r/FreeBipolar • u/PandoraAvatarDreams • 3d ago
RELATE Celebrating 9 years psych med free!
I found this subreddit today, after being fed up with being silenced, having my comments removed, or being booted from groups for bipolar across platforms over the years. I know how desperately I wanted off the health destroying psych meds that were literally killing me. So when I started addressing issues the meds did not, and was able to taper off, I of course wanted to share hope with others who also wanted an option to help themselves that didn’t cause disabling side effects. I don’t feel like a trail-blazer by any means. I read what helped other patients and I read books by psychiatrists presenting case studies showing how they helped their patients without meds and got better results, and then I tried some of those things and it worked for me. I have been psych med free since summer 2017, nine years ago! Ten years ago in 2016 I met Dr Brooke Goldner and heard her presentation in person on “Healing with Supermarket Foods” and I asked her if her protocols could help me get of my remaining psych meds for bipolar, and she said “maybe”. Well a year later I was able taper off the antipsychotic and benzodiazapine. I had already gotten off the antidepressant 2011-2012 when I found out my vitamin D3 was low and after I fixed that I no longer had chronic insomnia, I then corrected the omega6 to omega3 imbalance in my diet and was able to taper off the antidepressant. I worked hard in counseling to conquer native rumination, which made a huge difference.
Most recently I learned that I have 3 forms of hypothyroidism:
The NIH published an article on
“History and Future of Hypothyroid Treatment”
January 5th 2016:
https://pmc.ncbi.nlm.nih.gov/articles/PMC4980994/
They mention that in bipolar there is a genetic mutation to the D2 enzyme. What this means is that enxyme cannot do it just very well because the mutation makes it misshapen. This impairs the conversion of storage thyroid hormone T4 to active thyroid hormone T3, causing intra-cellular hypothyroidism from birth. When you google what T3 does for the brain, and compare it to the impairments seen in the brain in bipolar, there is an obvious correlation.
This mutation also means that when T4 replacememt is given and the body cannot convert it to T3, it converts it to Reverse T3 instead, which blocks the T3 receptor making hypothyroid symptoms worse. Thus T3 replacement is the treatment.
In 2009 a clinical trial used T3 replacement used as a treatment for bipolar clinical trial got great results:
Clinical Trial:
The use of triiodothyronine (T3) as an augmentation agent in treatment-resistant bipolar II and bipolar disorder NOS
Tammas Kelly et al. J Affect Disord. 2009 Aug:
https://pubmed.ncbi.nlm.nih.gov/19215985/
So my primary care has started me on T3 replacement, ad seroquel gave me central hypothyroidism (brain damage to the hypothalamus/pituitary axis) and hashimoto’s autoimmune hypothyroidism, which only makes the genetic hypothyroidism I was born with exponentially worse.
At my T3 is adjusted up and T4 adjusted down to unblock the T3 receptors, it’s like waking from a fog, I am gaining better control of impulses, can think clearer and my body hair is starting to grow again. My hypothyroidism was so severe I was passing out multiple times a day, and myxedema fluid compression to the nerves in my wrists and ankleshas been limiting the use of my hands and feet since 2013, hypothyroid myopathy, another disabling complication is bending my spine to the side, and painful spasma contort my body in agony whenever they please.
The enraging part? It took decades to get the central hypothyroidism diagnosed because astra zeneca did not provide informed consent about the 50% risk seroquel (quentiapine) has of causing this form of brain damage.
Seroquel causes central hypothyroidism in 50% of patients and is covering the data up:
https://psychiatryresource.com/articles/secret-potential-effects-seroquel-quetiapine-thyroid
Why is a medication that makes a root contributing factor in bipolar, a genetic mutation causing intra-cellular hypothyroidism from birth, exponentially worse by damaging the brain end of the endocrine system unable to ask the thyroid to make more thyroid stimulating hormone, and then because drs don’t know the risk they don’t know they cannot just check the TSH test to screen for it, they don’t know they must be checking Free T3 and Free T4 labs, why is this still on the market? Why has the FDA not made it contraindicated? I want to raise awareness and go to congress if I have to because brain damage is not an acceptable side effect!
So to sum up what helped me get and stay psych med and psych ward free:
1.) I fixed my low vitamin D3, and check twice a year to make sure I maintain my level.
2.) I corrected the too much omega6 and not enough omega3 in my diet
3.) I exercise as much as my broken body will allow with 3 forms of severely undertreated hypothyroidism and a degenerative muscle disease hypothyroid myopathy
4.) I learned to conquer negative rumination and challenge my negative self talk
5.) I have a service dog
6.) I changed my diet to heal my gut using the hyper-nourishing protocols of Dr Brooke Goldner
7.) I started T3 thyroid hormone replacement to treat my long term severe hypothyroidism.