Dr. Rafael Moguel, the Director of the Clinic of the Heart at the Amerimed Hospitals in Los Cabos is conducting CCSVI clinical trials for MS sufferers. If interested in participating in the trial contact:
Dr. Rafael Moguel at cathboss@gmail.com
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I would be interested in participating
Thank you
D.Braun
I am 54 year old woman with secondary progressive multiple sclerosis.
I have been diagnosed since 1992,however,in hindsight I can support evidence of CCSVI
since age 12.I am very interested in being diagnosed and then receiving treatment.
Thankyou for this possibility,I hope to hear from you again.
Sincerely,Anne Mac Donald
Dear Dr. Moguel,
I would be interested in your clinical trial of CCSVI. I cannot currently get any information from the Clinics of the Heart website but would like to know what you propose. I live in Canada.
Thank you,
Jill Ballam
CCSVI
I would be very interested in your protocol, length of CCSVI clinical trial etc. I would appreciate any information you could send me. Thank you.
Jill Ballam
jballam@shaw.ca
I would like to be considered a participant for this study as would my wife, Alison Masson (eastender_ali@hotmail.com). We both suffer from MS and would love to be a part of this study.
I am very interested in taking part in this trial – can you please provide more detailed information – thank you
Dr. Rafael Moguel
I am interested in your clinical trials for CCSVI. I have been tested for CCSVI at False Creek Surgical here in Vancouver, B.C., Canada where I live. I have PPMS, am 47 years old, female. My MRV showed narrowing of cerebral internal veins. When are your trials likely to start? Thank you for your time, Blanche Norton
Dear Dr. Rafael Maguel
At the present time I am 48 yrs old. Diagnosed with RR MS quite a few years ago, still mobile and independent. The MS is progressing I feel.
I am currently on LDN (Low Dose Naltrexone) as well as sleeping pills. And I am very interested in being included in a clinical trail for this dreadful
disease.
Another Canadian crying for treatment.
Thank-you for any consideration given and would you please be kind enough to include more information on the clinical trial. Thank-you
Dr. Rafael Maguel
I am 50 yrs old and was diagnosed with PPMS in 2008. I am still mobile, though I can’t run , and very interested in your trail. I would appreciate any futher information you can supply. I am a resident of Canada and have found that the hope for treatment is not a reality within our borders. Your consideration in this matter appreciated, Thank You
I am very interested in taking part in this trial – can you please provide more detailed information – thank you
I would be very interested in participating in your clinical trial. I am a 46 year old caucasian male of northern european descent, living in Southern Alberta which has a very high incidence of MS. I was diagnosed with RRMS in January 2004 and have been on Copaxone since November 2004. I am being tested for CCSVI at False Creek Surgical Center on June 3, 2010. I would appreciate more information and your consideration in the trial.
I am a 48 yr old female from Nova Scotia, Canada. I was diagnosed with RRMS in 2006; I’ve had symptoms for over 20 yrs now. Currently on Tysabri infusions and am trying to hang on to my job and independence. I am very interested in being a participant in your clinical trail. I look forward to hearing from you.
Kindest regards, Michelle MacNeil
Dear Dr. Moguel
How many people will you be taking into this trial? I already sent an e-mail to your e-mail address cathboss@gmail.com but didn’t hear anything. Will you be posting when you have completed what you can do and also your opinion and findings involving this procedure? I too am still very interested! I am making an appointment with my doctor to get all the scans done as soon as possible.
Thank You
I am very interested in being part of your clinical trails related to CCSVI. The wonders of WWW. I have a non-biological cousin living in the Grand Junction, States. Cyn is her name and she just sent me information regarding yourselves and her upcoming Liberation Surgery. very exciting it is. I to am diagnosed with MS so I am reading and reading many blogs and all the world wide information. I’m in the Uk. Most know nothing of CCSVI here, however they do after they’ve met me. I am sharing this news everywhere. I emailed you first now to read on. What I’ve read so far looks great.
Great stuff
Tracie Renshaw
trenshaw2000@yahoo.com
I am interested in the trials. More info please~!
Sarah
I would love to be part of this study. Please me send any infomation.
Thanks Amanda.
Amanda,
As you know, the CCSVI liberation procedure pilot group that Dr. Rafael Moguel and his team of specialists will be conducting on June 15th is based on 10 MS patients that have confirmed their wish to participate and ability to travel to Los Cabos, Mexico on or before June 14th with an expected stay thru June 18. The purpose is to confirm an CCSVI correlation plus findings of vein narrowing and angioplasty feasibility. At the conclusion of this experience, we will be able to determine the average cost of the complete diagnosis and treatment procedures. We will begin scheduling new procedures the week after the completion of the pilot group as our intention is to make this treatment available to MS sufferers without long waiting times nor the expense and discomfort of travel to Europe or Asia.
As you know, the CCSVI liberation procedure pilot group that Dr. Rafael Moguel and his team of specialists will be conducting on June 15th is based on 10 MS patients that have confirmed their wish to participate and ability to travel to Los Cabos, Mexico on or before June 14th with an expected stay thru June 18. The purpose is to confirm an CCSVI correlation plus findings of vein narrowing and angioplasty feasibility. At the conclusion of this experience, we will be able to determine the average cost of the complete diagnosis and treatment procedures. We will begin scheduling new procedures the week after the completion of the pilot group as our intention is to make this treatment available to MS sufferers without long waiting times nor the expense and discomfort of travel to Europe or Asia.
I am SO HAPPY and EXCITED about getting my life back again! I would love to travel to Los Cabos and be part of this program. Please send me information.
Barb Rud
I am also very interested in this procedure. Being just newly diagnosed I would love to hear from you…this offers me hope!
Thank you so much.
So is this where the results of your study wll be posted? It is so very pertinent to us that we can hardly control our selves! Time seems to be standing still for me and I am sure many of us.I keep coming back to this site and then I realise that only 12 hours have gone by since I last looked.I am in touch with about twelve of my fellow M.S.ers from around here and I promised to keep them advised as soon as I hear the results from your trial.
Our Canadian Govt.has lost touch with their constituents God Bless you for doing this We are praying for the results to cofirm the CCSVI theory.
Reg
Can I please receive some additional information for a friend of mine. He is 53 years old and was diagnosed roughly 26 years ago.
Thank You
Oscar
Please keep me informed. This procedure sounds like the best news I’ve heard in 9 yrs(since dx). Would love to take part in this breakthrough!
Thanks,
Rhonda
California
I am extremely interested in participating in a clinical trial. I am a 53 yr old woman, diagnosed 25 years ago. I am having difficulty walking and I have trigeminal neuralgia, for me the most horrible symptom of ms. My job as Executive Director of a non-profit is demanding and bottom line, I want my life back.
Thank you
Maureen Enegren
I am 41yrs old, and I have had MS for 7yrs. I would love to participate in your testing and treating CCSVI. If the study is over I am more then willing to speak with you about making an appt. as a paying patient. I am so excited and ready to be tested. I love the glimmer of hope..
Thank you,
Tammy Copeland
Alabama
i am a 64 year old male with MS. would like more info on your clinical trials. thanks you so much.
I was diagnosed with RRMS 5 yrs ago at age 42. I am very interested in getting this procedure done. I am willing to pay if the clinical trial is over. Please let me know
We have done much research into the treatment for ms in mexico.
However we would like to get some info on the admin side.
For example
What is available for the caretaker.
How many can accompany the patient,and can they rent a room at the facility.
if caregiver cannot lift Vickey is there help provided.
what are your costs for accomodations.
Transportation that is from the airport to the hospital.
Actual cost of procedure.
is the patient sedated during the procedure.
Any info you can provide will be greatly appreciated.
We look forward to hearing from you ASAP>
With many thanks:
Sincerely Kathleen Gagnon
35 Doug Kelley
Gatineau QC.
J9H 1K9
I was diagnosed with RR MS in 2005 and when I found out about this Liberation Treatment I was so excited about it when I found out that this is going help me and other people with MS. I would be a willing participant in your trial research. I have three young children that have to do a lot of stuff for me.
Hi,
I am interested in your clinical trial, I had the procedure done once in India already and I continued to experience relapses, currently my lower half of my body is immobilized. I believe my right jugular which was 80% blocked has re-stenosed. I live in Toronto. Thank you.
I am 45 yrs old, was diagnosed with MS 7 years ago. My biggest challenge is insomnia and walking. I have tried 3 different drugs so far(avonex, rebif and currently copaxone) and this disease keeps moving forward.
I am very interested in being part of your clinical trial.
I look forward to hearing from you, Gary
Denver Colorado