Experiences with

Vitamin D3

Hi all, I hope you are all doing as okay as you can be. I have thin lining issue due to adenomyosis and my age sadly. After I had 1 cancelled transfer and a heartbreaking recent loss, I would like to try vitamin e to try and increase my lining prior to my next FET🙏 Please can anyone advise what

I understand that many of us PD sufferers benefit from vitamin B1 therapy as outlined in Dr. Constantini's publications, current Facebook group , and per many posts herein . I know it doesn't help everyone, but I was curious if there are any theories on its mechanism of action? The reason I ask is I

Pyrroloquinoline quinone (PQQ) is associated with biological processes such as mitochondriogenesis, reproduction, growth, and aging. In addition, PQQ attenuates clinically relevant dysfunctions (e.g., those associated with ischemia, inflammation and lipotoxicity). PQQ is novel among biofactors that are

Apologies for yet another post.. but I truly feel like I'm being battered with one thing after another. I am trying to piece together what is B12 and what is something else. I've had tinnitus for months now, started after I began injecting. However, over the past few weeks this has changed to be pulsatile

Hi All, Im still looking for the answer..... does anyone have any experience of these, the info is overwhelming and I cant afford to make the wrong decision ,health wise or financially. Along with DIO2+, MTHFR ,+ CFS there has always been gut inflammation ,unexplained flat villi, (gluten free

Hi I’ve just had my thyroid results .. I’m not feeling too good have neuropathy flare 😞 I work NHS and I’ve asked about my results and they seem to think maybe my T3 is a little high for me as this neuropathy started soon after my increase ? I have also got a high ferritin which the GP thinks I shouldn

I recenrtly read in Health Unlocked that a woman, carng for her elderly mother who had Parkinson's, was treating her with Vitamins B7 and B12. The dosages were 100 mcg of B7 or B12 (3) times a day and 100 mcg of Vitamin B7.. or B12 once per day. I do remember the woman stating that her mother

To give a bit of back story, I first saw my GP for suspected thyroid issue in Jan 2021 at that time I was told my blood results were normal but I was Vit D deficient which was the explanation for my symptoms. Even though I felt fobbed off I took the findings for what they were as the GP is the expert

My ferritin saturation has dropped since b12 injections! What do I do? I feel so ill! We now think the only reason I was low in b12 was a very very stressful year!

Hi, I wrote previously about family member’s confusion/dementia symptoms on low dose methotrexate. Scans showed no signs of age related degenerative dx. So did my research & found multiple cases of debilitating cognitive decline even on low dose methotrexate, despite doctors not listening, at first.

This presentation by Dr David Morris, hosted by Cytoplan was posted to the PA forum recently by auldreekie Quite astonishing how many times Hypothyroidism and Hashimoto's AIT gets a mention. Enjoy https://healthunlocked.com/redirect?url=https%3A%2F%2Fvimeo.com%2F891099138%2F4150efa06b%3Fshare%3Dcopy

Hi, Can anyone help with explaining these results? Been feeling more and more run down, hair loss, weight gain I just can’t shift despite eating well and not a lot, added to which we’ve been unsuccessful in conceiving. Been to the GP several times and fobbed out with various excuses/explanations so

Started 10 months ago by waking up 1 morning by severe pain in lower right skull & around the rght ear & cheekbone. Finally an MRI in May shows bone marrow edema in these 2 discs, C1 & C2. Neurologist said he'd never seen this in that area. Only thing diagnosed beyond that is mild osteoarthritis & osteopenia

Hello, hope you are all well. I am currently taking Levothyroxine 50mg daily and have been since May, feeling slightly better in some ways so some positives. I have been reading about the thyroid only supporting 20% of T4 to T3 and the complex B12 can support this in addition. Does anyone have any experience

Just wondering if others have had issues with B12-raised hypertension? I've suffered with hypertension for a while (>5 years) and it has gone through periods of being controlled by medication, only to see the blood pressure start to climb again after a year or two, necessitating a change in medication

Good morning all I just wanted to update you on my previous post. All blood tests came back normal apart from very high B12 and Folate and a note under differential white blood count saying "RBC show mildly macrocytic picture" MCV & MCH were still abnormal but lower than a couple of weeks previously

I’ve been and am quite unwell and thought it was T3 but recent private blood tests show something else? (Tested 24 hours between Levothyroxine). * TPO 933?? I’m not sure how to proceed to get back to functioning and feeling normal. Been taken all recommended supplements, but perhaps I’m not absorbing

Just wanted to thank all the forum members who replied to my plea for help yesterday. Thanks for allaying my fears a bit, and giving me some hope that I might get through this, and not do something silly. I'm still in a pretty dark place (thanks to B12 deficiency), but as a result of reading your replies

I was interested to read a recent post regarding supplements and the timing of taking thyroid meds if one is taking certain supplements. I had a test in April which produced the following results: Ferritin 214 ug/L; range 30 - 518 Vit b12 active >150 pmol/L; range Vit D 160 nmol/L; range 50-250

Can I have some advice as to what I should do. Even though my energy levels seem ok, I have been feeling anxious, brain fog, suffering from palpitations and starting to feel low mood too. I wasn't going to get these bloods done until October but then decided I would - regardless of the cost - as I