Saturday, May 19, 2007

Types of multiple sclerosis

People with MS can expect one of four clinical courses of disease, each of which might be mild, moderate, or severe.

  • Relapsing-Remitting (RRMS): where symptoms fade and then return off and on for many years.
    Characteristics:
    People with this type of MS experience clearly defined but unpredictable flare-ups (also called relapses, attacks, or exacerbations) during which time new symptoms can appear and/or old ones resurface or worsen. The relapses are followed by periods of remission (recovery), during which time the person fully or partially recovers from the deficits acquired during the relapse. Relapses can last for varying periods (days, weeks or months) and there may be partial or total remission. The disease may be inactive for months or years. The vast majority of people presenting with Multiple Sclerosis are first diagnosed with relapsing/remitting. This is typically when they are in their twenties or thirties, though diagnoses much earlier or later are known. Around twice as many women as men present with this variety.
    Frequency: Most common form of MS at time of initial diagnosis. Approximately 85%.

  • Secondary-Progressive (SPMS): which at first follows a relapsing-remitting course and then becomes progressive. “Progressive” means it steadily gets worse.
    Characteristics:
    People with this type of MS experience an initial period of relapsing-remitting MS, followed by a steadily worsening disease course with or without occasional flare-ups, minor recoveries (remissions), or plateaus.
    Frequency: 50% of people with relapsing-remitting MS developed this form of the disease within 10 years of their initial diagnosis, before introduction of the "disease-modifying" drugs. Long-term data are not yet available to demonstrate if this is significantly delayed by treatment.

  • Primary-Progressive (PPMS): where the disease is progressive from the start.
    Characteristics:
    People with this type of MS experience a slow but nearly continuous worsening of their disease from the onset, with no distinct relapses or remissions. However, there are variations in rates of progression over time, occasional plateaus, and temporary minor improvements. Primary Progressive differs from Relapsing/Remitting and Secondary Progressive in that onset is typically in the late thirties or early forties, men are as likely women to develop it and initial disease activity is in the spinal cord and not in the brain. Primary Progressive MS often migrates into the brain, but is less likely to damage brain areas than relapsing/remitting or secondary progressive - for example, people with Primary Progressive are less likely to develop cognitive problems. Primary Progressive MS does not have separate episodes (relapses, exacerbations). Unlike RRMS where women are twice as likely to be diagnosed than men, PPMS is equally divided between the genders.
    Frequency: Relatively rare. Approximately 10%.

  • Progressive-Relapsing (PRMS): where the symptoms come and go but nerve damage steadily gets worse.
    Characteristics: People with this type of MS experience a steadily worsening disease from the onset but also have clear acute relapses (attacks or exacerbations), with or without recovery. In contrast to relapsing-remitting MS, the periods between relapses are characterized by continuing disease progression.
    Frequency: Relatively rare. Approximately 5%.

Sources:

  1. http://www.mult-sclerosis.org/whatisms.html
  2. http://www.nationalmssociety.org/site/PageServer?pagename=HOM_ABOUT_what_is_ms
  3. http://www.msif.org/en/ms_the_disease/types_of_ms.html
  4. http://health.msn.com/encyclopedia/healthtopics/articlepage.aspx?cp-documentid=100066440

Monday, May 14, 2007

5/14

I have my EEG appointment tomorrow at 9 a.m. These tests total approximatly 2 hours in length.

An electroencephalogram (EEG) is a test that measures and records the electrical activity of your brain by using sensors attached to your head and connected by wires to a computer. The computer records your brain's electrical activity on the screen or on paper as wavy lines. Certain conditions can be detected by observing changes in the normal pattern of the brain's electrical activity.

Evoked Potential (EP) tests
Evoked Potential tests are procedures for measuring the speed of impulses along neurons. These tests help point our lesions that are not causing symptoms by providing evidence of slowed nerve impulses.

Responses can be measured using EEG readings from electrodes attached to the scalp and occasionally other areas of the skin. They are in fact completely painless and entirely harmless. Based on input signals to the particular sense being measured, the time taken for that response to register can be accurately measured and compared to normal readings. The results are then analyzed on a computer and average speeds recorded.

Demyelinated neurons transmit nerve signals slower than non-demyelinated ones and this can be detected with EP tests. Although they may appear to function perfectly, even remyelinated neurons are slower than normal nerves and so historical lesions can be detected in this way.

There are three main types of evoked potential test: (and I believe will all be performed tomorrow)

Brain-stem Auditory Evoked Response (BAER)
The BAER test measures the speed of impulses along the auditory portion of Cranial Nerve VIII. This nerve arises in the Pons area of the brain-stem and therefore this test may be indicative of lesions in that area. The patient lies down in a darkened room to prevent visual signals from interfering with measurements. A series of clicks and beeps are played back to the patient. 67% of people with definite MS and 41% of people with probable MS will have abnormal BAER test results.

Somatosensory Evoked Potential (SSEP)
The SSEP test pertain to sensations in skin and deep tissue. These measure the conscution of impulses by applying electrical stimulus to the arms or legs. The current is switched on for 5 seconds and electrodes on the back and skull measure the response at particular junctions. The current is very low indeed and completely painless. The electrodes record neural signals when they reach the scalp. The speed of various nerves can be measured in this way and the points of slow-down (i.e. demyelinated lesions) approximated to because of the sampling at several places. 77% of people with definite MS and 67% of people with probable MS will have abnormal SSEP test results.

Visually Evoked Potential (VEP)
This noninvasive test measures the speed and amplitude of the of the optic nerve impulses. The patient has to focus on the center of a "TV" screen on which there is a reversing black and white checkerboard pattern shown at measured intervals. The patient wears a patch on one eye for a while and then on the other, so that the speed of both optic nerves can be measured. The electrodes placed on the back of the head to record cortical (outer layer) signals record when the nerve impulse is received. 85-90% of people with definite MS and 58% of people with probable MS will have abnormal VEP test results.

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5/23: I have an appointment at 9 a.m. for 3 MRI's (brain, c-spine and thoracic), but these will be MRI's with contrast. To gain better contrasts in the images, contrast agents such as Gadolinium are often injected intravenously (FYI: Gadolinium is a non toxic substance which does not contain iodine and has practically no side effects.) The gadolinium works by altering the local magnetic field in MS lesions and thus enhancing the MRI image. This helps to differentiate between new/active and dormant lesions. So, this would then illustrate whether this is my first attack or not.

Links for MS information

I thought you might want to read up and get some information to hopefully understand this disease more as some people have preconcieved notions and don't know what to expect. Any clarification is helpful for everyone, right? :) Here is some information on multiple sclerosis.. did you know sclerosis means scars?


This is information on COPAXONE, the Rx I will be on: http://www.copaxone.com/default.aspx


Additional resources:
  1. http://www.nationalmssociety.org

  2. http://www.webmd.com/multiple-sclerosis/guide/recognizing-multiple-sclerosis

  3. http://www.mult-sclerosis.org/ (Click "Explaining MS")

  4. http://www.rcep7.org/projects/handbook/msclerosis%20draft.pdf

  5. (New link as of 5/22): http://health.msn.com/encyclopedia/healthtopics/articlepage.aspx?cp-documentid=100066440

5/12

5/12: I had my neuroglogy appointment at 8:45 am. It is pretty much confirmed that I have relapsing-remitting MS (also called RRMS)-the most common form of MS that affects approximately 85% of newly diagnosed patients. RRMS is characterized by relapses that are usually followed by partial or complete recovery. I had about 5 vials of blood drawn this morning to do a few more test to rule out anything else (like Lupis).. but the neurologist is pretty much stating I have MS.

April 2007 - what is going on with the tingling sensation?

Hey, I just wanted to let you know I have turned into a human guinea pig, as far as going to the doctor to find out what is going on with my body.

About the early of last month, April, my right foot and leg started to have this tingling sensation. Then my left foot and leg started to do it. It was more annoying than anything, and not to mention abnormal. I don't know exactly how to describe the feeling, maybe when you are outside on a FREEZING day and go into a warm room and your legs are warming up and there is the tingling/numb sensation? I guess that is as close as I can get with describing it. Anyway, this feeling stayed around 24/7 for a week so I found a dr (Laura Martin) and made an appointment for 4/17 to explain the issue.

So, 4/17: I meet Dr. Martin and explained what has been going on. She, of course, askes a lot of questions and explains that she would like to run some tests.. so, I had my blood drawn. Believe it or not, I haven't ever had this done. Needles and Danielle are like oil and water-they just do not mix. I have to say, I did fine, especially since I went alone to the appointment knowing I would probably have to have blood drawn. The lab results on the blood were normal. Oh, I almost forgot.. that same day I also had back & spine x-rays. Those results also came back normal.

Moving along to 4/20: I went back for CT scans on my brain and spine. That machine was pretty neat. I asked the tech if he had ever seen Stargate with the time traveler thing.. he hadn't but that was what it reminded me of, except for the fact that I was laying down instead of walking through the ring like they did on Stargate. Anyway.. Dr. Martin called me to say there was a 'shadow' on my brain CT, and that they would like to do an MRI. I guess that means more testing?!

4/30: Had the brain and C-Spine MRI. That machine wasn't as cool as the CT scanner.. and much noiser.

Test results

So, my blood work says I am healthy (no thyroid problems, diabetes/blood sugar, animea, infection, kidney or liver problems), the x-rays/CTs show I don't have any herniated disks or anything out of alignment, EMG showed my lower extremities don't have any issues... so, other than the brain issue, I guess you could say I am healthy :)

MS isn't all that easy to diagnose, hence all of the thorough testing to rule stuff out.. and then I have only had one on-set (or a symptom) and usually you need two.

Everyone is glad that I just didn't say 'oh it will go away' and not go to the doctor when I started to get those tingling feelings in my legs and feet. I always say if you notice something just isn't right about your health and it lingers, go to the doctor. That is what they are there for. Why wait for something to get worse, right?!

May 5 & 8

~~~ Where do I begin?! ~~~ 5/5: I went back in to meet with my Primary Care Provider (PCP), Dr. Laura Martin so she could discuss all the test results (blood, x-rays, CTs). When she got to the MRI results she explained that 'this' is not confirmed, but the findings on the MRI are most likely related to demyelenation and multiple sclerosis. *gulp* She proceeded to explain that she would like to refer me to a neurologist for further testing.

During the visit, I told her that my legs were not tingling nearly as much that morning or the previous day. She still wrote me a 10 day Rx for oral steroids (Prednisone). Let me just say, these pills taste disgusting, but they did what she hoped they would... I no longer have tingling in my legs or feet. I wonder what would have happened if I would have waited one more day, would the tingling have gone away on its own? Then again, I just followed dr's orders.

5/8: I had my appointment with the Pain Management doctor, Dr. Shaeffer, who adminisered the EMG/nerve conduction study to rule out any problems I may have with my lower extremities/nerves. This involved two tests: 1) little electrical shock stimulation's to see how far the impulse goes and where it stops, and 2) acupuncture needles in leg muscles. You know how much I LOVE needles :) Neither of the two tests were as bad as I thought they were going to be, so that was good. I did notice the left leg was more sensitive to the acupuncture needles than the right, but all in all it went alright.

The results for the EMG was fine, just another thing to rule out a possibility or what ever.. if you can follow that :) Maybe this whole issue is some sick thought to try and get me over this needle phobia I have.. yeah, I don't think that is it either :)