Dear Dr. Dake...please can you take Melissa's stents out?

A forum to discuss Chronic Cerebrospinal Venous Insufficiency and its relationship to Multiple Sclerosis.

Dear Dr. Dake...please can you take Melissa's stents out?

Postby Jamie » Mon Jul 20, 2009 6:18 am

She's got far too much energy and I haven't got it in me to keep up with her.

Friday, Saturday, Sunday I went to bed first and was up second!

It's amazing how much you get used to the other person (the MS'er) becoming almost like a ghost in the house.

Mel was usually either at work or asleep with a few hour bursts of life every now and then, that pretty much left me and the dog to our own devices.

Now, of course I am joking and I am so very happy to see Mel like this but jesus woman, slow down!

I can't speak for everyone and Melissa was more skeptical than most (she did this essentially on trust that I'd understood it properly) but folks, this is a game changer.

She's tried most treatments and none gave her this almost instant response.

Additionally her prescription is definitely wrong, I'll confirm later but it seems that her eyesight and hearing have improved in just two weeks.

I've been holding off being too ebullient but f**k it, I'm too happy to keep it inside any more!

Viva CCVSI.
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Postby chrishasms » Mon Jul 20, 2009 6:23 am

123
Last edited by chrishasms on Sun Dec 06, 2009 11:06 am, edited 1 time in total.
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Postby cheerleader » Mon Jul 20, 2009 6:26 am

:lol: :lol: :lol: :lol:


You're really a card, Jamie (you have to be dealt with...)

I feel your pain. We had THREE social engagements this weekend...friends over two nights, out to friends house the third. Late nights, laughter, conversation. We haven't seen our gang in years...and they are thrilled to witness the change in Jeff. I'm exhausted this morning, still in my robe. Jeff jumped out of bed and just took our son to summer school. I have my partner again, and it feels like a miracle.

give Mel a hug for me, and take a nap Jamie. You'll need it-
Joan
Husband dx RRMS 3/07
dx dual jugular vein stenosis (CCSVI) 4/09
http://ccsviinms.blogspot.com
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Postby Jamie » Mon Jul 20, 2009 6:39 am

:)

Thought that'd wake you all up!

Apparently I'm on a diet now and we're going to use the treadmill......

:(
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Postby peekaboo » Mon Jul 20, 2009 6:40 am

WHOA!!! This is great news Jamie & Mel I got the tune Rawhide in my brain...rollin rollin rollin keep those doggies going RAWHIDE! I'm not quite sure if thats the exact way it goes but its the way its goin inside my head :roll:
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Postby Loobie » Mon Jul 20, 2009 7:46 am

As I sit in neck pain......I'M LOVING READING THIS
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Postby mrhodes40 » Mon Jul 20, 2009 9:52 am

:D :D :D :D WOW!! what a great update....
I'm not offering medical advice, I am just a patient too! Talk to your doctor about what is best for you...
http://www.thisisms.com/ftopic-7318-0.html This is my regimen thread
http://www.ccsvibook.com Read my book published by McFarland Health topics
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