ALS patient Roger, Talks About The Improvements After His Treatment with Global Stem Cells

Author: Global Stem Cells

I think on the improvement side, since we've arrived, certainly by eating with a knife and fork, and I can eat with a knife and fork and I can almost clean up the bottom of a plate up by using the knife and fork and not having to use my fingers to push the last pieces onto the fork. I can hold a bowl of soup and I can use a spoon to collect the soup out of the the bowl. One of the things as well that's been a big improvement is, before I came if I got a newspaper I couldn't hold the pages and turn the page over and pat the pages with my fingers, I had to put it down and sometimes use both hands to to find the next page, whereas now I can see it and it's not as good as it could be, but I can now turn the pages with either hand. Just going, I couldn't fasten the button on the top of my trousers, 80% of the time now I can manage it, and pulling your trousers up, as silly as it may seem, was very, very difficult, you couldn't get your thumb and your finger to hold together, tight enough to lift a pair of trousers up, I can do that now. I can actually. And putting a T-shirt on, or taking a T-shirt off, over my head, I can do that. In the last two days I've managed to do that once or twice on my own, without any help, and they're only small things but there are mountains to climb from where we've been.

When we first came there was no way I could get off a chair on my own, and now I can stand up and sit down 98% of the time without any help. The chair I've sat on now may be just a fraction lower to get off, but in general of an average dining chair, 98% of the time I'll be able to stand up on my own and that's, another thing that I couldn't do when we first came was sit on the bed lay down and swing my legs onto the bed. I have my legs lifted onto the bed, the last two nights I've sat down and I put my own legs onto the bed, with the muscles in my own legs, which it's quite rewarding. I've had no treatment at all before the stem cell treatment this is the first glimmer of hope that we had, apart from when I was diagnosed and you've given a very small tablet and, in our country and I think it's the same one worldwide, that gives you roughly 1 to 4 months of extended life and that's the only help you can get, and it wasn't until we found about the World Medical Center, that we had a little glimmer of hope that we might to get some help here. The the only thing I might add to that was that my wife found, it's like, vitamins, probably it is something called the Deanna Protocol, and it was developed in America, and it was developed by a surgeon whose daughter's was diagnosed with the motor neuron disease in the early 30's, and it helped her, and we went onto that about four nights before we came here, and I'm quite sure that was helping as well with the condition, but nothing is happening real quick, it's slow all the time. It was purely through my wife after we found the Deanna protocol we still didn't want to say, well, that's it, we give up now.

Basically we were handed to the life sentence we were told, it could be sort of six months or as long as two years, possibly slightly more, so we were both devastated and we were clinging at any help we could get. My wife looked on the internet, on forums for motor neuron disease, ALS, and she found that there was clinics in China, we found one in America and the World Medical Center here in Thailand, and she approached them. Unique Access was the first one to get back to us and then we read on some of the forums of people that have had treatment here, and it looked promising, and that's why we came to get in touch with you, and basically we couldn't get here quickly enough, because time is certainly something we haven't got plenty to spare of, once you're diagnosed you going down very quickly, and you need to save every minute you can get. We came in on the Monday morning and we started by having blood taken from me and infused with oxygen to detox my body, and then we went on to having, now then I can tell exactly, tell you exactly what it is, but basically it's a detox of your body to get rid of toxins in your body, so the treatment here can start work. The stem cells I understand that we get those injected into us intravenously and through lumbar puncture but we don't expect those to start work for at least two months. We don't expect any big improvements from the stem cells for at least two months. But moving on from that, you get the acupuncture which I found very, seems to be working very well, and you get the rTMS which is a stimulation of the brain, again to get the the neurons, or encouraging them to work.

But in the in the time we've been here I think probably the thing that's working the best at the moment is the occupational therapy, the physiotherapy and the pool therapy. I think all those therapies together, for the, probably looking where we're not quite through our second week, but I think we go home and we'll carry on with that therapy ourselves at home, and that will complement the stem cells when they start to work in two months time. When I first came here I couldn't hold a knife and fork to eat my dinner. Within a week I could cut my dinner up, meat, I could cut anything I want to do and I could virtually ate a full meal without having any assistance to to finish off. Though within the first week with the physiotherapy, acupuncture, and what was immediately effectiveness that was certainly some improvement in a week, and we've noticed the ongoing ever since I'm walking slightly better than I was when I came. I'd bet, I think if someone from home saw me, they would the wouldn't see a big difference, but myself and my wife we can see a difference.

ALS patient Roger, Talks About The Improvements After His Treatment with Global Stem Cells

Definitely. As far as the full package goes, that we bought, we came with great reservations because we don't travel, we haven't been on all of the abroad since 2003, so it was a massive, massive, step for us to come to Thailand. We didn't really know what to expect we looked at the facility on the internet, but the internet can tell you all sorts of things and then when you get there the facility can probably not even exist. You've lost your money and you're on your way back on penniless. That did not happen, we couldn't have been better looked after, we were picked up from the airport and brought to the hospital. We met the doctors on the sunday afternoon, we went back to a hotel until the monday morning. We came back on the Monday morning, we started then and we met the whole team, as far as the doctors, the nurses, and all the staff girl, including right down to the lady that comes in and cleans our room every day, they are absolutely 100% sound. They are a marvelous bunch, they really are.

The facility is always clean, very tidy, well looked after, and I can't say a lot more, cause I have no complaints. Our patient representative was Faith, from the first time my wife emailed on the sunday evening Faith had got back towards the following morning, I think it was 9 or 10 o'clock in it in the evening.... We got up the next morning at our usual time at past six, seven o'clock time, and there was an email waiting for us from Faith. From that time onwards Faith kept in touch every day and if you sent an email it was returned almost immediately. We could not complain at all at the response we've had from Faith and I'm sure all the other representatives would give the same service.

For anyone that's like ourselves, coming absolutely out of the cold, to come and have treatment here, don't have reservations. Come get it done. We believe it's the next generation of medicine. We had no hope, this is giving us hope. Excuse me. You've got to come and if you're in the same position as we where, where you've been given a life sentence of not too long, even if you can only buy yourself a few more years or one more year of a good quality of life, it must be worthy.

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