26 Mar '10 16:54>
Hi,
When was dx with MS I'd see my Neurologist every 4 months. When I have a relapse I get checked the next month if treatment was given. When I was on Avonex they had me come in every 3 months, to the MS Specialist, and have my blood checked for liver problems and find out how I was responding to the drug.
In Ireland, and Scotland I heard that many people only see a MS Nurse. I know they are well trained, as ours are too.
I see the MS nurse prior to going into the Neuro's office. She takes down the information, puts it in the computer, asks my problems and concerns, then the Neuro comes in and all is in the computer and chart in his hand. He gives an exam every visit, then orders blood work or MRI or whatever he thinks I need. He gives me the results of his findings and any past test.
I do admit, they are fast visits, because they see many patients, so the visit is about 15 minutes in a MS center or if a Neuro has his own practice the visit is much longer, due to less patients to see daily.
If you make a fuss in Ireland you may get to see the Neuro, or call him if you feel the medication is giving you any problems. You have to be your own advocate and be demanding when doctors are few. At least call and make known any concerns you have.
If you have a problem with the medication, go to the hospital and complain. Even your regular doctor can recommend you see the Neurologist if you need too. Good luck to you.
Lady2
Please see the Post on socilized medicine.....THIS REALLY SUCKS FOR PEOPLE JUST BEING DIAGNOSED WITH MS. THE GIRL FROM Ireland HAS A PROBLEM COMING USING INTERFERONS, AND NOBODY THERE HAS TOLD HER. INTERFERONS CAN DAMAGE HER LIVER AND KIDNEYS.
No matter what is said about the Health care in the USA, it's still the best in the world. Ask the sick of the other countries,, they are rushed about, and leave the office with very few clues on what is happening to them.....
The Red Neck
When was dx with MS I'd see my Neurologist every 4 months. When I have a relapse I get checked the next month if treatment was given. When I was on Avonex they had me come in every 3 months, to the MS Specialist, and have my blood checked for liver problems and find out how I was responding to the drug.
In Ireland, and Scotland I heard that many people only see a MS Nurse. I know they are well trained, as ours are too.
I see the MS nurse prior to going into the Neuro's office. She takes down the information, puts it in the computer, asks my problems and concerns, then the Neuro comes in and all is in the computer and chart in his hand. He gives an exam every visit, then orders blood work or MRI or whatever he thinks I need. He gives me the results of his findings and any past test.
I do admit, they are fast visits, because they see many patients, so the visit is about 15 minutes in a MS center or if a Neuro has his own practice the visit is much longer, due to less patients to see daily.
If you make a fuss in Ireland you may get to see the Neuro, or call him if you feel the medication is giving you any problems. You have to be your own advocate and be demanding when doctors are few. At least call and make known any concerns you have.
If you have a problem with the medication, go to the hospital and complain. Even your regular doctor can recommend you see the Neurologist if you need too. Good luck to you.
Lady2
Please see the Post on socilized medicine.....THIS REALLY SUCKS FOR PEOPLE JUST BEING DIAGNOSED WITH MS. THE GIRL FROM Ireland HAS A PROBLEM COMING USING INTERFERONS, AND NOBODY THERE HAS TOLD HER. INTERFERONS CAN DAMAGE HER LIVER AND KIDNEYS.
No matter what is said about the Health care in the USA, it's still the best in the world. Ask the sick of the other countries,, they are rushed about, and leave the office with very few clues on what is happening to them.....
The Red Neck