The Story of a Real New Zealander…
I have personally spoken at length with this young man who is living in New Zealand (aged 26).
This is a TRUE story…and he is sharing his story with New Zealand.
I’ve been contemplating about telling my story and going through this trauma again, but I am no longer willing to suffer in silence anymore.
If anyone is still recovering from post \/ related issues (neurological, physical) please let me know. Got the 1st jab in 13th of Sep, I was a huge pro-mask, pro v and pro science left-leaning supporter. Ever since I’ve been dealing with non-stop tinnitus, worsening vision, weakness in limbs, paresthesia, numbness, migraines, brain fog, significant hair loss, insomnia, and a long list of fked up symptoms.
Now I’m swept under the rug like I don’t even exist, numerous calls to healthline and reports to CARM with no follow-up, being gaslighted by doctors and nurses telling me it’s just anxiety, urgent pleads and emails sent to government officials like Andrew Little with promises of forwarding it to MoH and a reply in due time…then nothing, numerous emails to MPs with automatic replies and the worst of all, aunty Cindy’s assistant’s reply telling me to go report to CARM, when I have STATED in the email I’ve already done it numerous times.
Calling myself bitter, jaded and cynical is an understatement of the century. I am bloody furious they choose to ignore people like us and are afraid to acknowledge there are issues and nuances in this v thing. The MoH knows that if they provide treatments for us they automatically admit they are at fault, they even threatened doctors, nurses and healthcare workers about helping us. Just ask around, ask your healthcare worker friend if this is the issue right now. I know they are trying to reduce v hesitancy but at what cost? so much for the “greater good”!
I used to sing and play the guitar and was an enthusiastic and somewhat humorous amateur musician with a fine art background, now I can’t sing, play and produce because I have noticeable hearing loss and tinnitus, and my vocal chords are messed up. I can’t draw because my hands are shaky, my mind is literally blank and my imagination is non-existent. Before all of this, I had dreams and goals. This has cost me my relationship with my partner and my life, nobody understands unless they’re also suffering from symptoms after the v.
I’m currently on a second round of prednisone, trying to calm the tinnitus and inflammation, it’s only a temporary fix but I have heard it helped many others like me.
This has been a huge wake up call for me, this has been my red pill, this is my life now, and I don’t know if it will ever go away. This will be my fight, I will never back down, I have nothing to lose anymore.
Is there anyone out there in NZ just like me? Where is the safety net when things go wrong? Why is there no treatment for us?
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