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Viewing 6 posts - 13 through 18 (of 19 total)
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  • ashley
    Member
    Post count: 25
    in reply to: Had my acdf #6711

    Thank you so much. Good to know. I really appreciate your knowledge as it is a while from surgery date until my first appt with the ns.

    I have also not been able to eat a whole lot these last few weeks. Its a bit hard to swallow still and my dilaudid makes me feel sick. I have been taking childrens gummy vitamins because I am worried about not getting enough nutrients and the adult vitamins make me sick.

    To be honest I am lucky if I get a few popsicles a handful of grapes and some scrambled eggs in during a day.

    How important is nutrition in terms of fusing properly?

    ashley
    Member
    Post count: 25
    in reply to: extruded disc #6098

    Hi Dr Corenman,

    I am still waiting to have my acdf surgery but I have a question for you.

    As you know I herniated my c6,c7 after lifting my 20 lb baby repeatedly. No prior traumatic injuries except for a small fall.

    This injury occured when my baby had just turned 3 months old. About 2 months before I had my baby I started to have a lot of problems with my wrists, they kept popping in and out of joint, I would literally have to shake them back into place. They would collapse on me if I tried to put any pressure on them at all. They were loose.

    I asked my dr about that at the time and she said it was most likely due to relaxin preparing for the birth.

    To this day I still have these problems with loose joints. So I went back to my gp yesterday and she said it is most likely relaxin related. So that got me thinking.

    Do you think my sudden extruded disc after repeatedly lifting my baby could be due to the relaxin not going back to normal? Have you ever seen this, is this even a possibility?

    My dr is starting to think my herniation may have something to do with relaxin.

    Thank you for always being so helpful to me, I really appreciate your knowledge and your time Dr Corenman.

    ashley
    Member
    Post count: 25
    in reply to: extruded disc #5972

    When you say it could be coming from cord compression do you mean cord compression in my lumbar spine? Or cord compression from my cervical spine?

    Thank you.

    ashley
    Member
    Post count: 25
    in reply to: extruded disc #5969

    Dr Corenman,

    I went for a regular gp visit while I am still waiting to see my second neurosurgeon. I told my gp that I have started getting some numbness and tingling on my rt thigh and right groin area and the bottom of my toes of my right foot are sometimes tingling.
    So she checks my knee reflexes. My root knee had no reflex when hit. And my left knee was hyper reflexive.

    So she has now ordered a lumbar mri. Could these new symptoms be something to do with the extruded c6,c7 pressing on my spinal cord? Or is this something totally different and maybe has something to do with my lumbar spine?

    Any thoughts would be appreciated.
    Thank you so much.

    ashley
    Member
    Post count: 25
    in reply to: extruded disc #5926

    Thank you so much Dr Corenman,

    Your time and knowledge are very appreciated. I have chosen a surgeon here in Canada to do the ACDF surgery so I guess that’s half the battle.

    Thanks again,
    Ashley

    ashley
    Member
    Post count: 25
    in reply to: extruded disc #5913

    Thank you for your great explanations. You put things in clear, concise context for me.

    And yes I am sure genetics plays a huge factor in my injury. I am also only 5’3 inches and weigh only 100 lbs and I was repeatedly lifting my 15 lb baby with my upper body only 4 to 5 times a night when I was nursing.
    I guess my neck just eventually gave way. I wish I had been more careful but hindsight is 20/20.

    The first neurosurgeon I saw reviewed my mri but only said I would be needing a 1 level fusion. My extruded c6,c7. Yet I have a small bulge at c5,c6 also.

    Do you think a 1 level fusion would be sufficient?
    I guess what I’m really wondering is if you think I will eventually need the adjacent c5,c6 level fused inevetably?

    Or is that just a matter of wait and see?
    Obviously I want to avoid any further surgeries. If possible of course.

    Also for the last 5 yrs I have had some difficulty swallowing, sometimes double swallowing to get food down. Other times a pill may get stuck. It has been constant these past five years though. Not something that comes and goes like with MS. I have been to an ear nose throat specialist who found nothing.

    I did however get sent for the radioactive iodine test and they found a benign thyroid nodule in my neck. They thought this may be causing my swallowing difficulty. They also thought it may be due to GERD as I do have frequent heartburn.

    Anyway,I never had the nodule removed because it wasn’t too bad, however I know one of the side effects after acdf is difficulty swallowing.
    Do you think swallowing will be even more of a difficulty for me?

    Here in Canada it is quite a wait to get an appt with a neurosurgeon. My 2nd referral went in a month ago and I havent yet got an appt date for the initial meeting. It is very helpful to be able to ask you a few questions.

    Lastly, the first neurosurgeon said my c6,c7 extrusion has not only pushed my spinal cord off to the right but said the extrusion is also ascending and descending. I think he was concerned it might turned into a sequestration.

    Am I at any real risk of paralysis while I wait for an appt with the second neurosurgeon?

    I basically lie in bed propped up all day and no longer lift anything. Anything else you would recommend?

    Again, thank you for your valuable time. I appreciate it more than you know.

Viewing 6 posts - 13 through 18 (of 19 total)