Tag Archives: Syringomyelia




It has begun.

The pill-popping.

This is something I have been grappling with for months and months. Taking medication every day gives me an  unsettled feeling. There are many reasons why I do not wish to become a daily pill-popper. The main reason is that I do not want to put chemicals into my body that have the potential to make my physical well-being become dependent on them. Make sense?

Baclofen. Baclofen is a muscle relaxer and anti-spasm medication. Everything I have read and learned from my pharmacist is that Baclofen has terrible withdrawal symptoms similar to Benzo withdrawal or alcohol withdrawal (neither of which I have ever experienced, but have witnessed in other people.) Additionally, I have been avoiding medication like this because I read that muscle relaxers make you feel a little hinkey in the head. My family owns multiple rehab centers so I am familiar with medication addiction. Maybe that’s why I am leary of taking anything.

So far, (so far being 36+ hours) the Baclofen has been amazing. I am tooting that horn even though I am not on board with the pill-popping train. It actually works. It has only been a couple of days and already I feel looser, barely any tension, and very few spasms in my legs and none in my shoulder blade. The Baclofen is supposed to be taken with my Gabapentin for maximum effectiveness. I tried that last night and this morning and I feel great. My head does not feel funny at all. I’m happy to report that this doesn’t seem to be a typical muscle-relaxer in that regard. My dosage is quite low at 20 mg per day. It seems that 80 mg is a high dose and somewhat typical for MS, Syringomyelia, and other spinal cord issues. I’m happy to stick with the 20 mg per day. It is working.

Yoga time.

Recent Symptoms of My M.S. & Syrinx


Generally, I try not to complain or let anyone know I am having physical discomfort. Certainly not my daughter or boyfriend. For some reason, even though they know it happens every now and then, I hate to: 1. complain, 2. appear weak to the two people who need me the most, and 3. in my humble opinion, nobody likes to be around somebody who is always moaning, grunting, and ailing. It is just human nature.

On to some interesting symptoms that I have been noting in my journal.

1. Searing pain in cervical spine running into base of skull.

The details: It feels like a hot knife has entered my neck – inside the spinal cord – and is moved in one direction up toward my skull. It is quick and burning. At the moment it happens and for a few minutes afterwards, I cannot turn my head. Maybe I have a huge fear that I will suddenly become paralyzed. Not to mention that brief searing pain makes it feel like a bubble has been injected into my neck making it almost impossible to turn my head for a few minutes. Then, as fast as the pain came on, it instantly disappears.  Once I have that two or three minutes of discomfort (I am being gentle here with my choice of words) for the first time on any given day, I know it will come and go throughout the day for many days or a couple weeks. Then BOOM! It is gone and I forget all about it until the next bout.  This “searing pain” is not to be confused with the general feeling of “sunburn” that overpowers my upper thoracic and cervical for weeks at a time. That particular “sunburn” pain is not an instant searing feeling and then suddenly gone. The sunburn feeling lasts weeks and then I usually have intense fatigue after a couple weeks.

As far as the “searing” symptom goes, I have had two opinions on it by two excellent neurologists: Neuro One is my regular guy and he said it could be a symptom of the Syrinx beginning a slow spread toward the top of the spinal cord. Or it could signify future scarring/lesions.  Neuro Two is the specialist who is a researcher out of Stanford who has a small practice in Los Angeles who mainly treats M.S. patients, but loves to research wacky diseases of the spinal cord. She thinks it is a muscular or vascular issue since my arms are getting weaker as time progresses. Possibly Syrinx related.

2. Arms have been stricken by some invisible force causing complete immobility and pain so bad it causes severe exhaustion.

The details: So far, this has only happened, to this severity, while I am asleep. Overall, my arm muscles have become much weaker and extremely tender. This is all day, every day and I have adjusted my life to taking great care of how I use my arms. However, I must share that I feel fantastic when I stretch, practice yoga, and lift free weights. Regarding this brutally painful occurrence that comes on only during my sleep, I am acutely aware of my arm pain in general and sleep with my arms straight out – picture lying in bed making a T. Or I sleep with my arms running down the sides of my body. Sometimes I need a reprieve and will gently bend them, slightly, and rest them on my tummy. If I bend them, they don’t “fall asleep” in the normal sense of pins and needles. They become almost instantaneously numb and cold. If you cut of my hand or arm, I would not feel it. (This is why Neuro Two feels it is actually a vascular issue or muscular in nature.) One night, I awoke to see the pinky finger on my left hand sticking straight up like it had been bent backwards. I couldn’t feel it, I just happened to see it. I pushed it back down to align with my other fingers. This did not hurt me until the next day when my pinky knuckles hurt. Anyway, back to this invisible force. I am awakened by a deep, DEEP pain where my elbows bend, exactly where you might have blood taken or an IV inserted. This pain is so excruciating that I am unable to lift my arms because my bicep and triceps and my forearm muscles are mush and if I try to move even a pinch, they are in such pain that it brings with it a wave of nausea. It feels like a screw has been drilled into the middle of my arm at the bend. The pain from that invisible screw is one of the worst pains I have ever experienced. Ever. I honestly cannot imagine a pain worse than that though. Now if I lay there, and be still and do not try to move my arms, the only pain is in that “screw”. If I actually try to reposition my arms, I cannot. It is as if they are paralyzed, but the muscle pain is absolutely horrid. Like a big, bad, giant is standing on my little bicep and crushing it. This is now happening more frequently. It first began about four months ago with only my left arm. Suddenly it moved to my right arm and it isn’t happening occasionally. It seems to happen more often – about once or twice a week. The more frequent the incidents, the weaker and more tender my daytime arms have become. You see, I have nighttime arms that don’t work and daytime arms that don’t bother me that much.

I just made a doctor appointment with Neuro One. Hopefully he will share some reasons why this is happening.

3. Blurry vision.

The details: My long distance vision has gotten so blurry. This happened overnight. This blurry vision will last for a few weeks and then one day I’ll wake up and my long distance vision is perfectly clear again. I have been to the eye doctor numerous times and he keeps saying I have 20/20 vision. When I try to get into the eye doctor during a bout of blurry vision, he is booked or by the time the appointment comes around my vision has gone back to normal. I eat carrots… Why is this happening??

Again, I will share this with Neruo One. I do think it is a symptom of being closer to my mid-40’s than not!!

I have some other symptoms that have plagued me lately, but nothing that worries me like the searing neck and paralyzed arms. So off to a delightful weekend!

Different Doctors – Different Opinions

DoctorThe best patient is a well-informed patient. You are your own advocate. Ask questions. Write them down before your doctor visits. Show up prepared so you will receive the best advice and the most information that will benefit you that your doctor can provide.

Doctors give varying degrees of advice when it comes to Syringomyelia. Possibly because it is not yet well-researched. Read all that you can about the disease. Talk to doctors, talk with your peers with the disease through websites and forums, and learn what you can, not only from doctors, but on your own.

Checkout some of these sites for Syringomyelia and Chiari Malformation and read through them to see what new research has been done. Find a doctor who specializes in these two diseases of the spinal cord.

American Syringomyelia and Chiari Alliance Projecthttp://www.asap.org/

Chiari & Syringomyelia Foundation: http://www.csfinfo.org/

The Chiari Care Center: http://chiaricare.com/Related-Disorders/Syringomyelia.aspx

Mayo Clinic: http://www.mayoclinic.com/health/syringomyelia/DS01127

Cleveland Clinic: http://my.clevelandclinic.org/disorders/Syringomyelia/hic_Syringomyelia.aspx

When I was told I have Syringomyelia from my cervical spine to bottom of thoracic spine, my first neurologist told me that all physical activity should be stopped. Completely. He was referring to: running, weight-lifting, hiking, kayaking, aerobic exercise (except swimming – swimming is okay), carrying anything over 5 pounds, or carrying anything on my back or shoulders such as a backpack or a heavy purse. No pilates, no dancing, no rough-housing. He had a laundry list of stuff that I should no longer do. It was recommended that I not reach above my head. Don’t tilt my neck back. Don’t roll my neck. Be gentle with my body.

Neurologist number two said to keep swimming, use the StairMaster (no running on treadmill), lift weights 5, 8, and 10 pounds, keep hiking, keep kayaking, but maybe nix the idea of whitewater rafting and sky-diving. So I won’t sky-dive. I will however go whitewater rafting. She said it will get worse regardless of activity. She did not endorse insane activity like sky-diving or running, but did say that continuing to be active would alleviate some of the top symptoms of the ailment. Being sedentary can oftentimes make people feel worse due to loss of muscle mass, weight gain, and not keeping bones healthy. She also reinforced the following:  do not reach above my head. Do not tilt my neck back. Do not roll my neck. DO be gentle with my body.

For my own case of Syringomyelia, I agree with doctor number two. I do heed warnings from both doctors to stop running. Stop doing anything jarring. No rolling of the neck. However, I will say activities such as bowling, badminton, volleyball, and stuff like that I still enjoy. I am not jumping around and jarring my body. I see where people could get a bit more active and aggressive though.

Listen to your doctors. Get second and third opinions. A lot of people I have spoken to have a small Syrinx. Maybe from T2 to T3 or T6 to T8. Mine is from Cervical all the way down to T12. I have severe Coccyx pain (coccydynia). So I actually do try to be careful with the activities in which I choose to participate. Some people I have spoken to with a small Syrinx have severe disabilities with mobility issues. Other people go their entire lives without any symptoms at all. I have yet to encounter anyone with a Syrinx as long as mine who is completely debilitated. Some people I have talked with who have a long Syrinx go through flare-ups and waves of pain and immobility, but seem to bounce back from the flare-up quickly. I have noticed the people with the longer Syrinxes are the most active. Maybe because of the thought of paralysis…? Maybe the more active people did something during some activity that cause the Syrinx to begin with..?  I have no idea.

Talk to your doctors. Get informed.

A Little Reprieve

Whew. I have missed two seasons. For the last four months, I was working on putting together a health and fitness expo. I have had only one flare-up that lasted about eight weeks. Other than the normal deep spinal cord pain and muscle weakness, I have felt fantastic.

My spinal cord hurts deep inside with a sunburn feeling from the base of my skull to my lumbar spine. That is from the syrinx. It has been a constant pain for months. Possibly because I haven’t been swimming. Or using my Stairmaster regularly. BOOOO me! It was a birthday gift and aside from swimming and lifting (light) weights, the Stairmaster is my favorite exercise. Lifting weights is supposedly a no-no with the Syringomyelia. However, it is good for M.S. and other diseases in that family. Besides, it burns fat and keeps the skeleton and muscles in excellent shape. And after a few months of working and not taking care of myself… I need to get rid of some fat. Oh-my!

Between working my show and having some days of rest here and there, I did find time to enjoy this Southern California fall and winter weather.

Kayaking off of Ventura Harbor.

Kayaking off of Ventura Harbor.

Sea Lions & Sailing

Sea Lions & Sailing

Hiking with my Sherpa on the Santa Cruz isle.

Hiking with my Sherpa on the Santa Cruz isle.

Touring the gorgeous homes in Heritage Square. Los Angeles

Touring the gorgeous homes in Heritage Square. Los Angeles

Enjoying the holiday season with family and friends.

Enjoying the holiday season with family and friends.

1,000 Lights

1,000 Lights

That just about wraps up the busy year. I hope 2013 is a great year for everyone filled with an abundant amount of good health and joy.  Get up and keep moving. Stay strong. Move that body or lose that body.

Multiple Sclerosis & Syringomyelia in My Body!

Here is the short version of my M.S. & Syrinx story. I’ll call it Part 1.

I had tingling, leg spasms, weak muscles, vertigo, and severe fatigue off and on for about 12 years or so. Probably other symptoms I can’t think of right now…OH, oh, like Costochondritis, blurry vision, creepy crawly skin, electric shock in my feet and torso, and some other stuff. I’m very active I never really followed-up with the symptoms on a serious level. I figured I had the flu every couple of months for about four to six weeks each bout.

What sent me to the doctor was this weird sunburn like feeling between my shoulder-blades that has just gotten to be completely unbearable over the last three months. I decided to go see my mother’s Alzheimer’s neurologist because he is the head of a department at a swanky hospital here in my city. (And you know, swanky must mean he is good, right? I jest 😉 ) I offer him my symptoms and straight away he said, “M.S. for sure is my thinking, but please have an MRI as a formality.” In the MRI results not only does he find M.S., he finds this Syrinx that extends from T1 down to my Lumbar area. The MS is a pain in the budinsky just by itself. The Syrinx is now completely inconvenient because it is so long and full/thick in most places, that it might actually be causing additional pain, numbness, and vertigo. And in addition to that I am told I can’t kayak, do a lot of strenuous yoga positions, or swim vigorously. What?? Holy mother of… I’ll be a fatty in no time.

A syrinx is a sack of fluid, a cyst rather, that in my case has resulted from either a trauma or meningitis or a tumor, and over the years I have continuously damaged my back to the point where the Syrinx has grown larger and longer inside the spinal cord. It will continue to grow and fill with fluid until there is no more room for it which supposedly may cause the loss of the use of my arms or legs possibly. That could require a risky surgery. Apparently doctors dissuade surgery until the patient is almost at that paralysis point. So I’m just hanging tight with M.S. and the Syrinx for now.

P.S. I am 41 years old. How long could it take to be close to immobile? Can’t they just pull some CSF from around the cord to relive some pressure? I had a lumbar puncture last week and that little amount of fluid drainage made me feel AMAZING for about one week. The sunburn feeling was gone. Now it is back.

Moving Your Body


Having Multiple Sclerosis and/or Syringomyelia, I have found for myself, it is important to keep my body moving so my muscles stay strong. Hiking is one activity I have always enjoyed and still do. These days I don’t do very strenuous hikes due to the Syringomyelia, but certainly still enjoy longer trails with a low incline. My suggestion for a fantastic day trip for a nice hike for those in Southern California is to take a  boat ride out to the Channel Islands National Park to Santa Cruz Island.The morning ride out is usually foggy, but burns off quickly.


There are many trails to explore for the day and two of them are low-impact with a very low to moderate incline. Very manageable for MS or Syringomyelia peeps. When you get to the top of most any exterior hike on Santa Cruz Island, you will be happy you made the trek.


Gabapentin (Neurontin) Side Effects

I have only been on Gabapentin for three weeks and I have gained weight. Not sure how much weight, but a lot. A little, a lot. A dress I had worn three weeks ago wouldn’t even go past my shoulders yesterday. It must be water weight because it is all in my torso.

The Gabapentin stops spastic movements in the legs and stabbing, burning spinal cord pain caused by lesions. It is also used for people with Epilepsy so it is a multi-use pharmaceutical. Like every drug in America. HA!

The side effects I have felt since taking the Gabapentin are: fuzzy brain/thinking, not feeling very alert when driving, unfocused vision, (not blurry or doubled, but more just unable to focus on the person or thing I’m supposed to look at) lack of concentration, weight gain, and exhaustion.

NOTE: I have only been on 900 mg for 3 weeks and most of those side effects have subsided, except the weight gain. Hopefully that will level out. I sleep like a log at night and it is fantastic. I will not increase my dosage even if the doctor asks me to. At least not yet. I have noticed improvement in my spastic leg and pain quite a bit and about 50% in my spinal column. Due to the long Syrinx in my cord, I really do not want to increase the Gabapentin because who knows if it is helping anything other than the spastic leg. Why take the “normal” 1900 – 2100 mg per day. Who even says that is normal?? 

Good luck with your medication options.



Vegetarian Pasta Sauce – Fight Spinal Inflammation!


I made a very delicious ** mostly ** homemade pasta sauce tonight. Eating a vegetarian, mainly vegan, diet has really helped me feel less pain and fatigue with my Multiple Sclerosis and Syringomyelia. I like to believe it helps cut down the inflammation that I feel in my spine, neck, and body. The pasta sauce I made this evening is hearty and could actually be a meal on its own, but I like to make veggie pasta noodles to go with it.

To make the sauce:

One jar of sweet red pepper & basil marinara

One bag of Morning Star Meal Starter Crumbles

Two sweet, red bell peppers

One (or two, if you like) Maui sweet onion

1/4 cup of sun-dried tomatoes

3 on-the-vine-ripened tomatoes (or two cans of petite-cut or diced tomatoes)

1 clove of fresh garlic, minced or very finely chopped

Basil & Oregano to taste – approximately 1 tablespoon of each

Chop the sun-dried tomatoes, onions, red peppers, and garlic. Mix all ingredients together and simmer for about one hour. IF you are in a hurry, simmer until hot or pasta noodles are done. Since it’s meatless, it doesn’t really matter. The longer the simmer, the better the flavor though.

I use the jar of store-bought sauce and Morning Star Meal Starter to get me going. I love the flavor of the sweet red bell pepper sauce – yummmmm. So really, you could say that I’m just enhancing store bought sauce and it’s not really homemade. But what the hay! It’s so good with the sun-dried tomatoes and the other goodies. The Meal Starter really makes the sauce hearty and filling.

Hint, Target sells a mini, electric Proctor-Silex food chopper that holds just about 12 oz. I use it to chop the sun-driend tomatoes, peppers and onions for the sauce. Makes them juicy and blend in a little better. (Also a great little mixer for homemade guacamole.)

Enjoy your sauce. Enjoy your life, with Multiple Sclerosis or Syringomyelia, with less inflammation.




Also known as Hydromyelia. Which ever you prefer… it’s no good. Sometimes it is a speckle in your spine. Sometimes the size of an eraser. Maybe larger. Mine is is a long sausage running from the T1 (top of the thoracic spin) down to my lumbar spine.

Below are two links and a little information about Syringomyelia (sear-IN-go-my-lee-ya)



The fluid buildup seen in syringomyelia may be a result of spinal cord trauma, tumors of the spinal cord, or birth defects (specifically, “chiari malformation,” in which part of the brain pushes down onto the spinal cord at the base of the skull).

The fluid-filled cavity usually begins in the neck area. It expands slowly, putting pressure on the spinal cord and slowly causing damage.


There may be no symptoms, or symptoms may include:

  • Gradual loss of muscle mass (wasting, atrophy)
  • Headache
  • Muscle function loss, loss of ability to use arms or legs
  • Numbnessor decreased sensation
    • Decreased sense of pain or temperature
    • Lessened ability to sense that the skin is being touched
    • Neck, shoulders, upper arms, trunk — in a cape-like pattern
    • Slowly, but progressively, gets worse
  • Pain down the arms, neck, or into the upper back
  • Weakness (decreased muscle strength, independent of exercise) in the arms or legs

Additional symptoms that may be associated with this disease:

Signs and tests

A neurological examination may show loss of sensation or movement caused by compression of the spinal cord.

An MRI of the spine confirms syringomyelia and determines the exact location and extent. Often, an MRI of the head will be done to look for associated conditions including hydrocephalus (water on the brain).

Rarely, an spinal CT with myelogram may be done.


The goals of treatment are to stop the spinal cord damage from getting worse and to maximize functioning. Surgery to relieve pressure in the spinal cord may be appropriate. Physical therapy may be needed to maximize muscular function.

It may be necessary to drain the fluid build up. See: Ventriculoperitoneal shunting


Eat it

Eat it