did not cause the headaches. Perhaps blood flow is restricted or nerves affected. Good luck!
It is not your job to decide whether or not the Cleavland Neurologist should be or needs to be answering any question.
You forgot that type is hard to measure and it does seem a bit rude.
Nothing personal as you are a great contributor but right is right.
JCmcc.
The point is (and I too am guilty of this) that we, as a group of contributors, need to look at how we word things and to keep in mind that type is very hard to measure.
For the longest time I saw the statement, "Good Luck!" As a bit rude.
So, though you meant nothing, I could be taken as a write off.
Food for thought-not that big of a deal when we have, for example, contributing single mothers who have ALS.
Thanks Mike,
JCmcc.
i dont luck "good Luck" either. the impliction is that you will need it.
I can't seem to post a question here.....I see that you both are very knowledgeable and wondered if you'd be so kind as to offer up any comments/opinions/suggestions
on the following......Thanks if you can.....however, if you can't - I understand. Deb
Diagnosis of pseudo tumor two years ago after experiencing surges of pressure in my head accompanied by total lack of coordination, temporary total loss of vision, headache, shaking, often uncontrolable, depth perception loss, inability to put one foot in front of the other and always accompanied with a very stiff neck. These episodes would subside after about 5 minutes. Treated with Diamox with some success. Severe bout of kidney stones likely attributed to Diamox by a Nephrologist after testing. Referred to neurosurgeon for a shunt. With the absence of papilidema, loss of visual field and debilitating headaches, he won't put a shunt in. He questions the diagnosis. A cervical MRI to rule out a dural tear reveals C4-5 & C5-6 herniations, both central and compressing and flattening the cord. Narrowing of the canal to 6mm. Some signal increase in the cord suggesting myelopathic change. Two years of testing include blood work, cerebral angiogram, MRI's, CT scans, Xrays, VER testing, Visual Field, EEG's, Holter monitoring, EKG's, Evoked potentials, several umbar punctures with opening pressures consistently 27 - 32. Neurologist say herniations are likely the cause. Neurosurgeon says no, it's not. He said I would have had "catastrophic lumbar punctures resulting in paralysis". Any opinions, comments, experiences and invited.
Thanks for reading......deb