Getting blood test for nutrients not found in ... - Myositis UK

Myositis UK

1,264 members515 posts

Getting blood test for nutrients not found in common blood test

Eliotf profile image
1 Reply

I have a few questions for the group. First my background information: I am in the USA. My diet/eating habits probably won’t change. My eating habits are only ok. My blood is drawn all the time: cbc, wbc, etc and every 6 months my complete thyroid panel is drawn. I have hashimotos, CLL and they are well controlled and /or stable It’s the dermatomyositis and a few other disorders that seems to flare up. I will be going to a naturalpath & nutritionist/dietitian. My questions are: what nutrition blood panels & or specific tests can I run for a more fuller picture and to see the less common nutrients? Are those freeze dried ‘super greens supplements’ any good ? And of course I am also looking for micronutrients and finally the magic ingredient/pill.

Written by
Eliotf profile image
Eliotf
To view profiles and participate in discussions please or .
Read more about...
1 Reply
Mustgetaroundtoit profile image
Mustgetaroundtoit

Hi, from soggy UK! Very interested to see how you get on. I have Polymiositis/Dermatamyositis, Arthritis etc,etc... taking various drugs.I've been feeling rotten for some time, and feel that diet/herbal supplements etc may be worth looking into.

I have a blood test on Thursday looking at the same as yourself hopefully, so will see if I can find anything useful to report.

I'm also Gluten intolerant, which I think affects nutrient absorption and my state of health.

Any results and suggestions from my GP I'll let you know!

Kind regards.

Not what you're looking for?

You may also like...

mistaken diagnosis

Hi I’m just wondering if myositis can be mistaken for PMR ? I am asking because 2 GPS say i have...

Anyone have Drug-induced Myositis?

Hi, I've had a diagnosis of MCAS (Mast Cell Activation Syndrome), but I had an argument with my...

Anyone get calcinosis?

I'm still VERY far from getting a diagnosis (thank you, NHS) and I'd have given up long since if it...

IBM people, please post

I have just found my way to the new site. I hope all those with IBM will as well. I miss your...

Could I have dermatomyositis?

Firstly let me apologise for the length of this. I know it's not a good idea to ask for diagnoses...