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Newly diagnosed

Hi everyone

I was recently diagnosed (1 month)with CM after having a MRI to see what was causing my golfers elbow!!! I know but a true story.
I have a 10 mm descent and a shed load of symptoms with it. I had always thought that all but 1 symptom were due to other issues ie, I have 80% low tone deafness in left ear, so the constant falling over, balance issues, tinnitus in right ear and so on we're linked..... Oh how wrong was I.
My symptoms are balance issues, vertigo, tinnitus, cough headaches, numbness in right arm and hand, swallowing issues, double vision, sleep deprivation, right side of neck movement impaired, neck and back pain and a few others.
I have just had another MRI done on the whole brain and all the spine as the first MRI showed that the lower right side of my skull had no fluid due to the compression. I'm wondering if they have found a sprinx as when being moved on the bed  while doing the spine the movements went from around long movements to I would say no more than 2-3 inches. It almost felt like they wanted to get the top of the c6/7 with the thoracic.im now waiting for another appt where I will have a ns there also as I know I will be having decompression surgery.
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620923 tn?1452915648
COMMUNITY LEADER

  Hi and welcome to the Chiari forum.

Many of ur symptoms are the same I have had as well....and it is possible to have related conditions as well, and I feel it is very important to rule ALL of them out B4 surgery is considered as these other conditions can affect ur recovery.

A number of us with Chiari also have tethered cord...so checking ur entire spine is useful as well as many have ehlers-danlos and it can affect the disks in our spine, so bulging disks is not an unusual find.

Did u have a CINE MRI?

  
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620923 tn?1452915648
COMMUNITY LEADER

  If you had gone to the Drs sooner you may not have found one that could figure it out...I went to Drs since I was 17 with my headaches and was not DX'd until I was 48.....

First of all MRI's were not around for diagnostic purposes.....then, and now that they are more routinely used, it does not mean that ALL Drs know about Chiari and the related conditions...like ehlers-danlos which can affect the recovery.

It is a slow process with the medical community learning about this condition and how it is intertwined with others and how they can affect the outcome of surgery.

DX can be a long bumpy road as it can be finding the right Dr.....you seem to be lucky in that you found a Dr to DX and is aware of the condition.
  
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Avatar universal
Hi there
Yes I did have a cine MRI.
I'm lucky as I have private health care in England and my neurologist specialises in CM.
I wish I had gone to the doctors earlier as the 1 symptom that' I couldn't put anything to was the cough headaches and I have suffered with them for over 15 years..
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