This is a reprint from a recent study:
Dr. Metcalfe, who is based at Cambridge University in England, is currently looking for funding to further develop her theory that using a stem cell particle called a LIF would switch off the body’s auto-immune cells and help repair the brain.
In addition to being able to switch off the body’s autoimmune response, LIF also protects the brain and spinal cord — the areas affected by multiple sclerosis — and aids in repairing tissue, including brain tissue.
The research has not been smooth sailing. Metcalfe has found that LIF cannot survive outside the cell for more than 20 minutes before being broken down by the body, making it difficult to use as a therapy. However, she has found that nanoparticles could be the answer to the problem, as they can be used to help deliver the LIF therapy. By using antibodies with the nanoparticles, the therapy can be directed to certain areas of the brain — helping to repair damage caused by multiple sclerosis.
Metcalfe is now looking for research funding and hopes that one of the big pharmaceutical companies will step in. She hopes to begin clinical trials of the therapy by 2020.
We all know that summer heat and humidity are absolutely brutal on people with multiple sclerosis. And escaping it is almost impossible to do. But one area where everyone, ms or not dreads is getting into a car that has been sunbathing for a few hours and the internal temperature is usually somewhere in the 120 degree range.
There is a somewhat easy choice to reduce some of that direct sunlight. You’ve probably already seen them and perhaps laughed at some of the more goofy ones. If you’ve ever wondered if those car screens in the front window, and occasionally in the back as well, work? They do, and are very effective in keeping your car from becoming a roaster oven.
You can buy these screens at Walmart and other similar stores. And also keep your windows cracked open just enough to let any heat that may build up to escape. You can also invest in solar powered window fans that run off the power of the sun while your not in the car keeping the air moving so the heat moves out any cracked windows.
Try to stay cool and have a great summer everybody!
Do you know a literary agent or book publisher that would be willing to read my book? If so please email me and let me know.
That would be me!
Turmeric is derived from the spice curry used extensively in India. It’s health benefits range from helping to treat constipation to also being a huge anti-inflammatory agent. I personally had read so many great things about turmeric , including that some people believed it have something to do with India’s very small incidence of Multiple Sclerosis, that I just had to give it a try.
That was over a year ago and unfortunately I did not experience the health benefits that I had hoped to achieve. I am certainly not saying that it doesn’t provide benefits to other people but it doesn’t seem to do much for me except cost money. It may come down to each persons own body chemistry being a factor in whether turmeric has a positive effect or not. I know that researchers are discovering that many cancer drugs can work wonders for some people and have absolutely little if any effect for others.
In closing, if it works for you, by all means keep using it as long as your neurologist and general practitioner are aware of you using it as many supplements like turmeric can have undesirable effects when used with other prescribed drugs!
PS. I am still in search of a literary agent/publisher for my book if anyone can help by putting in a good word for me!
Multiple Sclerosis is a disease that is often accompanied by varying amounts of pain both muscle, through inactivity, and more often nerve pain because that is the nature of this awful disease. I’ve used all kinds of pain relief medications such as pills that often leave you with brain fog as well as having to deal with a whole host of other unsavory side effects including addiction and even death. I’ve also tried several kinds of pain lotions that do in fact seem to help a little but they are messy and difficult to apply to the point where even what relief they do provide seems almost not worth the bother.
Recently though I saw a commercial for a new aspercreme rub with 4% lidocaine added for additional pain relief beyond its other active ingredients. I was intrigued enough to go out and spend eight dollars on a 2.7 oz bottle to see if it actually worked? And surprise, surprise, it worked like a charm. I have not found any product, pill or otherwise, that reduced my pain in a matter of minutes like this product does.
At times I suffer from extreme lower back pain as well as sciatic nerve pain in the upper portions of both my legs and I almost can’t believe the amount of relief I get after just a few minutes from the time of application of this lotion. I’m sure that there are probably some side effects of over use of these products but I’m also pretty certain that they can’t be any worse then what most doctors prescribe for pain when it comes to MS.
Give it a try. If it doesn’t help, all you lose is a few dollars. Let me know if you try this and what your thoughts are!
That would be me!
I was reading another site and was stunned to read that researchers are studying Viagra as a treatment for Multiple Sclerosis. The following is what I found in a internet search and I’m still a bit surprised since this is the first I’ve heard of it.
Universitat Autònoma de Barcelona researchers have discovered that Viagra® (sildenafil) drastically reduces multiple sclerosis symptoms in animal models with the disease. The research, published in Acta Neuropathologica, demonstrates that a practically complete recovery occurs in 50% of the animals after eight days of treatment. Researchers are confident that clinical trials soon will be carried out in patients given that the drug is well tolerated and has been used to treat sexual dysfunction in some multiple sclerosis patients.
Multiple sclerosis is the most common chronic inflammatory disease of the central nervous system and one of the main causes of disability among young adults. The disease is caused by the presence of multiple focuses of demyelination (loss of myelin sheaths around the axons, affecting the ability of neurons to communicate) and neurodegeneration in different areas of the central nervous system. There is currently no cure for the disease, although some drugs have proven effective in fighting symptoms and preventing it from progressing.
A research team from the UAB Institute of Biotechnology and Biomedicine directed by Dr Agustina García, in collaboration with the research team directed by Dr Juan Hidalgo from the UAB Institute of Neurosciences, has studied the effects of a treatment using sildenafil, sold as Viagra®, in an animal model of multiple sclerosis known as experimental autoimmune encephalomyelitis (EAE). Researchers demonstrated that a daily treatment with sildenafil after disease onset quickly reduced clinical signs, with a practically complete recovery in 50% of the cases after eight days of treatment. Scientists observed how the drug reduced the infiltration of inflammatory cells into the white matter of the spinal cord, thus reducing damage to the nerve cell’s axon and facilitating myelin repair.
Sidenafil, together with tadalafil (Cialis®) and vardenafil (Levitra®), form part of a group of vasodilator drugs known as phosphodiesterase type 5 (PDE5) inhibitors, used in the treatment of erectile dysfunction and pulmonary arterial hypertension. Recent studies in animal models of central nervous system pathologies already pointed to the fact that in addition to vasodilation, these drugs could contain other neuroprotective actions and suggest their usefulness as possible treatments of both acute (cerebrovascular stroke) and chronic (Alzheimer’s) neuropathologies. Research published in 2010 in theJournal of Neurochemistry by the same research group from UAB demonstrated that one of these inhibitors reduced neuroinflammation and neuronal damage in animal models of traumatic brain injury.
At nearly the top of Mount Baker, WA.
Love reading your blog. I wanted to reach out to you to see if you know about the latest treatment option for Upper Limb Spasticity (ULS) a side effect many people who suffer from MS deal with.
ULS can occur weeks, months or years after being diagnosed with MS, and can make it challenging to do day-to-day activities, like getting dressed or putting on deodorant. People with upper limb spasticity may have rotated shoulders, flexed elbows, wrists, and clenched fists. Due to upper limb spasticity, arms become tight and are forced up against the body and uncontrollable muscle movements or spasms occur at inopportune moments. The muscles in the elbow, wrist and fingers are uncomfortably tight and stiff.
Now, there’s a new treatment option for Adult Upper Limb Spasticity. Xeomin® (incobotulinumtoxinA) was recently approved by the FDA for use in adult patients suffering from ULS. In clinical studies, treatment with Xeomin for adult ULS resulted in statistically significant clinical improvements in muscle tone, with a safety profile similar to that observed for other Xeomin indications.
We’d love to connect you with a national or local medical expert who can explain the impact of ULS in more detail and how Xeomin works in adult ULS.
Ever since I was diagnosed with multiple sclerosis back in 2000 my blood pressure has slowly crept up to a point where it was really starting to bother both myself and my family doctor. At first I was prescribed low doses of something that I don’t recall the name of but it made me cough to the point where it had to be changed to Losartan Potassium. And at first this seemed to bring my BP down to a more reasonable level. But it didn’t take long until the dose had to be doubled to 50mg and then doubled again to a 100mg which is where I’m at now and it still doesn’t seem to be enough to lower my blood pressure down to a safer level.
I think my doctor might also be starting to get concerned with this because he ordered a complete blood work up to see if something else may be causing my higher pressure levels. However as the results are now back they are all, for the post part, in the normal range with one exception. My glucose levels were high enough for my doctor to announce that I am now pretty much pre-diabetic.
In one respect this does not come as to much of a shock to me as just about everyone on both sides of my family are also either diabetic or like me, at some early stage of becoming diabetic. But in another respect I remember reading early on after my MS diagnosis that people who became diabetic rarely developed multiple sclerosis and vice versus as well. Another myth bites the dust.
There is a bright side to this diagnosis that if I watch my weight and my diet I should never develop full blown diabetes. Unfortunately this still doesn’t explain the hypertension. His guess is a combination of stress related factors along with the fact that I really don’t get enough exercise being at least part of the problem. And he stated that higher BP is somewhat common for people with MS. I do try and exercise as much as I can but it tires me out at a pretty fast rate and I live in a place where it rains a lot which also makes getting out more of a problem. And telling me that I am now one step closer to being diabetic certainly doesn’t help reduce any stress that I may be experiencing.
I have another appointment in a couple of weeks so I won’t know until then whether we are going to increase my current BP drug or try something new. Which means for now, the mystery continues!