The Life of a Human Zebra

  • Home
  • The Life of a Human Zebra

The Life of a Human Zebra An open and honest look at my life as I battle living with Ehlers Danlos Syndrome, Gastroparesis+

What is dysautonomia?Dysautonomia is an umbrella term used to describe several different medical conditions that cause a...
31/10/2024

What is dysautonomia?

Dysautonomia is an umbrella term used to describe several different medical conditions that cause a malfunction of the Autonomic Nervous System. The Autonomic Nervous System controls the "automatic" functions of the body that we do not consciously think about, such as heart rate, blood pressure, digestion, dilation and constriction of the pupils of the eye, kidney function, and temperature control. People living with various forms of dysautonomia have trouble regulating these systems, which can result in lightheadedness, fainting, unstable blood pressure, abnormal heart rates, malnutrition, and in severe cases, death.

Image credit
Dysautonomia is not rare. Over 70 million people worldwide live with various forms of dysautonomia. People of any age, gender or race can be impacted. There is no cure for any form of dysautonomia at this time, but Dysautonomia International is funding research to develop better treatments, and hopefully someday a cure for each form of dysautonomia. Despite the high prevalence of dysautonomia, most patients take years to get diagnosed due to a lack of awareness amongst the public and within the medical profession.

Some of the different forms of dysautonomia include:

Postural Orthostatic Tachycardia Syndrome (POTS) - estimated to impact 1 out of 100 teenagers and, including adult patients, impacted an estimated 3 million Americans before COVID-19. Recent research shows that the number of POTS patients is now estimated to impact at least 6 million Americans since the pandemic began. POTS impacts millions of people around the world too, but we don?t have good epidemiology data in other countries. POTS is a form of orthostatic intolerance that is associated with the presence of excessive tachycardia and many other symptoms upon standing. POTS can cause lightheadness, fainting, tachycardia, chest pains, shortness of breath, GI upset, shaking, exercise intolerance, temperature sensitivity and more. While POTS predominantly impacts young women who look healthy on the outside, researchers compare the disability seen in POTS to the disability seen in conditions like COPD and congestive heart failure.

Neurocardiogenic Syncope (NCS) - NCS is the most common form of dysautonomia, NCS impacts tens of millions of individuals worldwide. Many individuals with NCS have a mild case, with fainting spells once or twice in their lifetime. However, some individuals have severe NCS which results in fainting several times per day, which can lead to falls, broken bones and sometimes traumatic brain injury. Individuals with moderate to severe NCS have difficulty engaging in work, school and social activities due to the frequent fainting attacks.

Multiple System Atrophy (MSA) - MSA is a fatal form of dysautonomia that occurs in adult ages 40 and up. It is a neurodegenertive disorder with some similarities to Parkinson's disease, but unlike Parkinson's patients, MSA patients usually become fully bedridden within a 2 years of diagnosis and die within 5-10 years. MSA is considered a rare disease, with an estimated 350,000 patients worldwide.

Dysautonomia can also occur secondary to other medical conditions, such as diabetes, multiple sclerosis, rheumatoid arthritis, celiac, Sjogren's syndrome, lupus, and Parkinson's.1,3

There is currently no cure for dysautonomia, but secondary forms may improve with treatment of the underlying disease.4 There are some treatments available to improve quality of life, both with medications and lifestyle changes/adaptations, but even using all treatments available, many dysautonomia patients experience disabling symptoms that significantly reduce their quality of life. 1, 2, 3, 4, 5

Print out the 10 Facts About Dysautonomia flyer and share it with your community to help raise awareness!

Dysautonomia International encourages you to Learn More. You can make a difference in the lives of people living with dysautonomia by donating today!

Sources
1. National Institutes of Health Rare Disease Network's Autonomic Disorders Consortium

2. Dysautonomias: Clinical Disorders of the Autonomic Nervous System. Moderator: David S. Goldstein, MD, PhD; Discussants: David Robertson, MD; Murray Esler, MD; Stephen E. Straus, MD; and Graeme Eisenhofer, PhD

3. Dysautonomia, A family of misunderstood disorders. Richard N. Fogoros, M.D., About.com Guide Updated November 13, 2011.

4. National Institute of Neurological Disorders and Stroke Information Page

5. Clinical Disorders of the Autonomic Nervous System Associated With Orthostatic Intolerance: An Overview of Classification, Clinical Evaluation and Management. Blair P. Grubb, M.D. Associate Professor of Medicine and Pediatrics, Divisions of Cardiology and Neurology, Barry Karas, M.D. Assistant Professor of Medicine, Division of Cardiology, The Medical College of Ohio.

31/10/2024

I was just reminded that it is Dysautonomia Awareness Month, so here's a bunch of last min information on the last day

22/10/2024

Got home yesterday. Now I get to reorganize my ER and hospital go bags.

I've been in the the ER since yesterday and am being admitted. Breathing issues once again. And yes, my hair is once aga...
19/10/2024

I've been in the the ER since yesterday and am being admitted. Breathing issues once again. And yes, my hair is once again purple.

Yesterday I got to spend 4 hours at UC Davis doing a new gastric emptying study. It's the main test for gastroparesis. I...
15/10/2024

Yesterday I got to spend 4 hours at UC Davis doing a new gastric emptying study. It's the main test for gastroparesis. I haven't had one since my initial test 7 years ago. It must have been one of the most boring jobs my ASL interpreter has had.

I was admitted to the hospital on Thursday for another asthma flare. I've managed to avoid the ICU so far this time but ...
21/09/2024

I was admitted to the hospital on Thursday for another asthma flare. I've managed to avoid the ICU so far this time but an episode of ventricular tachycardia sent me to the cardiac care unit.

19/09/2024

Nucala Day

17/09/2024

When you show up to your dentist appointment only to be told the video interpreter tablet is charging and then the interpreted service unavailable. Thankful for my voice to text app. It's not perfect but better than nothing or writing notes.

Yesterday I had eye muscle surgery on both of my eyes. I have been dealing with severe multiple vision. This surgery sew...
14/09/2024

Yesterday I had eye muscle surgery on both of my eyes. I have been dealing with severe multiple vision. This surgery sewed the muscles in place. The surgery went well. The portion of my surgery when they woke me up to make fine tunes was pretty torturous. It will be 3-6 months until I reach the full benefit. I feel like I have sand in my eyes. I have some prescription eye drops that should help. Right now cold compresses are my best friends.

😂
03/09/2024

😂

😂😂😂
-
-
-
-
-
-
-
Image description: A two panel image shows a character, Michael, from the Good Place. He appears to be speaking quite emphatically. Captions read, "You're about as useful as my connective tissue. It's an EDSer insult. It's devastating. You're devastated right now." End image description

02/09/2024
31/08/2024

OSD is offering online ASL I and II for this fall semester again! It's FREE! It is for anyone who want to learn ASL to be able to communicate with a Deaf person.

The registration for Online ASL Classes for ASL I and II is now open until September 30th. The Online ASL Classes for ASL I and II will begin on September 16th and continue until December 30th. These classes are non-credit level courses. This is a "go at your own pace" class.

To register: https://courses.osd.k12.ok.us/
On the website, scroll down to read FAQ.

"The Ehlers-Danlos Society  · Please join us in sending a HUGE congratulations to Grace Nuhfer, who has won a silver med...
30/08/2024

"The Ehlers-Danlos Society
·
Please join us in sending a HUGE congratulations to Grace Nuhfer, who has won a silver medal for Team USA at the Paris Paralympic Games in the 100m butterfly S13!
Grace is scheduled to compete in three other races in the Paralympics: the 100 backstroke today, the 50 freestyle on Monday, and the 200 individual medley on Tuesday. Each event has a prelim race and a final race on the same day. Let’s get behind Grace and cheer her on!
Grace has Brittle Cornea Syndrome (BCS), a type of Ehlers-Danlos syndrome (EDS), and an ultra-rare disorder that affects less than 1 in 1 million people. BCS is a genetic connective tissue disorder that causes the cornea to be thin, fragile, and prone to rupture. BCS also causes blue sclerae and joint hypermobility.
In an Instagram post, Grace explained, “Thirteen years ago, I started my swimming journey. Not because I wanted to be like Michael Phelps, but because that was the only sport we found that I was allowed to safely participate in. The eye doctor said “no balls, bats, or rackets” and my connective tissue disorder made the other options, like dance and track, too painful to continue. Growing up with Ehlers-Danlos syndrome has not exactly been the easiest. There have been countless unexpected injuries, sprains, and random joint pain alongside numerous tests for glasses and hearing aids. Hours were spent at hospitals and in doctors’ offices just watching for changes and creating a better understanding of what we were up against.
"There are many different types of EDS. My sister, Elaina," and I have Brittle Cornea Syndrome, which only affects roughly 20 other people in the world. Doctors' appointments felt like a dog and pony show, a revolving door of resident doctors being told to guess what genetic condition was present. Each day presented a new question as we were subject to a multitude of tests and experiments. The biggest of all being Elaina’s cornea transplants (so far still successful after ten years!! she’s a rockstar).
"No one person with EDS has the same experience, just like no two zebras have the same stripes. Being diagnosed is so important as it allows for a deeper understanding of the individual condition and the ability to create a plan to help aid and protect everyday life.” - Grace
Follow Grace on Instagram: https://www.instagram.com/p/CoFhbLOuu0i/
Learn more about Brittle Cornea Syndrome: https://www.ehlers-danlos.com/.../brittle-cornea.../ "

Grace is seeing SILVER 🤩🥈

Grace Nuhfer secures a silver medal at her debut!

27/08/2024


Address


Website

Alerts

Be the first to know and let us send you an email when The Life of a Human Zebra posts news and promotions. Your email address will not be used for any other purpose, and you can unsubscribe at any time.

Contact The Practice

Send a message to The Life of a Human Zebra:

Videos

Shortcuts

  • Address
  • Alerts
  • Contact The Practice
  • Videos
  • Claim ownership or report listing
  • Want your practice to be the top-listed Clinic?

Share