Living with MS: What's good about MS? Answer to mrhmack's video.
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Uploader Comments (angelusa73)
Video Responses
This video is a response to MS Vlog # 2 What good things have come from your MS?
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All Comments (23)
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thank you
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amalia
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Dear Amalia,
I understand why MS might make you feel this way but I have to say that having MS allowed to get back to the way I was, appreciating the little things in life. I would love to go back in time and be that person that I once was, but I can't go back unfortunately...
Have a good night and take good care,
hugs
Angela
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no no ....! i like my self more befor i had MS
I HAte that every day !!!
amalia
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hi Agelusa
it is good to find yor comm.
how do you know that kerri is going to do it? if on thusday the specilist refuse to do it i might do it privatly .
my life quality is more important to me than Mony !
amalia
51amalia 1 year ago
Dear Amalia,
Kerri made a video where she speaks about her going to be the jugular veins unblocked. I will write you privately and give you the link to that particular video so you can see it too.
Have a good day!
Angela
angelusa73 1 year ago
hi
i will do everithing to have the Liberetion and open it !
my mum had 90 % block vein and she allmost died ...
she live in Israel .
if Kerri can do it in melbourne i can do it too /
thanks
amalia
51amalia 1 year ago
Dear Amelia,
it's good that you feel so hopeful now and I am so glad that you got in touch with Kerri! I promised you that I was going to contact you, didn't it? :)
Be hopeful, dear Amelia! I hope you will find a way to get the Liberation treatment in Melbourne just like Kerri!
Best of luck,
hugs
Angela
angelusa73 1 year ago
hi
i am traying to tell you way i am not happy .... i live in melbourne australia , if you have 60 % block vein in your neck like me there is nothing you can do ... they need more reserch ! i do not have time !!! i have too much pain ...
I am an artist and i can't do what i use to do
life become un bearabale some times
sorry .. i hope you are good were ever you are !
51amalia 1 year ago
Dear Amalia,
I completely understand how you feel. It's so frustrating to feel so sick, to know what's wrong with our body and not receive any help! That is why I have been giving support to Dr. Zamboni in many ways and I am doing my very best so people with MS will be heard!
I will try to you with a personal e-mail and I will let you know all about the changes that are happening about the world about CCSVI. We are not there yet, but we are moving...
Take good care. I am going to write you!
angelusa73 1 year ago