Vaderize03 posted: Give me a day or two, I can ask some of the Gastrointestinal specialists that I work with.
malkieD2 posted:In response to your thread request, and the private message you sent to me, I'll do some internal digging here to find out what is known about this company. I'll also research into the technique and therapy you are referring to, and see if it is safe and effect or not. I'll do it at work tomorrow, and will post the response here.
malkieD2 posted: ok, now for the bad news - I'm really, really struggling to be able to pass comment on the GemClinic in Russia, because all of the information I'm finding is in Russian (and as you well know, I can barely speak english, so I can hardly speak russian). However, in my continued research I'll see what I can find on my internal system at work - I'll post on wednesday. Hope all is well
Sherylin posted:I thought english was your native language, because you live in UK?
Lane_Winree posted:I suffer from UC, sort of Crohns to a lesser degree. I've been on treatments of Remicade for about five years now, and I can honestly say it's the only thing that keeps me healthy from day to day. It isn't a cheap drug, but it definitely costs less than $34K. Remicade is an anti-inflammatory that was initially used to treat rheumatoid arthritis patients. Research was done, and it showed that it could dramatically improve the lives of people suffering from IBS. It is so effective, in fact, it has become mainstream treatment for UC and Crohns patients in the US. The drug is administered intravenously on a set timetable. For example, I receive the treatment every seven weeks. Typically the infusion takes two to three hours. Sorry I couldn't help with the stem cell procedure you were looking into, but I thought I'd throw this out there for you.
Lane_Winree posted:I know the FDA here in the US is taking a good hard look at some alternative treatments, namely a self injection that has less side-effects than Remicade. Hopefully someone can come up with an affordable and safe treatment.
Lane_Winree posted:Keep us posted on this subject, I'll be interested to see where it goes. Lord knows I would love to not have to go in for an infusion every seven weeks. I've got a family friend who specializes in Crohn's, so I'll prod him and see if he knows anything about this.
Lane_Winree posted:My best wishes to your son. Hang in there, a lot of people are performing fantastic research of UC and Crohns treatments. I have a feeling that within the next five years something is going to pop up that'll change the way it's treated.