Haemochromatosis
Options
niknak7197
Community member Posts: 6 Listener
Hi Is anyone a Celtic warrior with Celtic curse?
Comments
-
Sorry @NikNak no Im not but you never know others maybe
-
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.
-
Scope
Specialist Information Officer and Cerebral Palsy Programme Lead'Concerned about another member's safety or wellbeing? Flag your concerns with us.'
Want to tell us about your experience in the community? Talk to our chatbot and let us know. -
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
-
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 and Cerebral Palsy Programme Lead'Concerned about another member's safety or wellbeing? Flag your concerns with us.'
Want to tell us about your experience in the community? Talk to our chatbot and let us know. -
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?
-
@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 and Cerebral Palsy Programme Lead'Concerned about another member's safety or wellbeing? Flag your concerns with us.'
Want to tell us about your experience in the community? Talk to our chatbot and let us know. -
No thanks they are despicable and heartless. I would never belittle myself to need help from them!!
-
Okay, the numbers are there should you ever need them.
Scope
Specialist Information Officer and Cerebral Palsy Programme Lead'Concerned about another member's safety or wellbeing? Flag your concerns with us.'
Want to tell us about your experience in the community? Talk to our chatbot and let us know. -
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 ?
-
I won't thanks but the world shall kill us all sadly!!
Brightness
Categories
- All Categories
- 13K Start here and say hello!
- 6.6K Coffee lounge
- 69 Games lounge
- 385 Cost of living
- 4.3K Disability rights and campaigning
- 1.9K Research and opportunities
- 199 Community updates
- 9.2K Talk about your situation
- 2.1K Children, parents, and families
- 1.6K Work and employment
- 767 Education
- 1.7K Housing and independent living
- 1.4K Aids, adaptations, and equipment
- 586 Dating, sex, and relationships
- 363 Exercise and accessible facilities
- 737 Transport and travel
- 31.6K Talk about money
- 4.4K Benefits and financial support
- 5.2K Employment and Support Allowance (ESA)
- 17.1K PIP, DLA, and AA
- 4.9K Universal Credit (UC)
- 6.2K Talk about your impairment
- 1.8K Cerebral palsy
- 868 Chronic pain and pain management
- 180 Physical and neurological impairments
- 1.1K Autism and neurodiversity
- 1.2K Mental health and wellbeing
- 317 Sensory impairments
- 818 Rare, invisible, and undiagnosed conditions