Multiple Sclerosis: 'I won't have to take drugs for life'

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  • เผยแพร่เมื่อ 15 ต.ค. 2024

ความคิดเห็น • 209

  • @Donna-zp7uv
    @Donna-zp7uv 3 ปีที่แล้ว +178

    After taking almost 2 MILLION dollars worth of MS drugs and relapsing and progressing on EVERY one of them in 22 years, I had HSCT in 2017 and it stopped the progression of my MS. Now I get better every day instead of worse! It’s only four days of chemo and was a cake walk compared to decades of this cruel disease. My only regret is not doing it sooner but here in the US we are made to suffer at the expense of big Pharma. I had to leave my country to save my life.

    • @markpowell6752
      @markpowell6752 2 ปีที่แล้ว +5

      Hi Donna can I ask how much did this cost?

    • @emilybarrett464
      @emilybarrett464 2 ปีที่แล้ว +5

      @@AH--173 why be so negative when its some peoples last option. Im currently being assessed for HSCT, and granted, its got alot of risks (my neuro said 30% mortality rate), but its not a useless treatment.

    • @frankgradus9474
      @frankgradus9474 2 ปีที่แล้ว +2

      @@emilybarrett464 If death is one of the options of HSCT treatment I'd still go for it. Death would be much better than the unstoppable slippery slope I'm on day in, day out now ...

    • @ernietollar7767
      @ernietollar7767 ปีที่แล้ว +2

      Thanks for sharing Donna. I'm earlier on in a PPMS diagnosis (58) hoping that HSCT is an option. I may do Ocrevus for a year or half year even ten hopefully HSCT. HSCT is being discoraged so far because I have PPMS. Although I trying to learn and take in different expert perspective as well as testimonial - especially from the PPMS camp

    • @theresau1070
      @theresau1070 ปีที่แล้ว

      This is so true . Keep us sick while big pharma gets rich.

  • @dawna4185
    @dawna4185 2 ปีที่แล้ว +28

    been watching her since early youtube days....she is an inspiration not only in makeup application and style but humanity as well...i wish her the very best on her journey and admire her tenacity to spread awareness of this horrible disease and treatments!

  • @lozmurphy7961
    @lozmurphy7961 3 ปีที่แล้ว +63

    I had AHSCT in Mosco in 2019 and it has given me my life back. No more wakening up in the middle of the night worrying if the strange feelings was a relapse. Best decision of my life. I wasn’t going to allow my daughter to be my minder at 13.

    • @proudman6651
      @proudman6651 ปีที่แล้ว +3

      How is it going now?

    • @tropisk.
      @tropisk. 10 หลายเดือนก่อน

      Vincristine is a vinca alkaloid with formula C46H56N4O10
      Vincristine Sulfate, USP is a white to off-white powder. It is soluble in methanol, freely soluble in water, but only slightly soluble in 95% ethanol.

    • @tropisk.
      @tropisk. 10 หลายเดือนก่อน

      C62H111N11O12

    • @tropisk.
      @tropisk. 10 หลายเดือนก่อน

      C6494H9978N1718O2014S46

    • @lozmurphy7961
      @lozmurphy7961 10 หลายเดือนก่อน

      @@proudman6651absolutely fantastic - I have had my 4 year MRI & no progression - still on no MS medication - life is great 😊

  • @melmatthews5876
    @melmatthews5876 2 ปีที่แล้ว +28

    I'm so delighted Nicola has found something that will probably work for her. I had been trying to find out how she was coping with her MS so this is very positive news. I wish her the very best and a complete and permanent recovery.

  • @NR-jr4sf
    @NR-jr4sf 2 ปีที่แล้ว +24

    Nic is so wonderfully articulate here and such an inspiration to share her story

  • @Lynneheal
    @Lynneheal 2 ปีที่แล้ว +52

    I have fought MS for nearly 50 years.

  • @emmaphilo4049
    @emmaphilo4049 2 ปีที่แล้ว +21

    Well done on raising awareness on this treatment. This is extremely important.

  • @theflicka28flicka24
    @theflicka28flicka24 2 ปีที่แล้ว +37

    The big pharmaceutical companies would rather people be forced to pay thousands of dollars for a lifetime supply of drugs rather than a (hopefully) one off treatment. I think Nic knows that too but couldn't say that on air.

  • @lozmurphy7961
    @lozmurphy7961 3 ปีที่แล้ว +18

    I had AHSCT in Mosco in 2019 and it has given me my life back. No more wakening up in the middle of the night worrying if the strange feelings was a relapse coming on etc. Best decision of my life. I wasn’t going to allow my daughter to be my minder at 13.

    • @carmenbalan2188
      @carmenbalan2188 6 หลายเดือนก่อน

      Hello ! How much în the price of this procedure in Moscow ?

    • @lozmurphy7961
      @lozmurphy7961 6 หลายเดือนก่อน

      In 2019 it was £45k I think it’s over £50k now.

  • @abab9622
    @abab9622 ปีที่แล้ว +10

    That’s amazing. I’m so happy for her! It’s a delight to hear the relief in her voice.

  • @mazdamaniac4643
    @mazdamaniac4643 3 ปีที่แล้ว +60

    This is genuinely good news. I had a friend that had to live with this for a few years until he sadly passed away.
    The 'treatments' seem bloody awful, folks have been campaigning for years for the development of better medications, while having to live with this horrible condition.
    If only the government put anywhere near as much effort into treating MS as it did for coronavirus...

    • @reptilenews8707
      @reptilenews8707 3 ปีที่แล้ว +2

      I chucked my 'Brabio' injection after a very bad reaction.
      When they gave me the original Copaxone' I decided just to go without and after two years little if anything has changed, thankfully.
      Pretty useless' is a good description of the NHS in my book.

    • @badfairy9554
      @badfairy9554 3 ปีที่แล้ว +1

      My friend was 35 when she died of MS.

    • @ghost8726
      @ghost8726 2 ปีที่แล้ว

      th-cam.com/video/6mcV_sOH8Gc/w-d-xo.html

    • @emilybarrett464
      @emilybarrett464 ปีที่แล้ว +9

      @@badfairy9554 sorry to hear that, but thats not very encouraging for us with MS to read. Like i hate it when i tell people i have ms, and the response is that they know someone that died of it. Might be s shock, but that’s hardly music to our ears.

    • @emilybarrett464
      @emilybarrett464 ปีที่แล้ว

      Probably because ms doesn’t have the same effect on the economy as a global, contagious pandemic does.

  • @Paul5520
    @Paul5520 2 ปีที่แล้ว +23

    Fair play to her. Hope it does something amazing for her.

  • @theresau1070
    @theresau1070 ปีที่แล้ว +18

    This disease is so difficult. I can’t deal with it anymore. I might get this treatment as well.

  • @__Wanderer
    @__Wanderer 2 ปีที่แล้ว +16

    spot on - ridiculous this isn't used yet in europe / uk - absolutely insane! This needs more coverage!!

    • @harmcity9934
      @harmcity9934 ปีที่แล้ว +1

      it is used in europe, check out lithuania, norway or sweden

    • @__Wanderer
      @__Wanderer ปีที่แล้ว +1

      @@harmcity9934 norway and sweden are in the economic union, not eu xD Perhaps I need to look into the Lithuania treatment options in that case. I live in NL and am stuck with the escalation model sadly :( they give me average drugs and wait for me to get worse before allowing something that works better...When i asked if i could get ocrevus my neuro said "oh I wouldn't do that, we had a patient that died from it"... great bedside manner

    • @harmcity9934
      @harmcity9934 ปีที่แล้ว +2

      @@__Wanderer i live in lithuania and it is compensated here so there should not be a problem, they also have it here for cash but it's roughly the same price as in mexico

    • @thres34
      @thres34 6 หลายเดือนก่อน

      Used in UK on private hospital for £90,000

    • @__Wanderer
      @__Wanderer 6 หลายเดือนก่อน

      @@thres34 seems like a more reasonable option. Most MS meds cost insurance / tax payer 10-20k per year for someone's entire life... a 90k treatment would be cheaper + likely allow someone with MS to work longer with fewer relapses... seems like a win win. I half believe pharma companies are holding back HSCT use because of this... Personally still on my first treatment (tecfidera/vumerity) - as soon as I see any changes on my MRI I want to escalate to something better...

  • @chrisismail
    @chrisismail ปีที่แล้ว +6

    My wife flew to Russia 4 yrs ago to have this treatment. It's amazing treatment.

    • @sandra2337
      @sandra2337 ปีที่แล้ว +1

      How is she now..

    • @cape2838
      @cape2838 7 หลายเดือนก่อน +1

      Yes how is she?

  • @amyg8176
    @amyg8176 2 ปีที่แล้ว +25

    The whole pixiwoo channel seems to be gone. I hope Nic is doing alright.

    • @QuietlyCurious
      @QuietlyCurious 2 ปีที่แล้ว +8

      That's how I ended up here. Was in the mood to watch old Pixiwoo vids.

    • @xcurvesx
      @xcurvesx 2 ปีที่แล้ว +6

      @@QuietlyCurious I was just looking for their videos right now and found this as well. They were the best!

  • @AnthonyD-yy2in
    @AnthonyD-yy2in 3 ปีที่แล้ว +13

    I hate MS! i saw it afflict my mothers cousin and one of my workmates, anyway on a positive note i hope more people will go ahead and take this treatment, at a 80% success rate things are looking pretty good for most of the people who try this.

  • @marazz53
    @marazz53 3 ปีที่แล้ว +26

    l was diognized with MS. l feel very tired and exhausted, fatigue.
    l go to Mater Dei Hospital for drip steroids every 4 weeks.
    l take Avonex injection every Friday at 6.00pm.
    l take the injection myself.
    To stop it from continuing killing me.
    Please pray for me... THANKS...

  • @reptilenews8707
    @reptilenews8707 3 ปีที่แล้ว +33

    2:26 Er, neurologists already KNOW about this treatment, as they did trials on it a decade ago.
    The problem with this country is FUNDING and always has been.
    I stopped taking my Copaxone after having a reaction to the cheaper 'Brabio' brand and I'd just had enough of injections.
    What I want and NEED is proper painkillers and anti-spasticity drugs like Sativex ( cannabis-based ), but they want you to try lots of other drugs first, which never work.
    WHY does this country always have a problem with giving out certain medicines, where others just get on with it?
    No wonder people go out and just buy cannabis from the street and who can blame them?

    • @carlosfurtado1164
      @carlosfurtado1164 3 ปีที่แล้ว +15

      Because doctors are being paid by pharmaceutical companies to perscribe these drugs, even if they don't work/have a lot of side effects.

    • @authenticmslife
      @authenticmslife 2 ปีที่แล้ว +5

      @@carlosfurtado1164 that's exactly right.

    • @ralsharp6013
      @ralsharp6013 2 ปีที่แล้ว

      Some of the drugs they give have side effects of dystonia, parkinsonism and tardive dyskinesia. 3 similar conditions on to of the already ms.
      A lot of the medication has aluminium Lake or aluminium advents..
      Just not nice of big Pharma to recommend to the doctors that we take this rubbish..
      A really good way to checkout possible side effects from medications, the studies are in PubMed. Example MS, supliaments, medication, adverse reaction pubmed.

  • @eskiemax5133
    @eskiemax5133 ปีที่แล้ว +5

    Praying for her!!!

  • @ntube9716
    @ntube9716 3 ปีที่แล้ว +12

    BREAKING: Disease talks for the first time, leaving scientists battled

  • @joycewright5386
    @joycewright5386 ปีที่แล้ว +4

    Wow I never heard of this treatment. I’ve been taking LDN for the past 7 years. It’s off label but all the MS drugs were too scary and unaffordable in the USA.

    • @aba1791
      @aba1791 ปีที่แล้ว +2

      Not all are unaffordable in the US. Theres federal assistance programs that covers the cost COMPLETELY with certain medical insurance. 100% FREE.

    • @pattischmitz2680
      @pattischmitz2680 ปีที่แล้ว

      @@aba1791they dont offer it in the US?

  • @noworriesnoproblems6382
    @noworriesnoproblems6382 3 ปีที่แล้ว +23

    My father had Ms I lost him at 18. This is unreal I hope it's as good as she says

    • @mindywatt8815
      @mindywatt8815 3 ปีที่แล้ว +12

      It is! I needed bilateral support or a wheelchair in 2014. After HSCT in 2015 I no longer even need a cane and recently walked over 10km in one evening. My life has been totally transformed.

    • @noworriesnoproblems6382
      @noworriesnoproblems6382 3 ปีที่แล้ว +3

      @@mindywatt8815 so after this treatment does it allow the the nerve cell coverings to repair, it doesn't just stop the damage?

    • @noworriesnoproblems6382
      @noworriesnoproblems6382 3 ปีที่แล้ว +2

      @@mindywatt8815 ps happy to hear it

    • @happyweekend2343
      @happyweekend2343 3 ปีที่แล้ว +5

      My father is 53 he's primary progressive, i always say your very lucky to be able to talk and eat compared to a guy who's same age as my dad in hospital completely immobile everywhere. MS effects some worse than others.... it's super interesting.

    • @sarastewart2633
      @sarastewart2633 2 ปีที่แล้ว +3

      That's so young to lose him. I lost my dad to MS when I was in my thirties. Terrible disease.

  • @Peeniemoon0714
    @Peeniemoon0714 3 ปีที่แล้ว +15

    Hoping to get this done one day!

  • @CarolCreates
    @CarolCreates 2 ปีที่แล้ว +11

    3:31. And there it is 🤷🏽‍♀️
    They will never have to take drugs again … pharmaceutical peddler’s wouldn’t want this loss of revenue.

  • @TheNails3
    @TheNails3 2 ปีที่แล้ว +5

    Yes Nic! So proud of her.

  • @clairehanson2036
    @clairehanson2036 3 ปีที่แล้ว +21

    I have ms and was given a lot of different medications which has resulted in me starting with anal cancer and having strokes. I take nothing now for ms I live with what I have been given

    • @alexandrar9021
      @alexandrar9021 3 ปีที่แล้ว +9

      So sorry to hear that. Do you have any idea which medication gave you the cancer?

    • @judtindouglas9051
      @judtindouglas9051 3 ปีที่แล้ว +8

      Look at a book called the wahls protocol

    • @clairehanson2036
      @clairehanson2036 3 ปีที่แล้ว +3

      @@judtindouglas9051 I will thanks

    • @judtindouglas9051
      @judtindouglas9051 3 ปีที่แล้ว +5

      @@clairehanson2036 also has a Ted talk on it, on TH-cam

    • @reptilenews8707
      @reptilenews8707 3 ปีที่แล้ว +6

      They use us as guinea pigs, which is why I don't take anything now either.
      Two years without treatment and still OK so far.

  • @straighttalker3459
    @straighttalker3459 2 ปีที่แล้ว +8

    I will be praying for her and that the US catch up to many of the treatments that other countries have already approved and proven viable

    • @TheFort87
      @TheFort87 4 หลายเดือนก่อน

      We have it (Northwestern). It’s just that without insurance or for foreigners, it’s much cheaper to do Mexico or Russia

  • @Truth1561
    @Truth1561 ปีที่แล้ว +3

    Russia abd Mexico aren't regulated aa closely as the UK, hence they just run with this risky treatment.
    My daughter was duagnosed 3 years ago and is stable on Tysabri. Shes lucky to gave a brilliant supportive Neuro consultant and specialist nurses.
    Shes run several half marathons since her diagnosis abd is runing the London Marathon for MS UK next year. I am so oroud of her!

    • @walksthroughlife900
      @walksthroughlife900 24 วันที่ผ่านมา

      Yes - completely true. The risky side to this is not reported at all. Very disappointing. The reporter is asking to speculate on things and while I like Chapman, she is just guessing and coming up with answers that are not true. Very misleading.

  • @hardworker645
    @hardworker645 3 ปีที่แล้ว +8

    God bless you

  • @kamalj7858
    @kamalj7858 2 ปีที่แล้ว +6

    Please let us know details where we can get treatment

  • @theresau1070
    @theresau1070 ปีที่แล้ว +3

    We all need to fight to have insurance company pay for this in the United States to help them. Ocrevus is 60 thousand . Why don’t insurance companies pay for this . What can we do to have help with this cost ?

    • @remnanttruth
      @remnanttruth ปีที่แล้ว +1

      My 42 year old brother had Ocrevus infusion. No improvement.

    • @aba1791
      @aba1791 ปีที่แล้ว +2

      Ocrevus is FREE with government assitance program. Ask me how I KNOW.

    • @theresau1070
      @theresau1070 ปีที่แล้ว

      @@remnanttruth I’m sorry . Hope he finds something that works for him.

  • @annacaggi6241
    @annacaggi6241 6 หลายเดือนก่อน +1

    Im going to have this done the end of may 24. I am so looking forward to this .

  • @cherryboo65b56
    @cherryboo65b56 ปีที่แล้ว +2

    They offer chemo based treatment in USA

  • @badfairy9554
    @badfairy9554 3 ปีที่แล้ว +8

    My friend died of MS. She was 35.

    • @badfairy9554
      @badfairy9554 2 ปีที่แล้ว +1

      @@chris1960 at the time the gov would not say one could die of MS.

    • @Every1ShouldSparkle
      @Every1ShouldSparkle ปีที่แล้ว

      ​@@badfairy9554You sadly absolutely can. People need to make sure doctors put it on the death certificates even if it is secondary cause. That means the numbers get added into the stats and that raises awareness, funding and research.

    • @badfairy9554
      @badfairy9554 ปีที่แล้ว

      Hi@@Every1ShouldSparkle that is what her husband said. The one thing that has changed is now in the UK the goverment understand that one can die of fatigue.

    • @Every1ShouldSparkle
      @Every1ShouldSparkle ปีที่แล้ว

      @@badfairy9554 Medics have always been able to put MS on death certificates

  • @sarcomakaposi2054
    @sarcomakaposi2054 4 หลายเดือนก่อน

    It's not just MS. Mexico was the first country to efficiently treat HIV and promote Hormone Modulation treatments for cancer instead of chemo. It's all about the money. Rich countries are holding off efficient treatments because it makes a lot of money to just sell drugs. Russia just came up with the first ever reversive treatment for glaucoma. We can't expect our country to provide us with everything we need anymore. We need to push for stem cell research, it's the key to cure most diseases.

  • @sadhanasarthak
    @sadhanasarthak ปีที่แล้ว +2

    I m also MS patient since 2022 oct

  • @sashamarie1972
    @sashamarie1972 2 ปีที่แล้ว +14

    There’s no money in cures. How evil is that.

    • @dermlover1
      @dermlover1 ปีที่แล้ว

      It’s disgusting.

    • @cujet
      @cujet ปีที่แล้ว +1

      There are plenty of diseases for which there is no cure. Curing what we can won't make a bit of difference to big pharma's bottom line.

  • @JulienArbor
    @JulienArbor 2 ปีที่แล้ว +5

    Is that theory that MS is a viral infection that hasn’t completely healed or a post viral disease like ME/CFS and Long COVID? What is the chemo killing off?

    • @olafbitter3999
      @olafbitter3999 ปีที่แล้ว

      MS is an autoimmune illness not an infection. Many things can trigger your immune system to attack your neurons. There are theories that following certain infections your immune system goes into overdrive and can attack your own cells, among them your neurons. This treatment targets your malfunctioning immune system. To put it simple it kills of the white blood cells then replaces them with stem cells that develop into your new white blood cells. After this treatment your immune system won't attack your neurons anymore.

    • @GO-xs8pj
      @GO-xs8pj ปีที่แล้ว

      th-cam.com/video/9hJA0lGsIKI/w-d-xo.html A TH-cam video about the possible link to ESB and CM virus and MS.

  • @sapanamodi5801
    @sapanamodi5801 6 หลายเดือนก่อน

    I am going for HSCT next week, my Ms makes me very hard to walk, keeping my balance. Update here after two months, how the treatment go.

    • @Pinkiev1
      @Pinkiev1 6 หลายเดือนก่อน +1

      How did it go?

    • @PrabhnoorSingh-o4f
      @PrabhnoorSingh-o4f หลายเดือนก่อน

      Plz tell abut your hsct

    • @Ooopss85
      @Ooopss85 21 วันที่ผ่านมา

      How'd it go?

  • @LaurieTurner-n7o
    @LaurieTurner-n7o 17 วันที่ผ่านมา

    80 percent is amazing!!!!

  • @DavidBaronStevensPersonal
    @DavidBaronStevensPersonal ปีที่แล้ว +3

    its a pretty revolutionary idea
    i believe it was the NHS that discovered this treatment.
    how ironic that it's not available through that very service for the people who paid for it to be developed.
    yall are becoming more american each day

  • @ckahlquist2129
    @ckahlquist2129 2 ปีที่แล้ว +8

    I'm going in two weeks.

    • @CarolCreates
      @CarolCreates 2 ปีที่แล้ว +5

      Hi, how did it go ❓

    • @ckahlquist2129
      @ckahlquist2129 2 ปีที่แล้ว +13

      @@CarolCreates I've been home for just over a month. The month I spent in Mexico was very difficult, physically, emotionally, spiritually even. At the end of that difficult month I walked without my cane for the first time in years. I no longer feel out of balance. There are muscle groups all over my body that are working for the first time in years. HSCT worked for me. I do not feel like I have MS I feel like I am now recovering from the effects of having had MS.

    • @ndobolo80star86
      @ndobolo80star86 2 ปีที่แล้ว +5

      Keep us update

    • @KS-wl6eu
      @KS-wl6eu 2 ปีที่แล้ว +2

      @@ckahlquist2129 Fantastic news. Spread the word and stay well

    • @yugdeepmeena7856
      @yugdeepmeena7856 18 วันที่ผ่านมา

      How r u now​@@ckahlquist2129

  • @edwinvanegas3682
    @edwinvanegas3682 ปีที่แล้ว +4

    The interviewer low key questioning how a country like Mexico can be a leader on fighting MS. She is so ignorant and full of herself. But happy for Nicola Chapman

  • @totalnoobfishing1753
    @totalnoobfishing1753 ปีที่แล้ว

    How did they administer the HSCT? IV or intrathecal ?

  • @myviews469
    @myviews469 ปีที่แล้ว +1

    How she doing now?

  • @The_Lazy_Crafter
    @The_Lazy_Crafter 2 ปีที่แล้ว +1

    Awwww we love her ❤️ 💕

  • @mybachhertzbaud3074
    @mybachhertzbaud3074 ปีที่แล้ว +1

    Truly hope this works for ya.😁 If it only halts progression, I think I'll pass.

  • @charro028
    @charro028 2 ปีที่แล้ว +2

    My beautiful Nic!!

  • @ernietollar407
    @ernietollar407 ปีที่แล้ว +1

    Is this used for PPMS?

  • @doomsday5375
    @doomsday5375 ปีที่แล้ว

    my wife has ms my wife is small she is only 7 8 stone they told her that hsct would kill her can someone give me some clarity weather it would help and how coild we build her ip to survive the chemo

  • @lightshift3431
    @lightshift3431 2 ปีที่แล้ว

    I think the news host was trying to hint that the expense is criminal...

  • @Knowdeepknowledge7475
    @Knowdeepknowledge7475 ปีที่แล้ว

    My brother have MS from 2022 , he cant walk

  • @happyweekend2343
    @happyweekend2343 3 ปีที่แล้ว +4

    This treatment won't work for people who have primary progressive/ It will probably work for newly diagnosed

    • @lozmurphy7961
      @lozmurphy7961 3 ปีที่แล้ว +7

      Sorry, but incorrect info there. HSCT works for all types of MS, the success rate and chances of improvements are lower than newly diagnosed yes but it does work at halting the progression rate. x

    • @ghost8726
      @ghost8726 2 ปีที่แล้ว

      th-cam.com/video/6mcV_sOH8Gc/w-d-xo.html

    • @CarolCreates
      @CarolCreates 2 ปีที่แล้ว +2

      She was diagnosed years ago.

    • @lozmurphy7961
      @lozmurphy7961 2 ปีที่แล้ว +4

      I was diagnosed 16 years ago and I’m now 3 years after treatment and no progress.

    • @CarolCreates
      @CarolCreates 2 ปีที่แล้ว +2

      @@lozmurphy7961 glad to hear that 🤗✨
      Tbh I don’t like the chemo aspect. Did u find it physically and/or mentally exhausting?
      Any side effects?

  • @daresaryan8229
    @daresaryan8229 ปีที่แล้ว +1

    Sweet and lovely lady 💖

  • @MrJoel125
    @MrJoel125 2 ปีที่แล้ว +4

    Freaking FDA sucks in the US

  • @jujutrini8412
    @jujutrini8412 ปีที่แล้ว

    Surely the years of drugs for MS must be more expensive than this new treatment which seems to be only for a few weeks. 🤔

  • @prathamxX
    @prathamxX 3 ปีที่แล้ว +4

    👍

  • @keitymarley733
    @keitymarley733 2 ปีที่แล้ว

    My sister is 32 years old and she has suffered from meniere disease for years and she always complains to me that I had to bought her Dr Madida herbs I saw on TH-cam and she is telling me last month that she is cured completely and don’t long have the symptoms like vertigo or dizziness, feeling of fullness in the ear or ringing, hearing loss, imbalance, motion sickness, nausea, or nystagmus.

  • @MrJoel125
    @MrJoel125 2 ปีที่แล้ว

    What's her TH-cam channel name?

    • @jayare6804
      @jayare6804 2 ปีที่แล้ว +1

      Try Pixiwoo or Nicola Chapman

    • @sarahtaylor7737
      @sarahtaylor7737 ปีที่แล้ว

      @@jayare6804 pixiwoo seems to have vanished off the planet. Very odd.

    • @pollyanna5354
      @pollyanna5354 ปีที่แล้ว

      ​@@sarahtaylor7737 Sam is back on TH-cam (Samantha Chapman Andrews)

  • @georgecoasta6923
    @georgecoasta6923 ปีที่แล้ว

    Walking myself was difficult for me because of my parkinson health situation but am happy that Dr Madida medicine on youtube I was able to get cured. Now I can walk properly🙏🙏

  • @majesticbutterfly
    @majesticbutterfly ปีที่แล้ว +5

    " Not the Russians or the Mexicans ??" Did this racist just say that ???? 😳😳😳😳😳

    • @mariajosea.m.5808
      @mariajosea.m.5808 ปีที่แล้ว +1

      I'm mexican, and i though the same 🤨. The interviewer feels rude since minute one.

    • @mr.makedonija2627
      @mr.makedonija2627 ปีที่แล้ว +2

      How is that racist?😂😂

  • @Gigiroo
    @Gigiroo 11 หลายเดือนก่อน

    Everyone has MS in a different way? No

  • @ankeu.a.wallace
    @ankeu.a.wallace ปีที่แล้ว

    #SharingIsCaring!!!
    👍🇺🇸😇💧💦🌊🌈🌎🌍🌏

  • @alann7077
    @alann7077 ปีที่แล้ว +2

    Typical... it's all about money...

  • @spiffymacadamia6405
    @spiffymacadamia6405 2 ปีที่แล้ว +7

    The way she compared the Brits and Americans to the Russians and the Mexicans was very poignant and biased. Her racism showed.

    • @maryjs4878
      @maryjs4878 ปีที่แล้ว +1

      Lol Americans Russians Brits and Mexicans aren't races.
      How was she being a racist??

  • @adamqjsmith
    @adamqjsmith 3 ปีที่แล้ว +1

    How much orgeano do u need for the sauce

  • @devilsadvocate9580
    @devilsadvocate9580 3 ปีที่แล้ว +5

    Not a fan of the skin head look, millennials baffle me

    • @zizia9060
      @zizia9060 3 ปีที่แล้ว +74

      She had chemotherapy, mate.

    • @devilsadvocate9580
      @devilsadvocate9580 3 ปีที่แล้ว

      @@zizia9060 oh

    • @Johanna040713
      @Johanna040713 2 ปีที่แล้ว +4

      😅

    • @Corn22
      @Corn22 2 ปีที่แล้ว +10

      she’s 41, not even a fuckin millennial mate.

    • @staceyvictoria8647
      @staceyvictoria8647 2 ปีที่แล้ว +1

      @@Corn22 she actually is but literally only just, Millenials were born 1981-1996 😁

  • @BarnyRumble
    @BarnyRumble ปีที่แล้ว

    It's either infection from bacteria or virus very hard to detect

  • @nat2040
    @nat2040 ปีที่แล้ว +1

    Goes to show what big pharma is all about Well done Nicola

  • @MrCharlesdick
    @MrCharlesdick 2 ปีที่แล้ว

    a "beauty expert" is not a thing.

    • @sarahtaylor7737
      @sarahtaylor7737 ปีที่แล้ว +2

      Yes it is. A very very lucrative thing.