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Meet, discuss & support other patients or families living with CAPS . Participate in group discussions. Contribute to topics, or just share what's on your mind
Conversations tagged diagnosis
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I thought I'd do a little intro, I turn 29 on the 16th of June and currently live in Western Australia. I first learned of Muckle-Wells when my brothers GP first brought it up. Though its really being my sister whose chased up info and got the ball rolling the most. This might have something to do with my darling little niece whose about 18 months old. My sister has since had her blood test as confirmed Muckle-Wells and not just my brother but also my Dad have blood tests pending. There is only me now, having got a referral, who has yet to start the testing process.
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karend published about 1 year ago | Originally written in EnglishDear Henrik,
I am also going to send you a more detailed personal email, but want you to know that there are other patients that are very young taking anakinra, and often the dose needs to be raised over a few months to reach the right amount of medication to fully cover all the NOMID/CINCA symptoms. I have heard from a few others that have infants that have experienced the same thing when starting anakinra, There are a few cases that the dosing of anakinra has been split into twice a day to fully cover the symptoms, which has helped, but is not commonly needed with most patients.
I will contact you via email, and will gladly send you CAPS booklets. Please let me know how many you may need. The NOMID Alliance is a non-profit, so we do not charge for the booklet, but if people want to make a donation to cover costs for shipping, we are always thankful! The CAPS booklet is available online to download for free at any time, until I can mail them to you by post from America. The link is: www.nomidalliance.net/downloads/finalCAPSb...
Thanks so much for contacting us, and I will reply in more detail to you right away about dosing, and practices with young infants, and also some contacts of specialists that may be able to guide your doctors with this process.
Best Wishes,
Karen Durrant
Thanks,
Karen Durrant
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paul published about 1 year ago | Originally written in FrenchPour Henrik
Bonjour et bienvenu sur le site.
je confirme les informations de Karen, il y a en France des petits malades qui ont des difficultés pour le traitement. Le spécialiste qui les suit a donc prescrit des dosages spécifiques à raison de DEUX piqûres par jour pour l'ANAKINRA.
en ce qui concerne ILARIS, je ne connais pas de cas, mais je vais m'informer, ce médicament venant d'être autorisé en France depuis un mois.
En France aussi, il existe des spécialistes pour le Muckle et Wells Syndrome qui exercent dans des hôpitaux parisiens sous l'appellation "centre de référence"
ces centres de références regroupent des spécialistes : rhumatologues, pédiatres, ophtalmologues, dermatologues, otorhino-logues...qui travaillent ensemble.
pour connaitre la maladie MWS, vous pouvez avoir des informations complémentaires sur le site orpha.net.fr qui est disponible en 5 langues.
vous pouvez aussi bien sûr regarder sur ce site.
je me présente, je suis Paul Rivière, dont vous trouverez mon profil sur ce site, et suis le Président de l'association Muckle et Wells Syndrome CINCA amws-cinca, et mon parcours du combattant est développé dans la rubrique "comprendre".
nous venons de mettre en ligne notre propre site (hier soir) www.amws-cinca.eu
il y a un lien entre ce site et le nôtre : regardez à l'endroit des associations, en dessous de l'association de Karen.
pour le guides des CAPS, en français, élaboré par le laboratoire NOVARTIS (qui vend Ilaris) et un centre de référence français, le CEREMAI. je vous l'adresse à votre adresse mail
bien amicalement et au plaisir de vous lire et je souhaite de tout coeur que votre petite fille dispose très rapidement d'un traitement approprié.
Paul
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carew52 published about 1 year ago | Originally written in EnglishI thought I'd better do an update. I've being approved to try Anakinra and have an appointment scheluded in a couple weeks from now to get started on it.
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CAPS community news
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Cryopyrin-associated periodic syndromes: otolaryngologic and audiologic manifestations.
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News, published 2 months ago
Cryopyrin-associated periodic syndromes (CAPS) represent a spectrum of CIAS1 gene-mediated autoinflammatory diseases characterized by recurrent systemic inflammation. The clinical spectrum of CAPS varies from mild to severe and includes the syndromes historically described as familial cold autoinflammatory syndrome (FCAS), Muckle-Wells syndrome (MWS), and neonatal-onset multisystem inflammatory disease (NOMID). This article presents the largest cohort of patients with CAPS. The objective is to describe the pathogenesis, otolaryngologic, and audiologic manifestations of CAPS. -
Drug halts organ damage in inflammatory genetic disorder
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News, published 3 months ago
NIH study shows benefits of long-term Kineret therapy in people with NOMID -
Cuts in Ireland drastically impacting young man with CINCA's future
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News, published 8 months ago
Aisling McNiffe's voice crackles when she talks about her son's school prospects. Jack, a chirpy, fair-haired six-year old with a fondness for Toy Story movies, is the only person in the world known to have both Down's Syndrome and CINCA Syndrome, a degenerative disease that causes crippling headaches, severe arthritis, skin rashes, deafness and blindness. -
Clinical Outcomes and Safety: A Registry Study of Ilaris (Canakinumab) Patients
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News, published 10 months ago
The purpose of this observational study is to collect additional information regarding long-term safety and effectiveness of Ilaris in the treatment of CAPS patients in clinical practice. -
Anakinra to Treat Patients With Neonatal Onset Multisystem Inflammatory Disease
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News, published 12 months ago
This study will evaluate the safety and effectiveness of anakinra (Kineret(Registered Trademark)) for treating patients with neonatal onset multisystem inflammatory disease (NOMID), also known as chronic infantile neurological, cutaneous and arthropathy (CINCA) syndrome. -
From the Australian Prescriber: New drugs Canukinumab
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News, published about 1 year ago
CanakinumabSome of the views expressed in the following notes on newly approved products should be regarded as tentative, as there may have been limited published data and little experience in Australia of their safety or efficacy. However, the Editorial Executive Committee believes that comments made in good faith at an early stage may still be of value. As a result of fuller experience, initial comments may need to be modified. The Committee is prepared to do this. Before new drugs are prescribed, the Committee believes it is important that full information is obtained either from the manufacturer's approved product information, a drug information centre or some other appropriate source.
(Aust Prescr 2011;34:55-9)
Ilaris (Novartis)
vials containing 150 mg lyophilised powder for reconstitution
Approved indication: cryopyrin-associated periodic syndromes
Australian Medicines Handbook section 15.2.2 -
Más calidad de vida con biológicos en niños con patologías autoinflamatorias
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News, published about 1 year ago
En el segundo gran grupo, el del síndrome de la fiebre persistente, no mantienen estos episodios tan marcados. Aquí se ubica el síndrome de CAPS o criopirinopatías. Las criopirinas son las proteínas que ponen en marcha el mecanismo inflamatorio. -
“Studies of the Natural History, Pathogenesis, and Outcome of Autoinflammatory Diseases (NOMID/CAPS, DIRA, CRMO, Still's Disease, Behcet's Disease, and Other Undifferentiated Autoinflammatory Diseases)”
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News, published about 1 year ago
Overall Status: RecruitingThis study will examine and test patients with neonatal onset multi-system inflammatory disease (NOMID) to learn more about the cause and course of the disease. It will study the disease signs and symptoms and the possible role of a gene called CIAS1, and it will develop a database to gather information on patients with NOMID in the United States and around the world. It will also serve as a screening protocol to offer eligible patients participation in a treatment protocol, if an appropriate one is available.
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NOMID in the news in Canada
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News, published about 1 year ago
Such is the case for seven-year-old Brampton resident Michael Spiridakis, who suffers from neonatal onset multisystem inflammatory disease (NOMID), a genetic disorder that causes uncontrolled inflammation in multiple parts of the body. -
Wood River teen pushes recognition of rare diseases
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News, published about 1 year ago
Radney, 16, has a particular interest in the subject of rare diseases because almost four years ago she discovered she has Neonatal Onset Multisystem Inflammatory Disease, also called NOMID.....


