Guest guest Posted December 2, 2010 Report Share Posted December 2, 2010 I called the neuro and told them of my worsening symptoms (the 4th kind of headache - the one that is getting worse on the right side of my head where it comes and goes hard) anyway, then I told them of my trouble walking - where I am limping and I can't hardly walk - that my legs seems like it is coming off and weak like. I still have the pain in my legs & all my other symptoms (the head pain and stuff) but these 2 things are worsening. I am afraid I will fall or just not be able to walk soon. So he said bc of the worsening of them, that he wants me to be seen in the ER to be evaluated. My problem with going there is that they don't believe me and think I am there for medication! I told the nurse this and she said tell them my surgeon wanted me to be seen and to call him if I have any questions. My other fear is that they will call him up and although he has his diagnosis of what is wrong with me (the chiari/cerebellar ptosis) that they will tell him there is nothing wrong with me and he will not want to see me anymore. They don't know anything about Chiari here where I live. I can go in there and tell them I don't want meds...I just need them to see what is wrong with me, but they still act like I am " seeking " ! They are the rudest people I have ever met in my life here at the ER. What should I do? They told me that I need to keep my appt with them in 2 weeks and my CT/MRI's too. I am definitely, but I don't know what to do about the ER. My husband has a problem with taking me there too. We wait for hours and hours and they are just rude and don't do anything for me. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 3, 2010 Report Share Posted December 3, 2010 I will say that the ER where I live is the rudest of all and lack even basic skill sets I feel you.When I my heart had stoped because of CM SCT I went thirty miles further to the teaching hospital where even thoug it took seveal hours a Dr. who knew about CM looked at me and gave me some good advice and even said it stoped because of my CM. I don't do what I was doing that day any more and I know you probaly do not have a choice but don't let them stop you from much needed atention.We all want to live long lives and with proper care we can.Try asking them if anyone is neuro or such when you go you might get lucky! Quote Link to comment Share on other sites More sharing options...
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