Showing posts with label my websites. Show all posts
Showing posts with label my websites. Show all posts

Tuesday, June 12, 2012

Migraine Awareness Month Post #12: "Let's Do The Monster Mash"

AwarenessMonth2012BC2
Today's prompt is:

Migraine Awareness Month Post #12: "Let's Do The Monster Mash."  Choose a movie monster that reminds you of Migraines and tell us why.
Today's creepy beasty blog post is featured on the Migraine blog Putting Our Heads Together which can be found here.

National Migraine Awareness Month is initiated by the National Headache Foundation. The Blogger’s Challenge is initiated by www.FightingHeadacheDisorders.com.
To help raise awareness about Migraine, please Tweet this post with the hash tags #NMAM and #NMAMBC and share it on your Facebook page. Thank you!

Friday, July 22, 2011

Michele Bachman News Reveals Surprising Truths

It took me a couple days of serious thought and research as I agonized over how to blog at Migraine.com about the media's take on Michele Bachmann's Migraine issues.  I already had a Migraine myself which will often remove the filter from my brain to my mouth.  Getting frustrated over the insinuations, misinformation and just plain junk "reporting" on the issue only served to make things worse.  I was afraid if I wrote what was really going through my head, it might get me in trouble.  o.0

As I read the comments on my Facebook page as well as Migraine.com and many of the bloggers who I follow, it became clear that there were a few things Migraineurs needed to get straight with the society we live in. The more people talk about this issue, the more obvious it becomes that there are some seriously unsavory truths that are being revealed, not just in our society as a whole, but in the Migraine community as well.  Some of these are truths I have not yet seen addressed by anyone else, yet scream out to be heard.

Here is my blog post: Michele Bachmann News Accidentally Reveals Hidden Truths

I know that this post could be written about any number of different diseases or conditions.  That is precisely why I wrote it as I did.  I am a blogger, not a journalist (despite the fact that this post made the #7 spot for Google News this morning).  I call 'em as I see 'em, and that's just what I did.

In it, I included a call to action.  Why?  Because the Migraine community as a whole is exhausted and in pain.  They're tired enough that 90% of them wait for someone else to write their legislators, write a blog post, comment on an article or even discuss these important issues online in any kind of a public manner.   This is a huge issue in the media right now however, and hay must be made when the sun shines.

Migraineurs are the ones who have the most to lose with all the insinuations and misinformation haunting the news as of late.  If we don't care enough about ourselves and each other to stand up for ourselves, then we'd better not expect anyone else to either.

Now is the time to either fish or cut bait.

What will you do??

Thursday, June 18, 2009

Cambia - New Migraine Medication is Approved

Cambia was approved June 17, 2009 by the FDA for use in the United States for the treatment of Migraine. It does not prevent nor lessen the number of attacks, but is designed to treat one already in progress. Cambia comes as a flavored powder to be mixed with water to form a solution which is drunk by the patient, preferably on an empty stomach.

Drugs.com reports that, "In randomized clinical trials, Cambia was shown to be effective not only in migraine pain, but also in treating photophobia (sensitivity to light), phonophobia (sensitivity to sound), and nausea commonly associated with migraine attacks. It was also shown to provide statistically significant onset of relief of migraine pain within 15 to 30 minutes." This is statistically much faster than the vast majority of oral Migraine medications on the market today.

Cambia is another hybrid medication. Hybrid medications like Cambia combine 2 or more previously known and used medicines. When used together, they combine and work synergistically together to create a formulation that is more powerful than the sum of either ingredient when taken separately.

The main ingredient - diclofenac sodium - has previously been known as Cataflam and Voltaren. It is an NSAID and carries all the normal warnings and contraindications of this class of drugs, but its safety profile was better than Triptans. In this case, diclofenac was blended with a unique buffering agent - potassium bicarbonate (usually used in higher doses to treat low potassium levels) which acts as the 'engine' that boosts the effects of diclofenac. Normally NSAIDs are taken with food to help prevent the gastric upset that is so common with this type of drug, but in this case the unique buffer makes it preferable to take without food, making the preparation an advantage for Migraineurs who suffer vomiting and nausea as a part of their attacks.

Unfortunately, Cambia comes flavored using aspartame and saccharine which may be a problem for some patients. As an oral preparation, patients with gastric stasis may still not be able to absorb Cambia well, although there is no research on this to date. Diclofenac has also been found rarely to cause drug-induced Lupus, and is contraindicated for patients suffering SLE, Lupus autoimmune disease. Other contraindications for the use of diclofenac include asthma or frequent runny nose or nasal polyps, porphyria, liver or kidney disease or swelling of hands or lower legs. Diclofenac can also cause bleeding or bruising problems.

Sources:
Genetic Engineering and Biotechnology News
Drugs.com
MedlinePlus
Medicine.net

Wednesday, January 7, 2009

About me




My name is Ellen Schnakenberg and I'm the chronic Migraineur behind Migraine Interrupted and several other blogs and websites devoted to Migraine, headache and chronic pain disorders.

I'm a 48 year old Missourian who began city life on the west coast, and now live on a quiet farm near Iowa. I am married to 'D' and together we have a grown son and daughter. 
A part time blogger, Migraine and chronic pain community and newsletter contributor, I was discovered online and then hired at the website WEGO Health and spent several years researching, writing and advocating with them as a community leader, as well as helping other health activists network and become better at advocating and educating patients utilizing various social media platforms. Much of the rest of the time I spent educating, advocating for and sharing my experiences with other everyday people who wish to become proactive in their own and their family's health care, including working with the media. 
I now work for Migraine.com as a patient advocate/educator and community manager, helping the amazing team of patients and doctors there develop a useful platform of support and education for both patients and physicians.  
I stay current on the latest and greatest information by attending American Headache Society's annual scientific meeting as well as their fall symposium, and actively participate each year in the (AHDA) Alliance for Headache Disorders Advocacy's Headache on the Hill in Washington, DC. 
I am also an Ambassador for the United States Pain Foundation.
Although I've been active in online websites and communities approximately 20 years, I've been blogging about Migraine and other health related issues since March 2008, starting with my first still located in the WEGO Health site. 
Due to multiple personal and family diagnoses I began to be asked to cover other health subjects including:
  • Cluster and other headache disorders
  • Dystonia and tardive reactions
  • Autoimmune diseases including lupus, Graves' disease, Hashimoto's thyroiditis, Sjogren's syndrome and others.
  • Nutrition, vitamin deficiencies, complementary and integrative health care  
  • Chronic pain
You can find me:

Twitter @ESchnak                        Putting Our Heads Together
Facebook                                     AHS ACHE blog
Learni.st                                       Headache Disorder Blog Network  
stumble.upon                                Migraine.com blog
Love.it


There are many good, informative websites now, unlike 30 years ago when my Migraine journey began. 

My wish: to add one more voice to those who no longer accept living in the dark. One more explanation of what Migraine is and is not. One more person to offer support to another looking for ways to live with Migraine disease. One more place to go for connections to other bloggers and websites who can help.

In my old life I worked with children, managed an Arabian horse farm/reproduction facility, was an emergency dispatcher and an award winning artist. I also volunteered with kids and animals, running successful programs for each of which I'm very proud. I am a medical First Responder, and still keep my spoon in many of these pots including CERT (Community Emergency Response Team), Search and Rescue teams, 4H programs and my church.

As you'll be able to tell from my blogs, I'm descended from photography and travel nuts and I love my horses, dogs and cats.
I hope that's given a glimpse of where I'm coming from. If you're a Migraineur or headache sufferer and want to learn more about these disorders and how you or someone you love can live well despite their symptoms, then I'd love to keep in touch. You can subscribe to this blog via one of numerous subscription methods by clicking the SUBSCRIBE TO button below the blog title. Additionally, I'd love to hear from you about Migraine or other headaches in the comments sections on my posts.

This page was last updated June 1, 2012