Vitamin D and M.E.: Hi :) - I'm just... - Myalgic Encephalo...

Myalgic Encephalomyelitis Community

2,086 members651 posts

Vitamin D and M.E.

Covenham profile image
4 Replies

Hi :) - I'm just wondering if anyone here takes Vitamin D as a daily supplement and if so, which brand and how much please?

I don't drink milk and avoid milk-based products, as I suffer with Bronchiectasis. I do eat oily fish several times a week and I also have fortnightly B12 injections.

I'd be very interested in anyone's response; thank you :)

Written by
Covenham profile image
Covenham
To view profiles and participate in discussions please or .
Read more about...
4 Replies
Brick1 profile image
Brick1

Hi,

I take Vitamin D daily. I use a company called Cytoplan as they are very good.

Hope that helps :-)

Lisa

ME65 profile image
ME65

Hi. Yes, I take vit D every day. I get mine from Nature's Best. It's £8.95 for 180 capsules of 1000mg D3. Here's a link naturesbest.co.uk/vitamin-d...

I have bought supplements from them for years, they are very good quality. You may also find CoQ10 and L-Carnitine useful along with the vit B12 injections that you have. This combination is recommended for helping with energy levels and it certainly works for me :-)

Good luck xx

sarkan profile image
sarkan

My son is on cod liver oil with vitamin d in it,iron supplements are also recommended to help alleviate fatigue.u need 2have a high protein diet including breakfast,graded exercise is recômmended if u can do that,u seem to have a lot of fish in ur diet already,tuna has the highest protein content xx

Covenham profile image
Covenham

Hi - I just wanted to say Thank You to those who put Replies on my Post; apologies for taking so long to acknowledge you. I really appreciated your comments - thank you 😊

Not what you're looking for?

You may also like...

Possible M.E.

Hi! I am new to this site. I have been looking for a while to find a community which may be able...
RachelHNC profile image

What cause your M.E.

What does everyone here think caused their M.E., not what the doctor said. I had a full time job...
Evelyn61 profile image

M.E. Association Petition on Change.org

Hi, Is everyone aware of this petition set up by the ME Association saying the NICE guideline is...
Mewser profile image

Could I have m.e.?

Hi, this is my first time using this service so go gently on me lol. I have an under active thyroid...
mills2k19 profile image

Anyone suffered from undiagnosedHypothyroidism symptoms after being diagnosed with M.E

I was diagnosed with M.E 30 years ago after contracting the Epstein Barr virus. I suddenly...
Annealise profile image

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.