Muscular Dystrophy Quotes

Her words felt like a new beginning, a turning of a page, and, ominously, rang like the beginning of a final chapter.

I haven’t been able to pray with the same unquestioned simplicity of hope since Dustin passed. My childhood ended the day my brother died. The naive hope that a miracle would save him, that he would one day walk, that a disease was a blessing in my family – that hope died with him.

They were not medical problems to rehabilitate. We were not medical problems. I was never going to undo the damage polio had done to my nerve cells and walk again, nor was this my goal. The disabled veterans coming home from the Vietnam War were never going to grow their limbs back or heal their spinal cords and walk again. My friends with muscular dystrophy were never going to not have been born with muscular dystrophy. Accidents, illnesses, genetic conditions, neurological disorders, and aging are facts of the human condition, just as much as race or sex.

My approach to parenthood was conditional, and the conditions were strict. I did not want to mother an imbecile or a paraplegic; whenever I saw fatigued women wheeling their stick-limbed progeny with muscular dystrophy for water therapy at Nyack Hospital, my heart didn’t melt, it sank.

There is a significant hereditary contribution to ADD but I do not believe any genetic factor is decisive in the emergence of ADD traits in any child. Genes are codes for the synthesis of the proteins that give a particular cell its characteristic structure and function. They are, as it were, alive and dynamic architectural and mechanical plans. Whether the plan becomes realized depends on far more than the gene itself. It is determined, for the most part, by the environment. To put it differently, genes carry potentials inherent in the cells of a given organism. Which of multiple potentials become expressed biologically is a question of life circumstances. Were we to adopt the medical model — only temporarily, for the sake of argument — a genetic explanation by itself would still be unsuitable. Medical conditions for which genetic inheritance are fully or even mostly responsible, such as muscular dystrophy, are rare. “Few diseases are purely genetic,” says Michael Hayden, a geneticist at the University of British Columbia and a world-renowned researcher into Huntington’s disease. “The most we can say is that some diseases are strongly genetic.” Huntington’s is a fatal degeneration of the nervous system based on a single gene that, if inherited, will almost invariably cause the disease. But not always. Dr. Hayden mentions cases of persons with the gene who live into ripe old age without any signs of the disease itself. “Even in Huntington’s, there must be some protective factor in the environment,” Dr. Hayden says.

Willpower doesn’t change everything. We can’t be just anything we want to be. My mother couldn’t will herself to be like she was when she was thirty or forty. She couldn’t choose to be normal — her muscles were degenerating.

There are a small number of debilitating conditions with a strong genetic basis, such as muscular dystrophy or Huntington’s disease. These are rare, affecting about one person in ten thousand or even fewer. They do not pose a significant threat to the survival of the species. If, however, we add up the numbers of people plagued by depression or ADD or the other common psychological problems people in this society struggle with, including alcoholism and anxiety, we will have identified no less than a third of the North American population. Genetic explanations for these conditions assume that after millions of years of evolution, nature would permit a very large number of disordered genes, handicapping a third of humankind, to pass through the screen of natural selection — a highly unlikely proposition.

TAT: I find I'm still left wanting to know how to tell if my patient has false memory syndrome. What's the test? How do I determine if my patient is suffering from this syndrome? Freyd: What are the tests if some body is suffering from " repressed memory syndrome?" TAT: Well, I can give you several symptom clusters - dissociative, cognitive, affective, somatic effects they're well documented. But, I'm asking you the question. You're telling me, David, as a clinician: you must be aware of the possibility your patients may have false memory syndrome. Okay, how should I be aware of that? How am I going to know? How do I test for it? Freyd: David, I'm going to ask Dr. Paul McHugh to talk to you because he is a clinician and I have stated from the beginning that I am not. TAT: I appreciate that, Pamela. But here's my issue with you not knowing. If I was talking to the Executive Director of the Muscular Dystrophy Association, who presumably is also not a clinician, I'll bet he or she could give me the signs and symptoms of muscular dystrophy. But in the case of false memory syndrome, so far no one seems to be able to say. Treating Abuse Today, 3(4), pp. 26-33

I need not point out that being redheaded is not a maladaptive condition. It’s a very lovely condition. It is an absurdity, offensive to both redheads and geneticists—a group that contains both family and friends—to suggest that red hair might be subject to a force of natural selection so powerful that oblivion awaits. Even actually maladaptive genetic traits, actual diseases with well-understood modes of inheritance, such as cystic fibrosis or Duchenne muscular dystrophy are not likely to go extinct, because carriers of a single copy live healthily and pass the faulty gene on to their children.

Our specialized stem cell experienced doctors are known for different types of muscular dystrophy disease and can deliver the best possible treatment. That’s the reason that makes us the best muscular dystrophy treatment in South Africa. As per our expert doctors, this disease has risen due to many symptoms such as enlarged calf muscles, breathing problems, heart problems, trouble swallowing, etc.

The victory feels hollow—not because I don’t believe that Peter is sincere in granting me this concession, but because of the dreadful circumstances that sparked the battle. If Diana had a visible handicap such as cerebral palsy or muscular dystrophy, or if she was missing an arm or a leg—even if she had a better-understood psychological condition such as schizophrenia or if she was bipolar, it’d be different. There are support groups for families dealing with these issues. People would understand. They’d offer help. But no one is sympathetic to the mother of a psychopath. To the mother of a girl who tried to kill her infant sister. A girl who let a toddler drown in a swimming pool. Or did Diana push the boy in?

But I always found that a bit awful of God. To withhold evidence, if the Cosmic Egg is so important. That’s how Hildegard von Bingen puts it—the Cosmic Egg. But yeah, it’s suspiciously stingy to give us nothing but a couple of self-professed messiahs every three thousand years. Prophets whose stories don’t align. Mary on toast. Somebody’s cured muscular dystrophy. It’s a lot to ask of us without collateral, don’t you think? Especially when there are so many competing stories, and the stakes are so high. Inferno or paradise. Forever.

I knew you’d know,” Mom said in a stabilizing, more confident, yet still husky voice. A smile broke across her face in the simple relief of her only remaining child not being shocked by the death of her youngest. She smiled genuinely, perhaps for the first time since cradling Dustin’s body as the fire truck alarm blared towards the house in response to her 911 call. Her son had died that morning in her arms as she tried resuscitating him with her own breath, but the first indication of her daughter’s reaction was calm. The child raised to expect death met the first moments of the news with seeming serenity.

Duchenne muscular dystrophy is a severe muscle wasting disease caused by mutations in the X-linked DYSTROPHIN gene. This is a large gene that encodes a big protein which acts as an essential shock absorber in muscle fibres. Boys carrying certain mutations in DYSTROPHIN suffer major muscle loss that usually results in death in the teenage years. Females with the same mutation are usually symptom-free. The reason for this is that muscle has a very unusual structure. It is called a syncytial tissue, which means that lots of individual cells fuse and operate almost like one giant cell, but with lots of discrete nuclei. This is why most females with a DYSTROPHIN mutation are symptom-free. There is enough normal DYSTROPHIN protein encoded by the nuclei that switched off the mutated DYSTROPHIN gene to keep this syncytial tissue functioning healthily

I think that people who stand up for what they believe in, no matter how unpopular, should be celebrated, not cast aside. I believe that my ideas about green highlighters and yellow highlighters could have served the Muscular Dystrophy Association well, if only they were given a proper and considerate airing.

In Portland, OR, “Jackie,” a homeless former social worker with muscular dystrophy, was hit with a misdemeanor theft charge for charging her phone from a plug on a planter-base on a sidewalk; she spent a day in jail when she missed her arraignment. The electricity she used to charge her phone was worth a fraction of a cent. She keeps her phone charged for her personal safety. Worried that a pleading guilty would put a black mark on her record that would interfere with her ability to get social housing, she pled innocent. After two court dates with two different public defenders, the DA dropped the charge.

I’m sorry about your little brother.” My throat gets tight. “Thanks.” “What was it—his illness? What did he die of?” “Muscular dystrophy.