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Haemochromatosis

niknak7197niknak7197 Member Posts: 6 Listener
edited June 2020 in Disabled people
Hi Is anyone a Celtic warrior with Celtic curse?

Replies

  • janer1967janer1967 Member Posts: 9,127 Disability Gamechanger
    Sorry @NikNak no Im not but you never know others maybe
  • LoveLifeLoveLife Member Posts: 4 Listener
    Yes, myself and my 9 other siblings. It's the most common disorder but you won't hear about it as big pharma have no drug cure just blood letting. Doctors are misdiagnosing people. It was discussed in Parliament before the plandemic. All newborns were to be tested. The video is online. 
  • Richard_ScopeRichard_Scope Posts: 2,725

    Scope community team

    Scope
    Specialist Information Officer - Cerebral Palsy

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  • LoveLifeLoveLife Member Posts: 4 Listener
    NHS is a private corporation.They have been bumping off folk for decades and decades with their morphine injections, not to mention their mustard gas chemo and all those jags given to our babies, aluminium and mercury causing autism, (my son is jag damaged) all those jags recently killing folk. There is no cure for haemochromatosis. Eat raw food diet, keep away from dead animals and the drug alcohol and doctors drugs, exercise - yoga and meditation, and spread love - get rid of any negative emotions like anger, forgive people. Donate blood to blood bank to keep iron down. We have an amazing genetic mutation that kept our ancestor's alive. Look after your temple. Take good care of yourself. Namaste x You have to unlearn everything that you have been taught. x
  • Richard_ScopeRichard_Scope Posts: 2,725

    Scope community team

    Well, they have saved my life on two occasions. I'm probably in on it @LoveLife. It's strange that you have brought all of this up. I was only talking to Bill Gates the other day about this very thing.
    Scope
    Specialist Information Officer - Cerebral Palsy

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  • niknak7197niknak7197 Member Posts: 6 Listener
    Wanted constructive advice not propaganda and saved us did it I think not. No a soul saving mutation just am a mutant!! Take it from Scotland?
  • Richard_ScopeRichard_Scope Posts: 2,725

    Scope community team

    @niknak7197
    From one mutant to another these helplines may help?

    Haemochromatosis Society helpline, tel: 03030 401102. This is run by volunteers, who I have no doubt will be keen to assist you.

    You could also try the British Liver Trust helpline 0800 652 7330, they also have local support groups.
    Scope
    Specialist Information Officer - Cerebral Palsy

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  • niknak7197niknak7197 Member Posts: 6 Listener
    No thanks they are despicable and heartless. I would never belittle myself to need help from them!!
  • Richard_ScopeRichard_Scope Posts: 2,725

    Scope community team

    Okay, the numbers are there should you ever need them.

    Scope
    Specialist Information Officer - Cerebral Palsy

    Want to tell us about your experience on the community? Talk to our chatbot and let us know. 
  • LoveLifeLoveLife Member Posts: 4 Listener
    I'm born and bred Scottish from Donegal parents, no 12, 2 siblings have died of it, one has cancer. Linked with bi polar, iron in the brain organ. 2 siblings that passed were given drugs for years. One they knew was overloading. Doc told my 71 Yr old eldest that she was a carrier when she is C and H gene. Silent killer. Why aren't the powers that shouldn't be educating healthcare and the masses? Have a lovely day 💗
  • niknak7197niknak7197 Member Posts: 6 Listener
    I won't thanks but the world shall kill us all sadly!!
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