Surviving and Thriving with Chronic Illness

POTS Care Opens!

The day has arrived! We are happy to announce the opening of POTS Care -- geared to help patients with Idiopathic POTS (often found with EDS, Chronic Fatigue Syndrome or Chronic Lyme disease). Dr. Diana, a former patient with POTS, is now part of a team helping those with this form of POTS that doesn't usually respond well to symptomatic treatment.
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As one of the first patients to come to PotsCare I encourage anyone who is suffering the symptoms of this condition and trying to find answers to come see Dr. Diana.  She and her staff will welcome you with open arms and you will receive personal care and attention you never though possible.  Your symptoms will never be dismissed and you will learn so much more than you ever thought possible about your condition than you knew of coming in.  I personally was not expecting to see how my myriad of signs and symptoms all related and how there was so much more to my suspicion of POTS that I wasn’t even aware of.  You can be confident that you will leave with much relief that everything possible has been examined with great care and thoroughness and the assurity that you will receive the best advice to manage your personal situation under the care of your own doctor and best of all you will finally feel validation and a great sense of gratitude for all the hard work that went into the opening of this wonder centre for suffering patients.  Dr. Diana has put her heart and soul into this venture, not to mention a lot of her family’s income so that people suffering NOW don’t have to wait decades longer.  Thank you Dr. Diana!!

My 18 year old daughter Morgan has been sick and in pain for seven years. Just diagnosed the last 3 years with POTS/ dysautonomia. It has had many changes and she has overcome a lot. She is constant nerve pain in her back which she doesn’t even discuss anymore( unless asked by Dr) she has severe pain within 5 minutes of eating or drinking anything but water. She forces herself to eat. Gallbladder was a zero% so it was removed in October. Surgery set her back again and didn’t help with pain. The biggest thing now is as she says ” she is stuck in her body” she can not stand at all or sit up right for more then 10 minutes without passing out. She is now in a wheel chair but can’t even always make it back from restroom at home with out going out. Cardiologists is happy that her waves and MVP looks better. Just added more fludrocortison and said to drink lots of milk- Help!! She is a senior ( homebound) and would like to be able to make it across the stage. How do I get her to become a Potscare patient. We like most are at a loss. Reaching out- Julie( bird mom)

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POTS would potentially consent to a backsliding transmitting heading, where signs come and go, for a considerable length of time. In so much occasions (about eighty rate ‘examined by Experts Dissertation Service ), a character with POTS enhances and transforms into practical, in spite of the way that a couple of lingering signs are common.

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Prettyill team you’re doing great work that you for care about people specially Dr Diana she’s very and nice personality BTW I will pay someone to do my essay i saw many users here can someone help me ?

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I may be the happiest one to read this news. I know how hard life can be when you have PTS. A close friend of mine is suffering from Lyme disease and I know how hard his life was for him. home extension

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it can incapacitate and lethargic to treatment and the fundamental cause can remain a riddle (“idiopathic POTS”). Patients with idiopathic POTS don’t more often than not react well to the customary treatment for POTS. Whiteboard Animation Videos A large number of these patients have connective tissue issue, high or low intracranial weight, elevated amounts of irritation, and outrageous and incessant weariness.

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