|
|
Pheochromocytoma
pheochromocytoma Information
What is progeria, pheochromocytoma, thyroid storm.?
Only if you have or know someone with a pheochromocytoma?
I would like to know what kind of symptoms you experienced before diagnosis. Please don't quote website information, as I can look that up for myself. Thank you
What does an episode of pheochromocytoma feel like?
I am writing a research paper, and I would love for someone with pheochromocytoma or who has a family member friend to describe how the disorder makes you feel physically and emotionally. Thanks
Surgery for pheochromocytoma,is it risky?
Do plasma free metenephrines check for anything besides pheochromocytoma? ?
I know this is mainly what is checks for but can it find other things if it's not a pheochromocytoms?
Where can i find a pheochromocytoma surgeon?
What is pheochromocytoma?
What is it?
Does anyone have pheochromocytoma? or know of anyone with this?
I have been plagued by all of the symptoms and am now awaiting the results of the tests. If it's not this then I don't know what I will do... THey have even said it's just " panic or anxiety attacks... I know that it's not that. I am not the panicky person and the symptoms are so real and scary. sweaty, shaky, weird feeling floods thru veins, blood pressure goes way up and pulse also. Headache and cold tingly hands and feet. Also mouth is numb and doesn't want to work very well. I have been tested for diabetes and have been taking my sugars and they are fine. They sent me home from the hospital with Ativan to take when these " episodes" start...I don't want a tranquilizar I want to feel normal. Any advise would be helpful.
Do I suffer from pheochromocytoma?
Weeks ago, I was suspected having pheo.Yet urine and blood diagnoses turned out to be negative.Nonetheless, I 've been asked to have a medical appointment for renal clinics.I am now really puzzled and haunted altogether.Is it possible that my diagnoses were false negative?
Do I have pheochromocytoma (adrenal gland tumour)?
I have symptoms of sinus tachycardia with occasional ventricular ectopic beats. BP was 180 100 then down to 140 100. I am 38. Doctors have put me on medication, but problems still persist. I have extremely bad headaches some days, but not always. Tachycardia palpitations occur most of the day. Drs say nothing wrong with your heart so we will treat the symptoms. I have type 1 Diabetes for 6 years. Anybody with medical background please reply. Worried I have pheochromocytoma after looking up symptoms on the net. I also have this weird sense of something really bad is about to happen too.
How do you differentiate pheochromocytoma vs. panic attack?
Does pheochromocytoma cause hairloss? (have other symptoms. doctors or nurses PLEASE answer!)?
doctors or nurses, please take a look at this and tell me if you think it might be possible that i have a pheochromocytoma. i know it's rare however...at around 17 i had an xray done because i started getting bad joint pains. they saw a mass on my adrenal glad, but never investigated it. then i developed inappropriate sinus tachycardia. i was given atenolol, and developed the very rare symptoms of lupus. i was on that for 5 years and was told by doctors that my lupus symptoms were all in my head and that i was crazy. i went off the atenolol and all the symptoms went away. i was diagnosed with drug induced lupus. this is apparently genetic. my grandma got it from beta blockers too For the latter 3 of the 5 years, my hair began to fall out by the masses. The first 2 years on the atenolol, it did not fall out at all.i've been off the atenolol for almost a year and my hair is STILL falling out by the masses. most of my lupus symptoms are gone. occasionally i'll get tingling in my hands and feet, or joint pain. once a month maybe. the tingling in my hands and feet has become more frequent in the last month or two. once every 1 or 2 weeks, i'll have it happen on and off for a day or 2. since i've been off the beta blockers for almost a year, i've had the inappropriate sinus tachycardia for a year. i have all the symptoms of it, and an electrocardiologist confirmed it today with an EKG and listening to my heart. He also gave me an event monitor and said to come back in 3 months. He said surgery won't help me, and medicine won't help much, but gave me a calcium channel blocker to help.My question is this...being that my hair is still falling out and we can't find any apparent reason, i have tachycardia although my mother and grandmother had it too. not sure what type , fatigue probably from the tachycardia, i dont know and the tingling in my hands and feet STILL, even a year after the lupus is supposed to be gone...could this all be caused by a pheochromocytoma? should i have that mass on my adrenal gland checked out to make sure that's not what it is?i believe the xray had said it was 2 centimeters big. that's small, but i think on your adrenal gland, that's sort of big..
Anyone here a pheochromocytoma patient?
Just want to know what were your first symptoms?
Could them reveal Paraganglioma and Pheochromocytoma?
My previous 24 hour urine collection and blood test particularly for pheochromocytoma were said to be fine. Later one, my doctor of renal clinics ordered the following blood tests for me but I didn't know what they were for.Among the blood tests they're Bone profile Renal function test Liver function test Glucose fasting Chol, Trig, DHL, LDL fasting Complete blood count with differentialCould they help reveal or diagnose a pheochromocytoma or paraganglioma?
|
|
