Day 18 – Something New. Many MS patients…
Day 18 – Something New.
Many MS patients complain about a high pitched ringing in their ear. I’ve had this so long that I had gotten used to it. Last night I noticed that the ringing was gone.
Tagged: MS symptoms RSS
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Gerry Peters
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Gerry Peters
Day 16
It’s now the 16th day since the procedure and have to tell you that I’m still feeling great. Have I noticed any new improvements? It’s hard to say. I know my reflexes are great, my eyes focus on objects quickly and I can notice growing muscle strength in my legs. People are humored by me when I get up to get something and do so quite quickly. My mind is still clear (at least that’s my opinion), I can talk without fumbling for words, and my balance is back to near normal.
Not bad for something that is described by many as placebo. I wonder when the placebo wears off?
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Lovella
.. and don’t forget how your face has changed. . .no droops. .just smiles. .it is so wonderful.
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Art
All good news Gerry. Now, about that motorcycle shopping….
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Gerry Peters
I just no if the face change is for the better. I used to get a lot more pity.
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Gerry Peters
you selling your bike? If you need to get it off your hands, then maybe, just an outside chance maybe.
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Gerry Peters
Pre-CCSVI Treatment Video #2
This is a little update of my MS symptoms. Hopefully this will give us some further benchmarks from which we can measure the success of my CCSVI treatment in Mexico. Enjoy the show!
Jayde, 
Joy-Lynn Archambeault and one other person are discussing. 
Art, and 
Ray Parker 5:52 pm on August 31, 2010 Permalink
Gerry;
That is incredible news that you are sharing with the world! I rejoice with you in the progress you have made and am sharing this with a close friend whose wife has first stage MS. I definitely prayed for you when Chrissie spoke about your going to Cabo. We are believing with you for a complete recivery.
Ray
Ray Parker 5:54 pm on August 31, 2010 Permalink
Gerry;
I am thanking the Lord for the good news that Chrissie brought to Church last sunday and so we remembered you in prayer. May the Lord give you a complete recovery because you have so much to share with a broken and suffering world.
Ray 6:05 pm on August 31, 2010 Permalink
Gerry;
I rejoice with you in the progress that you have made in your recovery and want you to know that Chrissie shared the news of your journey to Cabo and that since then I have prayed with you about the
procedure. May the Lord give you full recovery because you have so much yet to share.
Ray 6:06 pm on August 31, 2010 Permalink
Gerry;
You were prayed for in Cabo and it’s exciting to hear you speak of the answers.
Ray 6:08 pm on August 31, 2010 Permalink
Gerry;
You were well prayed for when you were down in Cabo and it’s praise time to hear of the good news!
Joy-Lynn Archambeault 6:47 pm on August 31, 2010 Permalink
Hi Gerry! Reading your story brings tears to my eyes as my mother has progressive advanced MS. I have been trying to get more information so we can get her in for this treatment as soon as possible. My parents are missionaries at Lake of the Trees Bible Camp in BC. I would be SO grateful if you could help me out by giving me any information that will help get her in for this treatment.
Congratulations on your Liberation! God Bless you and your family!
Jayde 8:28 am on September 2, 2010 Permalink
I’ve enjoyed sharing your journey with you. It’s so exciting whenever we hear a new improvement. I wanted to let you know that I’ve forwarded your YouTube videos to my cousin, who is a vascular surgeon in Canada.
Gerry Peters 9:04 am on September 2, 2010 Permalink
thanks Jayde and all:
On September 8th it will be one month since the procedure and I continue to feel stronger. There has definitely been nerve damage and so a smaller amount (about 1/3) of the pain medication is still needed. Other than that my energy is way up, my mind is clear and my reflexes have improved quite dramatically.
Thanks for forwarding this to your cousin.
Gerry Peters 9:31 am on September 2, 2010 Permalink
Hi Joy-Lynn
I’m glad my story can encourage others. I continue to improve in areas of strength and mobility. I would certainly encourage every MS patient to study this treatment option. I also hope and pray for your mother’s best.
I went to Los Cabos for a variety of reasons and I’m glad I did. What you can do is go to their website at http://www.cardioabroad.com/testimonials.php. You`ll read other testimonies of MS patients. If interested, just send them an email and ask your questions. You could certainly mention my name – it may get a quicker response.
I`ve found a lot of info on this facebook, http://www.facebook.com/pages/CCSVI-at-UBC-MS-Clinic-Information-and-Support/182832983940 This Facebook is local and full of info. If you ask a question there you will get a great response.
Another site I found useful was http://ccsvi-ms.ning.com There is a wealth of info, including videos, stories and locations that are having this treatment done.
Other than this, you can certainly contact me personally and we could talk. If you`re interested in that, email me or send a facebook message and i`ll give you my phone number.
Sure hope this helps some
All the best! Gerry