Alternative treatments for ALS 

DR. Bedlack, thank you so much for being open minded. The truth of the matter for me is that conventional medical practices is not meeting my expectations of efficiency. Your courage is commendable.

Love your sense of style

I wish more doctors took this approach when patients consider alternative therapies for their illnesses.

Dear doctor, thank you much for being so dedicated to help people with ALS. I wish we have thousands of doctors like you. I just found you a few days ago, and the more I watch your videos and listen to you, the more hopes I have for my mom to get better. She was recently diagnosed in Chile and Mexico with ALS. Would be so kind and tell me what would be the way and doses of Theracumin? She started getting acupuncture, she will work on her microbiota and I would love her to start with Theracumin. Thank you very again for giving hopes to many patients and family affected by ALS.

Just gonna exist, until I don't anymore. Keep pushing, until I can't any longer. Same as almost everyone else. Easing pain, stress, and taking something to combat fatigue, will have to work until it doesn't. I will live, until I die.

You refer to the website a lot, but not anywhere on your website can I find anything about curcumine or Theracumin? Where can I get the protocal for ALS with Theracumin?

Dr. Bedlack, I love how much dedication and effort you put for your people.

I was recently, July 2022, diagnosed with ALS and am seeking a second opinion. Mayo Clinic will be seeing me in September. Mayo has been seeing me for myasthenia gravis and recurrent thymoma. Theracumin sounds very interesting to me. I have had good results with circumin to relieve MG symtoms. If I do receive a diagnosis of ALS from Mayo, I would be interested in exploring clinical trial options. Thank you

I'm interested in knowing if there are any clinical trials involving HDAC inhibitors? My crude understanding is these drugs allow for more proteins that encourage neurons to grow such as BDNF.

I have been diagnosed with cervical spondiltic myelopathy. Next week I am scheduled for an EMG with nerve conduction to rule out MND.I have episodes of extreme weakness and complete loss of Rom.I cannot use my hands or lift my arms. As soon as I get prescribed steroids I improved.This has been an ongoing pattern with me since August of 2023.The neurologist giving me the EMG said she would not prescribe steroids.I just know that the Prednisone works for what I'm diagnosed y at this time.CSM is an ALS mimic. Steroids are cheap guess there's not enough money to be made have.

I would love to experiment with curcumin. What type of curcumin were they using? And how can I try Theracumin? For I was just recently diagnosed about a week ago. I have two little girls that I have to stay well for and I’m certainly not a quitter. I was a group fitness instructor for over 25 years and taught strength training and kickboxing. So I’m hoping that you could help me in anyway. Thank you

Will medical Marijuana help or will cbd..seems to help me..I don't know how much it helps

PEMF studies??

At least, he is open-minded - which is more than can be said for the pharmaceutical industries. I've noticed troubling signs that I may have ALS - reducing mental clarity, slurred speech at odd times - even when calm, a numbness and mild pain in both arms with my left arm being the worser of the two. The best I can describe the numbness is sort of like if you laid on that side for too long and your arm falls asleep. That's what it feels like. Reduced strength in both arms. I get random muscle spasms - largely in my lower-mid back which started... roughly a year or two ago, but perhaps they were not indicative of ALS at the time. I worry that perhaps these symptoms may be worsened by the fact that when I was in the hospital for kidney infection treatment, during the ongoing democide, I was forced against my will to get the PCR test. I wonder did that or any pharmaceutical drugs they gave me cause or worsen any of these symptoms? With that said, I dread that I may have ALS, but if I do - I will accept the death sentence and do my best to try to lose weight and spend as much time with my husband and family as possible and I definitely will continue to do intermittent fasting and refine my already organic non-GMO diet.

Do you have your patient's case?

Studies on raw plant based diet, juicing?

Hlw sir,I m from India(Uttar pradesh)..and my father is diagnosed with als in march 2021, and his condition is getting worst day by day he can't walk, can't speak and having swallowing disfficulty,we are loosing hope plz suggest something new🙏..and the form of curcumin you suggest i am going to start..and it's gives us hope..thanku sir🙏

Doc how to take curcumin, I milk or water, and whts the dosage. Thanks

Hello everyone. We filmed Dr. Bedlack on a variety of topics for Your ALS Guide. Unfortunately, he does not have time to answer individual questions outside of his clinic. You can find more information about alternative treatments as well as the link to his website that reviews alternative treatments in great detail at www.youralsguide.com/alternative-treatments-for-als. Please note that this video is for educational purposes only. Medical advice can only come from your treating physician. Hope that helps!

What happened to clenbuterol

Hello sir, I m from india (Kashmir).my brother is suffering from ALS for the last 2 years.He can't move by his own, can't speak fluently, but can eat yet.We want you to treat him n what cost it will take.plz respond.

Prayers

i have ALs C9 and have taken 5mg of stevia gummie every 6 hours with hemp gummie every 6 hours to . i sleep with by pap at night and wear copper socks i am past 5 years and still take care of my self and talk and mobil. have had to change what i eat so i dont choke. but it works for me. see you in 10 years haha

How to we get involved with the Duke University ALS group? I live nearby and would love to take my mom there. We have results from her Invitae test.