What do we do at POTS Care?
ฝัง
- เผยแพร่เมื่อ 4 มี.ค. 2024
- Dr. Diana Driscoll, optometrist and Clinical Director of POTS Care explains POTS (Postural Orthostatic Tachycardia Syndrome), and what happens at POTS Care. POTS Care is the only clinic dedicated to treating the underlying medical causes of POTS. What is causing your POTS? Have you heard of Inflammatory POTS? Dr. Driscoll explains options for patients -- and none of them involve trying to cover up the symptoms! #POTS #InflammatoryPOTS #Dysautonomia #DrDianaDriscoll #TheDriscollTheory potscare.com/ / potsrebels
Came to you in 2019 and you helped me so much. Thanks for your continued support to all this 💕
It was an honor to help you!
Just found out I have rapid gastric emptying, which I thought I had gastroparesis. I think my journey is leading to dysautonomia of some type! We were just dx with hEDS a couple years ago. Of course my primary dr, neurologist, and now GI dr do not see an issue, I have blood pressure issues, my eyes are changing so fast with 3 different prescriptions in less than a year. Now my teeth are disintegrating in my mouth and so many more symptoms ! I need help and my research has lead to you! I just got the parasym plus (mom found it on Amazon so hoping it’s the same as you sell) would love to see about the package, can’t afford much else from trying to find answers, I know you understand, 😊 so glad I found you!
YES
Very informative!
Loved the Talk Dr. D 😊
I'm so glad you enjoyed it! :)
How much is it?
Thank you for this. I missed the live. I wish I could afford to see you. Lyme etc chronic. Have pots symptoms which link over to mcas and EDS…life is passing me by. Almost 60. 💔
Gastroparesis is crazy making.
We have other options (such as consults and the POTS Care Package)! We are working to expand other options, too. Our goal is to help the masses. There are so many people suffering needlessly. If you are dealing with gastroparesis, please know we can usually help!
So what tests do I have to do ? I have pots for the last 15 years. I can’t go anywhere or go out so much anxiety on top my feet’s goes blue especially in the heat my heart rate hits 140-170 all the tests I have gone all came back negative but only table test came back positive. So what test do I have to do to find what’s the underlying cause so I can treat it my life is hell.
Hi Adam, we find every case to be extraordinarily complex -- and we've seen it all at POTS Care! A good place to start may be "The Driscoll Theory", then check out Inflammatory POTS information here: potscare.com/inflammatory-pots/ We offer case evaluations, should that be of interest to you.
Could it be inflammatory if your inflammation markers are normal in blood tests? My tests always come back normal, but I can't stand for long periods, always feel dizzy and like my legs are going to collapse in the shower, doing dishes or in line at a store, I have head pressure all the time, dizzy, light headed, can faint very easily with any stressful situation.
Yes, it is easy to miss many chronic inflammatory conditions when traditional markers (SED rate and hsCRP) are normal. 😢
That is me exactly
How do you get the package
It's here! potscarepackage.com/
I wish I can afford you!
It’s so expensive!!
After paying for all dr’s I’m basically empty, and I can’t even work, gotta lay in bed all day..
This illness is crazy!!
Your just handicapped all day with pain everywhere with no answers from any testings…
I’m just 22 years old and had my first child now..
I don’t know what the next day will bring me…
Fatigue is an understatement..
Pain in the eyes
Pressure in the head
Colds hand and feet
Heart by minimum 120 bpm when getting up, at 60 when laying down
Extreme anxiety
Brain fog
Did every test your test you can think of
MRI on almost full body
CT on almost full body
CT mylegram
Epidural blood patch
X-rays
EEG
Echo
Tracker on the heart for two weeks
Tilt table test
Blood work through the roof!!
Just about everything and everything was negative besides TTT the heart rate..
and all dr’s say no cure!!
Just increase salt..
What a craziness!!
I’m only 22 years old!!
I must get onto my feet back
I was so successful and went down the drain with this illness..😢😢😢😢😢
Don’t bother with her. Unless you have $10k, she won’t help you. Just more money hungry people feeding on the sick who are desperate.
We hate to hear how disabled you are by POTS and almost unbelievably, most patients are this sick! We have other options than full treatment and will be expanding these -- and we are continuing to release new information. Keep in mind that you are young and when the cause of problems is identified, you have opportunity to recover and to be able to work again. Never give up hope.
😢😢😢😢😢😢