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Saw this today and loved it. So glad Dr. Krzysztof is there to help people sick with Lyme Disease and to educate. May many follow in his footsteps.

I'm in Texas need help

Your enthusiasm is contagious, I'm now excited about this topic too.��

Thank you Fred! Dr Majdylo do you treat people with Lyme’s who also have Babesia? What type of treatments do you use? Thanks very much!❤

I was bitten in 2014/5 and still cannot get tested! I have Morgellons im in agony i have diagnosed Arthritis copd heart problems chronic lowe back pain paraesthetica in my legs. Why am i being left to die in agony?? Help.

Thanks brother Fred and Shelly she explained this stuff so well almost got me thinking I have some hope left I was back in emergency yesterday in Golden BC what are the doctor denied that I have limes and said it was Polymilgia and gave me a month's supply of the higher dosage did last month prednisone the girl that took my blood said they don't do Lyme test in Golden I reached out in desperation on Facebook found out there are lime cases an hour and a half South so I'm pretty frustrated he wouldn't get the test for me after seeing me 3 days after I ran out of my last prescription of lower dose was downhill really fast once I did the smaller doses was able to get 3-hour sleep last night before the pain woke me up great information from Shelly when she mentioned turmeric which I have been doing fairly regular for 8 years after I had a tick bite on my kneepit that just exploded it was swelling and pain and an old fella introduced me to it I've been using it for joint pain since as I do not like doing pharmaceuticals taking me a while to write this haha and I think maybe I can give some other people hope I will cut this short cuz I can Babble sometimes and I have some phone calls to make thanks again

Just found your channel on RUclips I've been suffering from extreme burnout and headaches for about 5 years and then about 2 months ago I pulled a tick off my dog the next day I pulled a tick from behind my ear now I'm in such severe pain it's crazy started seeing a new doctor he prescribed some hormone pills for me for a month ran out last week and it is again really bothering me I'm seeing a doctor this afternoon I'm going to ask him to give me some ivermectin what do nice folks think?

Does Gen Lyme also deal with co infections?

Thank you so much for all your work!

Fred, You are my hero, even though no one I know would take the time to read the book! 😢 Thank you so much for the work you do, and you deserve WAY more subscribers❣️

Reach out to Fred Diamond on Facebook or LinkedIn to request your complimentary e-copy of "Love, Hope, Lyme: What Family Members, Partners, and Friends Who Love a Chronic Lyme Survivor Need to Know."

Love this and will join them today, so supportive, thanks Fred!

Fred... this podcast is so encouraging for those of us that have battled Lyme for years with varying degrees of success in recovery. My mom, sister, and I were diagnosed almost 25 years ago in NYC by a wonderful doctor named Bernard Raxlen. He was the last doctor in a succession of 18 to 20 to examine my sister. She ultimately succumbed to her illness and passed away in 2015. Thank you for continuing to educate folks on this dreadful disease. ❤

Thank you!!❤❤❤

I'm in Texas and can't get help

Severe v injured and so glad I started high dose vit C last week I can feel my body coming back.

Loved this, am buying her book and am grateful for all the great tips about MCAS, thanks to both of you

Would you be open to additional data, insights, data analytics, etc, for your next book?

I have tried getting in touch with you before. I need to know who this California Lyme doctor is. I am being treated by a general practitioner and he doesn’t hear me. He doesn’t hear my depression. He doesn’t hear my solitude that I just stay in my house or my room. He doesn’t hear me when I say I can’t breathe good. He says it was only Lime and he gave me 30 days of Doxy Sillen.

Thank you for recognizing the financial burden of this disease and offering a free PDF for Lyme patients. ❤

The cash register is the #1 concern. Lost my brother to sepsis at J.H. and I can guarantee you not one drop of IV C was dosed to him.

Get methylene blue. It kills all infections and supports mitochondria. These people are just talking heads.

Thank you for the informative session. Is there any effort for finding novel agents for bart just like hygromycin was found for lyme? There could be low hanging fruits there. It seems bart especially is somehow much harder to kill than lyme. Previously test tube research has been done on bart but i dont see it make much impact in clinical practice. This seriously needs some good attention.

We need insurance to cover the labs that can best detect these infections

Loved this, very informative and gives me hope, thank you, I will be looking forward to many more.💚

Thank you SOOO MUCH about Lyme’s particularly Babesia. Plus I have Fibromyalgia, Hydrocephalus, Hashimoto’s but the Babesia has caused such brain fog it’s awful. Does Babesia etc also cause neuropathy? This podcast was tremendous & bless you both & your Alliance & researchers for caring!! Thanks again!❤

Thank you both for doing what you do for us!!! I went undiagnosed for 25 yrs with chronic lyme. Because dr.s were told they would loose their medical license if the diagnosed or treated us for lyme.

I am in central Wisconsin, a high infestation state of Lyme disease, and still, mainstream medical people are not educated correctly about Lyme, and that per CDC Lyme is diagnosed by “symptoms”, not by a positive tick blood lab (as those labs are at best about 45% accurate -which many medical providers here still don’t know). CDC Lyme webpage in middle of First Paragraph spells out Lyme is to be diagnosed by “symptoms”. I’ve had to point that out to more than one provider, and even then I got nowhere. This why, if you think you have Lyme and/or a co-infection, seek out a Lyme Literate Medical Provider (Dr, Nurse Practitioner, Functional Medicine Provider)! This is a must. Sadly, these Lyme Literate Medical Providers don’t usually take insurance, as insurance usually doesn’t cover much of Lyme treatments, but except perhaps an initial dose of Doxycycline, but, just how long will insurance cover an initial dosing treatment varies from insurance company to insurance. Plus, some mainstream providers only write a script for a day or two, vs writing a prescription for 3-4 weeks of this antibiotic, However, we know of a patient is in a chronic Lyme state, antibiotics are far from being what is all needed to get the patient better to some degree.

THANK YOU for this video! Both of you are amazing! This is the most comprehensive video of its kind I have seen on this topic! Thank you so much for shedding light on the numerous these coinfections and getting rid of them with various treatments. I’m getting anxious to heal faster from a live Babesia Mycroti and a few other latent Lyme+ infections like Bartonella, etc. I was diagnosed with 19 months ago, plus viruses that have resurfaced like EBS, shingles, and inflammation. I’m in freeze response from medical PTSD , brain issues, trauma, and CNS damage, I’m trying so hard to stay on the right track alone at 69, and function well enough to get the right help and deal with what needs to be addressed first, like my bills, paperwork, taxes, running a house I’m now allergic to, etc. As with most of us with chronic illness and pain, I’m dealing with depression and mental exhaustion. I’m trying my best to function normally, but I never know how I’ll feel or when symptoms may strike, and I’ve lost my family, money, and relationships. I’ve been undependable since i became ill 21 years ago from other toxins first, then mold, and now about 5 to 7 Lyme +, and latent viruses that have resurfaced. Most people DO NOT understand this, and I didn’t either! But, unless you or your child get it, you don’t “get it. To think that most of my childhood suffering from Bartonella, is a crime to children everywhere. I have found that people, including my loved ones don’t want to learn, and I’m concerned about the young children in my immediate, extended family, and children everywhere. Many have unnecessary illnesses that, if recognized by a GP, would save so much money, losses, pain, and suffering. I will share this with my loved ones, but I would bet no one will listen to this. I don’t have loved ones who care! My friends care, because they are aware, but, sadly, my loved ones don’t.🥲 Thank you for the website. Maybe add more information on how common this is, and that it’s not a bullseye rash nor just from ticks. Thank you for listening to my lengthy response❣️

Reach out to Fred Diamond on Facebook or LinkedIn to get the e-version of ""Love, Hope, Lyme: What Family Members, Partners, and Friends Who Love a Chronic Lyme Survivor Need to Know" for free.

I am 7 years from my "Target Date" excuse the expression Haa....Am now suffering from Arthritis in my hips and hands..Havin a hard time walking...My Dr told me."We dont have Lyme here in Arizona"...I told him I got it while in Maine..He told to go get a Maine Doctor..

Once again! Another highly beneficial resource! Thank you gentlemen

Great episode! Thank you for this Fred. I am going to share this with family & friends, to help them understand this awful disease more, and how to better be there for me, and to stress they too need to take care of themselves.

To get your free e-version of "Love, Hope, Lyme: What Family Members, Partners, and Friends Who Love a Chronic Lyme Survivor Need to Know," reach out the Fred on Facebook or LinkedIn.

I’m positive for bebesia duncan, mold and just found mold at home. Have you heard symptoms of hand/joint pain? That’s currently my main symptom. Thanks

I have just recently been introduced to these podcasts that I watch on RUclips. My Lyme went undiagnosed for 25 years. I spent the next 4 years working with this doctor who was LL. As I turned 80 I decided I’d had all I was never going to feel “normal.”

❤

So glad I found this!!!

Why not the hot tub? I have a hydro jet tub and take epsom salt soaks

I just started the Vital Plan by Dr. Rawls!!

'Promo SM'

I know all too well about the gaslighting of Lyme as I've had going on 15 yrs. two of which was the doctor to doctor stage. This was very informative, thank you. Lyme Loonies.

Another great, informative episode, Mr. Diamond! Thank you from Texas… I too was told that I was not sick…

“Love, Hope, Lyme: What Family Members, Partners, and Friends Who Love a Chronic Lyme Survivor Need to Know" www.amazon.com/Love-Hope-Lyme-Partners-Survivor-ebook/dp/B0B9Q8LX7G/

It’s my running theory that the African American demographic gets more Lupus diagnosis than Lyme. When you look at the symptoms and the fact that there is no specific test for lupus… it’s a clinical diagnosis. An African American friend of mine started a Lupus non-profit, and I wanted to understand his disease better, so I did my homework.

THANK YOU! THANK YOU! I want to thank my husband as well! He has been amazing! Most of my family dismiss Lyme and dont try to understand. Its a lonely journey especially when you get passed around like a hot potato. I agree eating clean is SO important to control inflammation and symptoms. Your gut health is compromised due to the treatment, and it can really mess things up. New symptoms pop up, and it feels like an endless whack-a-mole tournament. The psychological effects of the medical professionals is perhaps the most difficult aspect. In a wheelchair, unable to walk because of the excruciating pain, a neurologist at a university hospital diagnosed me with a form of Munchausens. I got so angry, and I decided to find my own way to get better. We Lymies take time, patience and love. Few have that, it seems. I appreciate your efforts more than you know. ❤

And not to mention, recognized by the CDC.

The e-version of Fred's book "Love, Hope, Lyme: What Family Members, Partners, and Friends Who Love a Chronic Lyme Survivor Need to Know" is always free for chronic Lyme survivors. Reach out to Fred on FB or LinkedIn for your copy. The gaslighting report can be found at www.ncbi.nlm.nih.gov/pmc/articles/PMC10778834/

I was told by infectious disease Dr. not to come back to him because I was given the 2 CDC recommended doxycycline regimens & nothing else he could do. Even though I was still having bad, constant femoral nerve pain/problems with difficulty sitting, walking, standing Told by a neuromuscular Dr. that chronic Lyme does not exist. Almost 2 years after a dog tick bite that tested positive for Borrelia & serum testing positive IgM & later IgG Tick Borne Relapsing Fever Borrelia....I havent found a specialist Dr. who wants to continue seeing me. And so far I've paid thousands since for specialists/out of pocket labs, & medicine/supplements & red light therapy. The medical system in US is broken, (probably because of Covid), even with health insurance. God help anyone who gets a Borrelia infection in nervous tissue.

I taught Regulatory Compliance at Northeastern