Experiences with

Potassium citrate

If im going to mtn bike hard that day Ill drink two liters of the electrolyte mix In one liter of water - Taurine 8g powder – Nutricost Brand Magnesium Chloride 500mg powder – Pure Brand Potassium Citrate 1400mg powder approx. 1 ½ teaspoons- Bulk Supplements Brand Beet Root Powder 1 Teaspoon –

Just wondering if anyone has had any similar experience and managed to find any alternative to Potassium citrate. Will 1234

(Magnesium citrate, plus : Electrolyte complex - Ingredients: Calcium salts of orthophosphoric acid, Potassium Chloride, Sodium Chloride, Magnesium Oxide, Potassium Citrate) Everyone always talks about being careful with T4, and takingT4 in the middle of the night always works well for me.

Currently on Potassium Citrate. Are there any new treatment’s?

I am thinking of H500 that contains H-500 Proprietary Blend (Potassium citrate, Magnesium citrate, Potassium ascorbate, Silicon dioxide, Sodium Borate).

POTASSIUM 3.8 --> 3.5-5.3 mmol/L Interesting, I put 1 teaspoon of Potassium citrate in every water bottle. about 1,700mg of potassium citrate. I buy potassium citrate by the kilo .

History of urinary tract infection I have had this infection for 3 years, Escherichia coli always comes out in the urine culture, except for one time when Proteus came out. For treatment I have used ciprofloxacin, amikacin, nitrofurantoin, levofloxacin (but there was resistance to it), Amoxicillin

I have been taking 1,000 mg of calcium citrate tablets daily, these supplements come in capsules of 100mg of elemental calcium each, therefore I’m taking 10 spaced throughout the day. My GP says why not take Calcichew 500mg twice a day instead? I’m hesitant because they are calcium carbonate. Have

Hello, I posted sometime ago. I live in Spain where I had a second thyroid ablation because of hyperthyroidism/Graves’ disease back in March 2024, the first being a year earlier. I then became hypothyroid some time in June/July and started at 75mgs of eutirox which was increased to 88mgs @ end August

PCa Friends, Due to cancer EXTENSIVE bone-mets ADT therapy and triplet therapy, the Dr. told us I have to take CALCIUM and D3 and so I went to the pharmacy and quickly bought NatureMade gummies (Tricalcium phosphate 500mg and Cholecalciferol-D3) cause my multi-vitamin didn't have enough. I'm nearly

I have quite bad RLS (every night) for the last 12 months - had it sporadically before for maybe 15 years. I am in the UK (England) Been consuming all the info on this forum for the last 6 months. The point of this post is to seek feedback on Prof Evangelou (Notts) who is mentioned on here as

Hi everyone, any thoughts re- latest results? Feels like the latest one is going in the wrong direction! Started a T3 trial with Roseway , back in July . I have an appointment with them this week.Results 21/6/24 TSH = 2.28 , T4 =19.5 (12 -22) 75%, T3 = 4.5 (3.1-6.8) 37. 0% After being on 75 mcg

Unfortunately I never got round to joining the PMRGCA uk ( brain sieve forgets to do a lot of things!) and so didn’t hear the speakers from the latest AGM. I have joined today! I was never prescribed calcium when I was diagnosed a year ago. I was told to buy Vitamin D 3000iu and I take it daily ( vitD3

Hello! I would be really grateful for some help, please. I have started on 50mg of eutirox since end July, after RAI treatment at end March. These are my latest test results, taken before food at 9.30 am Calcium, serum 9.2 Phosphate, serum 3.3 TSH 22.8 T4 free 0.89 T3 free 1.38 RT3 0.24 Anti

Morning all, I previously messaged about my husbands severe rls a few weeks back and since then and with advice from this forum he started taking magnesium citrate, vit D 3 and oral iron supplements despite ferritin >100 at night. His rls symptoms have improved greatly which is so good, the PLM and rls

My finger nails are in quite a poor way these days; they are weak and badly ridged. I’d be really grateful for tips on what others use/find beneficial. My diet is good, also vitamin levels. I’m on MTX subcutaneous 25mgs and have today started Tocilizumab subcutaneous. I take calcium citrate, magnesium

After Helen's last set of results we decided to take things into our own hands and start with some supplements after a long discussion with Greygoose and Jaydee 1507 we have been useing the following: 1. Magnesium Bisgycinate which has been changed to Magnesium Citrate as Helen became bound up, However

An atypical facial eruption in skin of color: A rare presentation of histiocytoid Sweet syndrome, 2024. https://www.jaadcasereports.org/article/S2352-5126%2824%2900087-0/fulltext - Normally red to purple lesions in Sweet's syndrome. - Doesn't disproportionately affect specific racial groups. "Although

Finally got an emergency blood test yesterday, results today, GP did not ask for potassium which my symptoms were an exact match to low levels! As expected with the high dose of steroids, results all over the place. Liver (Moorfields thought it was the steroids last week), kidneys now and thyroid TSH

when I last had a full blood count, I got the results back in a folder and a lot of things were below range, but the gp said not to worry they are ok,and my serum calcium level is below low reference limit, I have got osteoporosis now because my testosterone has never recovered, I have got some calcium