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Mcardles Disease: more detail

McArdle disease presenting as acute renal failure.(Disease/Disorder overview): An article from: Southern Medical Journal by Jayasree Pillarisetti, Awad Ahmed, 2007-03-01

The Migraine Brain: Your Breakthrough Guide to Fewer Headaches, Better Health by Carolyn Bernstein, Elaine McArdle, 2010-04-30

lists with details

Adult Outpatient Programs And Services Muscular Dystrophy Association Clinic
Metabolic Diseases of the Muscle. Phosphorylase deficiency(mcardles disease). Acid Maltase Deficiency (Pompe's disease)
http://www.njrehab.org/MDA.htm

Extractions: The JFK Johnson Rehabilitation Institute's Muscular Dystrophy Association (MDA) Clinic provides a multidisciplinary approach to the diagnosis and treatment of over 40 muscular dystrophies. Adult and pediatric clinics are held once a month throughout the year. Services consist of examination, testing and counseling performed by a physiatrist, physical, occupational and speech therapist. A social worker and registered nurse also assist in assessing the patient's/family's needs. After establishing the diagnosis and treatment plan, the patient is monitored two to three times a year through follow-up clinic visits. The clinic, partially supported by the Muscular Dystrophy Association through a grant, is one of 230 hospital-based clinics affiliated with the MDA. If you suspect that you or your child may have the diagnosis of muscular dystrophy, you may call for a clinic appointment. Appointments for the adult clinic can be made by calling (732) 321-7733 and the pediatric clinic can be reached at (732) 548-7610.
McArdle's Disease And Exercise
I can provide a lot more information about my life with mcardles disease, if requested.
http://neuro-www.mgh.harvard.edu/neurowebforum/NeuromuscularArticles/McArdlesDis

Extractions: This response submitted by David W. Brock, Ph.D. on 2/16/97. Author's Email: dbrock1111@aol.com I was diagnosed with McArdle's disease through a muscle biopsy as the University of Colorado Medical Center in 1975. I then volunteered to participate in an extensive series of research experiments in McArdle's disease. One set of experiments showed that I could do all of the exercise I wanted as long as I stayed below the cramp threshhold. I would ride a stationary bicycle with blood samples taken immediately before and after the workout. The samples showed that there was no rise in the level of creatine phosphokinase in my blood before or after the exercise, indicating that there was no muscle damage, as long as I eased off on the exertion at the first sign of cramping. Walking is probably one of the best exercises for a person with McArdle's disease, since it circulates the blood through the muscles. The main problem for a person with this disorder is that the muscles cannot burn their stored fuel, glycogen, so that their muscles must extract all of their fuel from the blood. Yesterday, I went on a vigorous five mile walk, and I did not have any problems. I did not see my urine turn brown, which would indicate myoglobinuria. The worst type of exertion for a person with this disorder to engage in is lifting heavy objects, such as moving furniture. I have often given myself severe cramps followed by myoglobinuria this way. This is because the muscles are stationary during heavy lifting and the blood flow is limited. I have found that I can lift heavy objects if I do some exercise to warm the involved muscles up first. The exact reasons why this helps are not known to medical science.
Mioti: Medical Condition
Maxillofacial Dysostosis, Maxillofacial Surgery. May Hegglin Anomaly, mcardles disease. McCune Albright Syndrome, McKusick Syndrome.
http://www.mioti.com/cat/condition/results.asp?Alpha=M
Mioti: Medical Condition
Condition mcardles disease. MEDLINEplus McArdle Syndrome. MEDLINEplus,a goldmine of good health information from the world's
http://www.mioti.com/cat/condition/condition.asp?Cat=McArdlesDisease
5 Listing Of Potential Topics Coris Disease Galactosemia McArdles
Coris disease. Galactosemia. mcardles disease. Von Gierkes Disease. Pompes Disease
http://www.uwlax.edu/faculty/weaver/pdfs/writing_emphasis.pdf
McArdle´s, Morbus McArdle, Glykogenose Typ 5, Phosphorylase Kinase Defizienz, P
Translate this page Info). mcardles disease, Private Seite eines McArdle Betroffenen inden USA (spezielle Info). Homepages Australien, Erläuterung. MDA
http://www.morbus-pompe.de/glyko_typ5/mcardle_info.html

Extractions: (McArdle Krankheit, Myophosphorylase Defizienz) Inhalt Beschreibung der Erkrankung: McArdle, was ist das? Medizinischer Text (* = Quelle: Muskelerkrankungen, Felix Jerusalem und Stephan Zierz, Georg Thieme Verlag Stuttgart, 2. Auflage, 1991) Deutsch Englisch McArdle Krankheit McArdle Disease Glykogenspeicherkrankheit Typ V Glycogen Storage Disease Typ V Glykogenose Glycogenosis Myophosphorylase Mangel Myophosphorylase Deficiency Auf der DGM-Homepage: http://www.dgm.org/muskelk/letters/letter3/kilimann.html http://www.ruhr-uni-bochum.de/pressemitteilungen-1996/msg00135.html
Untitled
An English physician named Dr. Brian McArdle diagnosed the first case of mcardles disease in 1951. At that time he reported on a 30 year old man who experienced pain followed by weakness and stiffness after exercise. also known as Glycogen Storage Disease Type V . Myophosphorylase Deficiency, McArdle Glycogenesis, McArdles Myopathy or
http://webportfolio.csuohio.edu/~ekutchman/Artifacts/ARTIFACT8/stand_8_mcardlepa
Page 17
Neuromuscular Disorders, Dystrophic Cardiomyopathy, mcardles disease, General Paediatricsand Paediatric Neurology General Paediatrics Muscular Dyshophy and
http://www.keele.ac.uk/depts/rjah/yearbook/Consultants_Services/consultants__ser
AGSD - UK Site - Guest Book
I was diagnosed with mcardles disease in 1999 after suffering all my life never knowing what was wrong with me.
http://www.agsd.org.uk/home/guestbook.asp

Extractions: Posted by Vicky on the My father was diagnosed with GSD in 1961. At the time, we were told that he was only the 3rd person to be diagnosed with this disease. While doing research on Dad, my brothers and I had to undergo a lot of testing, also. My mother was told that two of us showed symptons, but the doctors refused to tell her which two. For over 40 years, we have lived with this cloud hanging over us. It's been like waiting for a bomb to explode. Since my father was in a Veterans Hospital for three years and this was where the testing was done, I tried for several years after Dad died to track down his records. Apparently, the physician in charge took them with him when he left and has since died. I did track down one of the other doctors briefly. He remembered the case, but did not know the outcome. Because of Dad's delicate health, they convinced him the second tests proved the first tests wrong and this became a giant family secret. Only now is truth finally starting to come out as my youngest brother and I are unable to keep our strength up and our children are starting to show symptoms. Unfortunately, the scarcity of information only complicates the problem. When asking for help, I have been told I am "crazy,"; "What makes you so special?"; and, "You should just let your whole family die out!"
Curt Rogers
Curt Rogers. Disability mcardles disease, My name is Curt Curtis M .Rogers ,butjust Curt does fine. My online name is Gambit. I have mcardles disease .
http://www.withoutwheels.org/Profiles/crogers/

Extractions: Curt Rogers Disability: McArdles Disease My name is Curt "Curtis M .Rogers" ,but just Curt does fine. My online name is Gambit. As Paul does, I also play Golf Online and that is how I came across his site here "Without Wheels", and decided to write him and tell him my story. I have "McArdles Disease". Basically McArdles disease is a muscle disease that affects the skeletal muscles, which in turn if over stressed can affect the kidneys. In extreme cases as mine, they can completely shut down the kidneys. Well, I remember the days in elementary school, as far back has kindergarten. My School was about a mile and a half walk from home. Well, that walk would take me almost an hour to do. All through elementary school, I could not walk more then 50 yards without having to stop and sit down and rest. My legs would get this burning in them and they would feel like they weighed more then ten times then they actually were. The muscles wouldn't just move them anymore until I sat and rested. Running was out of the question. I remember them days in elementary school when we had them 40 yard dash's and stuff "Field Day" I think they called it. Well I would get up to them lines to run them dash's just knowing I could beat everyone and I did....for about 10 steps. I would push so hard that my muscles would completely lock up on me, but I would keep pushing "Something that I did not know could really hurt me then" until I made it to that finish line "Last every time I might add". Even the girls would beat me and I'm only talking about a lousy 40 yards. Needless to say, I would collapse just about when I crossed the line. Somehow I would manage to keep my feet under me and try to recover quickly. I hid it very well because it was embarrassing, at least to a 6 to 11 year old it was.
MEMBER TRIVIA
Answer. 1. mcardles disease 2. I loved sports and loved baseball. 3. I cando anything they can do. . 4. God was giving me my kidneys back! Answer.
http://www.withoutwheels.org/gazette/MemberTrivia/member_trivia.htm
Mda
I have mcardles disease. I would like to talk to others who have this.
http://www.mda.org.au/services/gbarchive/mar99.html

Extractions: Comments : Just purchased computer and learning how to use it. Found this site because I was looking for someone else who has Acid Maltase Deficiency. I was diagnosed in 1977 as having Limb-girdle dystrophy. Later changed to AMD. Would like to have someone to talk to about how they cope with this disease. Name carol tibus
Glycogen And Other Sugar Pathways
mutation f1) all organs affected f2) increased glycogen f3) Cardiorespiratory failure,death before 2 g) mcardles disease mutation in phosphorylase g1) muscle
http://umed.med.utah.edu/MS1/biochem/study/glycogen.html
New Alabama Chapter
It was then that I was diagnosed with Muscular Dystrophy a veryrare form called mcardles disease (phosphorylase deficiency).
http://www.vhl.org/newsletter/vhl2001/01coalab.htm

Extractions: to improve diagnosis, treatment, and quality of life for people affected by von Hippel-Lindau disease. Linda D. is our new chapter chairperson for Alabama. She shares her story, and her goals for the chapter. I am 48 years of age, one of seven children, with me being number seven and twin to number six. There are 4 boys and 3 girls in our family. I graduated High School and went into the paramedic program at the University of Alabama, Birmingham, Alabama. I worked for Carraway Hospital in the emergency room at the time and wanted to train for the Life Saver Helicopter that was just being introduced. In my second level of paramedic training I was sent to NIH in Bethesda, Maryland, for evaluation of muscle problems. It was then that I was diagnosed with Muscular Dystrophy a very rare form called McArdles Disease (phosphorylase deficiency). This ended my dream of becoming a flight medic or even a paramedic. Since I could not be a paramedic, I worked as an office manager with several companies, and then started my own cleaning business approximately 8 years ago. I have two children. My son, Patrick, is a Staff Sgt. in the Air Force in Louisiana. My daughter-in-law, Brandy, graduated from the Police Academy in June. My daughter, Candi, lives near me and helps me with my cleaning business. I have two grandsons, Justin (5) and Hunter (1), the joy of my life.
Definitions Of Genetic Disorders -P
disease/pgam.html. Phosphorylase Deficiency (MPD) (mcardles disease)http//www.mdausa.org/disease/mpd.html. Phosphorylase 6 Kinase
http://www.icomm.ca/geneinfo/def-p.htm
Creatine FAQ's
Creatine has also been used successfully to improve patients with neuromusculardiseases such as mcardles disease, neuropathic disorders, inflammatory
http://www.nutrasense.com/nutrasense/creatinefaqs.html

Extractions: To date there have been well over 75 research articles published about creatine in various journals, as well as a number of papers presented at various meetings such as the National Strength and Conditioning Associations Symposium. These studies reported no negative side effects. The only consistent side effect has been an average water weight gain of 3-5 lbs. Simply put, with the exception of carbohydrates, creatine is the most extensively studied nutritional sports supplement available to today's athlete. Even though creatine supplementation is most common with athletes it has a multitude of uses ranging from infants to the elderly. Creatine has been used successfully to treat infants with extrapyramidal movement disorders and creatine deficiencies in the brain. Creatine has also been used successfully to improve patients with neuromuscular diseases such as McArdles disease, neuropathic disorders, inflammatory myopathies, diomyopathy, mitochondrial cytopathy, dystrophies/congenital myopathies, and ALS - Lou Gehrigs disease. Study Shows Creatine Strengthens Elderly and Patients with Neuromuscular Disease - USA Today
THE LIGHTNING HYPERTEXT OF DISEASE.
McArdle Disease, McArdle's Diseases, McArdle Diseases, McArdle's Glycogenosis 5sMcArdle Diseases McArdle's Diseases mcardles disease Muscle Phosphorylase
http://www.pathinfo.com/cgi-bin/lh.cgi?tx=mcardles
Personal Training On The Net - Newsletter
Polycystic Ovary Syndrome. Strength for Rowing (click to view). mcardles disease.mcardles disease and Exercise. Niacin. Shin Splints. Clicking Hip (click to view).
http://www.ptonthenet.com/newsletter/june_02.htm
Department Of Kinesiology [FACULTY MEMBERS - Martin Gibala]
ranged from young healthy volunteers to special populations including neuromusculardisease patients (eg, myoadenlyate deaminase deficiency, mcardles disease).
http://kinlabserver.mcmaster.ca/kf/mg.html
Muscular Dystrophy Association | What's New
Treatment of mcardles disease by Dr. Ronald Haller 5/23/01; JerryLewis MDA Telethon 2000 Broadcast Journalism Awards 5/15/01;
http://www.mdausa.org/whatsnew/con_archive01.html

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