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Purtier Placenta???? Anybody used it in the forum??

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    Purtier Placenta???? Anybody used it in the forum??

    Hi all
    Very nice to come back to the forum after a long time. Had a very difficult time in Nepal. All the kids flew back from UK to see me and they stuck here for more than 4 months, they just returnedback to UK couple of weeks before only. I was very happy them to be here but son, daughter in law got Covid19, tiny grand daughters are trapped in a room. I was like a caged lion, luckily we all are safe now.

    My wife, elder son & elder daughter in law(from UK), younger daughter in law all got Covid 19. Elder daughter in law stayed hospital for 12 days in ICU. Luckily, I am still safe from COVID19.
    Couldn't go to doctor for follow up. Couldn't go outside from my room for a month. Now very difficult to even stand. Respiration; hardly can breathe, started bipap machine Prisma25s. Bipap made me bit easy, it's third day though.

    Because of pandemic couldn't back to UK, don't think I can come back to UK again, am bit depressed now. Someone talked me about Purtier Placenta. Does anyone know about it? Have you tried, does it have any good results??
    Please share me your experience, if anyone tried.
    Thank you!

    #2
    You sound a bit down my friend. Sunday is normally a very quiet day on here. So wait until tomorrow. Stay Strong we are here for you. 🤗👍💗
    Bulbar started Jan 2020. Mute and 100% tube fed but mobile and undefeated. Stay Strong 🤗😘🤗😁xx

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      #3
      Hello SATRUGHNA MANI LAMICHHANE - good to hear from you. Did you get the jab over there? Haven't heard of Purtier Placenta - had to look it up. Take care

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        #4
        SATRUGHNA MANI LAMICHHANE Don't waste your money on Purtier Placenta. If you have spare money, buy a plane ticket or two and bring family over to visit you, rather than line the pockets of people making false claims about their product.

        Love Ellie.
        ​Diagnosed 03/2007. Sporadic Definite ALS/MND Spinal (hand) Onset.
        Eye gaze user - No functional limbs - No speech - Feeding tube - Overnight NIV.

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          #5
          SATRUGHNA MANI LAMICHHANE so sorry to hear of all the health and other difficulties you and your family have been having, and your position about getting back to UK. Sorry I haven't heard of Purtier Placenta either, sounds like something to avoid from Ellie. Hope you can get some useful help. Love Heather
          Diagnosed July 2020, ALS bulbar onset.

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            #6
            Why can’t you come back to the UK? Is it Priti Patel and her department making it difficult for you or your MND? I wish good luck for you being able to come back to be nearer to your family so will have regular support.

            I too wouldn’t waste yours money on unproven medication. Lynne x
            ALS diagnosed November 2017, limb onset. For the 4 yrs previously I was losing my balance.

            I'm staying positive and taking each day as it comes.

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