• Skip to main content
  • Skip to secondary menu
  • Skip to primary sidebar
  • Skip to footer

PrettyIll

Header Right

Dr. Diana, both a doctor (therapeutic optometrist), and a recovered POTS and ME/CFS patient, offers help and hope for POTS, Dysautonomia, Ehlers-Danlos syndrome, Chronic Fatigue, Chronic Lyme, vascular abnormalities, Fibromyalgia, and Multiple Sclerosis. Dr. Diana is now working full time at POTS Care.

  • Home
  • The Driscoll Theory®
  • Videos
  • Meet Dr. Diana
  • Forum
  • Store

can anyone point me in the right direction

NEW STUDY! Parasym Plus™ for Multiple Sclerosis › Forums › PrettyIll.com Discussion › EDS/MS/Chiari › can anyone point me in the right direction

  • This topic has 16 replies, 3 voices, and was last updated 9 years, 1 month ago by Dr. Diana.
Viewing 15 posts - 1 through 15 (of 17 total)
1 2 →
  • Author
    Posts
  • February 15, 2014 at 11:35 pm #671
    ttpookinz
    Participant

    do you see anything that will help me get a diagnosis? I have intense arm pain, all over pain, constant pain for 15 years. chronic fatigue, eye issues, trouble walking, late night heart palpitations and so much more. it seems to get worse year by year but the doctors always say my labs look fine and to just lose weight and i’ll be fine. help. Help! HELP!!!

    Attached files

    February 16, 2014 at 6:22 pm #4869
    Barbara
    Participant

    Hi,
    Have you ever had an accident that started this off, or are you hypermobile ? Have you had an MRI of your head, or just neck. I would be interested in seeing your head MRI, if you have one, to see the state of your pituitary and to look for any excess cerebro-spinal fluid (CSF).

    I am not medically trained but I have been studying MRI’s for 6 or 7 years now. I can see several potential problems on this MRI but it is late and it will take me some time to examine and explain, so I will try and look at it again tomorrow.
    Barbara

    February 16, 2014 at 7:39 pm #4871
    ttpookinz
    Participant

    I don’t have a mri of my head. I have mri of my thoracic and lumbar spine. I was in a car accident at 17 and started having the true pain at the age of 23. but now I look back and realize I had a heavy head feeling and neck problems since I was little. This MRI was done laying down. My chiropractor says that in my x-rays(which are done standing) that it looks like my spine is shoved into my skull.
    My left arm hardly works and hurts so bad. I haven’t been able to work in years because of all the pain and weakness in my upper body. my heart races when I sleep at night. I have eye disturbances. all kinds of issues but I can’t find a doctor to take me seriously. they all want to put me on antidepressants and I have already went down that road. It doesn’t help. Neurontin doesn’t help either. This mri was done in 2009. the main things on the report that were not mentioned to me at the time were borderline canal stenosis and hypertrophy on the atlantodens articulation. I am so curious to know what you or anyone else thinks of this mri. I suspect that my odontoid is pressing on something when I am in an upright position.

    February 17, 2014 at 5:52 am #4873
    Barbara
    Participant

    I have annotated a copy below to highlight some of the matters that I think are important, then I will explain why.
    Barbara
    (UK)

    Attached files

    February 17, 2014 at 6:45 am #4874
    Barbara
    Participant

    So why can a ‘short clivus’ be problematic:
    It can allow the tip of the odontoid to prod or compress the brainstem, especially if the ligaments have been injured.

    So why are low-lying cerebellar tonsils (CT)a problem:
    This is a part of your brain that should be 5mm above the opening at the bottom of your skull, to allow free flowing Cerebro-Spinal Fluid (CSF). Low-lying CT can cause a ‘bung’ in the system and contribute to build up of pressure in the head. Over time, this pressure can flatten the pituitary gland, causing a whole range of problems, including weight gain! It may be that you need to get treatment to lose weight!

    What is a Retroflexed Odontoid and what difference does it make:
    The odontoid is the ‘peg’ part of the C2 bone, if it points backwards towards the spinal canal it is referred to as ‘retroflex’. A normal C2 odontoid points straight up and is less of a threat to the brainstem.

    What is the significance of a Pannus:
    A normal person, whose head is firm and secure, will not have a pannus. A pannus occurs where there is instability and therefore is a medical ‘sign’ of instability. It’s a pad which the body produces here against the tip of the odontoid, to help safeguard the brainstem from insult and, although it no doubt does help, that help is far from adequate for anything other than very mild instability.

    Why does it matter if the posterior arch of C1 encroaches the spinal canal:
    The spinal canal needs to be a smooth channel down which the spinal cord and CSF can pass freely, without obstruction. Anything interfering in this smooth passage can alter the fluid dynamics/flow, or impact on the spinal cord. I would also be asking why this is happening, i.e. has your atlas subluxed, or is it unstable ?

    What is the anomaly at C4/C5:
    There appears to be some change in signal here, where I would expect to see fluid, there is something making an impression on your spinal cord, is it from a disk ? I don’t know but if you look at the line of your spinal cord, it gives this object a ‘body swerve’ if you get my meaning, so it’s obviously aggravating the spinal cord.

    Hope some of this is useful, let me know if you need to know anything else.
    Barbara
    (UK)

    February 17, 2014 at 7:35 am #4875
    Barbara
    Participant

    Here’s some further points, suggesting cervical instability, I think your condition could be being aggravated by putting your head into flexion.

    I would try and avoid that by doing whatever tasks you can sitting down (so that your head is looking forwards and not down). Lift your work up to eye level too, i.e. raise laptops, use bookrests, adjust a gas-powered office chair to the appropriate height. If I were you, I’d be wearing a phladelphia collar with liners too.
    Barbara
    (UK)

    Attached files

    February 17, 2014 at 7:45 am #4876
    Barbara
    Participant

    I don’t have a mri of my head. I have mri of my thoracic and lumbar spine. I was in a car accident at 17 and started having the true pain at the age of 23. but now I look back and realize I had a heavy head feeling and neck problems since I was little. This MRI was done laying down. My chiropractor says that in my x-rays(which are done standing) that it looks like my spine is shoved into my skull.
    My left arm hardly works and hurts so bad. I haven’t been able to work in years because of all the pain and weakness in my upper body. my heart races when I sleep at night. I have eye disturbances. all kinds of issues but I can’t find a doctor to take me seriously. they all want to put me on antidepressants and I have already went down that road. It doesn’t help. Neurontin doesn’t help either. This mri was done in 2009. the main things on the report that were not mentioned to me at the time were borderline canal stenosis and hypertrophy on the atlantodens articulation. I am so curious to know what you or anyone else thinks of this mri. I suspect that my odontoid is pressing on something when I am in an upright position.

    What I think your chiropractor is suggesting is called ‘basilar invagination’ or ‘cranial settling’, if you want to look it up and see if that fits.

    You say your heart races when you sleep at night, have you tried raising the head of your bed, or sleeping upright ? Your symptoms sound like some of mine, I have to sleep upright, I have craniocervical instability, have you been checked for this ?
    Barbara
    (UK)

    February 17, 2014 at 8:07 am #4877
    Barbara
    Participant

    I have looked at the Grabb-Oakes measurement (which may be wrong if my scaling is wrong!) but it gives you an idea.

    If you look carefully at the brainstem, you can see an impression of the odontoid, I have put a thin red line on for your guidance.
    Barbara
    (UK)

    Attached files

    February 17, 2014 at 8:25 am #4878
    Barbara
    Participant

    You may find some more useful information in the post I made showing my head MRI annotated and the subsequent posts talking about possible treatments.

    http://prettyill.com/forums/viewthread/712/

    Barbara
    (UK)

    February 17, 2014 at 8:35 am #4879
    ttpookinz
    Participant

    Is surgery the only option for relief? Are there operations where they just remove the pannus from the odontoid? The pressure in my neck is killing me. I can hear trapped csf as it gets released sometimes. The doctors think I am crazy. I am obese. But when this all started I was perfectly thin and super active. I have been asking doctors,chiropractors, massage therapist, acupuncurist, etc. to help me for 15 years. Nothing they have suggested has ever helped. Some of it has progressed my symptoms. They all think I have Fibromyalgia. Thank you for your time and your opinion.
    I have suspected I have basilar impression and chiari.

    February 17, 2014 at 9:11 am #4880
    Barbara
    Participant

    Hi,
    Of course surgery is one option. I haven’t had surgery, I had a head and neck injury in 2002, here in the UK I have been unable to get surgery, instead they are using the ‘conservative’ treatment of a Philadelphia Collar (and for a few years a body brace) 24/7, it seems extremely cumbersome at first because it puts your head back in it’s rightful place (instead of hung forwards!) for maximum CSF flow (which of course your body isn’t used to!) but eventually you get used to it and as your symptoms improve, you’re GLAD of it. I don’t even notice it now.

    The thing is with the pannus, that’s your bodies defence, if anything needs removing it would be the rogue part of the odontoid but even then, without stability, your efforts are futile, you need to work on keeping it stable.

    Without a doubt you need a collar, not a soft collar either, as this doesn’t support your head, the best collar I’ve found is a philadelphia collar (but you do need to wash it daily and wear liners, for comfort!).

    Also ensure you get Vitamin C regularly throughout the day, and make sure you eat sufficient protein everyday because without either of these, your body will struggle to make collagen. You need your body to make the best collagen it can, to produce strong ligaments at the cranio-cervical junction because your head is held on by ligaments, there’s no bones holding it.

    If you have bone pain, get your vitamin D levels checked, a supplement can make all the difference. Massage helps me with the body pain but the collar severely reduced my overnight body pain. An epsom salt bath helps your body replenish Magnesium, which eases the muscle pain. If you get leg pain in bed, make sure you keep your legs 6″ lower than your bottom.

    If you have energy issues you are probably B Vitamin deficient too, a supplement of these helps, even if you eat well, as often our gut issues hinder absorption.

    Don’t forget, try raising the head of your bed, or sleep sitting up.
    Let me know how you go on
    Barbara
    (UK)

    February 17, 2014 at 9:21 am #4881
    Barbara
    Participant

    They all think I have Fibromyalgia. Thank you for your time and your opinion.
    I have suspected I have basilar impression and chiari.

    Have you checked out the symptoms checker which compares Fibromyalgia, Chiari and Spinal cord compression, at

    http://www.nfra.net/Symchart.htm

    This is what allerted me to the possible chiari involvement, years ago.

    February 17, 2014 at 1:59 pm #4885
    ttpookinz
    Participant

    Do you have Chiari Malformation as an official diagnosis? Do you think I would qualify for at least Chiari 0? I read some of your other posts. They are so informative. Thanks for being so giving with your time and opinions. I tried magnesium supplements, oils and baths about 2 years ago along with some natural antibiotics like colloidal silver and grapefruit seed extract. It almost killed me. I released so much toxins that I developed some kind of kidney stone and amazingly large tonsil stones. How do you clean your lymph system?

    February 17, 2014 at 4:10 pm #4886
    Barbara
    Participant

    After fighting with this lot for 6 years, in 2008 I flew across the Atlantic to The Chiari Institute in New York, as I believed I had found a man who really understood the problems I was suffering. He was a great educator and I watched all of his videos before going across. His name was Dr Bolognese, I have deep respect for this man, despite any bad press he has received in recent years. He has helped thousands, there are bound to be the odd few that haven’t enjoyed the same amount of success but overall he has done much good in this world, where others turned their backs.

    He diagnosed me with ‘Brain Compression’. His colleague Dr Milhorat carried out further testing (invasive cervical traction – NOT to be recommended!) and diagnosed ‘Post-Traumatic Cranio-Cervical Instability’ but I didn’t qualify for the Chiari diagnosis, as my cerebellar tonsils weren’t herniated by 5mm, so I was told they were ‘low-lying’. Dr Nishikawa, the morphometrics man, was very helpful too with his measurements and when I put my hypothesis to him, that I thought my brainstem was being pincered between my odontoid and opisthion, he looked at it and he thought it also.

    Here in the UK I consulted with Dr Raymond Perrin, after reading his book (available on Amazon) and after listening to Dr Diana (and reading her book!) about the involvement of CSF drainage. I’d wake up with hands resembling boxing gloves, they were swollen and I knew I needed some kind of lymphatic drainage (and help with the chronic fatigue I had developed). So I started The Perrin Technique, initially at his clinic in Manchester but also carrying out drainage massage and exercises at home. It has helped both with swelling and energy levels.

    You can watch 6 videos about Dr Perrin’s approach at:-

    Barbara
    (UK)

    February 20, 2014 at 7:17 pm #4890
    ttpookinz
    Participant

    I have an appt. with a neurosurgeon. Do you have any advice?

  • Author
    Posts
Viewing 15 posts - 1 through 15 (of 17 total)
1 2 →
  • You must be logged in to reply to this topic.
Log In

Footer

PrettyIll.com

This website was created to inform, educate and brainstorm with fellow patients and doctors. The content should not be used as a substitute for professional medical advice, diagnosis or treatment. Readers are encouraged to confirm all information with other sources and their physicians. The creator of this site will not be liable for any direct, indirect, consequential, special, exemplary, or other damages arising from the use of this website.

Twitter: @prettyill

What others say

“Dr. Diana will always hold a very special place in my heart for her selfless devotion to helping everyone, not just the Ehlers-Danlos community. I hate to think what my life would be without her insight and guidance.”

-- Chris Gross

Listings by topic

  • Chronic Fatigue
  • Consult
  • Contact
  • Coping
  • Ehlers-Danlos
  • Fibromyalgia
  • Hydrocephalus
  • Mast Cell Disease
  • Multiple Sclerosis
  • Orthopedic Issues
  • Pain Control
  • POTS
  • Speaking Engagements
  • Store
  • Uncategorized
  • Vascular abnormalities

This work may not be reproduced, copied or used in anyway without the express permission of the author -- that's me © Dr. Diana Driscoll 2020