Kitson Posts

[Kitson]

Kitson - You confuse me when you say the US has trials that are potentially fatal, but you would advise against anyone going to Mexico or China or wherever because of the risks. If you would like to rustle up some donations or feel we should charge a membership fee for our forum, we can eliminate forum sponsorships and very possibly lose some members who don't have extra money to participate. We have forum expenses and the sponsors help us defray the costs. Also, if you aren't interested in any of the sponsors, then simply don't click on an icon. How much simpler could that be? I have looked at other medical sites and some forums and we are not alone in allowing sponsorships. I find the information useful and the links handy to be truthful. We have started this forum to help others by having stem cell discussions and members who have had treatment give their stories. You don't seem to believe that stem cells can help with your condition and yet others with MS are seeing improvements. I also feel a good mental attitude is a must no matter what kind of treatment you seek. No one is claiming cures on here. Most members are not doctors. We do not give medical advise. As Harv says, today's information on stem cells is going to seem very pre historic in only a few years. No one is downgrading the U.S. The general consensus that I see is that the U.S. is simply not up to being ready to give treatment to people and many cannot afford to wait. You have an attitude of defeat. I would be laying on the couch with some respiratory problem as usual if I felt like you do. Instead, this year I am full of energy and enjoying my life again. And heavens forbid, I went to Mexico for treatment.

Costs how much to run this site? Puhleeeese

I run one 10 x bigger than this. I will send you the link via PM if you like.

This doesnt cost hardly anything.. your host? look for a better one then.
I looked it up.. you cant be paying much at all.
http://whois.domaintools.com/stemcellpioneers.com

The board is not updated ( leaves you open to hackers because of holes in secruity)

You have done nothing to customize the site

I see spammers signing up all the time, there is a simple way to prevent that.

You have no clue how to run a board.

yes this site does promote people going overseas to questionable clinics, you even host questions from people who workk ar these companies.

Discounts for members from this forum? Healthcare is like a blue light special?

 

[Kitson]

I think you are missing the entire point of this forum:
We are PRIMARILY here for people who have taken these risks, or are contemplating taking these risks.

To be sure, we are also here to discuss clinical trials that are available, new stem cell research, doctors, hospitals, clinics, and anything related to stem cells. We are also somewhat of a support group for anyone suffering from a grave illness, or anyone supporting someone who is. We are here to be uplifting or be a shoulder to cry on, whatever is needed.

But, again, I emphasize that we are people who have taken or who may take these risks.

A majority of people here are COPD patients who have taken that risk at a certain clinic in Mexico.

As you can see from my signature, I took TWO RISKS in Thailand and in Germany. Hasn't helped me yet. I spent a fortune last year, but does that make me a fool???

NO. It means that I have the desire to improve my existence, after trying every drug, therapy and treatment option available for my cardiac disease in the USA. Can you understand what I am saying? I HAVE TRIED EVERYTHING! I had a quadruple bypass when I was under 40 years old. I have had more than 15 stents! I had angioplasties. I have had cardiac radiation. I have had EECP. I have had 14 angiograms. I was rejected for transplant. I take enough cardiac medicine to knock out a cow.
I have Class IV angina. I get horrible chest pain by doing such "aerobic things" as: walking down the hall, letting the dog out the door, rolling out the trash can, propping up my pillows. Excruciating chest pain while performing such "olympic activities" as these!!

I am a "no option" cardiac patient. No option, meaning that the USA medical community has no options to offer me.

That is why I went to Thailand and Germany for stem cell treatment last year.

I WOULD DO IT AGAIN IN A MOMENT, IF I THOUGHT THAT IT MIGHT HELP ME.

We are here to help people, plain and simple.
Whatever it takes.

I think, however that "no option" applies to you.
You are simply being negative about what we are all about here, and, as such, I have nothing further to offer you.

I wish you well.

I do have options. one not being going to mexico or china.

The US has does do SCT for MS patients, one that I am going in for and it is succesful.

Sorry about your situation though, but not surprised considering on where you went.

What are you all about here? Discussions on the potential of Stem Cells or encouraging people to go to mexico and taking advantage of discounts.

By the way I have 2 recent articles of companies that post here that are in trouble.. as a matter of fact they closed one of the locations down.

 

[barbara]

Kitson - I have decided that you have a hidden agenda and that if you continue to bad mouth our strictly volunteer efforts, I will ban you which I only do to spammers at this point. You are a nasty know it all and I don't appreciate it considering the many hours that are spent working on this forum. As Jeannine says, start your own forum.With your attitude you ought to attract a lot of member. (Yes, that is singular). We are also working on a fund to help people who cannot afford the cost of treatment. Do you have any idea how much money that takes? There are no pop up ads or anything else to distract our members. Your information is totally biased that you give people here. You make confusing statements. In one post you are fine and in the next you are going to get treatment. You claim that others with MS have not been helped by stem cell therapy and that you know this for a fact. What a total crock. You don't know a thing about how these people are doing. What do you have against other countries anyway? Should many have to die before treatment is available here in the U.S.? Are you suggesting we need socialized medicine in the U.S. as you come across that way? Are you running for political office? Come clean with us because right now I see you as a very envious, disheartened person who is probably scared to death of the future. Again, I caution you to show consideration on this forum or I will ban you just like I do the spammers and the porn people. Nice company to be thrown in with wouldn't you say?

 

[Kitson]

Kitson - I have decided that you have a hidden agenda and that if you continue to bad mouth our strictly volunteer efforts, I will ban you which I only do to spammers at this point. You are a nasty know it all and I don't appreciate it considering the many hours that are spent working on this forum. As Jeannine says, start your own forum.With your attitude you ought to attract a lot of member. (Yes, that is singular). We are also working on a fund to help people who cannot afford the cost of treatment. Do you have any idea how much money that takes? There are no pop up ads or anything else to distract our members. Your information is totally biased that you give people here. You make confusing statements. In one post you are fine and in the next you are going to get treatment. You claim that others with MS have not been helped by stem cell therapy and that you know this for a fact. What a total crock. You don't know a thing about how these people are doing. What do you have against other countries anyway? Should many have to die before treatment is available here in the U.S.? Are you suggesting we need socialized medicine in the U.S. as you come across that way? Are you running for political office? Come clean with us because right now I see you as a very envious, disheartened person who is probably scared to death of the future. Again, I caution you to show consideration on this forum or I will ban you just like I do the spammers and the porn people. Nice company to be thrown in with wouldn't you say?

We are in the process of starting own forum. Good luck with yours.

By the way we have this site linked and your reply. Quite professional.


No worries, ban away. You hardly have any members right now at any rate.

A good forum is one that educates members about future treatments, possibilitie and trials. members can discuss.
One that is not biased and gives pro's and con's.
one that does not promote any clinic or even allow any of the clinics to advertise on the site.

I could go on.

Like I said good luck!