I received a call from the Nuerologist, I will be seen on the 6th of November rather than the 20th.
Gluclose results will be in on Friday, Will keep you all posted.
Thanks a bunch. You all are in my prayers
I want to Thank you all for your imput an support. This is just very hard to handle alone. I tried and I find myself crying. I just don't understand it or have the time for my body to feel the way it does. One minute I am fine and the next I just feel horrible. I am very afraid. Once again thank you all.
You all are in my prayers.
Marie
Hi there,
I too am undiagnosed and am waiting for my Neurologist appointment. Unfortunately I have tried to speed up the process but unless you are really on the verge of some massive attack or dying you just have to wait it out. My appointment is on the 26th Nov 2007 so only 6 days after you. I look forward to hearing what happens at your appointment :-)
Mel
Hi and welcome to our little support group! You sound like you have a competent doctor who is doing appropriate testing and then sending you to a neurologist to follow up. There are alot of us here on this website that are not diagnosed yet or have been diagnosed with other diseases that may mimic MS.
It is usually not a quick process to a diagnosis from what I have sean and heard but until you figure out what is going on with you, hang around here and share with us what is going on.
It is very nice to meet you and Have a nice night!
Kristin
You are our "prayer warrior". I love it!
Hi,
Welcome to our family. I'm sorry about all the problems you are having. I know nothing of the medical problems you may be having and why, but I'm more the family prayer warrior.
Like Johnny said, it all takes time. Try and be patient. I know how hard that is when something is wrong with your body but trust me doctors don't rush.
I'll be praying,
Carol
Thank you,
Johnny I am going to keep smiling. I have to wether I want to or not I have a six year old little boy and when he smiles at me, that smile is enough to keep me going. I guess I just have to prepare myself for a long journey. I am from Orange County. I don't know much about MS or Diabetes. Just what I have read on line. So anything you or anyone can share with me is very much appreciated.
Once again Thank you, and Good Luck You will be in my prayers. :)
Hi,
I'm sorry to hear your not feeling well. Believe me, better days are ahead.
You've several symptoms that could be symptomatic of MS, but they could also be caused by other things. It sounds like your doctor is taking a normal approach to things. Shes getting you in to see a neuro which often times takes forever. I would expect that between now and then if things get bad your PCP will get you in.
The neuro will do a standard exam, and probably will order some blood work to rule out a few possible things. A lot will depend on your MRI results. If there are lesions, then your neuro will certainly order more testing given that you have had some odd neurological issues. Don't "expect" that your neuro is going to look at the MRI and tell you whats going on. Thats the exception. A huge exception. Most neuro's I have seen don't venture much information until they are ready to make some kinda of diagnosis.
Could this just be Diabetes? Not sure. I have no idea how diabetes manifests itself. Until recently I had no idea how MS manifested itself, but you learn things pretty quickly when it sounds serious and they mention it as a probable cause of your not feeling well. I am not diagnosed with MS but have a lot of the symptoms. I am working towards finding the cause of my condition regardless of where it takes me. Like me, you know your not feeling right and you would like to know what's causing it. Diabetes or MS? Who knows. It could be a pinched nerve in your spin or any number of things.
I don't want to discourage you, but you wanted to know if you can speed this up and you can't. Appointments take time, getting the right tests done take time, getting back in to see the neuro takes time, more tests. I would expect that you might, if you push, find out whats going on within a year. It can take 10-15 years sometimes.
What you can and must do is to be your own advocate. If you have numbness or pain get in and make them find out whats going on. Sometimes PCP may not think there is anything much going on. I complained that my right leg hurt and arm had numbness for 3 years before getting in to see a neuro. I had to complain forcefully with my PCP that we were not trying to find the answers and I was sick of feeling this way. Stay on them to keep digging.
Keep a time line. A note book with month/year, you don't need specific days, but note times when your note feeling well, how you felt and if it impacted your normal routine. Arm numb, can't vacuum today.
Where are you from? Specifically, where did you live ages 1-12? MS is much more predominant in people that grew up in Northern climates. It still strikes all areas, but strangely those in the North are far more likely to develop it.
I'm going to let others say hello. You keep us updated on how your feeling and whats going on. There are a lot of good people around here, helpful and supportive. There is a retired pediatrician. She has a wealth of knowledge and she will certainly say hello soon. Until then, keep smiling.
Johnny