U described my life to a tee. I feel the exact same way. I did before surgery a little but since surgery my racy heart is worse, anxiety is bad, I even have high blood pressure now. Tremors, problems with left shoulder, arm, neck.etc...mentally I am detererating, memory, can't multi task nor explain things when having normal conversattions nor pay attention. Basically I have all the same issues u do...its driving mee crazy
OK so u know u have POTS< that explains ur anxiety issues....
May I ask, was ur NS a true Chiari specialist?
Were u checked for sleep apnea? Since u wake often, u should be checked if not yet,.....
AS for going back to work, u may have gone back too soon....even going part time can add to set backs....
Many with Chiari do have sinus issues, do see an ENT to see if that is what is going on with u......have they tested the fluid to make sure it was not CSF leaking?
At work, do u have florescent lights? If so, try tinted glasses to help as these lights can add to how u feel....it affects me, makes me dizzy, nauseated....like walking in a dream state...very odd.
Will u have a one yr post op visit with ur Dr?
I have the vision issues and the tremors also in my right hand....I was DX'd with Ehelrs-Danlos which I attribute my symptoms I have now to along with tethered cord, which I knew I had b4 my surgery.....
Post nasal drip has been an issue for me, and I take an antihistamine b4 bed which helps me sleep and with the drainage.
Also my nose runs almost all of the time. Completely clear and I am on an alergy medication.
I did not have these particular problems before hand. I had lived with the headaches for 15 years after being diagnosed for the first time. In March 2012 I began getting dizzy all of the time. I didn't want to eat and always felt sick to my stomach. I couldn't close my eyes without feeling like I was going to fall and my balance was gone. The only symptoms I have had both before and after are the problems with my eyesite, feeling kind of out of it and tremors, especially in my right hand. I had the decompressive craniectomy and cervical laminectomy, duraplasty and a portion of the C1 removed. I have had a hard time remembering words, term etc for my job. I can't come up with the right things to say or ways to explain things. I was back to work part time in August and full time in September. The problems with my thought process have been there for a while but are getting worse and worse. I was diagnosed with POTS in december after several spells of going to the ER feeling like I was dying. My heart was racing and I felt like I was going to pass out and then stop breathing. They did not want to see me and said if I was having post surgery problems that I need to see my PCP. They said the follow up MRI was good so it was not a problem from the procedure itself. I was told that I could have suffered minor brain damage as a result of the surgery and then I was written off, so to speak.
Hi and welcome to the Chiari forum.
May I ask, did u have ne of these symptoms b4 surgery...if not, what symptoms did u have?
What type of decompression did u have? lamenectomy, duraplasty?
How long are u back to work?When did these symptoms start?
And lastly what has ur NS said in regards to how u r feeling?