Multiple Sclerosis Community
misinformation
About This Community:

Our Patient-to-Patient MS Forum is where you can communicate with other people who share your interest in Multiple Sclerosis. This forum is not monitored by medical professionals.

Font Size:
A
A
A
Background:
Blank
Blank
Blank
Blank Blank

misinformation

I am sooooo frustrated! I just got up the nerve to call about the cervical myelogram and spinal tap to schedule it and was told now that they don't do both!! When I was at the doctors office the girl called there(the imaging place) and later called me to say that yes they can do both. I thought that I would just get them both done with 1 needle. I am so tired of all this bull ****!!!!!!!!! between the pain and the frustration along with the muscle spasms at night that even the zanaflex cannot seem to take away aqnd lets not forget the lack of sleep, I am at the end of my rope!!!!!!!!!!!!!!!!!!!!!!! Just letting off some steam. Thanks for listening.
Related Discussions
9 Comments Post a Comment
Blank
279234_tn?1363108849
Vent all you want! It is frustrating when they tell you one thing and you find out another. I'm sorry that you have to go through that. Hang in there!
Blank
572651_tn?1333939396
Hi, Welcome - I don't remember crossing paths with you yet.  From what you are writing, I am assuming that you are in limbo looking for answers.  Someone will correct me is I'm wrong but these are two different procedures - the myelogram is going to inject you with a contrast agent so that films can be taken.  The spinal tap (lumbar puncture) is to withdraw cerebral spinal fluid.  

I'm so sorry they can't just knock you out and do everything at one time - wouldn't that be great and maybe you could sleep too!  LOL

Exhaustion is a horrible thing to live with - I hope you get some answers and rest soon.

my best,
Lulu
Blank
Avatar_n_tn
I am new to this forum. I did however find out after my venting that the tech at the imaging place gave me the wrong info. My neurosurgeons  secretary told me that she spoke directly to the radiologist and he said that although they do not do it often it can be done. He told her that during the myelogram spinal fluid leaks out and they usually let it drain but it can be captured. I bit the bullet and told them to set the test(at least the myelogram) for next Fri. They will do the spinal tap too. I called the neurologist and left a message with his secretary that I am having the myelogram so if he wants the spinal tap he has to send them the script. I will know tomorrow if he is going to order it. I am pretty sure that he will want to because he believes that I have ms and it may be helpful. I know now from this site that sometimes the cf is neg yet you still have ms. as far as the problem I am having with the zanaflex wearing off bfore the night is over, they directed me to take another one if I awaken in spasm during the night. I wanted to just do that but I was afraid. I am supposed to take 2 a day but the one at night makes me so tired I don't take the one in the day. Oh one more thing THANK GOD the girl at the neurosurgeons office said she will tell the doctor I need something to calm my nerves before the procedure. The place won't do iv sedation so I will have to take a pill. I don't care as long as it calms me before the procedure!
Blank
Avatar_m_tn
i did not realize they still performed myelograms? considering what the MRIs of my neck have shown, i would love to have a myelogram road map of my neck to see if any nerve issues/damage is there. having a demyelinating disease and a diseased spinne in the neck, my mind cannot distinguish which is flaring up at time.

quite interrested in your myelogram results....
Blank
Avatar_n_tn
Hi, I did have a mri of my neck  and due to the fact that I have a titainum (probably spelled wrong) plate in my neck (due to previous surgery) they did not get a picture that shows the spinal cord behind the plate. therefore they want me to have a myelogram. I am not happy to have it. they are painful at least 20 years ago they were. I had a horrible experience 20 years ago when I needed a myelogram the day before back surgery. The tech at the mri place told me that they generally no longer need myelograms anymore because the mri does such a good job.
Blank
Avatar_f_tn
Hi, I have had a myelogram . I was so scared from all the talk and reading . It was not bad at all, I didnt feel the needle much cause they rub some numbing stuff before they stick you. I am scared of needles so I would of passed out if I wasnt lying down , but it was over so fast. It did show that I have some cyst and a collapseing bone, that all the mri's would not show, they never could see what was wrong.   But, I do have problems with my leg now it is cold , numb and foot feels like it is asleep all the time. Cramps come from nowhere at wants. I am taking 4 kinds of meds to deal with pain , I dont feel the pain in back ! that is why I went in the first place.
Blank
293157_tn?1285877039
Hi there... hope all the testing works out and let us know how it goes.. take care and try not too worry

wobbly
Blank
Avatar_n_tn
Please let me know if you ever obtained relief.  I had a myleogram done on Dec. 9, 2010.  I never had terrible pain thru procedure as I had in my legs and calf of my right leg in particluar.  It is January 25 - I have been given epidurals for my lower back-- lots of meds to try, most I am allergic to and my right foot is always asleep-- afraid to drive and the pain and spasms in my calf keep me up all night.

Alot of people say myleograms can't cause these problems.
I know what I am feeling and I know you feel the same way. Please respond.  Please.
Blank
Avatar_n_tn
First thing I want to say is if you are taking cholestrol medicine stop for 2 weeeks and see if your spasms subside. That is what the problem was for me and so many other people. My pain in my rear went away about 2 weeks after the test. Since my last post which was probably more than a year ago I have found out that I have what is called polyneuropathy. It is a painful disorder of the nerves. I had to have a nerve biopopsy to finally get an answer as to why my legs hurt so much. they believe that the brain mri looks like I have ms but I don't. I am just thankful to finally have a diagnosis. my future is a painful one but at least no one looks at me like it is all in my head anymore. I hope that you get relief and that you also get answers to your health problems. God Bless...... Carol
Blank
Post a Comment
To
Blank
Weight Tracker
Weight Tracker
Start Tracking Now
Multiple Sclerosis Community Resources
RSS Expert Activity
242532_tn?1269553979
Blank
Emotional Eating Control: How to St...
Aug 28 by Roger Gould, M.D.Blank
233488_tn?1310696703
Blank
New Cannabis Article from NORTH Mag...
Jul 20 by John C Hagan III, MD, FACS, FAAOBlank
242532_tn?1269553979
Blank
3 Reasons Why You are Still Binge E...
Jul 14 by Roger Gould, M.D.Blank
Top Neurology Answerers
572651_tn?1333939396
Blank
Lulu54
Dayton, OH
338416_tn?1260996698
Blank
jensequitur
Fort Worth, TX
987762_tn?1331031553
Blank
supermum_ms
Australia
147426_tn?1317269232
Blank
Quixotic1
Washougal, WA
1831849_tn?1383231992
Blank
kwarendorf
Great Neck, NY
Avatar_f_tn
Blank
essdipity