I Had HSCT for MS: How it went, and how I’m doing 4 years later! 

My experience was different. I had HSCT at Clinica Ruiz in Puebla in 2016 and I am very glad I did. Because I have Progressive MS and I knew going in that HSCT would not repair myelin, I had low expectations, but there was nothing else that could hopefully give me some improvement. I thankfully did receive several good benefits from it. My slow working brain and brain fog was completely eliminated just days after getting my stem.cells back. I had increasing overwhelming, debilitating fatigue as the MS progressed and that too was completely eliminated. When I was tired, my speech would get slurred. These things along with a few other things were resolved and have not returned. Over these past 7 years my mobility has decreased and other symptoms have increased due to the damage that was already done but I have no new symptoms. The care I received at Clinica Ruiz was outstanding and I have no regrets that I went to Puebla and had HSCT. I would like to point out that Dr. Ruiz is a Mayo Clinic alumni and has conducted peer reviewed studies on his protocol for his outpatient HSCT.

Thank you for sharing , I’m due to go for this treatment in a few days

Thanks for sharing your experience Michael.

I'm 2 years post Puebla. Glad I stumbled across your channel.

Thank you Michael for sharing your experience. Glad to hear your MS has stopped getting worse. Sending good vibes your way.

Thank you for the information and for your honesty!

I’m 100% bed-bound with a severe autoimmune complex since 2020. I have NMO antibodies but not a typical case of NMO. I haven’t gotten any treatment outside of IVIG and it’s not saving me, unfortunately. I was gaslit for a long time but terrible and unethical doctors. Anyways, I appreciate you sharing your story and I’m actually going heavy on an antiviral diet with antiviral supplementation. I don’t know if you’ve had any success with these sort of diet/supplement adjustments or if anything in those areas particularly hurts or helps.

Thank you for sharing your experience and being so candid.

Hey Michael! I just stumbled upon your channel earlier today and binged all your videos. I’m a 29 year Homeland Security/Emergency Management professional with MS (diagnosed 2019) in the National Capital Region. My biggest problem symptom is speech and dysphagia which is at odds with my career - it can make it difficult for me to be understood which is the most frustrating thing. You’re videos made my afternoon. I’ve been considering HSCT for a long time and your insights were helpful since I was looking at Clinica Ruiz for awhile. I wanted to asked are you still working? Our diets, attitude and lifestyle approach seem almost identical. I don’t have any major mobility issues, but do have a cane and haven’t had to use it. Exercise is super important for me in managing energy and fighting the brain fog, but it only helps so much..

❤Thank you for sharing- I’m sharing your experience with a friend who has been treated with stem cells and hasn’t had any results yet ❤ every word is helpful ❤

Thanks for sharing. I had hsct in 2019. I did not benefit from it too. I feel that the chemo might have damaged the nerves further. I would say it's probably more effective if one goes for the procedure before too much damage has accumulated in the body. Those people on Facebook only tell you the good stuff, and they'll block you if you're not in agreement with them. I think I regret that I went through the procedure, and I wish I hadn't done it. More people should know that hsct is a very high risk procedure with no guarantee you will get better.

It’s all attitude bud !! Keep on keepin’ on ! Thank you for sharing your insight, just started to get serious on researching SC therapy, the place in the caymans seems top-notch but right now you have to be “vaccinated” to enter there …..

Man so sorry to hear that you haven’t gotten the real win with hsct. Can I ask you about your regimen for MS as far as your diet and how much lower body movement you get? Thanks for putting in the effort and putting your videos out.

Another awesome content video! Thanks so much. I am newly diagnosed & on Kesimpta! I wanted to ask my neuro this month about his thoughts on stem cell. Your info & positivity are admired:) Thank you from CO

Thanks a lot for sharing your experience. Sorry you haven't had full recovery. When you had the treatment were you walking assisted with a cane? You mentioned the treatment was about 50,000 dollars? Did it include everything? Thanks a lot and God bless you!!

Thank you for sharing

I just had HSCT for my PPMS in Puebla (Cyclophosphide = Rituxan) :aimed at halting the disease. Something much different, and aimed at regeneration, is MSC: Mesenchymal Stem Cells. By Neil H. Riordan, PhD practiced in Panama is aimed at regeneration and is not bunk.

Thanks for sharing

Hi Marco, I think you are definitely on to something hear I would really appreciate it if you would give me more information about your theory? I’m going for the treatment soon and I’m not sure if I should do this before during or after treatment? If there is a way to get in touch please let me know Kind regards Leah😊

Have you heard of allogeneic blood-cord derived mesenchymal stem cells? They are able to renew and heal the damaged myelin sheath (more potent than autologous as i can understand).

Thank you for sharing your story. I'm sorry it didn't work as well for you as it does for some. Are you progressive or relapsing/remitting? I've read that can make a difference with this treatment sometimes, too.

Have you tried HBOT? I believe we may need more 60 sessions to see some benefits. Do you take vitamin D regularly

Thank you for sharing!🙏 #09msdiagnosis

Hey man just curious but why didn’t you just use the mesychemal stem cells from placenta and Whartons jelly of baby’s umbilical cord without going through radiation and all of that? It’s simple like just administration of IV, no need for chemo etc. did you know about it?

Hey Mike, i'll write to you like I did to Deepa(another HSCT user), You were on the right track with the HSCT, probably the rejuvenation was helping. My guess is you where feeling good at first, and progressively went back downhill. I think you were just missing a step! You see, if your Immune System(IS) attacks the Mylene, that's fine, stem cells will help in replacing that Mylene. However, the problem persists, your IS still goes for that Mylene. Thus, HSCT is treating a symptom and not the cause. A Prolong Fasting Session, 5Days+, will allow you to turn over in Apoptosis many of those defective Immune cells. Upon the slow re-integration of the right foods, new Immune cells are generated from a cleaned out slate of DNA. Too boot, all cells of the body become more robust, including DendroCytes(DC). The steps are as follows, in the first 2-Days of fasting your glycogen depletes. Remember you're going from Insulin/Glucose as fuel to Ketones/Lipids. Your energy will drop but it'll come back. Day 3: Autophagy and Apoptosis, the checking of cell integrity. Those unworthy... Apoptosis, programmed cell death, as their part are needed to continue cellular growth in these rough times. Day4: Un-spooling of DNA to repair broken parts and fix any methylation issues. Day5: To be sure you made it to the end. After 120hrs no food, start eating again, but small portions every 4hrs, and by small, I mean small for say 2 days... From there, Diet on LowCarb/HighFat(LC/HF) on an 18/6 Intermittent Fasting(IF) protocol for 3months. Repeat, another 5 days, and slowly re-feed(2nd 5Day fast is so much easier, but I bet your first one was a killer). This will fix Gut Health, Hormone unBalance, reduce Blood Pressure, etc. Good Luck to you. Take notes throughout the process if you try this, Google search Autophagy, get tools to monitor blood glucose, and go for it. My girlfriend has MS, she doesn't even want to quit smoking... Thanks for sharing your experience!

How did you get diagnosed so young?

Did your insurance cover it all

I use to surf in Mexico. I’m scared of the drug cartels. Probably wouldn’t go back.

Must be expensive

Do you take sny DMT 'S