Tagged: CCSVI RSS

  • tanya

    tanya 7:49 am on August 8, 2010 Permalink | Reply
    Tags: CCSVI,   

    We’re sitting in the hospital, waiting to see the neurologist. I think Mexico time might be kicking in… So, experiences of Mexico non-CCSVI related…. Last night after we got back to our room at 9pm, we realized we still hadn’t seen the ocean. We could hear it roaring and crashing and so went for a little walk down to the water. It was pitch black and we really couldn’t see much but the white when the waves would crash. But the sound was unbelievable. Mom and Dad sang “How Great Thou Art”, while I hummed and scanned for kidnappers (I’m being careful Chris.) After seeing them again this morning, we are pretty sure they are 9ft waves. No one swims in it because the undertow is so great – but boy are they beautiful. Mom and I walked down again this morning and went just far enough for a wave to skim our feet. Well, apparently the tide was coming in, because the next wave came rushing in and crashed up to our thighs! Our skirts were sopping wet! So, we backed up a few feet and the next wave came in even farther and crashed up at our thighs again. Pretty fun…

    The other neat thing is that right outside of the hospital is the main street through town. The whole left hand lane is shut down with bicyclists. When we asked the fellow at the desk what was happening, he said that every Sunday they shut down one lane of the whole road for people to ride their bikes for exercise. It is the neatest thing to watch. Tons of local families riding their bikes up and down the street. Very nice entertainment and something I think Canada should consider!

    Well, we sit and wait. Dad just quoted Romans 8:24-25. “But hope that is seen is no hope at all. Who hopes for what he already has? But if we hope for what we do not yet have, we wait for it patiently (in Mexico).” Emphasis mine. Perfect verse for today.

     
  • tanya

    tanya 8:49 pm on August 7, 2010 Permalink | Reply
    Tags: CCSVI,   

    Ok! No procedure tonight, but it will be at 9am tomorrow. They felt it was getting too late to do it safely tonight. But did that possibility surprise us! Tomorrow he will meet with the neurologist to assess current symptoms, then they will skip the ultrasound altogether and go straight to the venograph (camera in his veins) and then angioplasty. So we should have news by lunch – unless Mexico time kicks in!

     
    • Lovella

      Lovella 8:57 pm on August 7, 2010 Permalink

      I hope you can sleep tonight. . Does Gerry stay at the clinic overnight?
      Hugs

    • Lorie

      Lorie 9:21 pm on August 7, 2010 Permalink

      Good Night you three, sleep tight. We will all be praying for Gerry’s procedure and the steady hands of the Cardiologist. We love you.

      God Bless,
      love Lorie

  • tanya

    tanya 6:27 pm on August 7, 2010 Permalink | Reply
    Tags: CCSVI,   

    Procedure Yet Tonight? 

    We just had a wonderful visit with Andres the administrator at the hospital and Dr. Moguel, the cardiologist. We are amazed at what wonderful people they are. Where else would the doctor come in and sit and chit chat with you for an hour sharing stories, answering questions. He was wearing shorts, t-shirt and crocs. So relaxed and calm. They wheeled Dad in for the MRI and then Dr. Moguel asked what we would think about having the procedure yet tonight. he leaves for a conference on monday and would really like to have a full day afterwards here in case there are any complications. So, they have left to talk about the logigistics of this… and dad doesn’t even know yet! Haha! We have been told to expect Mexico time and for everything to take way longer than expected, but this is slightly the opposite! It is now 8:25pm here and we are imaging being here until after midnight now, but it’s worth it if we can have it all said and done! Mom and I walked down the street and picked up a wonderful meal of a famous local restaurant called MacDonalds. I was mortified that we were eating there and not somewhere authentic, but mom was so hungry and so we grabbed what was easiest. Anyway, now we wait… So, stay posted and we’ll let you know as soon as we here something!

     
  • tanya

    tanya 4:25 pm on August 7, 2010 Permalink | Reply
    Tags: CCSVI,   

    We’re Here! And the Testing Has Begun! 

    Well, believe it or not we are sitting in the waiting room of the Amerimed Hospital already! Let me start at the beginning…

    We had a wonderful flight, only 4 hours long and no turbulence. Dad did great. Getting through immigration, collecting our baggage and then going through customs was a little difficult. Dad was in his wheelchair and mom and I were lugging all the luggage while trying to push him in the wheelchair. To say we are ready to be done with that thing is an understatement!

    After making it through the room with all the timeshare people trying to push you into talking with them, we walked out the doors to see a big sign that said “CCSVI” on it. I started to cry… unbelievable that we are here for this.

    On the way, Andres, the hospital administrator phoned the driver asking to speak to mom. He told her to check in at the hotel, get our bags into our room and then take a taxi to the hospital tonight. We were only scheduled to come tomorrow morning so this was a bit of a surprise. He said they had time to do some of the testing tonight to ensure that he can have time to do the procedure tomorrow.

    So, without any time to check out our hotel room, look at the beach or glance at the pool, we are here now with mom filling in pages of paperwork. Dad will have the MRI tonight and then the rest tomorrow! We are hungry and tired, but realize it will be a bit of a marathon for two days and then we can relax.

    Dad says he’s tired, but fine. :) This is about the time that he normally settles onto the couch for the night, so to still be going after the travelling is requiring more of him than normal. You can pray this isn’t overdoing it here today in preparation for tomorrow’s all day event. But we are thrilled to be here and feeling like it is all a little surreal!

    We’ll check in later tonight!

     
  • tanya

    tanya 4:48 pm on July 19, 2010 Permalink | Reply
    Tags: CCSVI, ,   

    Gerry’s Pre-Treatment Video 

    Check out my Dad’s pre-treatment video! This records his symptoms of MS before we head to Mexico in 2 and a half weeks to have the blocks in his veins cleared. We’ll then be able to record a post-treatment video to (hopefully) document the improvements! This is a very accurate representation of his symptoms. We made sure there was no exaggerating going on. Thanks for watching! Tanya
     
    • Lovella

      Lovella 7:13 am on July 20, 2010 Permalink

      Thanks for the pretreatment video. We watched it this morning and saw it as Gerry’s reality. It was good to be together as siblings last night ..spending time together and looking forward to Gerry’s future. We went for a short walk while he rode with our other brother Ken in the gator. Soon ..he’ll be doing those walks on his own.

    • Lovella

      Lovella 7:17 am on July 20, 2010 Permalink

      I’m Gerry’s sister. We were together as siblings last night at Ken and Mary’s. .(another brother). We had such a good time together. .anticipating the future after the procedure.
      We went for a short walk and Gerry rode in the gator beside us. We look forward to seeing him walking without his cane. . .
      Great video Tanya. . thanks for sharing it with us.

    • joanne

      joanne 7:33 pm on July 20, 2010 Permalink

      I havnt seen you in many years and watching your video brought me to tears, i pray everyday for you to get better (as much as you can) and am sending u my love and support.

    • gerry

      Gerry Peters 8:03 pm on July 20, 2010 Permalink

      thank you Joanne. You’re just great!!

    • Rick

      Rick 5:13 am on July 24, 2010 Permalink

      Gerry has been training me look after our CR website with pdf’s. What a great teacher you are Gerry thank you for your time and patients with me.

      I watched your video very well done and informative for me I don’t really know much about MS other than it slowly robs you of the quality of life that was very well translated in your video.

      Know that I’m praying that this procedure is a great success for you and your family Gerry

    • gerry

      Gerry Peters 8:00 am on July 24, 2010 Permalink

      Thanks Rick. You’ve become a real techie. For those that don’t know, CR stands for Celebrate Recovery

  • gerry

    Gerry Peters 9:23 am on July 18, 2010 Permalink | Reply
    Tags: CCSVI, discrimination   

    CTV British Columbia – MS patients claim discrimination in treatment access – CTV News 

    Here’s a CTV BC News video clip about the class action law suit.  CTV British Columbia – MS patients claim discrimination in treatment access – CTV News.

     
  • gerry

    Gerry Peters 9:25 am on July 14, 2010 Permalink | Reply
    Tags: CCSVI,   

    Here’s a recent testimonial from an MS patient that received treatment at the Cabos clinic with the Doctor that I’m seeing. http://ccsvi-ms.ning.com/profiles/blogs/ccsvi-liberation-procedure-in-2. If you have a little time, it’s worth the read.

     
  • gerry

    Gerry Peters 8:09 am on July 12, 2010 Permalink | Reply
    Tags: CCSVI,   

    MS Story II 

    Because people have been asking us…

    …here’s the continued story from My Story of MS and the CCSVI Treatment.  Much has happened since and decisions made.

    Heidi, myself and our daughter Tanya will be flying to Los Cabos, Mexico, on August 7 where I will begin thorough testing and treatment on the following day, August 8, 8:30am, at the Clinic of the Heart(More …)

     
  • gerry

    Gerry Peters 5:47 pm on July 10, 2010 Permalink | Reply
    Tags: CCSVI   

    Here’s a short but great article in the National post: http://www.nationalpost.com/Hope+those+with+false+hope/3163985/story.html

     
  • gerry

    Gerry Peters 5:36 pm on July 10, 2010 Permalink | Reply
    Tags: CCSVI,   

    Interested in understanding more? A great Macleans Article is at: http://www2.macleans.ca/2010/05/31/not-available-in-canada/

     
c
compose new post
j
next post/next comment
k
previous post/previous comment
r
reply
e
edit
o
show/hide comments
t
go to top
l
go to login
h
show/hide help
esc
cancel