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My life since discovering LCHF

Oh my gosh Poshtotty - what a wonderful, wonderful story. !! How amazing. You've made me smile.

I've found LCHF marvellous too for general energy and wellbeing, as well as BG control.y only gripe is rather awful hair loss, but it should grow back.

How wonderful.
 
That really is brilliant @poshtotty .

Can I ask how long it took for those particular LCHF benefits to kick in?

Thank you. I started LCHF in March last year and gradually weaned myself off all RA meds, starting with the nasty Methotrexate, until I was entirely free of all RA meds by July last year. So almost 12 months. By November last year my disease activity had reduced to the 3's. Curiously my RA has responded better to the LCHF than my diabetes has done. My only intention was to improve my T2. The improvement in my RA was purely accidental.
 

Thank you. Yes, I've also suffered hairloss. Mine is thickening up again which I attribute to Vit D twice daily
 
What an inspiring story. I missed it first time around (I'd not been diagnosed when it was first posted) and it's just a real tonic to hear of your success.

Well done, and thanks @poshtotty .

Thank you. LCHF really does work, and perhaps not in the ways we expect it to!
 
Keep up the good work - I'm so pleased for you and love hearing about success like yours!! X
 
Thank you @Debmcgee. It was written a while ago but have been able to maintain, if not improve since. I enjoy reading your progress and you have my admiration. Keep up your good work too
 
What a very inspirational story! It is a constant experience, how medical professionals are so reluctant to accept health improvements that are so significant, it never fails to amaze me why they aren't curious and eager to discover how we have made such huge health improvements. Never once has my doctor asked how I have healed myself, when I try to tell him, he just dismisses what I say, saying it's simply weight loss, any diet would do it, and am I still refusing to take statins?
 
Simple - there's no money on food cures for the pharmaceutical companies....they want us to be ill
x
 
Thank you for such an inspirational story and I am so glad that you found that pair of heels!

I have been LCHF since the 10th February (I decided to give up high carbs for lent.....anyone seeing the irony here!). I had a blood test on the 3rd March which gave me an HbA1c of 118 and a BG reading of 17.7!

So much has changed from my official diagnosis on the 15th March it seems like a lifetime ago. I am now testing my BG regularly (thanks to the advice on this forum) and my last 7 day average was 5.9.

I am eating fabulous food, And now have the ability to fast for a day And feel well And not be starving hungry.

I have energy so much energy, my days are now packed instead of dragging myself through them with the desire to get back on the sofa for a snooze ASAP.

I have joined a gym And love swimming, Aqua aerobics, working out, And a rather funky dance class in the dark with glow sticks that brings back my miss spent youth! Yes me the old excercise dodger loves to work her body who would have Guessed!.

I have lost 14 kilos since the 10th Feb, And am currently sitting here in a pair of trousers that I used to wear when I was 6 kilos lighter than I am now so my body has changed shape.

But best of all that foggy feeling that feeling of I feel really down but do not know why that General feeling of "Meh" has gone.

So glad that i discovered a) this WOE and b) this forum.
 
Thanks @Lindy1706 and @AtkinsMo. Although I posted this back in 2014, I'm happy to report that I'm still in remission with my RA

Interestingly, I've also found that although I don't visit my GP very often, whenever I do, he always seems to have plenty of time for me. I've convinced myself its because I'm saving the NHS a lot of money on medications!

LCHF is no fluke! Let's all keep up the good work.
 
Well Poshtotty what a wonderful story. I was on Methotrexate (has anyone noticed the first four letters are M E T H!!!!) until last Monday when I was taken off it because of a cough. Obviously I will be offered it again when the cough goes. I don't know if I want it. I was taking it because of Psoriatic Arthritis and had noticed some improvement in my condition. But I still don't know if I want it back!

I have a whole book of complaints PA, Heart disease (aortic valve replacement and triple bypass), Psoriasis (about 50% coverage), Cervical Spondylitis, fused Pelvis, Fibromyalgia, ME, IBS, Diverticulitis and a few more. Oh yes...forgot diabetes I started eating LCHF on Tuesday of last week after joining the forum with the hope of reducing my BS readings (in the high teens) so I have a long way to go! I have not found it difficult so far but my dear Husband cooks anything I want to eat so I am very lucky. I have yet to clear this with my GP!

I sincerely hope I have half the improvement you have had Poshtotty.

BTW.. I was pointed to your post by AndBreathe, many thanks to him/her.
 
I was also on methotrexate for about 15 or so years for psoriasis and psoriatic arthritis. For most of that time very large doses (30mg) that had to be taken by injection because of the stomach side effects. I believe it stopped doing me any good many years ago but the docs wanted me to stay on it to compliment the biologics I also take. Due to paperwork snafus I lost access to my current biologic (stelara) for about 6 months and everything fell apart. I looked like I had second degree burns to about 80% of my body with the psoriasis flare. PASI score of 90. My CRP was at 33. The methotrexate did nothing so I stopped taking it, no change. Once I went back on stelara I cleared up almost 100% within about 3 weeks. Methotrexate has caused damage to me, including making my hair thin and brittle. This is not a vanity thing so much as a realization that hair is a huge indicator of overall health. What is also interesting is that during this period of time when my immune system was left to go nuts, my diabetes exploded out of control and yet my arthritis did not really flare at all. Weird. It does point to type 2 being, at least in my case, immune mediated as it stayed under control with little effort from me the whole time I was on biologic immune modifying drugs. Now that the beast is loose, however, it is not being easily controlled at all and I am struggling. LCHF with the addition of metformin and forxiga is the only thing that seems to help but it is not 100% effective any more.
 
Wow! What a brilliant story!
I’ve got RA & steroid induced diabetes amongst other inflammatory illnesses. I’m also on Methotrexate and have suffered no side effects on it as yet. I’m at the beginning of my LCHF journey and you’ve so inspired me!
 
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