Stem-cell Therapy ---- Lungs

Posted , 14 users are following.

I was just wondering if anyone in USA or Canada has heard of this and what they thought?  I have talk to a Dr. and a Nurse from the States and they say it does work, but cost a few thousand . No one has called me back in Canada yet. Before I spend the money, just want to make sure it's safe and will help. Thank you in adavance 

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  • Posted

    I think you should first look it up on Clinicaltrialsdotgov. There is a good hospital in Little Rock, Arkansas which does perform this procedure. 
  • Posted

    For those in the UK:

    Strangely enough, I asked my doctor about stem cell transplant thingy today. She'd never heard of it, but is going to enquire if the NHS are doing any clinical trials at the moment, and said she'll get back to me.

    I'll keep the forum posted on what she finds out.

    Jo

  • Posted

    Just googled stem cell therapy for copd in Canada and there is a ton of info that you could read about it.  Good luck! 
  • Posted

    Bitnd objective & realistic is most difficult when one is desperate, particluarly where improving quality or length of life is concerned  ... but very necessary when there is currently clear evidence of the profit motive being the dominant force. 

    A couple of years ago, while struggling up the stairs of a hotel with oxygen cyclinder in hand because the lift had failed, the hotel owner declared that I no longer needed to suffer as COPD was now curable with stem cell surgery. Yes, she had been looking on the Net while I was out and had found all sorts of clinics in South America, India and E Europe offering the 'magic cure' for a mere 10 to 15 grand  Small beer (to her).

    Not unnaturally, I have since made my own extensive enquiries so though not an expert, I am much better informed.

    Bottom line is that while stem cell surgery is the bees knees for various bits of the body, the lungs are totally different and my consultant (who keeps close tabs on all developments in COPD care) reckons it'll likely be 20 years yet before such a system could be perfected for lungs. 

    Meanwhile then, I strongly advise you to verify any claims of benefits spefically for those with COPD direct with the patients who have had this treatment rather than rely on 3rd party forum posts, some of which are clearly from "plants" on commission for the "clinics".

    As always, remember the old addage "a fool and his money are soon parted" !!

    • Posted

      Emmgee speaks my mind. As to patient recommendations in the U.S., no doctor who wishes to keep a license can reveal a patient's name without permission. No one gives permission without significant remuneration. This makes them actors reading or typing the doctor's scriot
    • Posted

      Thanks aitarg35939. Much appreciated !

      Funny, isn't it, that after yesterday;s flurry, the posts suddenly stopped ? Now what was I saying about 'plants' ?

    • Posted

      And here we are 2 years later, emmgee, and boy are you right about things dying off for a long time.

      I just realized something which I failed to point out to non-American considering med treatments in the States. If a doc says something will be a few thousand, ask for a price sheet. Then - crucial - ask if there will be other fees. Just as a sample for cancer surgery:

      - your doc, the oncologist

      - the surgeon

      - the anesthesiologist or nurse anesthetist

      - the radiologist

      - charges for each speck of med used (anesthesia drugs & anything else)

      - hospital operating room charges

      - recovery room charges

      -room charges or, even worse, ICU charges by the second [it seems] followed by room charges

      - off-hour charges

      - respiratory therapy charges, up to hourly tho most I've had so far is 6 x day/night ... with me cancelling all the 4 a.m. treatments because I can't get back to sleep

      And that's by no means all, just giving you a taste.

  • Posted

    Hi Patricia! I am from Ontario, Canada. I am very interested in this also, but my doctor tells me it has not been approved in Ontario. Good luck ...and keep us posted.
  • Posted

    We seem to have strayed from stem cells and COPD. I see my haematologist shortly. He is a professor and is in demand to speak at conferences all over the world  all the time and he never charges me (nice guy and super smart about things like stem cells) Ataxathin is the red stuff in your salmon - harmless and good for you. - Side effects and so on is a vexed issue with drugs - BUT if using something that the human body usually digests just keep doses low unless you do plenty of research. When I had my stem cell transplant I asked the doctors for a multi vitamin. I burst out laughing when I saw the size of the tablet - tiny. Common sense is a good guide or better yet get yourself a good naturopath or naturopathic doctor. Checking these things is their job! Probably a simple thing is to stuff yourself with fresh fruit and vegetables - organic if you can - ALWAYS wash well and grow as much of your own as you possibly can - you will notice a real difference to your health - if you have family, pets, do them the same favour - anybody can grow fresh herbs - take out the pretty tree and plant an apple and so on - good luck!!

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