Is Chronic Lyme Disease curable?
Katina Makris tells of her Chronic Lyme & Fibromyalgia Healing Journey
After getting more and more sick for 5 years, learning she had Fibromyalgia & Chronic Lyme Disease, Katina had to ask herself questions like “is fibromyalgia curable” & “is lyme disease curable”
When you hear so much negativity, then after being diagnosed with Fibromyalgia and finally learning you also have chronic Lyme disease, you have to ask yourself if either and both of these are curable. Katina Makris wanted to help others learn from her experience so that they could recover faster using what she learned from her own Chronic Lyme and Fibromyalgia Syndrome recovery. In this interview she talks about how the illness led to her life falling apart and how she hit rock bottom only to turn it all around.
Katina’s story is a testament to the human spirit and the power of having a positive mentor. Listen carefully to the realisations Katina made about how to recover from Chronic Lyme Disease and Fibromyalgia Syndrome.
Katina Makris has published her book Out Of The Woods and has a website to help other people with Chronic Lyme Disease and Fibromyalgia here: https://www.katinamakris.com/
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I found this interview very inspirational. Thanks Katina!
Wonderful talk. Very inspirational.Recently I attended a talk about the 1918 bird flu.One of the scientists mentioned that it wasn’t the weak that died but more the strong young fit adults.He believes that their immune system was so strong it killed the virus but then did not shut down unfortunately killing the person as well.Sounds like us. Fighters to the bitter end.
Yes indeed, most of the illness symptoms is actually caused by the immune system fighting the infection.
Indeed, people with ME/CFS/FMS are often too tough for their own good – time to be more gentle and nurturing with oneself!
I found this very inspirational and informative – Thanks!
Very inspirational, thank you Katina and Dan. I am trying to watch a video a week and read a page of your book Dan, hard for my brain to cope with the info but I am feeling a bit better for hearing all the positive stories and finally some hope for the future.
Great to hear! Did you download your copy of Discover Hope?
Yes Dan I am currently reading that and I have just purchased your book “cfs unravelled”. My specialist said I was the worst he had ever seen. 12 months testing to confirm cfs, they said it was a virus that hit at my heart which had excess fluid and I have very low blood pressure and very low heart rate which struggle to be above 40bpm, I spend most of my time kissing walls and floors with vertigo and dizzy, worst part was when I was diagnosed the doctors all said nothing we can do for you, just go home… Read more »
It’s frustrating to get so little help.
However, the advice of ‘rest’ is sound of course, but in my experience seldom followed.
It’s important to learn that REST is something that goes beyond lying in bed – it has to do with FEELING like you are resting.
You might like to check out Katie’s recovery interview, she explains it well: https://cfsunravelled.com/katie-shares-how-she-broke-out-of-mecfs-relapse-cycle-to-make-full-recovery-from-mecfs/
Thank you Dan, I will check that video out. Rest I did at the time, became bed ridden so no choice. I have been meditating for a long time, at first I thought no difference but persevered and I can feel the difference now. I am learning more and understanding so much more thanks to you xxx
Katina’s story resonates with me. I am terribly sick with late stage Lyme disease, co infections, biotoxin illness, autoimmune issues, ME, etc. I regret doing antibiotics. Here is my question: what do I do to find a knowledgeable homeopath ? I live in a state that has very few . Money is holding me back. I am home bound since 2012, but sick was before that. Tick bite was in 2000 Any advice.
My view is that normalising ANS function is key for recovery from ‘chronic’ lyme disease.
For specific questions around homeopathy, you would be better of asking Katrina via her website! 😉