mepolizumab, reslizumab, lebrikizumab, tralokinumab, dupilumab

this contact form speed dating gone wrong rencontre ayem nabilla para que se utiliza el hombre solo herramienta spring break 2018 hookup rencontre gratuite 60 numero de site de rencontre gratuit aries woman dating gemini man The UMABS have arrived!


There is a group of new medicines hitting the market that may help patients with EGPA / CSS.  Since Asthma is such a large component in many patients with CSS these are mostly targeted at the asthma market.

These are various targeted biologic therapies that are currently in late-stage development for asthma, including GlaxoSmithKline’s Nucala (mepolizumab),  ( Teva’s Cinquil (reslizumab), Roche’s lebrikizumab, AstraZeneca’s tralokinumab, and Sanofi and Regeneron’s dupilumab.

Most of the new drugs in the asthma pipeline are interleukin inhibitors targeting inflammatory pathways.  Interleukin inhibitors are immunosuppressive agents which inhibit the action of interleukins. Interleukins are a group of cytokines which are synthesized by lymphocytes, monocytes, macrophages, and certain other cells. They function especially in regulation of the immune system.

I have attempted to gather information here about these new medicines and given links to find out more information.  I have Churg Strauss Syndrome (CSS) which has been renamed eosinophilic granulomatosis with polyangiitis (EGPA).   I live in  the USA, so my research is pertaining to the US market and focusing on CSS/EGPA.  A google search could give you more information pertaining to your country.  I do not work for these drug companies, nor am I in the medical profession.  I am a patient, a researcher and a life long teacher.

Mepolizumab under brand name Nucala in the USA

Nucalaapproved by FDA in November of 2015


Mepolizumab is a humanized IL-5 antagonist monoclonal antibody. Mepolizumab is produced by recombinant DNA technology in Chinese hamster ovary cells.

US- FDA-Approved Indications:

NUCALA is an interleukin-5 antagonist monoclonal antibody (IgG1 kappa) indicated for add-on maintenance treatment of patients with severe asthma aged 12 years and older, and with an eosinophilic phenotype.

Mepolizumab is an interleukin-5 antagonist (IgG1 kappa). IL-5 is the major cytokine responsible for the growth and differentiation, recruitment, activation, and survival of eosinophils.  Mepolizumab binds to IL-5 with a dissociation constant of 100 pM, inhibiting the bioactivity of IL-5 by blocking its binding to the alpha chain of the IL-5 receptor complex expressed on the eosinophil cell surface. Inflammation is an important component in the pathogenesis of asthma. Multiple cell types (e.g. , mast cells, eosinophils, neutrophils, macrophages, lymphocytes) and mediators (e.g., histamine, eicosanoids, leukotrienes, cytokines) are involved in inflammation. Mepolizumab, by inhibiting IL-5 signaling, reduces the production and survival of eosinophils ; however, the mechanism of mepolizumab action in asthma has not been definitively established.

This is where it can help CSS patients.  If your asthma is the eosinophilic phenotype then Mepolizumab can lower the EOS in your airway which can lead to better asthma control.   This is not to be confused with Xolair which works on IGE / allergic type asthma by lowering the IGE level in patients.  Also note how it states “add-on” not replacement.

Dosage and Administration:

Nucala is given subcutaneously, 100mg administered once every 4 weeks under a doctors supervision.

At this time Mepolizumab is considered investigational and not medically necessary for all other conditions, including but not limited to:

  • aspirin-exacerbated respiratory disease (AERD)
  • atopic dermatitis
  • eosinophilic esophagitis
  • eosinophilic granulomatosis with polyangiitis (EGPA) (Churg-Strauss syndrome)
  • nasal polyposis
  • hypereosinophilic syndromes (other than severe eosinophilic asthma)

At this time (5/11/2016) this is a kinda grey area for CSS patients.   You can in the USA get insurance approval for Mepolizumab for your EOS type asthma but NOT for CSS.  SO, usually you can (if you qualify) receive this medicine through your asthma or pulmonary doctor.

Now there are current studies going on using Mepolizumab at a dose of 300mg, every 4 weeks.  The study is due to conclude in August of 2016 then we can all await the results and see if Mepolizumab will be allowed at a higher dose for CSS patients.

Early, very non scientific, reports of CSS patients with the EOS type asthma using Mepolizumab has been very positive.  I can say that I have been able to lower my prednisone and am now off all asthma inhalers after just 4 months of Nucala / Mepolizumab.  Others have has similar results, although once your prednisone is lowered other CSS symptoms may become more prominent and this is why this is an add on medicine at the current 100mg dosage and not a total replacement medicine (in my opinion).   There are side effects, as in most of our immune suppressing medicines and it is up to the patient to really investigate these before making medicine choices.

Reslizumab under the name Cinqair


logoNOW APPROVED for use in the USA 4/26/2016.

CINQAIR® is a new anti-interleukin-5 approved as an add-on treatment for adults (18 years and older) with severe asthma and elevated eosinophil levels.

CINQAIR (reslizumab) is a humanized interleukin-5 antagonist monoclonal antibody (IgG4k).  Reslizumab is produced by recombinant DNA technology in murine myeloma non-secreting 0 (NS0) cells.

Reslizumab is an interleukin-5 antagonist (IgG4, kappa). IL-5 is the major cytokine responsible for the growth and differentiation, recruitment, activation, and survival of eosinophils. Reslizumab binds to IL-5 with a dissociation constant of 81 pM, inhibiting the bioactivity of IL-5 by blocking its binding to the alpha chain of the IL-5 receptor complex expressed on the eosinophil surface. Inflammation is an important component in the pathogenesis of asthma. Multiple cell types (e.g., mast cells, eosinophils, neutrophils, macrophages, lymphocytes) and mediators (e.g., histamine, eicosanoids, leukotrienes, cytokines) are involved in inflammation. Reslizumab, by inhibiting IL-5 signaling, reduces the production and survival of eosinophils; however,the mechanism of reslizumab action in asthma has not been definitively established.


CINQAIR is an interleukin-5 antagonist monoclonal antibody (IgG4 kappa) indicated for add-on maintenance treatment of patients with severe asthma aged 18 years and older, and with an eosinophilic phenotype (1).

Limitations of Use: CINQAIR is not indicated for:

• treatment of other eosinophilic conditions

• relief of acute bronchospasm or status asthmaticus


•  intravenous infusion only.

• Should be administered in a healthcare setting by a healthcare professional prepared to manage anaphylaxis

• Recommended dosage regimen is 3 mg/kg once every 4 weeks by intravenous infusion over 20-50 minutes

Reslizumab is also indicated for an add on in Eosinophilic Asthma so that is where CSS/EGPA patients can benefit from it.  Patients are just beginning to receive this medication in the USA so I do not have any patient remarks on it yet.


being studies by Rorche and GeneTech not FDA approved in Phase III clinical trials

Lebrikizumab is a humanised monoclonal antibody designed to specifically block the action of interleukin-13. Roche is also conducting clinical studies of the injectable therapy in chronic obstructive pulmonary disease, atopic dermatitis and idiopathic pulmonary fibrosis.

About Lebrikizumab

Lebrikizumab is a novel humanized monoclonal antibody designed to specifically block the action of interleukin-13 (IL-13), a cytokine that is a key contributor to airway inflammation and asthma disease processes in some people. Clinical studies in asthma, chronic obstructive pulmonary disease (COPD), atopic dermatitis (AD) and idiopathic pulmonary fibrosis (IPF) are ongoing.

About Eosinophils

Eosinophils are inflammatory cells that can be present in increased numbers in the airways and blood of people with asthma (eosinophilia). Airway eosinophilia has been associated with key features of asthma. IL-13 plays an important role in attracting eosinophils from the blood to the airway, hence contributing to airway eosinophilia.

About Periostin

Periostin is a protein that has been identified as a key biomarker of inflammation in certain types of asthma. Its presence can be measured with a blood test. In people with asthma who have high levels of serum periostin, IL-13 appears to be a major contributor to their airway inflammation. An elevated serum periostin level has also been shown to be a predictor of airway eosinophilia, a prominent feature of asthma.

In February 2016 Roche reports mixed Phase III data for lebrikizumab in severe asthma.

Do your research on this one.  I am not finding a proposed marketing name in the US and the drug trials have very mixed reviews.  Interested to see how phase III trials go and what illnesses it is finally approved for.


being studied by AstraZeneca and Abbott

Interleukin (IL)-13 is a pleiotropic cytokine believed to be an important mediator in the development and maintenance of the human asthmatic phenotype through its role in key underlying mechanisms including inflammation , airway hyperresponsiveness (AHR) , fibrosis  and increased mucus production . Elevated IL-13 levels have been identified in the sputum of a proportion of subjects with asthma including those with severe disease treated with systemic corticosteroids.

Tralokinumab (CAT-354) is a human immunoglobulin (Ig)G4 monoclonal antibody which potently and specifically neutralises IL-13  and has been shown to inhibit a range of IL-13-mediated effects in pre-clinical studies. Tralokinumab is in clinical development for the treatment of asthma,

July 2015 — a study was done :

Efficacy and safety of tralokinumab in patients with severe uncontrolled asthma: a randomised, double-blind, placebo-controlled, phase 2b trial.   In this study it was found Tralokinumab does not significantly reduce asthma exacerbations.

This drug is still in the testing phases for asthma and other inflammatory illness.



being developed by Regeneron and Sanofi

Dupilumab is a monoclonal antibody designed for the treatment of atopic diseases. It binds to the alpha subunit of the interleukin-4 receptor (IL-4Rα).[2] Through blockade of IL-4Rα, dupilumab modulates signaling of both the interleukin 4 and interleukin 13 pathway, which have been implicated in the pathophysiology of allergic disease, particularly asthma and atopic dermatitis.

Dupilumab is first systemic therapy to show positive Phase 3 results in patients with moderate-to-severe atopic dermatitis, a serious, chronic inflammatory skin disease marked by widespread rash, itching and associated psychosocial comorbidities.  U.S. regulatory submission for dupilumab planned for third quarter of 2016.

So, how does this drug enter the world of CSS you may be asking yourself.  Well, a clinical study was done, Effect of Subcutaneous Dupilumab on Nasal Polyp Burden in Patients With Chronic Sinusitis and Nasal Polyposis, which showed some positive results.  As we know many CSS/EGPA patients suffer from Nasal Polyps and Sinusitis.

In 2013 there was a study of  Dupilumab in Persistent Asthma with Elevated Eosinophil Levels with promising results.

My Conclusions on the UMABS:

I think there is great promise here to help alleviate some of the symptoms of CSS and I am very excited to see how much research is being done.  We as a CSS/EGPA community because of the rarity of our illness depend on drugs being marketing to other communities and then being studied and used off label for CSS/EGPA (this was true for Rituxan many years ago).  As always it is up to you as a patient to do your research before beginning any new drug therapy, each have their burden of side effects and as always insist on careful and continued monitoring while on and after any drug therapy.

 A really good follow-up article to read

Novel targeted therapies for eosinophilic disorders by Michael E. Wechsler, MD, MMSc, Patricia C. Fulkerson, MD, PhD, […], and Amy D. Klion, MD

From 2012 but a great Table graphic explaining Biological drugs in asthma treatment.

PDF links to handouts and prescription information (including known side effects):



want to read more about CSS/EGPA?

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It’s hard…. what Dr’s never tell you

Although this is written for CVID (people who are receiving IG replacements) — this really is an article for anyone with a chronic, incurable illness.
After reading this I felt like the feelings I was having recently are not mine alone.
“It’s hard.That’s what they don’t tell you when you get diagnosed. They tell you things like “It’s manageable.” Of course, that is what they’re supposed to do. They’re doctors. But nobody ever tells you that it’s hard”….. click on the link to read more.…/post/living-with-cvid.aspx

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CSS /EGPA December Awareness Post

December’s Churg Strauss Awareness Post is up and ready for sharing.

Join Dennis L. on his journey.

Is That A Horse Or A Zebra?

by Dennis L.


When I asked myself why I volunteered to write something about my history with  Churg Strauss Syndrome (CSS) (also known as eosinophilic granulomatosis with polyangiitis [EGPA] or allergic granulomatosis,)  I heard a voice that sounded like many doctors we’ve all seen and heard: “Could be the medications.”

Then I asked myself what angle should I take and I heard some of those same voices: “I don’t know, let’s run some more tests and see what develops.”

I underwent seven sinus/polyps surgeries prior to my diagnosis of CSS in 2005. The last surgery was in late 2004, from which I had trouble bouncing back…literally! Active in youth sports coaching for years, my attempt to return to basketball practice left me on the sidelines, dizzy and exhausted. I thought that maybe that nasty three letter word ”age” might have slowed my recovery, so I went about the business of living and working, acting as if everything was okay.

Two weeks later, I was hospitalized due to shortness of breath. imagesPulmonary Infiltrates showed up in both lungs, I was treated for pneumonia with antibiotics and oxygen, while giving the same “no” answer to that pleasant question: “Are you coughing up anything?” After two weeks of being unable to convince the pulmonary doctors that I did not have pneumonia, I heard from my primary care doctor about an article he had just read in The New England Journal of Medicine concerning CSS…First time he had heard the term, First time I had heard the term. He checked with the ENT who had performed the sinus surgery and found my Eosinophil Blausen_0352_Eosinophil count was excessively high. My primary care doctor had no hospital privileges so we worked together to get the disbelieving doctors to drop the antibiotics and start a high dose of Prednisone. Two days later, I walked out of the hospital without the aid of any added oxygen.

As I tried to reduce the Prednisone, other symptoms presented themselves; neuropathy in arms, legs, and feet, skin rash on legs, fatigue and blood clots. I was sent to the Medical University of South Carolina, where I was immediately started on around-the-clock IV’s of cyto500aCytoxan and steroids for four days. After dismissal, I received IV treatments of Cytoxan once per month for six months, along with being placed on oral dosages of Methotrexate and Prednisone.


Subsequent to that initial fun, I’ve had a number of illnesses: pulmonary embolisms, prostate cancer, phlebitis, cataracts in both eyes, and possible kidney and abdominal involvement.

I’ve also had many personal setbacks since 2005: my wife decided to leave after 34+ years together, the loss of work and the need to go on disability, personal bankruptcy, and the deaths of my parents in the past three years.

Understanding that not everybody’s symptoms, tolerances, or life situations are identical, I

'There are some things they don't teach you in medical school. I think you've got one of those things.'

believe there are two major stages in dealing with life with this disease. The first stage consists of sitting on the sidelines letting doctors, nurses, and tests run your life, becoming an accomplished actor when you know that something is not right with your body. Others don’t believe it so you use your acting skills to move into denial…maybe even believing you don’t really have CSS and everybody else must be right.

The second stage takes a more positive and proactive approach, believing and hoping that you do have some power over this unique syndrome. Actively question doctors and test results. Don’t accept snapshot results…make sure your medical team is looking at trends. Change doctors who don’t try to answer your questions. Believe that there are people out there who can help you. Get back in the game as much as possible…don’t let everything keep you on the bench!

Now to explain the title: in my recent search for another opinion, I was referred to a new nephrologist. He was a pleasant young man. We had a good discussion on autoimmune diseases and the need to treat them differently. He then related a quote from his medical professor: “If you hear hooves, it may not be a horse, it may be a zebra.” With autoimmune diseases, you need to be sure your medical team is looking for both the horse and the zebra!images-1

Kevin Selig  was diagnosed in January 2014 with Churg Strauss Syndrome and fought a courageous battle against the disease. Kevin passed away on Saturday, June 21, 2014, at the Mayo Clinic Hospital in Jacksonville, Florida.
We in the CSS community were saddened by the loss of such a vibrant human being and reminded how our illness often goes undetected until too late.  Glenys , a very brave CSS warrior, set us into motion to bring awareness to our disease with a challenge to raise awareness of Churg Strauss Syndrome by posting a story on the the 1st of every month in an effort to let the world know we exist and we want to help others obtain earlier diagnoses. 

Link to other CSS awareness posts in memory of Kevin Selig

General CSS/EGPA and Vasculitis Information

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What’s worse than being ill 24/7?

Every Month I have the honor of hosting a post by someone in the the Churg Strauss Syndrome Community telling the world about what’s it like to live life with CSS.

CSS is what is called an invisible illness, we carry most of damage within our bodies and tend to look ‘normal’ on the outside.  The damage is deep and I am humbled by my fellow CSSers on how they keep going on day after day.  How hope burns so bright and even though our disease is considered to be an rare illness, we are all hopeful of new medical treatments in the future.

Here I present Emma’s story.

What’s worse than being ill 24/7?

Being ill 24/7 yet nobody believing you!

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September 2015 – CSS awareness by Shawna

On the 1st of every month, I host a post by a member of the CSS community so that we can get the word out about CSS and help people get earlier diagnosis.

This Month’s post is by Shawna and she lets us into to her world and how she has had to alter her life in order to live with CSS.  Her wonderfully honest post is not about the medical tests and the process of diagnosis but rather how she has had to change herself in order to live with CSS and how this has impacted her both mentally and physically.

Shawna shows us how when life does not go as planned we just need to stop and look around us to find joy and love.

Please read, enjoy and share.

September 2015 — by Shawna


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Asthma Treatment Medication

11696307_10207073310935985_2105916589720375038_oThis is an informational post about Asthma medications and treatments.  Always consult a doctor before beginning, changing, or discontinuing any asthma treatment.  Asthma is a serious condition that without proper management  can lead to death.   I am NOT a medical professional, these are just useful sites I have found.   The cover photo is from a drug company and  does not list all options, please read on and click on the links to see what other medications are available.


Some of us have had Asthma for many years and forget why we take a particular type of medication for Asthma.   Here is some great background and reinforcement reading and charts that I found today.  For me it is always a great reminder of why I take some medications for my Asthma associated with my CSS, how these medications affect me affect me, and what other options there may be out there.


Here are some good graphics explaining asthma inhalers and a very text chart from the American Lung Association of different types of asthma medications (it’s from 2009 so does not have the latest and greatest) but it’s  a nice read or reminder.



Extremely nice PDF chart with pictures of each medication and dosages available from the state health dept of Minnesota. (use your ‘zoom in’ button on your PDF reader to make it more readable)



images-1From National Asthma Council Australia  here is another chart.

Look around their site it’s full of great information

Lastly a 32 page PDsup-doc-homeF guide written for doctors called the Pocket Guide for Asthma Management and Prevention.  The intended audience is doctors and nurses and it was updated in 2015 which makes it very relevant.  It states it is based on the global strategy for asthma management and prevention.  I learned a lot from this guide — I like to know how my physician thinks and what it is based upon.     The main site for the Global initiative for Asthma is

I didn’t start my morning by  intending to write this post, but I awoke with an asthma attack and was wondering about my medications so it lead to this post.  I hope everyone find something new or educational and please feel free to share and comment with your useful asthma links for other readers.


to return to the Karen in Wonderland Blog Posts

to return to more information about CSS / Vasculitis

to return to other monthly CSS awareness posts




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CSS awareness post August 2015 by Sheila Eddy

A NEW Churg Strauss Awareness Post for August is up and ready to be shared.  Read about Sheila’s Journey and how ‘The Cough’ lead her to her CSS diagnosis.

IMG_2392Follow this link to Sheila’s journey….

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The Ugly Side of Competitive Chronic Illness

4850038-3x2-700x467Is having a Chronic Illness really a competition?  

Logically you would think not, but in some patients eyes it is…

I can’t believe I even have to mention this happened in a Symposium for people with Vasculitis. I was greatly hurt when I overheard these comments and at one point I was close to verbally slapping someone as I felt the need to protect a young adult patient that I greatly admire.

First, let me say Vasculitis is a roller coaster. Sometimes we find ourselves heading up the

Silhouette of roller coaster; sunset

Vasculitis is a roller coaster

highest hill. We may look great, we may feel pretty darn good but we know our illness is a chronic one and we never know when the down cycle is coming. Other times we are in the down cycle. We feel like hell, amazingly enough, many of our aches, pains and organ damage cannot be seen on the outside. We may cover the bruises, the rashes the sores that are not healing properly. You can NOT look at me and tell me what my Oxygen level is, You have no idea that I may have just stepped out and done my pocket nebulizer in private. You do not know the hell I may have been through or the hell that may be ahead of me.

I have enough difficulty with people I do not know judging me, so the last thing I expect to encounter or over hear at a gathering for patients, their families and doctors is someone judging other illness or feeling the need to belittle their experience and express verbally how ‘lucky’ that patient is that they are not as sick as the judging person perceives them to be.

I am angry! I am sad.   I can’t stay quiet about this. Vasculitis is not a competition. There are no winners for being the perceived ‘sickest’. We are all victims and are trying the get the best quality of life that we can. How can you look at someone in year 5 of this chronic illness and just because they ‘look good’ judge them as never being that sick. Maybe their tracheotomy scar is hidden by that pretty scarf they wear, or they have worked their butts off learning to walk again after that stroke that had years ago.

I for one look darn good on the outside. I work at making sure I look good when I go out. Don’t tell me I should be happy that I can eat when you see my few pieces of fruit on my plate at breakfast. You have no idea that I spent 30 minutes throwing up in my hotel room 19808_582940935142261_8881695349126739132_nand then took a Zofran, washed my face and headed down to the conference with a smile on my face hiding whatever pain I may be in.   You were not in my room at 1am when my asthma got so bad that I had to do back to back nebulizer treatments and then the albuterol in my system made it so I could not sleep. Yet I drugged my tired, aching body out of my room to be at the 9am session. Yes, I smiled and I laughed. For me that is the best medicine. I could curl up in bed and feel sorry for myself or I could complain about everything or be angry at how this illness has altered in my life. You have not walked in my shoes, you have no idea what my shoes look like.

I was shocked to hear a few attendees take time to belittle others about their illness. Signifying that ‘they’ were sicker. This is NOT a one up game people. How dare you say some young adult was ‘lucky’ when you have no idea of the hell she has been through and how she just keep going and has not and will never give up. Did you look?  Did you see the scars she carries? Did you even spend a moment and talk to her and really listen to what she may have been through before you belittled her illness and called her, “lucky”. She may choose to move on and move forward rather than wallow in self pity or dwell upon her past medical history.  She is living in the moment.11168468_841650835900962_5996818757295356416_n

Sure, I get jealous of those patients that may be off prednisone or are in remission. That jealousy can turn to anger that WHY have I not be given the gift of prednisone free days or why remission may always be a unreachable goal for me. Sure I have those feeling but to overhear on another occasion someone openly ask another participant are they sure they even have Vasculitis because that patient is currently off prednisone.

It is nice to hear from other patients what medications they are on because you might hear about something new or you might feel good that is they lowered a certain medication, you may also be able to do that in the future. To use a ‘what meds are you currently taking’ question and then turn it into an attack on a person… so wrong and so sad. The accuser never even knew this patient has had heart surgery related to her Vasculitis. The sad part is this patient was attending their first VF symposium and finally felt like they belonged and had people around them that understood what personal hell they may be going through.   I feel sorry for the accuser for being so angry at the world that they never took time to listen.. really listen. If they did maybe they have learned a thing or two.

We should not have to justify our chronic illness. We should not have to make ourselves look bad just so others would not question our condition. We are allowed to look good, laugh and have fun.   Please, if you are one of these ‘judges’ or ‘one up addicts’… STOP IT!

We are allowed good spells. We can go out and climb a mountain, run a race, or ride our bikes. We should not have to hide the fact that we enjoy life and are trying to make the 11329875_770964676349497_5327448943496000336_nbest life possible for ourselves. We should not have to hide it. We never know when our health is going to change, so please stop the judging if we are having a good spell and enjoying all that life has to offer.

We are a Vasculitis community and should act as one. We should help each other through the tough parts and hold each others’ hands when things get miserable. We should share information and not be ashamed to hide our successes. We NEED people that are in remission or on low dosages of medications to stay in the social media groups and not be scared away because they ‘no longer seem ill’. It is important to see their accomplishments and hear their stories. They can give positivity to the social media groups, which is greatly needed at times. All scary, all the time is never good unless you are in a Stephen King novel.   Vasculitis becomes less scary when we hear about how people may be off or on minimal medications, or are out in the world accomplishing things. Maybe if we listen we can get ideas of how to alter our lives to get the most out of it.

We are given one life. To have Vasculitis sucks but we need to learn to be kind to ourselves and others with this crazy roller coaster of a chronic illness so we can learn to move forward.

Thank you for listening and I apologize if you were one of those victims of people needing to be sicker or belittle you. The Vasculitis community is a great group and please stay active and you will find you place with like-minded individuals. The beauty of social media is that there are now many groups for Vasculitis patients. Some are for specific disease types, some for general questions, some for social and fun which allows member to swear away from all Vasculitis all the time, some are for Alternative therapies or healthy cooking and some are for religious and prayer circles.   You can choose to belong, read or participant in any group you feel draw toward. If you don’t find one, think about starting your own group or blog.   I started this blog because I felt the need to share my positive focus even in the face of this life altering illness. You may agree with me, you may not – you can choose to read or follow my posts. I may not agree with you on some topics but that is OK. Diversity is what makes life special.

Just a few words of caution about social media:

#1 – Don’t spend all your time online, go out and live life not just observe it or read about it on the internet. If you are ignoring your own family due to a drama on the internet maybe you should re-evaluate how you are spending your time.

#2 – People on the internet can falsify who they are or the extent of their illness.   Be careful.   If your ‘spidey sense’ says something may not be right, you have the power to unfollow or block that person. Sometimes the best thing is just ignore them, without attention the internet ‘fakers’ tend to go away or find another group. (I know this may contradict the meaning of this post… but meeting someone in person and on the internet is two very different things) Trust me.. been there.. lived through that hell and have finally moved forward.

#3 – NEVER, EVER send people money over the internet that you do not know or can not verify! Direct people to local groups that can assist them or help them with medical assistance.





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Information from the Vasculitis Patient-Powered Research Network

During the 2015 International Vasculitis Symposium we had the opportunity to connect with patients and their families. One of the questions we received about joining the Vasculitis Patient-Powered Research Network most often was about data security.

We provide detailed information about the security of your data and how it will be used on our website at:

Interested in joining this Research Network and being an active part of research into Vasculitis?  How can you help?  Funny you should ask.  Join the V-PPRN (Vasculitis Patient Powered Research Network).  I find it kinda fun if you do it through their portal called V-Bold.  Then it seems more fun and you can earn ‘points’ to get some of that cool SWAG you saw from the convention and you can even get enough points by just answering surveys about how you feel or about a recent flare that you get to have a one on one conversation with a researcher (kinda cool…).

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Kathryn tells her CSS/EGPA story

The July Awareness post is finally up and I hope you enjoy the CSS life story written by Kathryn.  She shows how CSS totally changed her life and the frustration of years of not knowing what is going on on with your own body.

Kathryn shares how her belief if God has helped her through and after her initial support system (her husband) abandoned her, she found a much stronger support system through her sister.

Please read and enjoy

Kathryn’s Story


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