How Craniocervical Misalignment Effects Fluid Flow

Dr. Scott Rosa, who is doing compelling upper cervical chiropractic research, discusses his latest research in the area of neurodegenerative brain disease, cerebellar tonsillar ectopia (CTE), altered cerebrospinal fluid (CSF) and arterial/venous flow dynamics and their correlation to the cranio-cervical junction and atlas misalignment.
Interview topics:
Introduction and research history
Mis-alignment at cranio cervical junction
Head-neck trauma
Cerebellar tonsillar ectopia (CTE)
Cerebrospinal fluid (CSF) obstruction
Neurodegenerative disease
IGAT - Image Guided Atlas Treatment
Atlas Orthogonal
Fonar MRI imaging
Pathology
Glymphatic System requires free flowing CSF
CSF flow patterns are similar in neurological disease patterns
Mechanical & structural compressions decrease arterial & venous blood flow
CSF impact on pituitary gland
Denticulate ligaments - MS lesions at site of attachments

[@NonyaSmith]

These findings should be on the 5 o'clock news! They speak to sooo many illnesses.

[@suzanneanderson1206]

Exceptional, fascinating presentation of your ongoing research Dr. Rosa. Thank you for all that you are doing to help those who suffer from these issues. You are making the world a better place.

[@sharonhagemann9563]

Scott Rosa thank you for walkimg the talk

[@AndyJK45]

Interesting that the scan shows a change of CSF flow so soon after correction. That fits with the way I felt following my first atlas correction.

[@NonyaSmith]

Same here.

[@rainbow20112011]

Which upper cervical technique was performed on you?

[@grojandroid]

I want to humbly suggest that anyone who experiences recurrent low lying cerebellar tonsils, syringomyelia, mis-alignment of the CC junction, AO etc. be evaluated for hypermobility. Even in the presence of a known precipitating trauma. Hypermobility runs in about 10% or more of the general population, though not all have trouble as a result that we know of yet. But I would especially examine those recurring sports injured patients... as a hypermobile patient myself (diagnosed with hypermobile Ehlers-Danlos Syndrome in 2012 at 45), I've become all too aware that we are essentially like "walking car accidents" even in the absence of much or any head/neck trauma. (I "loosened" my own head just biking on skinny tires a couple of years ago and going over too many bumps.) Our connective tissues are so weak that we can have loose heads and necks even in the absence of concussion, but especially in the presence of it or any whiplash or other stress or injury. In fact, it was a fellow patient with AO in a support group who tipped me off to this video. (Thanks Steph!) And also alert the good doctor(s) that there is a brand newly recognized (since March 2017) but still poorly known brand new diagnostic category called Hypermobility Spectrum Disorders, essentially "subclinical EDS" if you will, and covers the less bendy among us. Many of whom probably run around and play sports like soccer and American football etc. (We are an active lot until our bodies betray us.) I have friends who are literally trying to keep their good heads on their shoulders as I type this, but who did nothing more than ride a roller coaster in their youth. It's an easy thing to see and screen for. (Google "flying bird hand sign", or see my When Else to Suspect page below.) Even if they don't have a form of Ehlers-Danlos Syndrome, or an HSD, it could explain why they are so easily injure or re-injure in some cases. (We also have comorbid endocrine imbalances and so much more, all readily explained by the "corking" you described, along with tethered cord.) Also, our community is finding upright (functional) MRI to be vital to diagnosing these problems as you have, as well as the even newer digital moving x-ray technology I'm sure you've heard about. That said, we do require great care under surgery, as our tissues are quite fragile, and don't suture the same as "normal" people's, and we can have major "allergic" like reactions to the anesthetics and the procedure itself thanks to commonly comorbid Mast Cell Activation Diseases or disorders. Learn all you might like about all of this and more here: ohtwist.com

[@AndyJK45]

There is a big overlap here. Hypermobility patients are much more prone to these malalignments, and getting the malalignment to stay corrected is much harder. However correcting the malalignment is still essential for recovery.

[@HCRHSHH]

what can be done to treat hypermobility?

[@NonyaSmith]

@@HCRHSHH Supposedly something called prolotherapy. I really don't know if its legit, but there are tons of video testimonials on the Caring Medical YT channel from the chiropractors patients. This guy has been doing this dextrose injection therapy into laxed ligaments in the neck (and elsewhere) for a long time with success in his patients.

[@HCRHSHH]

Jan Droid how have you been doing since? Have you done surgery ?

[@JanGroh]

@@HCRHSHH I"m fine, as I both a) stopped biking so much, and b) take 6000/day Vitamin C plus 1000/day Magnesium (I'm lucky to tolerate both as well as I do) and have for seven years. These have served to help tighten up my neck again as my tendons and ligaments re-strengthened about 40% since my onset cascade in 2012 that got me diagnosed. I'm not "cured", but managed. I also avoid things that would loosen my head or neck as much as possible now, so no surgery needed. (I wore a collar for a bit too.) Others aren't so lucky, even without biking or accidents. (I know several who are nearly internally decapitated just from "living" with EDS.) Tough sitch.

[@kaelou3408]

So what is happening now with his services, has he opened up to accepting more patient’s? Has he trained other’s to do this? This is needed by so many!!

[@kelleyrogers6013]

Thank you for saving my son from 4 yrs of worsening symptoms!

[@depressorfull]

Is there any way I could get into contact with him by email? I have symptoms of ventral brain stem compression but no one is believing me.

[@kelleyrogers6013]

Introvert yes he has email listed on his website. Google Scott Rosa D.C. Rock hills NY.

[@kelleyrogers6013]

Introvert and they didnt believe my son because they dont understand it. So they say you are lying or a psych issue. Im sorry it happened to you too.

[@depressorfull]

I've emailed him and his receptionist said he would get in touch but it's been 5 days... sigh

[@kelleyrogers6013]

Introvert He is very busy. You can keep trying or tell me the area you live and I can google for a more local guy for you. We ended up going to someone local. Dr Rosa did initial evaluation of my sons MRI though. It was around 150$. He found the problem. But a local ao doc did the procedure in texas.

[@doroparker4072]

Wondering if this will help spinal stenosis, a bulging disc, degenerative disc issues, scoliosis, RA. osteoporosis and sciatica. I'm posed to have surgery soon, nothing has helped, i saw a chiro and had PT plus a very painful injection in my spine

[@Ausman5]

Is there anyone in Australia doing this treatment from a local practitioner?

[@ExplorePanama]

You mentioned chronic headaches, but what about chronic migraines? My wife has suffered from chronic migraines for decades. Could your treatment possibly help?

[@kellyoconnell5976]

I would love to know if there is an atlas chiropractor in my area? Fairfield County. Can I email Dr Scott Rosa? The video was very interesting and for me to listen for an hour who has MS is pretty remarkable. Lol

[@HappyFern07]

If mechanical compression of jugular vains, how can this be corrected?

[@karenc.7728]

I just learned of Dr. Rosa & found this video. I’m wondering if a misaligned atlas & axis can cause issues with the mandible & the bite?

[@marionharris5952]

Yes

[@godwinthehuge7169]

Could someone give me a QRD

[@bassventura6144]

I’m so scared right now I see him Thursday I hope he can help. I’m at rock bottom

[@wesporter2176]

How did it go? I did NUCCA it helped a lot at first but then it was a slow steady climb.

[@bassventura6144]

@@wesporter2176 seems like it’s getting a little better it’s a long climb I’ve been with symptoms for 4 years. He was super helpful in identifying the issue that dozens of other drs could not so I’m happy about that.

[@El_Superhombre_Blanco]

@@bassventura6144 hey..how are you doing? Someone told me that the first visit with Dr Rosa costs 7 thousand dollars, is that true?

[@bassventura6144]

@@El_Superhombre_Blanco yes it did.

[@lawrencetaylor5407]

@Bass Ventura How are you feeling since you last post (4months ago)? My girlfriend hasn't been able to stand up for more than 30 seconds in the past 2 years and I'm beyond worried.

[@Learnguitartoday]

can an atlas misalignment cause syringomyelia?

[@Learnguitartoday]

@@NicholasPeters1 interesting, is he going yet? Let me know what happens, I wasn't born with my syrinx bc I had MRIs to prove it from years ago however it just randomly popped up and now i have it with no known cause

[@El_Superhombre_Blanco]

i have a syrinx too. I believe it was caused by instability compression in my neck or something to do with Cerebrospinal fluid hyper or hypo tension. I cant find any doctors to help me.

[@jordannicole6608]

Who is the woman doing to interview?

[@newlanddewinter4692]

A patient.

[@brendaz9222]

Would this help Autism?

[@bobgeorgeff]

The title of this video should contain the word “Affects” not “Effects.”

[@SkeensSeattleUSA]

This video is way to long and lacks organization. The information is interesting however lacks scientific references.

[@AndyJK45]

Here is plenty to keep you going: www.karger.com/Article/Abstract/365470 There are a further series of papers down the side, and by the time you trace the links through PubMed, Im sure you will have a fine collection. :)