Experiences with

Lazersporin-C

I started my medication journey in June 2024 and really struggled with adverse effects. I would like to post some experiences so that people starting their journey do not feel alone. Side Effects from Medicine: Stage 1 ( week 1 to week 8 ) This is a combination of ethamutabol/rifampicin/pyromiazide

Morning all,Following on from my post yesterday - my blood test results on 25th April were TSH 5.9mu/L B12 193ng/L Folate 2.9 ug/L T4 12.8pmol/L Vit D 25.8. I was prescribed 50 micrograms thyroxine ( various brands given - currently using Accord brand). Initially I was prescribed folic acid for 4

Hi everyone, I am planning to do Medicated FET in January and wondered if anyone could please give me some advice. Is it worth taking extra vitamin C? I am now taking the following supplements. - Proceive - extra Vitamin D (2000 IU) - Optibac (two a day) I’m going to start taking these few

There’s an old saying that it’s what’s on the inside that counts, and that’s very true in relation to your health, including that of your skin. For most people, their skincare routine is all about what cleaners, toners and moisturizers they use. But, that’s only a very small part. Your diet is not only

[i]After every night there will be light[/i] 💓 Hello everyone out there, sick people and relatives. 👋😊 I wanted to give you all an update on my rehabilitation. 🤕 I have been at home since June 24th after a 16-day stay in hospital following an encephalitis of unknown origin (probably autoimmune

I’m new to taking meds for my ADHD and have a lot of questions! I felt absolutely nothing with 5mg adderall 2x day last week so my dr said to double it and take 10mg at once. I tried that for two days and still didn’t notice much, maybe a slight decrease in appetite and staying awake later but I’m still

Could someone help me with my blood test results please? They were done about two weeks ago, and I have seen the Dr. since to discuss the results. My TSH level had gone from under I to 3.7, I presume because she had cut my Levothyroxine down from 125mg to 100mg. I had been suffering some hot flushes.

Please accept my apologies if this question is off topic to this forum. A recent blood test shows that my Phosphate is slightly below range (see attached photo). My daily diet consists of eggs, chicken, milk and fish. I also supplement magnesium, Vit D, Vit C, Selenium and a few others to support my

Hi Everyone, I`m in the ongoing battle with PMR inflammation ,and Predisolone side effects . Is there a consensus about useful supplements to take . I`m already on Multi vits/minerals , vit c , vit b complex , cod liver oil . Omeprazole . I`m worried about bone density and have been suggested alendronic

I am preparing for my next endo appt in about a month so I thought I would privately test my TSH, T4 and T3 to see where I'm at. I tested at 9am and stopped my B complex a week before. TSH 0.3 (0.27-4.2) 0.76% T4 15.3 (12-22) 33% T3 4.1 (3.1-6.8) 27.03% I've been taking 100mcg Levo for about

Had my iron tested for the first time 8 months ago when my ferritin was a lowly 22. I've been taking iron supplement (with vitamin C -and a probiotic- more recently) as suggested by Sue and others on here since then and had a retest last week. Ferritin is now 78, so improving. I'm not noticing any improvement

Hi all I discovered in May that I had Intestinal Metaplasia and this was a real shock. I’ve had abdominal pain, stomach cramps, diarrhea, bloating, difficulties with digestion, excess gas (sorry!) for a long time. Also feeling of fatigue and low energy and mood. Then I only had blood test last week

Hi from Australia! i have joined this forum after searching for alternative treatments to chemo for my dad (83) CLL 8 years on. I am very open minded with a slight bias against chemo after watching my mum suffer and pass from breast cancer. So not wanting my dad to have chemo unless it’s a last resort

So I thought I would finally post my recovery on here. I’ll backtrack a little bit. Some of you may remember in 2010 I was in a car accident and I had undiagnosed cervical/ jaw dystonia for a decade and my B12 issues started then, pernicious anemia runs in my family and I never felt the same after that

I have been reading the posts about Iron Bisglycinate for a while now and thought that is wasn't for me because I have had bad reactions to iron before and I had a transfusion of iron a couple years ago and my ferritin is still over 200. But, because of the urging on here, I tried it and it is amazing

Please try 1000 mg time released Vit C it stops atrial fibrillation

Hi all..... So, I've been following the forum for years. I rarely post because I haven't had much to contribute. First off, let me express my most sincere thanks to all of the regular contributors that this forum has been blessed with. I could list them but you know who they are. I must mention

Hi. I was recently diagnosed with hemochromatosis based on slightly off bloodwork and genetic test. Neither of my parents had hemochromatosis but both were carriers and I inherited the gene from both. My ferritin is currently 111 (I previously always had very low ferritin and actually had one transfusion

I'm currently on loads of different supplements to try and help boost my immune system, reduce inflammation and for joint health. Recently when I'm having a flare up the joint pain isn't getting as bad as it used to, I'm wondering whether it's the supplements helping or that bechets is so unpredictable

I've been following advice on here and taking iron bisgycinate usually with some orange juice before going to bed on alternate nights. However I haven't noticed any improvement in my RLS and I want to change to taking a vit C tablet instead of the juice as I can probably take that more consistently.