What is cidp mayo clinic?

If you’re reading this, chances are you may have stumbled upon the mysterious acronym ‘CIDP’ and a rumor circulating that it’s connected to some place called ‘Mayo Clinic’. But fear not, dear reader! This article will explain what CIDP actually stands for (Chronic Inflammatory Demyelinating Polyneuropathy) and why on earth we’d ever care about The Mayo Clinic.

Neurology 101: What is CIDP?

To begin with, let’s break down what Chronic Inflammatory Demyelinating Polyneuropathy means. Long story short, it affects your nervous system- specifically your nerves’ ability to communicate between your brain and other parts of your body. Picture those old school telephones with wires connecting different switchboards- when there’s interference or damage on one of those wires (or in our case, nerve fibers), communication gets all fuzzy.

But wait there’s more! That inflammation can lead to damage around myelin,(the fatty substance that surrounds & protects nerve fibers) resulting in a wide range of symptoms – from numbness/tingling sensations in hands/feet/muscles/tongue/throat to difficulty walking/breathing/swallowing/talking/writing/lifting objects… basically anything you do that requires well-functioning nerves.

Subheading

To give an idea on how rare this ailment is (lucky us!) according to several sources both reliable (The National Organization for Rare Disorders) and questionable(My Aunt Susie who claims sniffing pepper makes her immune)- only approx 40k Americans suffer from it!!

Look Who Told Ya “How yo Get To Zebra Lane??”

And if all these medical shenanigans weren’t enough already- they’ve gone ahead & made diagnoses more difficult by ruling out more common ailments. Here’s a taste of what doctors will (probably) rule out before even considering CIDP:

  • Multiple sclerosis
  • Lupus
  • Lyme disease
  • Heavy metal poisoning

Those are some serious zebra conditions, & in comes an even rarer yet equally dangerous ailment known as CIDP. Ain’t I the bringer of good news?

Mayo Clinic- More than just a Spread!

So with all this information and medical jargon being thrown around, you might be wondering: Why is it important that CIDP is associated with Mayo Clinic? What on earth do they have to do with it?

Glad you asked! TheMayo Clinicis not only one of the most recognized medical facilities worldwide- but it’s at the forefront when diagnosing & treating rare neurological conditions like our invisible enemy..CIDP.

Subheading

Founded in Rochester Minnesota in 1865 as “St Mary’s Hospital” by Dr William Worrall Mayo( now ya know how he got his name)- attracted other top physicians throughout years :which included several members from Mayos family whom performed experimental surgeries crouched over steel tables so their arms wouldn’t stick to them /(life was harder back then y’all)//…

So…what does Mayo specifically do for CIDPers?

Well, first thing -they follow diagnosis procedures recommended by world-renowned neurologists consisting of:

  1. Electro Myography Test (aka EMG)
  2. Nerve Conduction Studies (NCS) &
  3. Spinal Fluid Analysis

Basically, they measure your nerves’ irritation levels using electric currents via needles+electrodes+pads-> because apparently toddlers weren’t enough to make us squeal.

Yippee! You’ve Been Diagnosed With C-I-D-P!!!

Your doctor will then assess results of all these tests to establish whether or not you’ve won the “Who has CIDP” lottery. If diagnosis is confirmed, get ready for a whirlwind trip down treatment lane.

Treatment?? Yay…?

Mayo Clinic and other leading medical facilities largely follow the same regimen when it comes to treating Chronic Inflammatory Demyelinating Polyneuropathy:

  1. Doctor prescribed medication
  2. Physical therapy
  3. Intravenous immunoglobulin (IVIg)
  4. Plasmapheresis
Medications

The types of recommended medication may vary depending on which stages your CIDP’s at- but usually include immune suppressant drugs that’ll keep those darn inflammation levels in check; IV MP is another immunosuppressive agent used.

^^^^(“Immune suppression” might sound unglamorous, don’t be too hasty-A-listers like Angelina Jolie have undergone Mastectomy due her predisposition for breast cancer cells )^!!

Intravenous Immunoglobin? What in Tarnegolions name is.. that?! Someone pass me a dictionary!

Let me break it down for y’all- Basically, doctors inject purified antibodies from blood donors into YOUR system via vein under watchful eye 24-hour monitoring ; That way any shenanigans can quickly be caught & fixed after this 5 day barrage!

PlasmaPhere-whata?

This process sounds just as complicated as its name: plasmapheresis – Ridding your polluted plasma/scones from scorching chemicals and replacing them with ‘healthy’ scoops till ur supply seems sufficient. (its been hailed by some viewers –mostly patients– akin to juggling flaming swords while riding oil slicked motorcycle)

You spend anywhere between 2-&6 hours in dialysis-like chairs where bloods pumped out of one arm & back in opposite. Tip: You can make your blood type known to staff- so they don’t mix it up with someone else’. Cheers to reducing awkward encounters, people!

What’s the Take Away?

In conclusion, CIDP Mayo Clinic has become an inevitable duo that should not be taken lightly when dealing with such a serious neurological condition. Catching and diagnosing this disease early on is crucial in starting promising treatments options and interfering with progression of the chronic ailment.

So if you or anyone close to you happen to be experiencing any symptoms such as muscle weakness, numbness or gradually declining mobility – seek out medical attention immediately. Remember: the sooner we act upon our body notifications for help, less severe are likely its consequences!

REFERENCES

  1. Chronic Inflammatory Demyelinating Polyneuropathy – National Institute of Neurological Disorders and Stroke
  2. Rare DiseasenDay.org
  3. Intravenous Immunoglobin (IVIg) Therapy – American Academy of Neurology
    4.National Organization for Rare Disorders (NORD)

Random Posts