I was liberated 2 weeks ago and it's amazing to get big parts of my life back! I started learning about CCSVI from you and I thank you! My 3rd birthday is March 4th!
have not heard from you in a while. hope you are doing great. I'm 42 and have had MS since '02. going for liberation in LA next month. just wanted your advice and updates. take good care brother- you have given me a lot of hope for the past year
Hi! just wanted to let you know spoke with a nurse for my nuero and she knows about CCSVI and informed me I should talk with the neurologist re such. From what I gathered he has not brought the procedure up as he believes there has not been enough research re procedure. I am confused, do you think it is just a smokescreen? Next month I will see him and you can bet I have questions.
I was diagnosed with MS back in 1983.Recently I came across ccsviclinic.ca. They are screening in Fargo, ND. Called (404)461-9560 and spoke to Nurse Lisa. Their Liberation Package includes pre-op video consultation with their doctors, flight costs, visas, accommodation within their hospital premises. The treatment includes stent, medications, reports & post-op followup for next 6 mths. Email:apply@ccsviclinic.ca. Getting liberated mid-November. Thankful to CCSVI Clinic for making this happen!
@Irishbear76 I showed your videos to my MS wheelchair bound girlfriend. She was really touch by what you had to say. She and I are really interested in pursuing if she is a candidate for this procedure. We are in Missouri so we don't know of any physician testing and doing the procedure yet. However we are will to travel. If you can tell us what we should do 1st we'd really appreciate it. Thanks for the inspiration, hope, advocacy, and great videos. God bless ya!!
@Irishbear76 I showed your videos to my MS wheelchair bound girlfriend. She was really touch by what you had to say. She and I are really interested in pursuing if she is a candidate for this procedure. We are in Missouri so we don't know of any physician testing and doing the procedure yet. However we are will to travel. If you can tell us what we should do 1st we'd really appreciate it. Thanks for the inspiration, hope, advocacy, and great videos. God bless ya!!
Irish, I showed your videos to my MS wheelchair bound girlfriend. She was really touch by what you had to say. She and I are really interested in pursuing if she is a candidate for this procedure. We are in Missouri so we don't know of any physician testing and doing the procedure yet. However we are will to travel. If you can tell us what we should do 1st we'd really appreciate it. Thanks for the inspiration, hope, advocacy, and great videos. God bless ya!!
Irishbear you are a true inspiration... many thanks for giving hope and intelligent comment on this issue... I am in the UK and fighting to get this procedure. I am hoping to get this done soon but guess I'll have to travel overseas and pay for the procedure but hey, if I get any improvements it'll be well worth it. Beg, steal or borrow (well maybe not steal!). I am a real technophobe so dont have the facility or knowledge to post videos but just love watching the videos posted.
I have watched several of your videos and I'm so excited that you had the liberation treatment! I think I have about the same level of disability that you have. I hope that I'll be able to do it someday- have a 3rd birthday! I have a question...did you pay for this out of pocket, or did your insurance cover it?
I have watched several of your videos and I'm so excited that you had the liberation treatment! I think I have about the same level of disability that you have. I hope that I'll be able to do it someday. I have a question...did you pay for this out of pocket, or did your insurance cover it?
congratulation! I am also on the NY waiting list for 2011, but like 521cr, I would love to get this procedure performed sooner. I have haed an MRV and an interventional radiologist said I have moderate stenosis in both jugular veins. I am going to get on more lists to hopefully get the procedure sooner. My email is stephcalebcat@gmail.com thanks.
I am in Kansas. Would you give me information on how to look into scanning and treatment in Indiana? I can't find scanning and treatment in this area. I am wheelchair bound and getting to new york or cali doesn't seem plausible although I have a call in to Albany, NY.
Happy birthday! You seen very happy and full of energy. Can't wait to see all your new tricks. Faith is huge. It's so interesting, since I joined this community over a year ago (what a year!) the whole vibe here has changed, from not only love and support, but 'real' hope and striving for actual recovery. It's wonderful. I think we all see that as possible now. Thanks for the vid - Glamanda
@irishbear76 Haha! I just read this now, for some reason it went to my junkmail folder. How did you know about the 'real' secrets of my success?! ;-) CCSVI is exciting. I only wish that diet and vitamin D (for which there is mountains of evidence) gained the same enthusiasm among MSers. I'm a bit scared of the procedure (long story) and I'm getting well anyway, so happy to sit back and wait for it to become mainstream. By then I might have eaten my way to foot venous flow!
This is awesome news! Saw in the comment that you will likely go on an oral med when they come out. Have you ever looked into LDN? LDN has gone through the same issues that CCSVI is in the Company of those that make $ off of MS. I've been on it 6 years and love what it has done for all of my health.
Oral, inexpensive, minimal side effects and no risks. Nobody will make lots of money off of it, so it will not get FDA classification to treat MS. Check it out ldnscience. org, ldnaware. org
(ah, sharing the links is the issue with posting... see if this works, just know, put the org with the above sites...
Just because they do not see it doesn't mean it is not there.
The Doppler and MRV cannot find some of them. THey are hidden in valves or in the azygous that you cannot see/hear with Doppler. MRV is limited as well.
I am finding that people have been found to have them in venogram when they couldn't be found in less invasive ways.
That is my news flash. If you tell me someone has a venogram and they did not have any stenosis, my first response would be MISDIAGNOSIS
@irishbear76 You haven't done your research, over 45% of clinically definite MS patients in the Buffalo study tested negative for CCSVI, so it clearly is not the universal cause of all MS.
@OneLife1Voice I have done my research, you have half the info. Dr. Zividanov addressed this during the open forum. The numbers were so low because they were not using the right protocol. the Zamboni protocol is this. DOppler ultrasound. Venogram . (This is the gold standard). Zividanov admitted to this. The Buffalo study was seriously flawed. I will not be able to reply and get into a big discussion about this right now because I have a guest. Talk to you another day God bless. Mark
@irishbear76 Georgetown has stopped treating CCSVI. . Zamboni's study did not specify it's exact treatment protocol, i.e. balloon size, length of time of inflation, etcBefore CCSVI can be demonstrated to be true or false, there must be observations of many many MS patients and controls and pictures from venography of every person's jugular veins and azygous. Plus, there must be some kind of standard established for the procedure.
I get the impression that vascular specialists damn well decide what they are going to do and with which tool (this is an inside joke to anyone who has ever known a vascular or cardiothoracic surgeon).
Seriously though, I believe balloon size is variable to the job. My doc told me he used a 16.
I think CCSVI should be studied and researched COMPLETELY.
In regard to standards. Vascular surgeons have established standards of practice. NOt new 2 them
So extremely happy for you!!!!!!!!!!!! I have ppms and live in the area you were treated in. Can you tell me if the name of the interventional radiologist is Gerard Duprat? Will I need to get a referral from my GP? I am on a list for Albany, but would be thrilled to be able to have it done in Indiana. I won't be able to have it done in Albany until 2011. LCR
I am still doing well. I had to take my contact lenses out and put my glasses on. I have been falling asleep in my contacts, because I have been wearing them so late because I am still freaked out by my clearer vision! I literally do not want to take them out for a second.
Physically i feel great. I am going to make a follow up video on Friday for my 7 days post-procedure
A sneak preview: MS symptoms are diminishing quickly. Walking quicker, raced my wife and daughter yesterday!
@irishbear76 All I have ever found is that CCSVI is not being done in the US...or is it just subject to finding a doctor who will check to see if you have any blockage? May I ask if it was a simple process for you or was it a lengthy time process to get this help in Indiana?
@irishbear76 Mark, Thanks for the response. It sounds good to stay on the meds but I just would like to leave them in my past. Great comment, I wonder often whether my immune system or my mind will go crazy first. It just makes me wonder, are the meds really beneficial or has it been that we needed a repair all this time. I know, more money in endless drugs.
@tazscott14 It's great to hear all these good stories, fingers crossed for continued improvement. I hope that all the people who are getting the CCSVI treatment will look into LDN now. These two are compatible and if they both work well, all the better. LDN modulates your immune system, it's cheap and has no lasting side-effects. It's miles better than any toxic drug. Dr. Tom Gilhooly in Scotland who is the UK's CCSVI pioneer has been a LDN expert for years.
YEAH!!!! So awesome to see this video. And so happy to see & hear how much CCSVI has helped you. Thank you so much for posting your videos and keeping the hope ~ faith and love flowing.
Wow! This post must be the most positive, love inspired place on utube after reading some of these posts inspired by your wonderfully positive spiritual energy Mark. I am so happy to hear it was successful for you. Things can only get better. Incremental improvements. Do you have any idea of what percentage, if any, of azygous veins that have restenosed after the procedure?? That was all I had unblocked....to my surprise. Hard to find info on the net.
I do not know any statistic on which veins go back more easily to their collapsed pre-liberation state. I was shocked to find my azygous was okay! I only had a 60% block on one jug and when he ballooned that narrowing, my eyes kicked ablaze and I got a surge of "wakefulness" I had not experienced for quite a bit. I even have less anxiety after the procedure. Weird things!!!! are happening.
I love you, dear friend.
Take care of yourself and tell yourself NO STENOSIS!
thanks for spreading the message.. I think the MS Society is not doing anything enough.. Oh did you heard, they are going to give 5 million dollars to create a new drug... This shows you that the MS Society got their money in the big pharm business and they're trying their best to prove CCSVI doesnt work... I think the National MS Society is a business, not a charity..
Wonderful news, Irishbear! Keep getting the word out there - still 99.9% of MSers to get tested and treated. Glad to hear that the Fighting Irish are fighting for CCSVI acceptance.
I'm so glad this has worked out well for you Mark, they're starting to look into this most everywhere and hopefully once more and more people have this procedure it can be available worldwide.
I guess for the meanwhile I'll have to carry on with Tysabri which is working ok for me thankfully. I would like a shot at this though but unfortunately I can't afford to have it until it's made available on the health service. All the best for your recovery going forward :o)
Note* My family called me Marky until I insisted they stop at the age of 17.
2nd note* They said "screw you" and some still call me Marky
I was in the exact same boat you were in. I had not the means to get it done and then WHAM! I found out they were doing it in my area and my insurance covered it.
I got off lucky. I will fight to make sure EVERYONE GETS A SHOT!!!!!!!
I'm so glad this has worked out well for you Mark, they're starting to look into this most everywhere and hopefully once more and more people have this procedure it can be available worldwide. I guess for the meanwhile I'll have to carry on with Tysabri which is working ok for me.
:o) Really haven't stopped grinning since I heard you came through so amazingly. I agree what you say about your eye. It was my left eye I had probs with and my left jugular the worst. Yes so clear, vibrant and beautiful - I was not imagining it eh? So so so pleased for you Mark.. so upset for our friends who are struggling to get this done. And the earlier people get the venogram the better - it's just gotta happen now! Kerri
I had forgotten what you said about the colour "green" after your procedure.
I noticed everything was crisp. It was not just definition and colour but my depth perception and so many things are better with my vision.
I am going to repeat Rhomberg's sign and heel to toe later. I have a creeping suspicion it has improved. Who am I fooling? I could pass a field sobriety test now!!!!!!!!!!!
You inspired me, Kerri. My first YouTube friend to be Liberated.
Mark You were one of the first people I saw on utube talking about CCSVI and You convinced me to go for Liberation. |For this I will be eternally grateful. Thank you Mark.
Its so wonderful! I'm so happy! oh my, this is it, isn't it? I'm so excited! Thank you so much for your videos! I was on pins and needles and praying that this would do you good! I'm so glad!
Good for you Mark! Your faith in CCSVI is obvious and well-placed. I am so glad you are seeing some positive results from the procedure and I look forward to similar videos from you in the future outlining your road to recovery from MS! God bless!
So glad to see you have already had some positive changes, the clock is ticking and it's only matter of time before loads of other great changes appear, your body now has the chance to heal. Luv to you...xxxx
@irishbear76 Thank you, Mark! I will try to stay strong and keep fighting too! It is so hard to deal with the symptoms of ms...even after a 1 and 1/2 year remission! Hopefully, I will see the light at the end of the tunnel soon!
It's great to see that you have finally had your liberation that you have made possible for so many others! Thank you for all that you have done and HAPPY LIBERATION!! GOD BLESS!
"I've had double vision since my first attack".... *gasp*... tears.. me too :(. I still have double vision, and I've had it since my initial attack as well. Wow!!! To hear this makes me want to go get liberated, big time!!! I see my GP Monday, let's see what she has to say.
I wonder if liberation will resolve my burning mouth syndrome too? Wouldn't that be wonderful? *dream* :)
I'm SO SO thrilled for you! Lots of xoxoxo!!! Thanks for this video!!!
@irishbear76 LMAO about maple syrup! Hahah!! I bet that's what's been coursing through my veins all these years! No wonder I feel so sluggish every day ;).
Keep smiling and enjoy being 'liberated'! =) This is a great day!!!
@irishbear76 LOL Mark, of course I know you're kidding around :) Keep laughing and loving! I'll have a Keith's in your honor instead, how about that? I'm not a Moosehead fan :p!
Congrats Mark!! So happy to hear it all went well, which we knew it would..Jesus certainly is paving the way..Sooo happy for you and your family...God Bless...All honor and Glory is His!!
Mark! You knew everyone was waiting patiently to hear about you,. thank you for posting as soon as you could! This is awesome news, its so great to see you so happy and that excitement is contagious! Truly truly you have been among one of the huge trailblazers for CCSVI and thank you! It's so exciting to see everyone who is able to get on board and be counted. I'm hopin and praying many more of us will be there soon!
So happy for you!! I was thinking about you all day yesterday! Thank you for sharing about your experience....calms my nerves knowing Im going in just a few days from now!! make sure you rest!
BRAVO..you have been reborn!! Happy new birthday :D very very happy for you...can't wait for my turn to leave the darksider and be on the light side :D Good for you bud...
I think it will help everyone individually and I know in my heart not EVERYONE will have dramatic results, but ANYTHING we can get back is a blessing RIGHT?
Keep being LOVE and everything will fall into place.
I would love to do anything that comes to mind to bring Liberation to my MS family.
I would stand on my head and pee in my own mouth like that monkey on YouTube if that is what it takes. LOL (I change my mind. I just threw up in my mouth a little).
Yes! I am very happy for you Brother. Drink a lot of water my friend, it will help. It is an amazing gift we've been given to be helped. Looking forward to you healing and feeling even better.
Mark!! I am so happy for you! You sound great!!! I've been checking your page all day! Thank you so much for everything you've done, and I hope things get better and better for you!! MUCH LOVE! GOD BLESS!
Yay Mark! Just want you to know that we love you too!!! You have been amazing through all this CCSVI development. Thank you for your pledge to continue fighting the fight! Every one of us needs to remain committed and strong like you. :D
I am soo HAPPY 4 u and I am soo happy for US (MSers unable to access anything for CCSVI, because of various reasons - no hands on help, no money, no medical support) as the Liberati have just acquired another General!
We will change things. The more of us that have it done and show how effective it is, the harder it is for BIG PHARMA to spread lies as if they were truth.
I am happy with the results and cannot wait until ALL ARE LIBERATED!
Yaaaaaaaaaaay!! Had trouble watching this coz of the traffic - 29 views up to 86 in 10minutes - good news travels fast in the MS world! Great to hear of your improvements Mark - I'm sure with rest and time more will come your way :o) Enjoy being a member of the Liberati hun! x
I was so worried about you! so happy to hear you're feeling good! Now... as I said when I shared this... REST!! RELAX!! you've just had a procedure and our bodies don't take well to invasion sometimes. oh, my eyes are 3 rx's back :) Glad you're home!
Whoo Hooo!!!!!!!!!!!!! You look kind of hyper dude..I wonder why LOL Congrats and so happy. I hope that I get the same results on the 14th! Thank you for always being there for all of us. You are one of the reasons I really did my research!
Love you to and yes the universe does send back what you put out.
I am SO happy for you Mark.........I knew it would go well and just improve for you....You so deserve it....Your family must be so damn happy with you....You have brought all of this to us and encouraged and empowered us to make a change in our lives and in the world about this....Thank you for everything and GOD bless you friend....Great days ahead.........Happy 3rd birthday....HAPPY LIBERATION!!!!
Mark,
I was liberated 2 weeks ago and it's amazing to get big parts of my life back! I started learning about CCSVI from you and I thank you! My 3rd birthday is March 4th!
MsHopeforhealing 11 months ago
@MsHopeforhealing
I am glad to hear about regaining large parts of your old life.
This has been an adventure!
Keep informing others and you are welcome.
Blessings,
Mark
irishbear76 11 months ago
Mark,
have not heard from you in a while. hope you are doing great. I'm 42 and have had MS since '02. going for liberation in LA next month. just wanted your advice and updates. take good care brother- you have given me a lot of hope for the past year
1911prince 1 year ago
@1911prince -
Sorry for the late reply.
Life has been hectic since I moved to Colorado about 3 weeks ago.
I am assuming your liberation is forthcoming or has happened recently?
I would love to hear from you.
Take care,
Mark
irishbear76 11 months ago
Hi! just wanted to let you know spoke with a nurse for my nuero and she knows about CCSVI and informed me I should talk with the neurologist re such. From what I gathered he has not brought the procedure up as he believes there has not been enough research re procedure. I am confused, do you think it is just a smokescreen? Next month I will see him and you can bet I have questions.
Friends,
Jeanne
jeannelovesjon1 1 year ago
Well done Mark. Hope you keep getting better and better. Bravo!
lynne4cobis 1 year ago
I was diagnosed with MS back in 1983.Recently I came across ccsviclinic.ca. They are screening in Fargo, ND. Called (404)461-9560 and spoke to Nurse Lisa. Their Liberation Package includes pre-op video consultation with their doctors, flight costs, visas, accommodation within their hospital premises. The treatment includes stent, medications, reports & post-op followup for next 6 mths. Email:apply@ccsviclinic.ca. Getting liberated mid-November. Thankful to CCSVI Clinic for making this happen!
rebecawatson57 1 year ago
wow!! what is your doctors name???
noizkisses 1 year ago
wow!! what is your doctors name???
noizkisses 1 year ago
This has been flagged as spam show
@Irishbear76 I showed your videos to my MS wheelchair bound girlfriend. She was really touch by what you had to say. She and I are really interested in pursuing if she is a candidate for this procedure. We are in Missouri so we don't know of any physician testing and doing the procedure yet. However we are will to travel. If you can tell us what we should do 1st we'd really appreciate it. Thanks for the inspiration, hope, advocacy, and great videos. God bless ya!!
marvinb22 1 year ago
@Irishbear76 I showed your videos to my MS wheelchair bound girlfriend. She was really touch by what you had to say. She and I are really interested in pursuing if she is a candidate for this procedure. We are in Missouri so we don't know of any physician testing and doing the procedure yet. However we are will to travel. If you can tell us what we should do 1st we'd really appreciate it. Thanks for the inspiration, hope, advocacy, and great videos. God bless ya!!
marvinb22 1 year ago
Irish, I showed your videos to my MS wheelchair bound girlfriend. She was really touch by what you had to say. She and I are really interested in pursuing if she is a candidate for this procedure. We are in Missouri so we don't know of any physician testing and doing the procedure yet. However we are will to travel. If you can tell us what we should do 1st we'd really appreciate it. Thanks for the inspiration, hope, advocacy, and great videos. God bless ya!!
marvinb22 1 year ago
Irishbear you are a true inspiration... many thanks for giving hope and intelligent comment on this issue... I am in the UK and fighting to get this procedure. I am hoping to get this done soon but guess I'll have to travel overseas and pay for the procedure but hey, if I get any improvements it'll be well worth it. Beg, steal or borrow (well maybe not steal!). I am a real technophobe so dont have the facility or knowledge to post videos but just love watching the videos posted.
Kanny989 1 year ago
Irishbear, who is the doctor you went to in indy-I am a chicago resident and would rather not trave to mexico to be liberated.
emdmdd 1 year ago
It is now Sept how are you doing!!!?? Great to see you on this video you look like your doing excellent. God Bless
carol4nn 1 year ago
I have watched several of your videos and I'm so excited that you had the liberation treatment! I think I have about the same level of disability that you have. I hope that I'll be able to do it someday- have a 3rd birthday! I have a question...did you pay for this out of pocket, or did your insurance cover it?
mrsrhendrie 1 year ago
@mrsrhendrie
\Thank you.
Yes, insurance covered it.
I have MS but I ALSO HAD a vascular problem.
THey fixed it and remarkably my MS symptoms have DRAMATICALLY LESSENED, MOST HAVE DISAPPEARED.
The results were many times better than I could have anticipated.
Thanks for watching my videos!
Mark
irishbear76 1 year ago
I have watched several of your videos and I'm so excited that you had the liberation treatment! I think I have about the same level of disability that you have. I hope that I'll be able to do it someday. I have a question...did you pay for this out of pocket, or did your insurance cover it?
mrsrhendrie 1 year ago
hey irish! i am glad your ccsvi treatment worked out for you! i am heading to delhi, india for my treatment in 2 weeks.
god bless and i'll see you on the otherside!
kiwee33 1 year ago
@kiwee33
Good luck and God bless you.
irishbear76 1 year ago
congratulation! I am also on the NY waiting list for 2011, but like 521cr, I would love to get this procedure performed sooner. I have haed an MRV and an interventional radiologist said I have moderate stenosis in both jugular veins. I am going to get on more lists to hopefully get the procedure sooner. My email is stephcalebcat@gmail.com thanks.
stephcalebcat 1 year ago
I am in Kansas. Would you give me information on how to look into scanning and treatment in Indiana? I can't find scanning and treatment in this area. I am wheelchair bound and getting to new york or cali doesn't seem plausible although I have a call in to Albany, NY.
mzdjpb 1 year ago
Happy birthday! You seen very happy and full of energy. Can't wait to see all your new tricks. Faith is huge. It's so interesting, since I joined this community over a year ago (what a year!) the whole vibe here has changed, from not only love and support, but 'real' hope and striving for actual recovery. It's wonderful. I think we all see that as possible now. Thanks for the vid - Glamanda
missalgernon 1 year ago
@missalgernon
Glamanda of the Glamazon tribe located in the outback of Oz.
The Glamazons sustain themselves on berries, red wine, cheap sex, sleeping pills, and LF accordian music.
(Post on wikipedia?)
Seriously though, I have noticed the same thing.
A group of people who had no hope are now harbingers of such HOPE that they are now ATTACKED by the hopeless.
Epic novel in the works?
I want you to check this avenue with your lifestyle changes.
CCSVI and your healthy lifestyle=health4U
irishbear76 1 year ago
@irishbear76 Haha! I just read this now, for some reason it went to my junkmail folder. How did you know about the 'real' secrets of my success?! ;-) CCSVI is exciting. I only wish that diet and vitamin D (for which there is mountains of evidence) gained the same enthusiasm among MSers. I'm a bit scared of the procedure (long story) and I'm getting well anyway, so happy to sit back and wait for it to become mainstream. By then I might have eaten my way to foot venous flow!
missalgernon 1 year ago
@irishbear76 I meant 'good' not 'foot' of course! I really put my good/foot in it :-)
missalgernon 1 year ago
Glad youre good man !! Fantastic news. Good one !!
I will follow in time ! Have to push them along here .
Tony (",)
thaikaching 1 year ago
so much trouble trying to post a comment!!!! Great news!!!!
girlgeek333 1 year ago
This is awesome news! Saw in the comment that you will likely go on an oral med when they come out. Have you ever looked into LDN? LDN has gone through the same issues that CCSVI is in the Company of those that make $ off of MS. I've been on it 6 years and love what it has done for all of my health.
girlgeek333 1 year ago
Oral, inexpensive, minimal side effects and no risks. Nobody will make lots of money off of it, so it will not get FDA classification to treat MS. Check it out ldnscience. org, ldnaware. org
(ah, sharing the links is the issue with posting... see if this works, just know, put the org with the above sites...
girlgeek333 1 year ago
@girlgeek333
Got the LDN info.
I am definitey keeping my options open.
Thank you.
Mark
irishbear76 1 year ago
Congrats! I had the doppler scan but it came back normal.
MSconquer 1 year ago
@MSconquer
Many of them do come back normal.
Not sure why, but sometimes blockages cannot be assessed with Doppler.
irishbear76 1 year ago
@irishbear76 Well don't you think if this was the cause of MS ALL MSers would have this blockage. News flash, they don't.
OneLife1Voice 1 year ago
@OneLife1Voice
Just because they do not see it doesn't mean it is not there.
The Doppler and MRV cannot find some of them. THey are hidden in valves or in the azygous that you cannot see/hear with Doppler. MRV is limited as well.
I am finding that people have been found to have them in venogram when they couldn't be found in less invasive ways.
That is my news flash. If you tell me someone has a venogram and they did not have any stenosis, my first response would be MISDIAGNOSIS
irishbear76 1 year ago
@irishbear76 You haven't done your research, over 45% of clinically definite MS patients in the Buffalo study tested negative for CCSVI, so it clearly is not the universal cause of all MS.
OneLife1Voice 1 year ago
irishbear76 1 year ago
@irishbear76 Georgetown has stopped treating CCSVI. . Zamboni's study did not specify it's exact treatment protocol, i.e. balloon size, length of time of inflation, etcBefore CCSVI can be demonstrated to be true or false, there must be observations of many many MS patients and controls and pictures from venography of every person's jugular veins and azygous. Plus, there must be some kind of standard established for the procedure.
OneLife1Voice 1 year ago
@OneLife1Voice
I am not sure about that.
I get the impression that vascular specialists damn well decide what they are going to do and with which tool (this is an inside joke to anyone who has ever known a vascular or cardiothoracic surgeon).
Seriously though, I believe balloon size is variable to the job. My doc told me he used a 16.
I think CCSVI should be studied and researched COMPLETELY.
In regard to standards. Vascular surgeons have established standards of practice. NOt new 2 them
irishbear76 1 year ago
So extremely happy for you!!!!!!!!!!!! I have ppms and live in the area you were treated in. Can you tell me if the name of the interventional radiologist is Gerard Duprat? Will I need to get a referral from my GP? I am on a list for Albany, but would be thrilled to be able to have it done in Indiana. I won't be able to have it done in Albany until 2011. LCR
52lcr 1 year ago
@52lcr
Sent you a PM.
irishbear76 1 year ago
Can you tell me how u r doing today?
ndavidcara 1 year ago
@ndavidcara
I am still doing well. I had to take my contact lenses out and put my glasses on. I have been falling asleep in my contacts, because I have been wearing them so late because I am still freaked out by my clearer vision! I literally do not want to take them out for a second.
Physically i feel great. I am going to make a follow up video on Friday for my 7 days post-procedure
A sneak preview: MS symptoms are diminishing quickly. Walking quicker, raced my wife and daughter yesterday!
irishbear76 1 year ago
@irishbear76 All I have ever found is that CCSVI is not being done in the US...or is it just subject to finding a doctor who will check to see if you have any blockage? May I ask if it was a simple process for you or was it a lengthy time process to get this help in Indiana?
ndavidcara 1 year ago
Hi Mark,
Great news. I am glad to hear that everything went well. Congratulations on your Liberation!
Just one question- are you going to DROP THE DRUGS? What have you been told about staying on or getting off of the "MS" medications?
Take care,
Bill
tazscott14 1 year ago
@tazscott14
IF I were on meds I would stay on them;
Thanks to elevated liver enzymes, I have not been on therapy for a while.
I will probably take one of the oral meds when they come out.
You never now when you are going to re-narrow so I need to be prepared for the immune system to go crazy. I th ink of MS drugs as double protection.
Not giving you medical advice, just telling you what I will do.
Blessings,
Mark
irishbear76 1 year ago
@irishbear76 Mark, Thanks for the response. It sounds good to stay on the meds but I just would like to leave them in my past. Great comment, I wonder often whether my immune system or my mind will go crazy first. It just makes me wonder, are the meds really beneficial or has it been that we needed a repair all this time. I know, more money in endless drugs.
Take care and keep us posted,
Bill
tazscott14 1 year ago
@tazscott14 It's great to hear all these good stories, fingers crossed for continued improvement. I hope that all the people who are getting the CCSVI treatment will look into LDN now. These two are compatible and if they both work well, all the better. LDN modulates your immune system, it's cheap and has no lasting side-effects. It's miles better than any toxic drug. Dr. Tom Gilhooly in Scotland who is the UK's CCSVI pioneer has been a LDN expert for years.
Lucretia1419 1 year ago
YEAH!!!! So awesome to see this video. And so happy to see & hear how much CCSVI has helped you. Thank you so much for posting your videos and keeping the hope ~ faith and love flowing.
You are a blessing!
88whynot 1 year ago
@88whynot
Thank you.
You are a blessing as well.
I cannot tell you how many of these comments have gotten me choked up!
Love is beautiful. Life is beautiful. God is beautiful.
My vision is clear in more than one way at this moment.
blessings,
Mark
irishbear76 1 year ago
I'm happy for you, your one of the reasons why I'm getting this done, Good luck !!!!!
Eric83ism 1 year ago
@Eric83ism
You are one of the reasons I am fighting for it after having it done:)
irishbear76 1 year ago
Wow! This post must be the most positive, love inspired place on utube after reading some of these posts inspired by your wonderfully positive spiritual energy Mark. I am so happy to hear it was successful for you. Things can only get better. Incremental improvements. Do you have any idea of what percentage, if any, of azygous veins that have restenosed after the procedure?? That was all I had unblocked....to my surprise. Hard to find info on the net.
Love ya mate, Rick.
rickileeway 1 year ago
@rickileeway
Rick,
I do not know any statistic on which veins go back more easily to their collapsed pre-liberation state. I was shocked to find my azygous was okay! I only had a 60% block on one jug and when he ballooned that narrowing, my eyes kicked ablaze and I got a surge of "wakefulness" I had not experienced for quite a bit. I even have less anxiety after the procedure. Weird things!!!! are happening.
I love you, dear friend.
Take care of yourself and tell yourself NO STENOSIS!
irishbear76 1 year ago
thanks for spreading the message.. I think the MS Society is not doing anything enough.. Oh did you heard, they are going to give 5 million dollars to create a new drug... This shows you that the MS Society got their money in the big pharm business and they're trying their best to prove CCSVI doesnt work... I think the National MS Society is a business, not a charity..
watzgoodinthe711 1 year ago
@watzgoodinthe711
Money is the motivating force for BIg Pharma.
Love is my driving force.
I love people and want MS patients to have access to ANY and EVERYTHING that gives them relief.
Love kicks money's arse every time.
If you feel the MS Society is driven by anything but love, cast them away from thee :)
Methinks you have discerned this and doesn't trust them anymore?
Me too.
Mark
irishbear76 1 year ago
@watzgoodinthe711
Do not trust them anymore (I edited the sentence and did not correct the syntax)
irishbear76 1 year ago
Wonderful news, Irishbear! Keep getting the word out there - still 99.9% of MSers to get tested and treated. Glad to hear that the Fighting Irish are fighting for CCSVI acceptance.
nicknewf11 1 year ago
@nicknewf11
I will do my best to get momentum behind this worthy movement!
irishbear76 1 year ago
Congratulations, Mark this is the Lord's work. enjoy your liberation
Rick
33rojrsr 1 year ago
@33rojrsr
I have felt His presence and know that He has moved HIs Divine Hand over my life to bring hope to his children.
I will minister to his flock with MS until the day I die.
I promised.
Mark
irishbear76 1 year ago
Good on you mate!!!!!!!!!!!!!!
Get on with, & enjoy life.
This is the only thing that had made sense to me, since diagnosis.
MrMarkafisher 1 year ago
@MrMarkafisher
We are in the "Liberati" now!
I will make sure I talk about CCSVI until they listen.
You are great, mate!!!
Mark
irishbear76 1 year ago
I'm so glad this has worked out well for you Mark, they're starting to look into this most everywhere and hopefully once more and more people have this procedure it can be available worldwide.
I guess for the meanwhile I'll have to carry on with Tysabri which is working ok for me thankfully. I would like a shot at this though but unfortunately I can't afford to have it until it's made available on the health service. All the best for your recovery going forward :o)
marky147 1 year ago
@marky147
Note* My family called me Marky until I insisted they stop at the age of 17.
2nd note* They said "screw you" and some still call me Marky
I was in the exact same boat you were in. I had not the means to get it done and then WHAM! I found out they were doing it in my area and my insurance covered it.
I got off lucky. I will fight to make sure EVERYONE GETS A SHOT!!!!!!!
Mark
irishbear76 1 year ago
I'm so glad this has worked out well for you Mark, they're starting to look into this most everywhere and hopefully once more and more people have this procedure it can be available worldwide. I guess for the meanwhile I'll have to carry on with Tysabri which is working ok for me.
marky147 1 year ago
:o) Really haven't stopped grinning since I heard you came through so amazingly. I agree what you say about your eye. It was my left eye I had probs with and my left jugular the worst. Yes so clear, vibrant and beautiful - I was not imagining it eh? So so so pleased for you Mark.. so upset for our friends who are struggling to get this done. And the earlier people get the venogram the better - it's just gotta happen now! Kerri
kezzcass 1 year ago
@kezzcass
I had forgotten what you said about the colour "green" after your procedure.
I noticed everything was crisp. It was not just definition and colour but my depth perception and so many things are better with my vision.
I am going to repeat Rhomberg's sign and heel to toe later. I have a creeping suspicion it has improved. Who am I fooling? I could pass a field sobriety test now!!!!!!!!!!!
You inspired me, Kerri. My first YouTube friend to be Liberated.
I will "Kerri" the torch.
irishbear76 1 year ago
Mark You were one of the first people I saw on utube talking about CCSVI and You convinced me to go for Liberation. |For this I will be eternally grateful. Thank you Mark.
colmmc881 1 year ago
@colmmc881
It was my pleasure. I am sick of them killing off our immune system and calling it a "treatment", while we feel like crap all the time.
I have great confidence that my venoplasty put my MS on hold for a good, long time.
I will just have to follow up if symptoms return. (Positive thoughts, though)
I appreciate your gratitude, but all I ask is a favor.
Spread the word about CCSVI to all who will listen and some who will not.
Blessings and you are certainly welcome.
Mark
irishbear76 1 year ago
Congratulations, you are a great role model for all of us MS sufferers
kilkennycreamale 1 year ago
@kilkennycreamale
Thank you.
That is a very nice thing to say.
Take care,
Mark
irishbear76 1 year ago
So so so glad you're back! Best news ever. xxxxxxx
joobaable 1 year ago
@joobaable
Thanks, and I am still feeling good :)
irishbear76 1 year ago
Its so wonderful! I'm so happy! oh my, this is it, isn't it? I'm so excited! Thank you so much for your videos! I was on pins and needles and praying that this would do you good! I'm so glad!
Take care and god bless!!
MsGirlOnline 1 year ago
@MsGirlOnline
All I am 100% on at this point is vision.
I am not really allowed to put this old body to the test for another day or two.
I am curious to see how your veins look. You have had a rough year or two and I am positive YOU would see a lot of difference.
I am still going to sleep with my head up and my CPAP machine on to keep my veins open as long as possible.
Mark
irishbear76 1 year ago
Awesome! I am so close to South Bend! I hope that I can get this procedure done!
saffron491 1 year ago
@saffron491
I sent you a PM, friend.
irishbear76 1 year ago
Good for you Mark! Your faith in CCSVI is obvious and well-placed. I am so glad you are seeing some positive results from the procedure and I look forward to similar videos from you in the future outlining your road to recovery from MS! God bless!
vbeachy 1 year ago
@vbeachy
You can take that to the bank, so long as God wills it that I am here to do it :)
irishbear76 1 year ago
Energy bouncing back and forth in the universe!! That's awsome!!
Congratulations with the surgergy!!!!!!!!!!! And I love YOU! You are amazing!
Prissie28 1 year ago
@Prissie28
Love to you, Astrid.
Yup. It is like the Beatle's sang,
"And in the end the love you take is equal to the love you make."
What you put out into the universe comes back to you.
irishbear76 1 year ago
So glad to see you have already had some positive changes, the clock is ticking and it's only matter of time before loads of other great changes appear, your body now has the chance to heal. Luv to you...xxxx
MYLIFEWITHMS 1 year ago
Great, now it has to get known to the die-hard political driven neurologists.
Alexknobsob 1 year ago
@Alexknobsob
I am pretty sure that fighting Neurology may become one of the centerpiece things for me to do on this earth.
I will not let you down.
They will not stop this.
x M x
irishbear76 1 year ago
WoW!! Congratulations!! You are so inspirational!! This proves that dreams do come true!! Thank you for doing these videos!! Wishing you the best!
WithCourage2008 1 year ago
@WithCourage2008
You are welcome. I like your videos too.
You are so young, I want you to get this done, too.
I will fight for you.
Mark
irishbear76 1 year ago
@irishbear76 Thank you, Mark! I will try to stay strong and keep fighting too! It is so hard to deal with the symptoms of ms...even after a 1 and 1/2 year remission! Hopefully, I will see the light at the end of the tunnel soon!
~Anna
WithCourage2008 1 year ago
@WithCourage2008
I wish you the best, Anna! :)
irishbear76 1 year ago
It's great to see that you have finally had your liberation that you have made possible for so many others! Thank you for all that you have done and HAPPY LIBERATION!! GOD BLESS!
SNO4FUN 1 year ago
@SNO4FUN
I will not rest until this is available to all of us.
My vision is so clear (bout to start crying again).
Mark
irishbear76 1 year ago
Tour ding awesome! another radio show? GOD is with us and nothing can defeat him!
ThePennygirl 1 year ago
@ThePennygirl
You lead the way. I will do what you ask of me.
Love ya, kid!!!!
M
irishbear76 1 year ago
Congratulations Mark. I'm so pleased that your improvements are happening now. Just watch for any slippage cos it could happen. Life is wonderful!
lordluddy 1 year ago
@lordluddy
Already wondering when my veins will collapse back into their MS position.
It is congenital. My veins have been screwed up my whole life.
I NOW KNOW THIS IS THE KEY.
I will work until they figure out how to open them and keep them open.
This is only the first step in my journey.
mark
irishbear76 1 year ago
"I've had double vision since my first attack".... *gasp*... tears.. me too :(. I still have double vision, and I've had it since my initial attack as well. Wow!!! To hear this makes me want to go get liberated, big time!!! I see my GP Monday, let's see what she has to say.
I wonder if liberation will resolve my burning mouth syndrome too? Wouldn't that be wonderful? *dream* :)
I'm SO SO thrilled for you! Lots of xoxoxo!!! Thanks for this video!!!
dmplaura 1 year ago
@dmplaura
No problem.
My vision changed within 30 minutes of the procedure.
I only had a 60% blockage.. I wonder how thick my blood is!
Probably like Log Cabin Maple Syrup YO!
Good luck at the GP.
M
irishbear76 1 year ago
@irishbear76 LMAO about maple syrup! Hahah!! I bet that's what's been coursing through my veins all these years! No wonder I feel so sluggish every day ;).
Keep smiling and enjoy being 'liberated'! =) This is a great day!!!
dmplaura 1 year ago
@dmplaura
You would be more of a Maple Leaf seeing that you are from the Great White North.
Don't be a hoser, eh?
You know what I am talking ABOOT.
I am so surrey if you think I am making fun of you.
I just f**king love Canadians!!!
Especially dark moon princess Canadians.
Have a Moosehead in my honor.
Mark
irishbear76 1 year ago
@irishbear76 LOL Mark, of course I know you're kidding around :) Keep laughing and loving! I'll have a Keith's in your honor instead, how about that? I'm not a Moosehead fan :p!
dmplaura 1 year ago
@WONKAVISION2
I sure hope so.
I am happy with how I feel now. If it gets even better. I can handle that.
:)
irishbear76 1 year ago
Oops! MSlexia vision & speling:(
AzUdo2day 1 year ago
@AzUdo2day
MSlexia LOL.
irishbear76 1 year ago
Thanks for sharing your experience with us Irishbear... looking forward to hearing more from you soon:) Take care~.~
AzUdo2day 1 year ago
@AzUdo2day
U2
irishbear76 1 year ago
Thanks for sharing your experience with us Irishbear... look forward to hearing more from you soon! Tace care~.~
AzUdo2day 1 year ago
Thank you I am hoping and praying for good results!
lavmac56 1 year ago
Can't wait to hear about ur improvements.
yay . :)
so happy for u.
Vivianne766 1 year ago
Congrats Mark!! So happy to hear it all went well, which we knew it would..Jesus certainly is paving the way..Sooo happy for you and your family...God Bless...All honor and Glory is His!!
Jackie
JackieCanada64 1 year ago
Great news! I wish you continued healing.
mslawlor76 1 year ago
@mslawlor76
Thank you.
I will keep you all updated.
Mark
irishbear76 1 year ago
Nice and no plecebo Mark but we shall see long term.
qualisarx 1 year ago
@qualisarx
Yeah. I just could not believe how quickly i noticed something.
You feel like maybe you are imagining things.
You see instant improvement in a couple of areas.
Peace be with you,
Mark
irishbear76 1 year ago
Congratulations!!!!!!!!!!!
You've given me great hope for my own procedure! Just waiting for that call with a date!
auscursdad 1 year ago
@auscursdad
I sure hope you see the difference I am seeing.
Man, this is surreal.
Blessings,
Mark
irishbear76 1 year ago
Mark! You knew everyone was waiting patiently to hear about you,. thank you for posting as soon as you could! This is awesome news, its so great to see you so happy and that excitement is contagious! Truly truly you have been among one of the huge trailblazers for CCSVI and thank you! It's so exciting to see everyone who is able to get on board and be counted. I'm hopin and praying many more of us will be there soon!
God Bless ya Mark!
Eileen
bluerosegg 1 year ago
@bluerosegg
Eileen,
I will not stop until this is available everywhere for everyone.
I will keep running this big, fat mouth :)
I am feeling good and I want everyone to feel this way.
Take care,
Mark
irishbear76 1 year ago
So happy for you!! I was thinking about you all day yesterday! Thank you for sharing about your experience....calms my nerves knowing Im going in just a few days from now!! make sure you rest!
tarahvirgil 1 year ago
@tarahvirgil
You have nothing to worry about.
The doctor explained that you have just as much risk at becoming ill from the IV stick to give you the medicine as the actual procedure.
This guy knew what he was doing too. You can spot just how sharp he is after the first minute or two.
I am drinking lots of water to flush out the contrast dye and trying to rest.
I am real excited though.
I will start working out on Monday to really see what I have back.
I will keep posting.
Blessings,
M
irishbear76 1 year ago
BRAVO..you have been reborn!! Happy new birthday :D very very happy for you...can't wait for my turn to leave the darksider and be on the light side :D Good for you bud...
peace and light
Jayn
jayne4ccsvi 1 year ago
@jayne4ccsvi
I am hoping you can get this done real soon.
I think it will help everyone individually and I know in my heart not EVERYONE will have dramatic results, but ANYTHING we can get back is a blessing RIGHT?
Keep being LOVE and everything will fall into place.
Warm regards,
Mark
irishbear76 1 year ago
@irishbear76 oh so am I...thank you my friend...keep resting and heal for your family..peace love and light to you
jayne4ccsvi 1 year ago
Bravo! I am so glad you got it done! Hope no more problems for all of us that get it done, Bless you! I am scheduled in Sept.
lavmac56 1 year ago
@lavmac56
Cheers to September!
I want you to feel the way I do right now!!!
Mark
irishbear76 1 year ago
Wow Mark , Congratulations..... Have you ever thought of doing mild stand up promoing CCSVI...... you can communicate ?
boatjohn1 1 year ago
@boatjohn1
I will promote CCSVI anyway I can.
I would love to do anything that comes to mind to bring Liberation to my MS family.
I would stand on my head and pee in my own mouth like that monkey on YouTube if that is what it takes. LOL (I change my mind. I just threw up in my mouth a little).
Mark :)
irishbear76 1 year ago
congratulations!! Thanks for all your work and please do keep on going! Yes I agree, keep faith alive!!! :) Much love and light, Angelo
thepasture 1 year ago
@thepasture
Thank you, Angelo.
I will keep going until every MS patient out there is treated or at least offered treatment.
This is very clear to me.
I send you much healing love, brother.
Mark
irishbear76 1 year ago
congratulations!!
thepasture 1 year ago
awesome!! am in so happy man.. u look great and you sound great too!!
Its hard to express how happy i am in words but man im HAPPY!!
love ya bro!
Omario
omexmc80 1 year ago
@omexmc80
Love you too, Omario.
You were first brother. You pioneered the way for me.
You were in my heart the day I was liberated.
WE did it seperately but God made sure we were liberated together, in a sense.
Our kids will hear about how Uncle Mark and Uncle Omario were liberated in 2010 and that is when the REAL FUN BEGAN.
Scrape me off the ceiling dude!!!
Love ya, brother,
Mark
irishbear76 1 year ago
Congratulations, we keep fighting!
margreet0 1 year ago
@margreet0
We keep fighting until the very last of us is Liberated.
They do not know who they are messing with.
MS'ers have to fight just to get out of bed.
Ending the ignorance and misinformation is child's play compared to what we have been through.
WE keep GOING!!!!
VIva la Liberation!!!!
irishbear76 1 year ago
@margreet0
Until the very last MS'er is treated!
irishbear76 1 year ago
@irishbear76
Yeah!
margreet0 1 year ago
ps. welcome to the liberated club!
ccsvimomma 1 year ago
@ccsvimomma
It is great to be in it!!!!!!!!!!!
irishbear76 1 year ago
sooooooo Happy for you! All of us together will move this mountain. I have faith.:o)
ccsvimomma 1 year ago
@ccsvimomma
WE can do anything together as a family.
That really gets the warm and fuzzies going :)
irishbear76 1 year ago
o my goodness love love love love love love love love !!!!!!!!
mandi7and10 1 year ago
@mandi7and10
It is really great to be alive.
I knew that before though.
I guess I always had my life back, once I had hope.
Keep it alive, foster and nuture that hope.
Do not forget to LOVE, too!!!!
HOPE and LOVE
HOPE and LOVE
irishbear76 1 year ago
Comment removed
DojoDansa 1 year ago
Congrats... I loved your video.
keepingonwMS 1 year ago
@keepingonwMS
Thank you very much!!
irishbear76 1 year ago
Yes! I am very happy for you Brother. Drink a lot of water my friend, it will help. It is an amazing gift we've been given to be helped. Looking forward to you healing and feeling even better.
Stephen
msmessnv 1 year ago
@msmessnv
Gulping H2O as I read your comment.
(Twilight Zone theme song plays in the background)
irishbear76 1 year ago
Mark!! I am so happy for you! You sound great!!! I've been checking your page all day! Thank you so much for everything you've done, and I hope things get better and better for you!! MUCH LOVE! GOD BLESS!
laurenvparrott 1 year ago
@laurenvparrott
God bless and love to you LAUREN!!!!
I must say, I feel very good. I am shocked at how quickly I started to notice things.
Niles, MICHIGAN is 6 miles from Notre Dame Stadium.
Just sayin' :) :) :)
Mark
irishbear76 1 year ago
Welcome to the club my friend :) I am SO happy for you :) YAY!!!!!!!!!!!!!!!
Everything is so clear & beautiful & vibrant :) Keep healing my friend & drink LOTS of water :)
Gtlr123 1 year ago
@Gtlr123
Yes, ma'am!! :)
irishbear76 1 year ago
WA HOO
ThePennygirl 1 year ago
@ThePennygirl
OH YEAH!!!!
irishbear76 1 year ago
Comment removed
DojoDansa 1 year ago
Yay Mark! Just want you to know that we love you too!!! You have been amazing through all this CCSVI development. Thank you for your pledge to continue fighting the fight! Every one of us needs to remain committed and strong like you. :D
DojoDansa 1 year ago
@DojoDansa
Thank you, that was very nice to say.
Blessings!!
irishbear76 1 year ago
I am soo HAPPY 4 u and I am soo happy for US (MSers unable to access anything for CCSVI, because of various reasons - no hands on help, no money, no medical support) as the Liberati have just acquired another General!
brp4wheels 1 year ago
@brp4wheels
We will change things. The more of us that have it done and show how effective it is, the harder it is for BIG PHARMA to spread lies as if they were truth.
I am happy with the results and cannot wait until ALL ARE LIBERATED!
Shalom,
M.
irishbear76 1 year ago
Yaaaaaaaaaaay!! Had trouble watching this coz of the traffic - 29 views up to 86 in 10minutes - good news travels fast in the MS world! Great to hear of your improvements Mark - I'm sure with rest and time more will come your way :o) Enjoy being a member of the Liberati hun! x
jaydee1508 1 year ago
@jaydee1508
Feels good to be here :)
Thanks for coming by to see me.
I will rest and hopefully I will feel even better.
Blessings.
Mark
irishbear76 1 year ago
I was so worried about you! so happy to hear you're feeling good! Now... as I said when I shared this... REST!! RELAX!! you've just had a procedure and our bodies don't take well to invasion sometimes. oh, my eyes are 3 rx's back :) Glad you're home!
BrendaRaven1 1 year ago
Whoo Hooo!!!!!!!!!!!!! You look kind of hyper dude..I wonder why LOL Congrats and so happy. I hope that I get the same results on the 14th! Thank you for always being there for all of us. You are one of the reasons I really did my research!
Love you to and yes the universe does send back what you put out.
Andrea
MSVlogSupport 1 year ago
@MSVlogSupport
Andrea,
Thank you.
Man, I DO FEEL HYPER. I have not had this kind of energy in quite a long time.
Here is to you feeling this way too on the day after yours (the 15th)
Love ya,
Mark
irishbear76 1 year ago
I am SO happy for you Mark.........I knew it would go well and just improve for you....You so deserve it....Your family must be so damn happy with you....You have brought all of this to us and encouraged and empowered us to make a change in our lives and in the world about this....Thank you for everything and GOD bless you friend....Great days ahead.........Happy 3rd birthday....HAPPY LIBERATION!!!!
auntoni51 1 year ago
@auntoni51
Oh, sweet Ione.
You always say the nicest things!
I am glad it went well and I really want you to get it, Ione.
I think it is possible you could get such relief.
I will pray for you and keep you in my heart.
With love,
mark
irishbear76 1 year ago
Dear Mark,
I am so happy you were liberated! Your healing journey has started! :)
I wish you the very best, dear friend and I look forward to hearing about your improvements!
Good luck to you!
lots of hugs,
Angela
angelusa73 1 year ago
@angelusa73
Thank you, Angela!
I am very impressed with the "after". I look to test my balance in a few days and then every week, thereafter.
Hugs,
Mark
irishbear76 1 year ago
AWESOME news!!! Great job with the updates. I need to figure out how to get this treatment here in NC.
nobogeys72 1 year ago
@nobogeys72
Did you try 9gabbycats on YT?
She has excellent resources in finding doctors who will do it all over the US.
Give that a try and I pray everything works out for you.
Blessings and warm regards,
Mark
irishbear76 1 year ago