This Is MS Multiple Sclerosis Community: Knowledge & Support

1. If an MS patient has a very high degree of disability (EDDS is well above 8 ) do you think it could be possible to only have an IJV with 50% narrowing in the proximal third (compression by the Bulbus Caroticus)?
This 50% narrowing was said not to be severe enough to treat with angioplastic. Does that mean this MS patient can forget about ever being 'liberated'?

It is not your field of expertise maybe but can you think of a reason how and why an MS patient could benefit from stemcell therapy after angioplastic for CCSVI?

. Can many MS laesies in/at/on the brainstem (sorry, I'm not a native speaker Embarassed ) cause a higher risk during and/or after angioplastic?

The first nero specialty was for spinal issues checking for pinched nerve. He saw something in the MRI w/contrast and did not know what it was exactly. He said it could be a blockage of blood flow to the spine, but was not MS. Could the azygos blockage show up on the upper back MRI?

When I was getting the ultrasound, the tech was looking on the right side and she had been rubbing the carotid artery and had made me very sleepy and I was nearly out. That same sudden drowsy feeling happens to me all the time. I can be awake and doing things and then I feel as if someone has slipped me something and I feel extremely drowsy. If I'm home, I will pass out for a couple of hours, sometimes fight the entire day to stay awake. If I'm not, I fight to stay awake until I am home.

My question, can this be explained by the blockages they are finding with CCSVI?

Dear Dr Sclafani,

Two weeks ago, I had angioplasty by Dr Thomson in Melbourne, who like yourself, is a skilled, relaxed and caring IR. He ballooned at 5 points including within a stent at the valve of the IRJV, which had been placed by Drs Ludyga and Simka in Poland, in November 09. The other points of ballooning were within both jugulars and the azygos.

For a week after the Thomson treatment there were noticeable changes similar to those experienced by many others - energy, better balance, less spasticity etc. Some of the changes have subsided and I sense this might mean that the veins have collapsed and I require a few more stents or something more permanent to keep them open.

However the most extraordinary outcome from the Thomson treatment related to my legs. For as long as I can remember I have had fat, puffy, tree trunk legs and ankles which I assumed was a deformity but worsened by 'MS'. Two days after treatment - no more tree trunk legs! Instead, shapely, normal, athletic legs that if you squinted a bit, might rival those of Michael Johnson. My wife could not believe her eyes - she clearly did not marry me for how I looked in shorts! I was walking around all day with my Jobst knee-high stockings falling down, around my ankles. The absence of edema, without a tight and constrained feeling to my legs and ankles, also made it easier to move.

Questions - have you seen similar 'leg' results in others and/or does this make 'medical sense' to you?

Inbox :: Message
From: hopeful2
To: drsclafani
Posted: Sun Apr 18, 2010 2:22 pm
Subject: Zip Code Wrong? Quote message
Dr. Sclafani:

The zip code you gave for letters of support (SUNY IRB, c/o ... Kings County Hospital...Brooklyn, NY) was 11215. But I thought 11203 was the zip code. (I sent the letter, with changes, to 11215.)

You may not want letters of support after all, and I won't tell a soul---but I thought I'd tell you in case this was an unintentional mistake.

Take care,

rubbing on the carotid artery reduces pulse rate by a feedback mechanism in the autonomic nervous system. . Given that MSers have abnormal autonomics, it is possible that one would not adapt to pressing too hard on the carotid. Thus the sleepiness.

just my educated guess
I do not think that pressing on the vein would cause any immeidiate effect.

Patients with nerve conduction problems like MS can have any of their nerves affected by the MS. Thus the nerves that are a component of cardiac conductivity can be affected by MS

it would be irresponsible for me to respond to this question

dear greek
your fete of feta cheese may leave you with a fetid aroma

but George.....people take this stuff seriously

so lets be clear: the Greek is one of my patients and his rye humor has not been affected by his MS

you sound like one hot tamale.

i do not think that vasodilation is going to help you one bit. But i am not a dietician, just a purveyor of ccsvi, trying to put things into the context of the zamboni concepts.

I did a search of chili and cerebral blood flow and only came up with a bunch of stuff on cerebral blood flow in llamas studied in Chile

sorry i cannot be of more help.

but i say, eat what you love

If I had what you described, i would probably also make a decision to take the risk for you sound like your options are very limited. Short term restsenosis means either that the angioplsty did not adequately treat your problem, or your problem cannot be adequately treated by angioplasty. Your conclusion that restenosis make migration less likely is possible, but migration will really depend upon how much it dilates after stenting, exactly where the stenosis is, how long the stenosis is, and a host of other issues.

While i do not want to have a migration in one of my patients, i do not think that is my greatest worry. it is more what to do if the stent clots off. will it be possible to re-established flow through the clotted stent. But for you that is a bride or stent that you havent arrived at yet.

I would love to see a picture of you pre and post procedure venograms.

Okay, so to clarify, when I have the extreme drowsiness, at the times when I'm just living life and not getting ultrasound, do you mean that this might actually be the MS and not something to do with my veins? I do suffer severe fatigue as well as sleep issues. Mainly actually falling to sleep, Sleep specialist told me that MS has affected my "sleep trigger". Doesn't matter how tired I am at times, I will have no ability to sleep. But when I am finally sleeping, I can sleep 10-12 hours on average. So, MS has a sense of humor getting me too tired and leaving me with no ability to sleep and making me severely drowsy as if I've been drugged, just all depends on the moment...