2+ Month CCSVI Post Op Up Date: Ginger MacQueen

[AWDESIGNS8]

how long have you had ms before you got this done and when you take a mri do you have any lesions ccsvi is just taking the symptoms away not the lesions in your brain or spine is that correct i'm all for ccsvi when you can get rid of the lesions then we can say ccsvi is a cure i want that to happen

[marklross2]

Wow! I hope the improvements will keep coming! I am on the list at the Hubbard Foundation in San Diego (hubbardfoundationDOTorg) for evaluation and treatment if I am a candidate. I hope to join the ranks of the liberated soon!

[npiltan]

good for you thats what I call new hope

for how long you have ms?

[npiltan]

good for you thats what I call new hope

[jimmybryght]

Can I have some MILF and cookies?

[derekdadey1]

Call CCSVI Clinic; (404)461-9560 to schedule your screening today in Fargo, ND or email us at apply@ccsviclinic.ca. Yes, get screened within the US. No waiting….find out more at ccsviclinic.ca

[MillionsStrong4MS]

Keep up the great work!!

[ginnwild]

You give me great inspiration! I am going for my procedure this Thursday and really looking forward. I am hugely indebted to you for your active voice and informative memos. Keep up the good work!

GinnWild

[gingermacqueen]

@ginnwild Welcome to the dark side!!!!

[npiltan]

good for you wish you luck wish me luck

[dely1112]

Love hearing your good news, hope the weakness improves while you strengthen your body!! YEA on not having permanent damage, how exciting!!! I will LOVE to lose this foot drop! Hugz!!

[boazingy]

Danged technology! I am lost. I can't see how to comment without doing a reply.

Ms. McQueen,

Thanks for the update, As you were making this vid, I was in the hospital in Katowice, having the procedure. I often think of you on your bike, and was hoping to be riding my own this summer, but alas... My 3.5 year old asked me the other day why I have flat tires, and never ride my bike. Sigh.

I'm back to Katowice in October for round two.

You do look great!

[amarcelous]

How bad off were you befefore you hAD YOUR SURGERY

[msclinicaltrialsinfo]

Good news! You go girl! Keep us posted!

[62blanco]

Ginger, Thanks for yr latest post!! Am glad u continue on the road to health/optimisim! Looks beautiful on u!

[lavmac56]

You look absolutely amazing! 

[ericet19]

I'm so happy to see how this is turning out for you and for all MS affected people who one day soon I hope will get liberated like you. Thank you for doing this and for giving everyone hope that things can get better.

[watzgoodinthe711]

what stage of MS are you in? i'm glad to see your getting better... good luck

[gphx]

You overcame so many difficult obstacles to get your ccsvi done which is truly impressive. So nice to see the smiles.

[irishbear76]

Thank you for the update.

Sounds like the Liberation Procedure kept you from getting pretty bad real fast.

I just wish everyone could get it right NOW.

I appreciate your efforts in spreading awareness.

Take good care,

Mark

[SHIRLEYRENSHAW]

BRAVO!!! Looking goooood!! :) I do not believe that the MSSs and others working together will ever happen!  This has become a turf war and why would the MSSs ever admit they were wrong!!! It would be so great if I was wrong on my gut feelings and if I am wrong I will eat these words gladly!!!!!!

[brp4wheels]

You look wonderful! Thank u 4 being so vocal 4 all of us.

[Vivianne766]

Huh ! Providing you guys and the CCSVI movement with a "table" and "chairs" is probably the biggest thing MS society has done so far. :(

Hey Ginger, you look great.

Hope you'll get even healthier everyday and stay happy. :)

[elysegail]

YOU LOOK MAR

VELOUS. TELL ME ABOUT THE KALE SMOOTHIES. EMAIL ME ON FACEBOOK. THANKS GINGER, KEEP UP THE INCREDIBLE WORK YOU DO FOR YOU AND ALL OF US!!

[milorad173]

Ginger, you are great!! I sill wait......

[9gabbycats]

OMG! You look freaking GREAT! I'm so happy for you Ginger! When I saw my therapist yesterday and had the testing she too told me that she isn't seeing neruological damage so much as she is now seeing fatigue weak muscles. Where as before she thought she was seeing neurologically damaged muscles, but apparently that's not what was going on! Such good news for us! Lots of love and prayers for your continued health and well being! Thank you for being my lead!

[MSVlogSupport]

First I am just going to say what everyone else has said, Girl friend you look HOT HOT HOT!! So glad that you are able to do so much in such a short period of time. I am so hoping that here in the states I will be able to get liberated ast well

Hugs,

Andrea

[CTYankeeMS]

Wonderful to hear your great progress!  Keep up the fight.

[tmcgreg1]

Great job! Such an inspiration. I will keep you close when I get to Sofia in July. Meantime I have heard a lot about your kale smoothie..... where can I get the recipe? I would appreciate it very much if you could send the recipe or direct me to where I can find it.

[rickileeway]

You're looking radiant Ginger. I'm so happy for you.

Rick

[smokeybearsmum]

cool i have rrms but it hit me really hard i am currently in a wheel chair my edss 7.0 i have ive had it since 2006 and ive been in a chair since a yr ago so im curious to what im gonna feel...but like i said itll be a bonus hey its rave u have me on facebook..... but ya im glad to hear yer getting better and better everyday ...... and boy yer looking good!!!!

[kezzcass]

Yeah that is weird about your right side. I do still get that too when I overdo exercise. But I guess it takes a while to rebuild when it has been a 'lazy' side for so long. You look fantastic. That is awesome about the MSS - so hope that continues in a positive direction. Kerri

[curmudgeonine]

Great news about you, and encouraging news about the MSS. Thanks, Ginger - you're looking GREAT!

[mamadawnna]

So glad to hear you continue to do well Ginger! I think it show's you are gracious to take the olive branch extended by the MSS I'm not sure I could.

[angelusa73]

Thank you so much for the update, Ginger!!!! You look great and you told us that you feel great and this is wonderful news!

You got so many things done and I am sure that many more will come!

Take good care and good luck with the exercise!

Hugs,

Angela

[falsecreekcare]

You look wonderful! Thank you so much for keeping us updated.

[thepasture]

you look great\! What was that about Alberta getting the ccsvi therapy approved?

[gingermacqueen]

@thepasture . if you go to my latest blog you can read all the info and details there .iamsickofms.blogspot.com

[ChaozFear]

You made it to

ccsvi-stories.blogspot.com

Congrats! :D

[omexmc80]

wow, u look great! :)

[smokeybearsmum]

what kind of ms do u have?? im going in ten days to get liberated getting me really excitied to have the liberation treatment u seem to have great results...

[gingermacqueen]

@smokeybearsmum Hey! I was DX'd with RRMS although since 2007 until 2009 I was certain I was moving into SPMS as I was constantly sick. NO REMISSIONS. Sick 100% of the time 24/7 and getting new symptoms to boot! If you saw my CBC/thenational documentary on TV you could see that the reflux on my left side was SO BAD and I think I was really heading for a BIG HEALTH CRASH had I not got liberated when I did. Good luck to you!! Dont have too high expectations, though. :D