Cece's turn

A forum to discuss Chronic Cerebrospinal Venous Insufficiency and its relationship to Multiple Sclerosis.
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NZer1
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Post by NZer1 »

Cece thanks for your reply.
Has Dr.S been talking about this on his tread, I have not been following it and I must take time to catch up.
I am imagining that he is thinking full time more about the difficult and unusual cases, to get a better understanding of what treatment is going to be required.
Take your time and be well.
Nigel
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drsclafani
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Post by drsclafani »

Cece wrote:We only just got back in. We'd been out for six hours...a bit much for the day after angioplasty!
For those that do not realize, the temperature in NYC yesterday was upwards of 93 officially. My wife's car clocked the T as 97. Humidity was above 80%.

So your six hours was quite a feat my friend
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Post by munchkin »

It's great that Dr.Sclafani was able to treat the issue. Maybe this time is the keeper. It's sounds like you made it through a hot and humid day with flying colours.
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Post by Cece »

Today we stayed local, it was much easier.

Walked across Prospect Park, got pictures by a waterfall and an arch tunnel. Made it to our destination, Brooklyn Botanical Gardens. I was charmed by the Shakespeare garden. I was also charmed by the existence of children in NY. They are noticeably absent in Manhattan.

Now we are going to to eat at either Bark Hot Dogs or Stone Park Cafe. I have a sinking feeling my husband will be picking the Hot Dogs....

I am not as tired as I was yesterday or the day before or the day before that, for that matter. (The travelling day.)
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Post by Cece »

NZer1 wrote:Cece thanks for your reply.
Has Dr.S been talking about this on his tread, I have not been following it and I must take time to catch up.
I don't think he has been talking about it particularly. It wasn't anything unusual, as far as I understand, just simple restenosis of the valves. Now I wonder if the right side will close up at some point in the future? Durability....
I am imagining that he is thinking full time more about the difficult and unusual cases, to get a better understanding of what treatment is going to be required.
Take your time and be well.
Nigel
He is thinking full-time. Striving for excellence.
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Post by Cece »

We have left Brooklyn behind and are now in the Times Square hotel, ready for the symposium patient day tomorrow!
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MrSuccess
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Post by MrSuccess »

TIMS couldn't get a better person to be attending that meeting ........

I look forward to reading your take on it all , Cece.



Mr.Success
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Post by fogdweller »

Cece wrote:We have left Brooklyn behind and are now in the Times Square hotel, ready for the symposium patient day tomorrow!
Please start a separate thread dedicated to that. You probably were going to anyway. I sure will look forward to it!
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Post by Cece »

I will definitely be sharing my impression of patient day...but do we have anyone attending the two doctor days who is willing to tell us everything??
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Re: CCSVI Symposium

Post by NHE »

Cece wrote:I will definitely be sharing my impression of patient day...but do we have anyone attending the two doctor days who is willing to tell us everything??
Or better yet, record it so we can listen for ourselves.

NHE
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Post by Cece »

drsclafani wrote:Yes Cece
although you have a copy of the images, perhaps it would be good for you and your fans to review here as you suggest.

The sequence was as follows
1. prep and drape
2. time out
3. cath in left femoral under local anesthesia
4. advancement into right jugular, venogram, ivus, 18 mm angioplasty to thirteen atmospheres, repeat venogram
5. advancement into left jugular, venogram, ivus, angiopasty to 14 mm at ten Atm, repeat venogram
6. advancement into azygous vein, venogram of ascending azygous followed by zero, twenty, seventy and ninety degree views of the azygous arch
7. IVC venogram
8 ascending lumbar venogram
This is from my procedure back in February. Left jugular was originally ballooned to 14 mm at 10 atm. This time it was 10 mm as the most appropriate balloon size. He's grown more conservative. Only after it did not fully resolve, he went up to 12.
Image
There's what my left jugular looked like pre- and post-ballooning back in February. When I get home, I'll have a cd drive, so I can look at the new images from the procedure this week.

That first one looks dreadful, doesn't it!
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Post by Cece »

Once again I am leaving NY with brightened colors. The blue and red from my little cutesy icon are popping out at me. So are the red fish on my toiletries bag. (It's blue sharks, chasing red fish. Technically it belongs to my children.)

time to go....
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Donnchadh
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Post by Donnchadh »

Cece,

Has Dr. Sclafani approved your residency yet? lol :wink:

Stay well!

Donnchadh
Kitty says, "Take that, you stenosis!"

Got MS?.....Get Liberated!
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Post by CD »

Cece, have a pleasant and safe trip home. I hope all your veins stay open and flowing for good. Enjoy the colors and brightness in the eyes of your children, and husband too. Do you have those blue eyes too?
CD
Where there is a will, there is a way. "HOPE"

CCSVI Procedure December 2010
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Post by Cece »

Yes, CD, I have blue eyes, my husband has brown, and we kept waiting for a brown-eyed child to turn up but all three came out with blue eyes. It was so good to hug my kids again after getting back!

Donnchadh, alas, no...but what an opportunity it has been to learn here in his thread. :)

I looked around at the symposium and I did not see Dr. Neuro Olojist anywhere. Perhaps he is off somewhere playing with mice.
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