duchenneinfo.com
Duchenne Info | A site to assist anyone searching for information about Duchenne Muscular DystrophyA site to assist anyone searching for information about Duchenne Muscular Dystrophy
http://www.duchenneinfo.com/
A site to assist anyone searching for information about Duchenne Muscular Dystrophy
http://www.duchenneinfo.com/
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Michelle Jones
12363 D●●●●●●●ains Rd
Joh●●●own , Ohio, 43031
United States
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Michelle Jones
12363 D●●●●●●●ains Rd
Joh●●●own , Ohio, 43031
United States
View this contact
Michelle Jones
12363 D●●●●●●●ains Rd
Joh●●●own , Ohio, 43031
United States
View this contact
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Duchenne Info | A site to assist anyone searching for information about Duchenne Muscular Dystrophy | duchenneinfo.com Reviews
https://duchenneinfo.com
A site to assist anyone searching for information about Duchenne Muscular Dystrophy
Our Fight - Living with Duchenne Muscular Dystrophy: June 2012
http://ourfightdmd.blogspot.com/2012_06_01_archive.html
Our Fight - Living with Duchenne Muscular Dystrophy. Saturday, June 23, 2012. On May 25th Jocelyn had a blood draw for genetic testing to see if she is a carrier of the DMD gene. The test results came back postive stating: Mutation detected. A deletion mutation in the DMD gene empassing exon 46 was detected. We have not told her the results. We are going to wait for her to ask. I'm worried about telling her. I hate that she will think about it for several years to come. I just want her to...Next time I r...
Our Fight - Living with Duchenne Muscular Dystrophy: April 2012
http://ourfightdmd.blogspot.com/2012_04_01_archive.html
Our Fight - Living with Duchenne Muscular Dystrophy. Thursday, April 19, 2012. I will be doing a medical update on Logan's April 3rd follow-up appoitment soon. After every appointment I receive a copy of the dictation from our doctor. I'm waiting on that report before I post my update. Subscribe to: Posts (Atom). Cincinnati MDA Muscle walk March 24, 2012. View my complete profile. 5/25/2012 - Blood draw on Jocelyn for genetic testing to see if she is a carrier of Duchenne Musclar Dystrophy. 10/5/2011 - H...
Our Fight - Living with Duchenne Muscular Dystrophy: Heartless people
http://ourfightdmd.blogspot.com/2012/06/heartless-people.html
Our Fight - Living with Duchenne Muscular Dystrophy. Saturday, June 23, 2012. Last night I received an email stating that I had a new comment on one of my blog posts. The post came to me anonymously. The post says this:. Anonymous has left a new comment on your post " Hope. My response to this anonymous post is going to educate. It is obvious that whoever wrote the post is not informed with the condition of Duchenne Muscular Dystrophy. Acts as a cushion, as well as a kind of glue. Duchenne is typically d...
Our Fight - Living with Duchenne Muscular Dystrophy: May 2012
http://ourfightdmd.blogspot.com/2012_05_01_archive.html
Our Fight - Living with Duchenne Muscular Dystrophy. Wednesday, May 30, 2012. I understand some of your confusion from the visit. We will make sure to give you more concise and clear information in the future. John Lynn Jefferies, M.D., M.P.H. Wednesday, May 23, 2012. There truly is a lot I need to know with Logan's condition and I hope that I can just remember them all. Please keep Logan in your prayers as we continue through this journey. Tuesday, May 22, 2012. Wow, it's been a while. It seems like...
Our Fight - Living with Duchenne Muscular Dystrophy: January 2012
http://ourfightdmd.blogspot.com/2012_01_01_archive.html
Our Fight - Living with Duchenne Muscular Dystrophy. Tuesday, January 3, 2012. I hope that everyone had a great holiday season. We sure dd! Christmas day is so exciting. I love watching the excitement of my turkey's. They woke up around 6:00 AM. I love it that Jocelyn came in to wake us up. "Mommy, Daddy Santa came it's time to get up." Then about 15 minutes later we hear the sound of Logan ripping. New Years Eve we celebrated with my side of the family. I had a really great time. Every year we d...Like ...
Our Fight - Living with Duchenne Muscular Dystrophy: Hope
http://ourfightdmd.blogspot.com/2012/05/my-mom-and-i-took-trip-up-north-to.html
Our Fight - Living with Duchenne Muscular Dystrophy. Tuesday, May 22, 2012. The information I received that is near to my heart and gives me hope for Logan is in the exon skipping. I have attached a link if your interested in reading:. Http:/ www.muscular-dystrophy.org/about muscular dystrophy/research faqs/612 what is exon skipping and how does it work. All we have is hope, These clinical trials give me hope that Logan will be have a good quality of life. May 22, 2012 at 3:17 PM. View my complete profile.
Our Fight - Living with Duchenne Muscular Dystrophy: Clarity
http://ourfightdmd.blogspot.com/2012/05/clarity.html
Our Fight - Living with Duchenne Muscular Dystrophy. Wednesday, May 23, 2012. I'm glad to have the clarity and it does seem at this point there is no need to be alarmed. I'm hoping that if there is something going on the holter test (the 24 hour monitoring device) will show something and we will proceed with the MRI. This will enable Logan to get the appropriate treatment he needs and hopefully prolong the effect of cardiomyopathy. Subscribe to: Post Comments (Atom). View my complete profile. 12/22/2011 ...
Our Fight - Living with Duchenne Muscular Dystrophy: November 2011
http://ourfightdmd.blogspot.com/2011_11_01_archive.html
Our Fight - Living with Duchenne Muscular Dystrophy. Friday, November 11, 2011. Jocelyn has been very supportive of Logan. Last night she decided that she would also wear some night night shoes. She got a pair of her boots and wore them all night. She is such a sweet girl and loves her brother. I'm so proud of her for being there for her brother. I love both of those turkey's and together we will get through all of this. Enjoy the pictures I would have to say they are pretty cool. Sunday, November 6, 2011.
Our Fight - Living with Duchenne Muscular Dystrophy: March 2012
http://ourfightdmd.blogspot.com/2012_03_01_archive.html
Our Fight - Living with Duchenne Muscular Dystrophy. Friday, March 30, 2012. On May 10th Logan will have an echo cardiogram. Then we will have our first appointment to see the cardiologist. I'm also anxious for this appointment. Logan has had 3 episodes were it has been noticed or he has complained of his heart beating rapidly. So I'm anxious about getting this checked out and to talk with the cardiologist about how Duchenne will effect his heart. MDA Muscle Walk - Why we walk. Our team - Logan's Hope.
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duchenneheroes.ingmarvanzutphen.nl
Introductie
700 kilometer - 7 dagen - 4 landen - 1 DOEL. Welkom op onze website voor Duchenne Heroes. Na de geweldige en indrukwekkende ervaring van Duchenne Heroes 2009, gaan wij in 2010 opnieuw meedoen aan Duchenne Heroes. Duchenne Heroes is een zware mountainbike tocht die in 2010 voor de 5e keer wordt gehouden, met als doel aandacht vragen en zoveel mogelijk geld ophalen voor Duchenne. Klik hier voor mijn verslag van Duchenne Heroes 2009. Het sponsorbedrag is op het moment 6.640,52.
Home — Duchenne Heroes Italia
Hai dimenticato la password? Hai dimenticato la password? 34 Eroi già iscritti. Lasciati ispirare e unisciti a noi! Il Duchenne Heroes è un evento di solidarietà alla sua terza edizione in Italia. Un’esperienza unica, emozionante: sette giorni in cui si percorreranno oltre 500 km lungo percorsi e panorami mozzafiato con un unico obiettivo: raccogliere fondi per finanziare la ricerca sulla Distrofia Muscolare di Duchenne. Non puoi perderti questo evento! Ti sentirai un altro dopo quest’esperienza! Insieme...
Home – Duchenne Heroes 2018
9 - 15 september 2018. Singletracks and steile heuvels. Heb jij je startbewijs en ben je erbij. Weekend-Heroes ingeschreven. € 268.224,84. Wat gebeurt er met het geld.
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duchenneheroes2008.blogspot.com
Duchenneheroes 2018 Riders for Pelle
Duchenneheroes 2018 Riders for Pelle. Van 9 t/m 15 september 2018 vindt de 13e editie plaats van de Duchenne Heroes, dé mountainbiketocht die opnieuw helemaal herwerkt wordt. Schrijf je in en ervaar deze 7-daagse mountainbiketocht tvv. het onderzoek naar de spierziekte “Duchenne-spierdystrofie”. Fortbiken against Duchenne - 6 uren van het Fort van Borsbeek. Meer info en inschrijving. Zaterdag 20 januari 2018. Doen: inschrijven voor Fortbiken against Duchenne. Vrijdag 19 januari 2018. Trooper is dé manier...
Duchenne Info | A site to assist anyone searching for information about Duchenne Muscular Dystrophy
A site to assist anyone searching for information about Duchenne Muscular Dystrophy. Skip to primary content. Skip to secondary content. A One Stop Shop for Duchenne Muscular Dystrophy is here! September 23, 2011. This slideshow requires JavaScript. The information is for informational purposes only and isn’t endorsed by the authors of this website and shouldn’t be used to diagnose or treat your child. Http:/ www.cincinnatichildrens.org/svc/alpha/n/neuromuscular/default.htm. Saving Our Sons One Story at ...
Blog de duchennejo - Fin - Skyrock.com
Mot de passe :. J'ai oublié mon mot de passe. Les lois sont comme les proverbes : on en trouve toujours une qui justifie la violation de l'autre. Henri maret. Ps3 a vendre. Plus d'info 0494/76.27.64. Mise à jour :. Ce que Mr.Grumpy écoute. Requiem for a Dream (LotR TTT Trailer). Abonne-toi à mon blog! Rien Un fil venant de nulle part n'alant nulle part, perdu parmi des millions de millions d'autres fils identiques mais dont le possesseur se croit le centre de l'Univers. Ou poster avec :. Ou poster avec :.
The Foundation to Eradicate Duchenne – Working for a Cure!
Working towards a cure. Working towards a cure. Working towards a cure. 11th Annual Jeffrey Steele Concert. Green’s Grocery, Leipers Fork TN. 6:00 pm - 9:00 pm. 18th Annual Dining Away Duchenne. 15th Annual FORE Duchenne. Westfield Golf Club, Clifton Virginia. The Story of the Foundation to Eradicate Duchenne. November 3rd, 2016. FED Praises Vamorolone Development Deal. The following statement was issued today by Foundation to Eradicate Duchenne co-founder and President Joel Wood:. March 24th, 2016.
Blog de duchennemiguel - miguel en force - Skyrock.com
Mot de passe :. J'ai oublié mon mot de passe. Bienvenu sur mon sky regarder les tof et lachez des coms. Mise à jour :. Abonne-toi à mon blog! Moi et ma femme. N'oublie pas que les propos injurieux, racistes, etc. sont interdits par les conditions générales d'utilisation de Skyrock et que tu peux être identifié par ton adresse internet (67.219.144.114) si quelqu'un porte plainte. Ou poster avec :. Retape dans le champ ci-dessous la suite de chiffres et de lettres qui apparaissent dans le cadre ci-contre.
duchennemusculardystrophy-2.wikispaces.com
DuchenneMuscularDystrophy-2 - home
Skip to main content. What is duchenne muscular dystrophy? Duchenne muscular dystrophy (DMD) is one of a group of muscular dystrophies characterized by the enlargement of muscles. DMD is one of the most prevalent types of muscular dystrophy and is characterized by rapid progression of muscle degeneration that occurs early in life. Who discovered the duchenne muscular dystrophy? Mostly affects boys (rarely girls). Often brothers or male relatives have same problem. May develop a sever.
duchennemusculardystrophy.wikispaces.com
DuchenneMuscularDystrophy - home
Skip to main content. Create interactive lessons using any digital content including wikis with our free sister product TES Teach. Get it on the web. Duchenne muscular dystrophy that it keeps on loseing muscular cells. You are born with it becuase it starts about two to six years old and its dominants. That you can not use your mucuals whehn your yung and you will be prillised. They can be equally and because it can happened to anyone. It will happen in the arm and legs. Help on how to format text.
