Comments for Don't Let Gerry Drag His Feet http://gerrypeters.com/hope Gerry Peters - MS - CCSVI - Life - Hope Fri, 06 Jan 2012 04:23:32 +0000 hourly 1 http://wordpress.org/?v=3.3.2 Comment on Interesting study on MS by Lovella http://gerrypeters.com/hope/?p=528&cpage=1#comment-1377 Lovella Fri, 06 Jan 2012 04:23:32 +0000 http://gerrypeters.com/hope/?p=528#comment-1377 Gerry, I couldn't get into the website to read the article. It requires a log in. Gerry, I couldn’t get into the website to read the article. It requires a log in.

]]> Comment on CCSVI Bill will take place in House of Commons by Loreena Weideman Buhl http://gerrypeters.com/hope/?p=525&cpage=1#comment-1200 Loreena Weideman Buhl Tue, 06 Dec 2011 04:27:07 +0000 http://gerrypeters.com/hope/?p=525#comment-1200 Hello, My name is Loreena Weideman Buhl and I am currently doing online research for a Canadian TV documentary "The Italian Cure" about CCSVI and I came across your wonderful blog. I absolutely love the title of your blog ;) Would you be willing to let Zoot Pictures/Emma Pictures use your blog and videos? This is the blurb from "The Italian Cure": The Italian Cure is a one hour documentary that delves into the science, controversy and drama around Liberation therapy, produced by Zoot Pictures Inc. in association with the Canadian Broadcasting Corporation to be broadcast on The Nature of Things in 2012. Please take the time to verify the truth of this email at the following website, www.zootpictures.com/?s=inproduction. I can be reached through my YouTube page or my personal email address - loreenawb@gmail.com. Thank you for taking the time to read this message and for your help. Loreena Hello,

My name is Loreena Weideman Buhl and I am currently doing online research for a Canadian TV documentary “The Italian Cure” about CCSVI and I came across your wonderful blog. I absolutely love the title of your blog ;)

Would you be willing to let Zoot Pictures/Emma Pictures use your blog and videos?

This is the blurb from “The Italian Cure”: The Italian Cure is a one hour documentary that delves into the science, controversy and drama around Liberation therapy, produced by Zoot Pictures Inc. in association with the Canadian Broadcasting Corporation to be broadcast on The Nature of Things in 2012.

Please take the time to verify the truth of this email at the following website, http://www.zootpictures.com/?s=inproduction.

I can be reached through my YouTube page or my personal email address – loreenawb@gmail.com.

Thank you for taking the time to read this message and for your help.

Loreena

]]> Comment on CCSVI Information by Robert Minshall http://gerrypeters.com/hope/?page_id=419&cpage=1#comment-1136 Robert Minshall Sat, 24 Sep 2011 00:48:07 +0000 http://gerrypeters.com/hope/?page_id=419#comment-1136 Just received an e-mail from Newport Beach and they are including 4 nights at the Hyatt plus some food. Man I love competition. Just received an e-mail from Newport Beach and they are including 4 nights at the Hyatt plus some food. Man I love competition.

]]> Comment on On February 8th it will be 6 months sinc… by Brian Marson http://gerrypeters.com/hope/?p=472&cpage=1#comment-708 Brian Marson Wed, 09 Mar 2011 01:05:12 +0000 http://gerrypeters.com/hope/?p=472#comment-708 Its great to hear you continue you do so well Gerry! Thanks for keeping us all so well informed and for inspiring so many others- Brian Its great to hear you continue you do so well Gerry! Thanks for keeping us all so well informed and for inspiring so many others- Brian

]]> Comment on On February 8th it will be 6 months sinc… by Mayda http://gerrypeters.com/hope/?p=472&cpage=1#comment-707 Mayda Tue, 08 Mar 2011 23:23:52 +0000 http://gerrypeters.com/hope/?p=472#comment-707 i'll be going to Cabo in a few weeks. I presently live in central Mexico. walking a thin line of hope and skepticism. i also have secondary progressive MS. on permanent disability since July 2006. diagnosed with Relapse Remitting in 1996. i'm so glad you found such good results. i’ll be going to Cabo in a few weeks. I presently live in central Mexico. walking a thin line of hope and skepticism. i also have secondary progressive MS. on permanent disability since July 2006. diagnosed with Relapse Remitting in 1996. i’m so glad you found such good results.

]]> Comment on If you have had the CCSVI Procedure, I w… by Betty Henehan http://gerrypeters.com/hope/?p=464&cpage=1#comment-569 Betty Henehan Fri, 17 Dec 2010 03:03:18 +0000 http://gerrypeters.com/hope/?p=464#comment-569 I had it done 1 month ago at Pacific Interventional. I haven't seen much change. I had an ultrasound yesterday here in Upstate NY and left jugular is still closed. Right jugular is better. I had it done 1 month ago at Pacific Interventional. I haven’t seen much change. I had an ultrasound yesterday here in Upstate NY and left jugular is still closed. Right jugular is better.

]]> Comment on CCSVI Information by Joy-Lynn http://gerrypeters.com/hope/?page_id=419&cpage=1#comment-521 Joy-Lynn Tue, 07 Dec 2010 20:11:47 +0000 http://gerrypeters.com/hope/?page_id=419#comment-521 Hi Gerry! Thank you again for all the information you gave me for my mom. She is currently in Mexico. They arrived yesterday. She is having her treatment today! I am so excited to hear how she is doing. I just thought you might be interested to know what the cost is now with accommodation and everything except food. Its now$11,525. The hospital sets up all the details for the accommodations at the Marina Fiesta Resort. If you google search it you can find some really amazing pictures and info on the resort. Anyway- Thank you again and God Bless! Joy-Lynn ==================================== thank you Joy-Lynn. We would love to know how your mom is doing. Could you let us know? Gerry Hi Gerry!

Thank you again for all the information you gave me for my mom. She is currently in Mexico. They arrived yesterday. She is having her treatment today! I am so excited to hear how she is doing. I just thought you might be interested to know what the cost is now with accommodation and everything except food. Its now$11,525. The hospital sets up all the details for the accommodations at the Marina Fiesta Resort. If you google search it you can find some really amazing pictures and info on the resort.

Anyway- Thank you again and God Bless!

Joy-Lynn

====================================

thank you Joy-Lynn. We would love to know how your mom is doing. Could you let us know?

Gerry

]]> Comment on My Story of MS and the CCSVI Treatment by Gerry Peters http://gerrypeters.com/hope/?p=186&cpage=1#comment-510 Gerry Peters Fri, 03 Dec 2010 18:34:48 +0000 http://gerrypeters.com/hope/?p=186#comment-510 thanks for sharing Jessica. Sorry for the loss of your brother. It's a good reminder for MS sufferers to research well before going to just any clinic that is providing this procedure. thanks for sharing Jessica. Sorry for the loss of your brother. It’s a good reminder for MS sufferers to research well before going to just any clinic that is providing this procedure.

]]> Comment on My Story of MS and the CCSVI Treatment by jessica forester http://gerrypeters.com/hope/?p=186&cpage=1#comment-508 jessica forester Thu, 02 Dec 2010 22:28:00 +0000 http://gerrypeters.com/hope/?p=186#comment-508 The CCSVI Liberation Treatment could be the cure but fact remains that the rate of re-occlusion is stuck at 50% and MS patients being treated in the European and Asian countries end up suffering as they did, 3 months ago. While Big Pharmaceutical Corporations and governments in the US and Canada are coming up with new ideas to stop any advancements to the CCSVI theory (Like the superbugs, etc.), millions continue to travel to countries like India and Poland to get this simple procedure and no valuable data is recorded to support the CCSVI theory. Unless we get our position strong enough to support the CCSVI Theory, we will never be able to beat the Pharma Corporations or start the treatment here and many will keep suffering and dying even after having the procedure done. I lost my elder brother last month because of a blood clot in his stent. He got liberated 5 months ago in Poland. We need to prove to the government that this works. Non-profit organizations like the CCSVI Clinic http://www.ccsviclinic.ca/ are tirelessly working to develop safer protocols with teams of world renowned surgeons even though they are feeling the negative pressure from you know who. This Atlanta based Organization has started Clinical Trials for CCSVI and we need to support these groups because they are our only hope to fight for the truth. Without the valuable data that they are collecting offshore, the procedures will not be allowed here, in our own countries. The CCSVI Liberation Treatment could be the cure but fact remains that the rate of re-occlusion is stuck at 50% and MS patients being treated in the European and Asian countries end up suffering as they did, 3 months ago. While Big Pharmaceutical Corporations and governments in the US and Canada are coming up with new ideas to stop any advancements to the CCSVI theory (Like the superbugs, etc.), millions continue to travel to countries like India and Poland to get this simple procedure and no valuable data is recorded to support the CCSVI theory. Unless we get our position strong enough to support the CCSVI Theory, we will never be able to beat the Pharma Corporations or start the treatment here and many will keep suffering and dying even after having the procedure done. I lost my elder brother last month because of a blood clot in his stent. He got liberated 5 months ago in Poland. We need to prove to the government that this works. Non-profit organizations like the CCSVI Clinic http://www.ccsviclinic.ca/ are tirelessly working to develop safer protocols with teams of world renowned surgeons even though they are feeling the negative pressure from you know who. This Atlanta based Organization has started Clinical Trials for CCSVI and we need to support these groups because they are our only hope to fight for the truth. Without the valuable data that they are collecting offshore, the procedures will not be allowed here, in our own countries.

]]> Comment on For those wanting to see my pre-treatmen… by Penny http://gerrypeters.com/hope/?p=447&cpage=1#comment-480 Penny Mon, 15 Nov 2010 00:33:53 +0000 http://gerrypeters.com/hope/?p=447#comment-480 Congratulations, Gerry! It's so imspiring to see the wonderful transformations. You give hope (to someone who's also had it for "30 years") that it's not too late! Thanks for sharing! Congratulations, Gerry! It’s so imspiring to see the wonderful transformations. You give hope (to someone who’s also had it for “30 years”) that it’s not too late! Thanks for sharing!

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