:-\ Unfortunately many of us here do understand the situation and the emotional fears you feel about the situation. And yes, I'd agree, totally RIDICULOUS even a bit retarded but those are the hoops we've been given so we just have to keep jumping through em for now.
So ranting? Nah, just expressing what is on your chest to others who 'can' understand what you are feeling. For the rest of us, well we just hope and pray that our words in this black and white impersonal forum can reach out and give you a hug.
Hang in there, try, as hard as it is, not to let this all get your dander up as that will only worsen the symptoms. As Carolyn says, do be an advocate, NO is an answer that we can not accept.
Wolf
I understand...and please feel free to rant!!!
My experience was much the same...I was left to progress for 6 months b4 anyone did anything about it and I do blame a lot of my pain now (post op) on the damage that was done during that period. So what I am saying, is keep pushing them and don't give up no matter how they make you feel. I should have pushed hard in hindsight but it was more difficult for me b/c I didn't even have a dx...
Don't take "NO" for an answer....push for those tests!!
Carolyn
So I had called the Dr on Friday morning and didn't get a call back. I called them this morning and I guess my progression of symptoms in 3 days wasn't as scary to them as it was to me! They put me on a cancellation list which I can't imagine getting me in any sooner than Thursday, but fortunately nothing got worse over the weekend.
They always like to tell me that every neurologist in the area is booked for months, which is only half true...some are, some aren't, but my insurance is going to get angry with me for hopping around. So I'm afraid that I'm going to go in Thursday, maybe convince him to run the necessary tests, and then not be able to get back in for 6 weeks again...and continue to get worse in that 6 weeks. Ridiculous!!
Just had to rant - I'm sure you all understand my frustration.
I had the same experience except mine was the left side. Even post op, I still have issues with turning my head sharply to the left, thank goodness shoulder checking when driving is mainly on the right.
It started to go from my neck, down my arm and then fairly quickly (matter of months) affected my left leg too. Keep in mind that I was doing activities that I shouldn't b/c I had no idea that it was Chiari causing it. I agree with the others, keep your head turning to a minimum and avoid neck stressing activities. I think you were right in calling your dr, hopefully they will agree to see you sooner.
Carolyn
HI...I have to agree with Wolf....I was told no driving and am still not behind the wheel...I also had drop attacks...but, u do not want to do nething that will aggravate ur symptoms and this obviously does.
Sometimes the symptoms do progress rapidly.....sometimes very slowly.....and sometimes it may level off for a while.
If u get new symptoms call ur dr right away.
and as Wolf said..do be careful if u feel u must drive
"selma"
It sounds to me like you need to quit turning your head to the right until a Dr can get a look at what is causing it.
Post op I had similar symptoms that caused my PCP to insist that I not drive at all, no exceptions. I either agreed to it or he went to the state to have my DL revoked. It was a pain but looking back I agree with his actions totally. Why? - Shortly after I started having those type of problems the drop attacks began happening. If I'd had a drop attack while driving .... don't want to even think about the very real possibility that I could have killed someone.
Please do be careful!
Wolf