DNA, food allergies and vitamin deficiencies.

Before the end of the year I had a bunch of bloodwork done which included DNA testing, standard tests such as cholesterol; and hormone, vitamin, and allergy tests.

I got all the test results back last week. I believe all the information I now have will help me in the treatment of my disease.

The DNA results are interesting. I have information that can be given to my rheumatologist as well as other doctors to help make decisions about medications based on my genes.

I found that I have two food allergies. I am allergic to milk and egg whites. In the past month or so I eliminated both milk and eggs on the autoimmune protocol diet (AIP diet) so keeping them out of my diet permanently should be fairly easy.

I did some reading about milk and egg allergies and how they manifest, and there is some evidence that they can cause an autoimmune response. So hopefully keeping them out of my diet will settle my immune system down some.

My vitamin levels are out of balance as well which is not uncommon in RA patients. My vitamin D is very low, as is my vitamin A, and my vitamin C level was almost nonexistent. I couldn’t believe it because not only do I eat copious amounts of fresh vegetables and fruits, but am religious about taking my vitamins and supplements. Thanks RA for yet another fun aspect of the disease.

I’ll be starting a prescription vitamin blend based on my needs and genetic make up. So my levels will be brought to the best level for me not the broad government standards. It will also have a substance to help me absorb them since my body is not doing it well enough on its own.

Once my vitamin D, C, and A are brought up my hormones and other levels should become balanced and I should feel a lot better!

I’ve stayed on the AIP diet through the elimination phase and just added legumes/beans back to see how my body responds.

I also have a call into my rheumatologist because I believe I had a reaction to the last Kevzara injection I did on Tuesday. I’ve had similar site reactions like I did with Humira, and had a significant rash/hives within 24 hours of the last injection.

We’ll see if she wants me to continue treatment or hold off. I would be willing to take a break from meds and pursue the AIP diet knowing that the 2 food allergies could have been impacting me greatly.

I still believe remission is possible and that my body has the ability to heal and be well.

I’m definitely persistent enough to keep trying.

Gut health and hope

I know I’ve talked about gut health imbalances and the link to autoimmune diseases.

Believe me I’m skeptical of products that make claims that they can fix or cure my disease. I’ve researched and tried numerous products and foods with no success.

On July 4th I started taking Plexus slim after having lunch with a friend. I believe our meeting was meant to be because she did not meet me to discuss the products she distributes. Our conversation evolved and before long we were talking about my RA.

She told me about her best friend that has MS and RA and how she’s used these products and gotten off meds and is in remission.

This wasn’t a testimonial from someone who is thousands of miles away but someone who is a person that I could call if I wanted to. I was intrigued.

So I started using Plexus slim to only introduce one thing at a time in hopes of balancing my microbiome. There are numerous scientific studies about RA and gut health. A lot of RA patients have an overabundance of one particular “bad” bacteria and not enough good bacteria.

I started this before Humira could possibly work and noticed a difference within a week.

I firmly believe the product is working.

Humira takes time to work and I had only one injection before taking Slim and setting results.

My pain and inflammation is much improved.

I’ll be discussing this with my rheumatologist since she recognizes that we are seriously behind in research here in the US.

I’m still having issues with Humira and side effects. I’ll take another injection this Friday but if the side effects continue she wants to discuss another biologic.

I’ll be discussing taking a break from meds altogether and seeing if I can go into remission on my own.

I’ll be smart about it and certainly she can track my progress by blood markers.

If you’re interested in talking about the products I’m happy to have that conversation. I will be distributing them now myself. That’s how much I believe in the link to gut health and autoimmune diseases as well as other issues.

Weird side effects…

Because life just likes to mess with me lately… I spent a few hours in the ER with what appears to be an unusual side effect to the Humira I injected 2 weeks ago. I thought it was an allergic reaction but the doc and my rheumatologist think it’s an unusual side effect to the meds.

I admit I was a bit frightened because my lips started burning out of the blue, almost immediately my arms began to burn, and a rash started at my knuckles and went all the way up my arms to my neck. It burned really bad but was not itchy.

So they gave me a steroid through the IV and guess what? I had a rare side effect from it. 0.01% of people get it…go figure.

I was supposed to take my 2nd Humira shot tomorrow but my rheumatologist said to hold off and let my body settle down. I will take the shot next Friday.

In the meantime as a precaution I’m getting epi pens that I’ll need to carry with me.

On the bright side…the steroids will ease my pain for a few days.

What a journey. #makeitcount