Yolanda Hadid Opens Up About Her Battle With Lyme Disease, Awarded Lifetime Achievement Award for Advocacy


Yolanda Hadid is contining to be a strong advocate for Lyme Disease. Right after announcing her the release of her book, she has been awarded with a Lifetime Achievement Award by ProHealth, Inc.

The press release states, “We’re honored to award Yolanda Hadid with a Lifetime Achievement Award for her efforts to foster awareness about chronic Lyme disease and for her courage and willingness to share her story publicly, as she also battles to recover from Lyme.”

Hadid shared the story about her initial diagnosis with Lyme with Pro Health.

“Before I got sick, I was a hardworking multi-tasking butterfly that could do anything. Nothing was ever too much for me! I was a single mom raising three kids in Santa Barbara. I was a busy bee, always going, 24-7.

Then, I started to have flu-like symptoms that were cyclical; I would have severe joint pain, and it was as if I would get a bad flu every two weeks. But when you are such a high functioning person, as I was, you always find an excuse for the symptoms. I told myself that I was working too hard, or that I was driving too much, or that I wasn’t getting enough sleep—things like that. So I went through a whole denial stage at first.

I went to Germany and tried lamb stem cell therapy, which ended up helping me remarkably. Literally overnight, the joint pain disappeared. But I continued to have severe fatigue, as neurological and brain symptoms started to set in. For instance, I started to not recognize people, was suddenly bothered by noise and began to have memory issues—that sort of thing. I saw many doctors, all of whom tried to treat the symptoms rather than get to the root cause of what was wrong with me.

I did that for maybe a year before moving to Malibu in 2011, right before I got married. Then, I remember being in the gym one day, getting ready for my wedding, and all of a sudden I realized that I couldn’t do one more push-up. I looked at my husband-to-be (David Foster) and said, “You know what? I’m done. I can’t work out one more day.” Five years have passed, and I haven’t been to the gym or worked out like that since.

In the meantime, while I was in Malibu, I continued to see doctors but everyone around me was saying things like, “You are (feeling badly because) you’re doing too much; between getting ready for your wedding, doing your show in Holland, and so on…you are overworked.” But I knew this wasn’t true, because I used to thrive on that kind of lifestyle. I told them, “That’s not what is wrong with me.”

The doctors at that time gave me a whole rundown of antidepressants and medications; things like Ritalin and Adderal, to try to speed up and improve my brain function, but none of their treatments resonated with me or made me feel better. Yet I knew something was really wrong, because I would get circles, or rings, under my eyes every 3-4 weeks that would come and go. I would tell the doctors that it was as if something like a bacteria, was growing in my brain. But the doctors would tell me that I was wrong.

At times, I would go to the hospital with severe migraines, but the doctors would always just send me back home and tell me that I had chronic fatigue syndrome. However, I knew that because of the cyclical symptoms that I had, that it wasn’t chronic fatigue syndrome; that there was something in my brain that was causing symptoms to come and go.

Then I went to Belgium to see one of the top chronic fatigue syndrome specialists in Europe, and he ran some tests on me. Six weeks later, he called me and said, “You have chronic neurological Lyme disease. You need to get a port and start intravenous antibiotic therapy.” And that’s where my healing journey really began. This was in 2012.

At the time, I didn’t know much about the difficult detoxification reactions that could happen with intravenous antibiotic treatment. These reactions occur when microbes die in the body and release neurotoxins into the bloodstream. If I had known then what I know now, I’m sure it would have been a totally different experience for me (because I could have prepared for those reactions).

Once I started the antibiotics though, it was as if my body just shut down. I would be sweating on bathroom floor, feverish, sick, and in the end, the medications didn’t really get me much better. And, as I started researching—and I’m a pretty matter of fact kind of person—I realized that there is no cure for Lyme.

Once I really started educating myself about it, I thought, okay (the research shows that) they can’t kill Lyme in a test tube, which means that popping antibiotics for long periods of time doesn’t make sense. Doing antibiotic therapy never really felt right to me, anyway.”

Yolanda also shared how she is currently doing with her Lyme battle.

“I’ve pretty much traveled the world and exhausted every possibility of being able to figure this disease out. In the end, I took the road of “underground medicine” and studied and tried just about any and every (treatment) out there outside of conventional medicine that I thought could rebuild my body and make my immune system better. Those were a crazy five years, but now, I’m pretty stable compared to where I once was.

I continue to see a renowned integrative Lyme specialist, Dietrich Klinghardt, MD, PhD, every six weeks, for treatment. I also have a health advocate who works with me daily. I do a variety of treatments to eliminate the infections and rebuild my body; drips, shots, homeopathy, low-dose immunotherapy—many different things. I feel that if I keep hitting the infections from different angles that it will be beneficial and I hope and pray that one day, I will just wake up and be ready to get on with my life.”

She also shared how her children Bella and Anwar are doing with their Lyme battle.

“They are doing good. They are also under the care of Dr. Klinghardt. Looking at them keeps me extra motivated every day. They are young, and much more resilient than I am, fortunately.”

But Hadid is still motivated to find a cure.

“When I get words of ignorance from the world, it makes me stronger and just creates in me a desire to fight harder. I feel very strongly that God gave me the gift of being able to deal with all of the adversity, criticism and nonsense around me. It doesn’t make me angry. Somehow, I have the ability to just let it roll of my back and keep trekking forward.”

Yolanda has been doing some soul searching on vacation in Tahiti. Check out her photos below.

❤️Sun kissed, Tahitian style………. #Maruru #Tahiti #Summer #IslandLife

A photo posted by YOLANDA (@yolanda.hadid) on

❤️Choosing to make the rest of my life, the best of my life……… #Sunrise #salute #Intentions

A photo posted by YOLANDA (@yolanda.hadid) on

Photo Credit: Bravo



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