NEW STUDY! Parasym Plus™ for Multiple Sclerosis › Forums › PrettyIll.com Discussion › EDS/MS/Chiari › Who has neck pain with pain at the bottom back of their heads that radiates down to their shoulders?
August 30, 2012 at 3:25 pm #2824MJParticipant
I’m so glad the deafness cleared up! I’m still suffering a bit from tilting my head like that, but it was worth it to get the picture. I have not been tested for mast cell activation. No one is taking me seriously or even trying to help me – I am not being tested for anything. I need to find a doctor, as mine just relocated. The only thing I have a confirmed diagnosis of is Classical EDS. And I have POTS ‘unofficially’ confirmed, with my Naturopathic Doctor doing a poor man’s tilt table test in her office. I’m pretty sure I have Mast Cell issues, Dysautonomia, CCI and CCSVI, just to name a few.
I looked up diagrams of neck veins, and I believe that vein is the external jugular, and I believe that the internal jugular is also over-sized. You can see the enlarged vein branching off a bit, but then it disappears. I think that is the internal jugular and the swelling stops when it goes behind the muscles and becomes ‘internal’.
Also, I believe I read that there is a valve about 4 cm above the clavicle, which is where the vein appears to stop. So, it could be that the part of the brainstem that controls valve function is being ‘pressed’ on by something with certain head movements. It could also be that the part of the valve that prevents the back-flow of blood is somehow becoming impaired. There are so many possibilities. It may even be related to the heart.
Thank you SO much for chatting with me about this Barb. I posted the pictures, and although 50 people viewed them, no one replied.
MJSeptember 14, 2012 at 2:22 pm #2927EDSlifeParticipant
I have EDS hypermobility and have this pain. I just thought it was related to being tired & stressed. What type of doctor do you see to get a diagnosis for any of this?September 15, 2012 at 10:03 am #2928Give My Daughter the Shot!Participant
That is a big question – what type of doctor. I am not sure where you are located but I would STRONGLY recommend just getting to the ‘top of the foodchain’ as far as doctors go. I, myself, have yet to pull this off for several reasons. It is, however, a huge goal of mine to get to the top; of the foodchain (as far as doctors) and quit the exhausting ‘are you my mother’ tail-chasing.
My genetic doctor dx me w/EDS though. The prob is that any specialist who doesn’t understand EDS and how it impacts EVERYTHING is really not such a good fit. I love my cardiologist and was careful to request one who specialized in genetic disorders due to my EDS – only to find that he specializes in congenital heart defects. There is a big diff in a congenital defect and a genetic disorder of collagen. Ugh! It’s a major struggle and that is why I recommend getting to the heavy hitters.
Clair Francomano, Paul Cheney, Hal Dietz, Pocinki, Grubb, etc. CHeck with EDNF or Marfan national support groups for doctors who would be familiar. SAve yourself years of phychological abuse by doctors and get yourself to where you need to be by seeing a doctor who understands.
Again, this information is hypochritical (coming from me since I’ve yet to accomplish following my own advice) but in my heart I know its best. If not for all of my current obstacles I would have already followed my own advice. Due to rarity of my situation, I have in the past sought treatment by the exact type of microspecialist (top of the foodchain) doctor that I mention – merciful God. Just now I am so bound by so many obstacles I cannot comply with what has been the proper decision for me in the past. I have yet to see the specialists whom I know would be in my best interest considering the current state of my health and the accompanying diagnoses.September 16, 2012 at 12:56 pm #2930EDSlifeParticipant
I live in Memphis,TN. My daughter and I were diagnosed by a genetisit at Vanderbilt three years ago. Most doctors here arent familiar with EDS or know enough that they dont want to see you! Still havent found a rhuemy for myself. Wondering if we should just make the trip to Baltimore for both of us and get as much info as I can! My four year old has a good cardiologist that deals with EDS. Her rhuemy is pretty amazing as well. I have had much better luck with the pediatric side than adult and even that is minimal. How do they test for POTS?October 11, 2012 at 6:59 pm #3043JulsParticipant
I’ve had these awful headaches, they come on in an instant & it feels like I’m being electrocuted. That usually last for a few seconds (5-20) then a tremendous amount of pressure. I have pressure & pain at the cavity where your neck meets your spine & through my shoulders & between my shoulder blades bad!! I’d beg my hubby to DIG his fingers in that cavity at the base of my head & ask him to try & punch his fingers around my spine… My neurologist said I probably had “occipital neuralgia” and put me on Gabapentin…gave me awful chest pain. I told him about reading “The Driscoll Theory” and asked about Diamox… He was reluctant but let me try it. The first pill I took helped SO MUCH!!!!
Thank you Dr. DianaOctober 30, 2012 at 2:41 am #3089capriParticipant
Me… I was told it was part of my occipital neuralgia, there’s ligaments/muscles w/e that travel that path from the base of the neck to the scapula area.
Speaking of bad necks, I also have ringing/hissing in my ears that comes and goes. Sometimes I’m able to stop the hissing and ringing based on the direction I tilt and hold my head. Very weird… and majorly annoying.November 6, 2012 at 4:03 pm #3106SunshineParticipant
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