Skip to Accessibility Tools Skip to Content Skip to Footer


MS Research

Emerging Treatments and Therapies

  • By Editorial Team

    Share your experience with emerging treatments and therapies in MS. Get the conversation started.

  • By Bill B.

    I read a very interesting and encouraging article in the latest (Aug/Sept 2014) issue of Neurology Now magazine that discussed some great results in using statin drugs (specifically Zocor) in reducing brain atrophy in people with progressive forms of MS. Has anyone else seen anything about this? I know this is early research, but it could help lead to better treatments for SPMS and PPMS.

  • By Zigby

    ATL1102 for MS
    ANP (Antisense Therapeutics ltd) is currently investigating provision of ATL1102 under an Early Access Program (EAP) on
    compassionate use or on a named patient basis in markets where the drug would qualify for use on
    these grounds including those where the Company can charge for drug access resulting in a possible
    early income stream. These investigations are moving forward positively with the Company having
    identified a potential existing source of ATL1102 material for use in an EAP. Assuming all the material
    will be available and suitable for use (to be confirmed in ongoing technical diligence and business
    follow up) ANP estimates there would be sufficient quantities for one year’s treatment for
    approximately 200 patients1.
    ANP is in discussions with an experienced European based group to set up and run the program in
    Europe for ANP. Pricing for such EAP access for patients to use ATL1102 would be determined with
    the insight of the European firm, however as a point of reference the hospital price of TysabriTM in
    Europe ranges from A$25-$33,000 per patient per annum2. ANP expects to update the market on the
    progress of this use of ATL1102 in the coming months as key components are confirmed.
    As outlined earlier, ANP’s plans are to conduct a Phase IIb trial of ATL1102 with a funding and
    development partner. The Company is currently engaged in the process to attract a partner.

  • By afizmyf8


    My brother lived with MS for 11 years and for the last 2 years he has been researching HSCT (Hematopoietic stem cell transplantation) which is the transplantation of multipotent hematopoietic stem cells, usually derived from bone marrow, peripheral blood, or umbilical cord blood. This procedure is not approved in the U.S. although it has been researched and tested since the 1990’s, because the big pharmaceutical companies don’t want it approved! They will lose BILLIONS of dollars a year from MS patients not needing medication ever again. HSCT has a 86-91% success rate– not putting MS in remission but ERADICATING it completely!! My brother had to travel to Mexico for the procedure (it is also performed in Russia and Thailand) and costs about $85,000. Yes that is a lot of money to come up with and insurance companies aren’t going to help pay for it, but it is definitely worth it to be MS free for the rest of your life. My brother was unable to drive and could not walk without a can and a month after the procedure, he is walking without a cane! Definitely do some research about HSCT!

  • By talonsgirl

    I was actually going to have an autologous stem cell transplant at StenGenX in San Diego CA….issue is the $15,000 price tag….while that covers everything but your plane trip, it’s too spendy for my pocketbook. In this form of transplant they take the dormant stem cells from your fat, they take millions of cells, they take them from fat because they are dormant and have not been exposed to MS. They separate the stem cells from the fat and the plasma (holding onto the plasma) clean off the stem cells then activate them using there drugs and yoyr plasma. They then will introduce the srem cells 4 ways into your body. 1) Into you vein through plasma, 2) thay give you a vasal dialator, and make a nasal spray and you use the spray to inhale and the stem cells will make it through the blood brain barrier through the dialation of your arteries in your nose, 3) you will get a spunsl injection around your S1 area and )4 you will get a bladder washing of cells to help with the damage done to your bladder. This is a 2 day orocedure, they put you up in the hotel across the street so it’s easy to monitor you, and at the end of the second day you can go home…..I tried a go fund me to get the money to help fund this but no ho from the thousands of people across the country throygh the chirch.

    • By Erin Rush Moderator

      Thank you for sharing, WVDarren! Ongoing research into potential causes of MS is very important. Best, Erin, Team Member.

  • By RobW

    My dad unfortunately passed from a heart attack about a month ago at the age of 71. He had battled MS for the past 15 years of his life. He had such a great attitude. I miss him dearly. Dad had secondary progressive MS.

    The reason for this post is that approximately 4 months ago, Dad had a UTI and when tested it was some type of “super infection”. Upon receiving the phone call to go to the ER to get treated intravenously, he did so, and came home that evening better than he had been in 10+ years. This lasted several weeks. Energy, enthusiasm, mental clarity, you name it. We asked his GP if he could get another round of this treatment about a month later and the physician responded with a “no, your dad would have to be diagnosed with still having this infection and we can’t be giving super infection antibiotics to everyone, as this is a last line defense for the general public.” I don’t want to get anyone’s hopes up, but I am convinced, concerning my dad, the treatment he received, at least temporarily kicked MS’s a## for several weeks. It also wasn’t the day of clarity or so that some dying people have days before their demise. This was immediate, long and sustained. Although he didn’t get up from his wheelchair and walk, he sure as heck benefited from this treatment.
    I hope this helps someone and God speed to everyone that suffers from or has a loved one that suffers from this suck a## disease.

    • By Shelby Comito Keymaster

      Hi @robw, I am so sorry about the loss of your father and offer you my deepest condolences. I can’t imagine what a painful loss that must be for you. He sounds like such a strong and admirable man. Thank you so much for sharing a bit of his story with us, and also for sharing his positive experience with the intravenous treatment! That is definitely exciting news, and I appreciate you sharing what you discovered here. I hope you come back and continue to share his and your story with us. Please know that this community is here for you!
      Best, Shelby, Team Member

  • By Kim Dolce Moderator

    @heymanhowsitgoing, the attached 2017 Canadian study says tanning beds can raise D levels by an average of 42 points. Tanning beds use mostly UVA rays and some UVB to the tune of 95% UVA to 5% UVB–about the same as natural sunshine. During the winter months in Canada, natural sunlight does not contain enough to keep our D at a healthy level. So phototherapy and tanning can each help, especially for those who can’t absorb D oral supplements through the gut:

    • By WVDarren

      Check the cofactors including magnesium, vitamin K, zinc, boron & vitamin A, etc that are needed for vitamin D use by the body. Vitamin D alone may not help.