Stem Cell Treatment Results

Posted , 10 users are following.

Well, It's been 6 months since I had my stem cell treatment and I can't say that it has helped me. Maybe because I have Bronchiectasis that adds a whole new issue to COPD. My lungs maybe repairing it self, but the weakening of the airway walls (the difference from Bronchiectasis and COPD) will not improve.  I knew that going into the procedure. My hope was an improvement of lung function and less shortness of breath.

But I still have lung infections and are hard to get rid of, so bottom line....think twice before having the procedure if you have Bronchiectasis.  It is still considered research, so insurance will not pay for it.

Elizabeth49611

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  • Posted

    Hi

    I have had bronchiectasis since 1996. My biggest problem is getting the mucus out. I even have a vest help loosen the mucus. But hasn't been a lot of help. I'm so frustrated. I'm in and out of hospital due to pneumonia. Also past four months menapause symptoms makes me feel miserable! !! I'm 42 yr old have one son. I miss alot out with being able to do stuff with my son. My guilt is horrible put it on myself.

    Thanks for listening

    Good luck

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    • Posted

      Kris,

      I know how you feel.  I started having lung problems in my late 30s.  That was 26 yrs ago.  I was diagnosed with Asthma, then COPD and then after a CT scan 5 yrs ago, bronchiectasis.

      I retired last year, and my mind wants to do alot of things and be active, but my lungs really slow me down. 

      You may want to start to think 'outside the box'.   Check into supplements (Turmeric helps with iflammation), essential oils, etc. I take a spoonful of Manuka honey each day (it has antibiotic properties).  I also take Azithromycin (antibiotic) every other day. It's a long term antibiotic.

      Also, do you have a flutter valve? I use it thru out the day.  Along with the use of my vest, it helps loosen the mucus.  After using it, I position myself with my head lower than my waist and cough, gravity helps the mucus come up.

      Hang in there, you are not alone, Elizabeth

        

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  • Posted

    After talking to a Doctor's Nurse at a Clinic in Florida about the stem cell procedure and her telling me what the outcome and cost would be I talked to my Pulmanary Doctor at the UofM in Michigan and he told Me that he felt the procedure was not recognized as any benificial good to the patient

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  • Posted

    Dear Eliabeth.   Thank you very much for  bothering to come in to this site to report on your treatment.It is so useful to hear from someone who has actual experience
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  • Posted

    Helo Beth,

    Damn sorry to hear we where all really hoping that it might work for you,I got back on the Azthromycin again and I do fine a big difference,but as we said in earlier post hard to belive that they can't find something for this BX,well hope you stay as well as can be expected with this.

    Regards,

    Charlie

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  • Posted

    I would also like to thank you for helping us all by providing information. Hopefully one day they will come up with something for us. I really had hope in the stem cell procedure too. I have asthma, pseudamonas and bronchiectasis. I always wonder how many people have these 3 things?
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  • Posted

    I am sorry to hear that. My mother is getting her second treatment this week. Due to osteoporosis she could not do the bone marrow.  With her PF and bronchiesctasis we have seen some improvement - coughs up a lot of green, but no infections.  I know from my research that it can take up to one year for the stem cells to work. We will keep praying for you.
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    • Posted

      Terri,

      Where did your Mom have the treatment done? I live in the states and had mine done at The Lung Instutite.  They use my own stem cells.

      It's good to hear that some one has improved with the treatment, hopefully, she will continue with the improvement.

      elizabeth

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