Making An Ebook For Ebook Promotion - 914 Words

Writing an eBook is quite a feat in itself, but the project doesn’t end when you press the publish button. In fact, the hard work often starts when the book is finished. Marketing an eBook like a professional can be a rather tricky and time-consuming task. But with the below tips, you can get the job done smoother and have fun in the process. Before you start Before we start examining the key strategies you need to implement for eBook promotion, you need to consider a few things. Essentially, you must decide on the marketing budget you want to use and the specific strategies you want to use. First, you need to decide how much money are you willing to spend on marketing the eBook. Marketing costs can easily vary from $0 to above $1,000. Therefore, you don’t want to rush into your project only to realise later what you’ve spent. Spending more money doesn’t automatically guarantee results; so don’t feel like you have to spend money in order to achieve higher reader numbers. 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The Secret Circle The Captive Chapter Two Free Essays

string(58) " was swinging at an angle, and Diana turned to follow it\." Somewhere on the way downstairs Cassie stopped feeling guilty. She didn’t know exactly how it happened. But it was necessary, if she was going to survive this. We will write a custom essay sample on The Secret Circle: The Captive Chapter Two or any similar topic only for you Order Now She was doing everything she could to protect Diana-and Adam, too, in a way. Adam must never know about Faye’s blackmail. So Cassie would do whatever it took to protect them both, but by God, she wasn’t going to feel guilty on top of it. And she had to handle Faye somehow as well, she thought, marching behind the tall girl, past Diana’s father’s study. She had to keep Faye from doing anything too radical with the skull. She didn’t know how; she’d have to think about that later. But somehow she would do it. If Faye had looked back just then, Cassie thought, she might have been surprised to see the face of the girl behind her. For the first time in her life Cassie felt as if her eyes were hard, like the blue steel of a revolver instead of the soft blue of wildflowers. But right now she had to look neutral- composed. The group on the driveway looked up as she and Faye came out the door. â€Å"What took you so long?† Laurel asked. â€Å"We were plotting to kill you all,† Faye said breezily. â€Å"Shall we?† She gestured toward the garage. There were only traces of yesterday’s chalk circle left on the floor. Once again the garage was empty of cars-they were lucky Diana’s father worked so much at his law firm. Diana, her left fist still closed, went over to the wall of the garage, directly behind the place Cassie had been sitting when they had performed the skull ceremony. Cassie followed her and then drew in her breath sharply. â€Å"It’s burned.† She hadn’t noticed that last night. Well, of course not; it had been too dark. Diana was nodding. â€Å"I hope nobody is going to keep arguing about whether there was any dark energy or not,† she said, with a glance back at Deborah and Suzan. The wood and plaster of the garage wall was charred in a circle perhaps a foot and a half in diameter. Cassie looked at it, and then at the remnants of the chalk circle on the floor. She had been sitting there, but part of her had been inside the skull. Diana had told them all to look into it, to concentrate, and suddenly Cassie had found herself inside it. That was where she’d seen-felt-the dark power. It had begun rushing outward, getting bigger, determined to break out of the crystal. And she’d seen a face†¦. She was grateful, suddenly, for Adam’s calm voice. â€Å"Well, we know what direction it started in, anyway. Let’s see if the crystal agrees.† They were all standing around Diana. She looked at them, then held her left fist out, palm up, and unclasped her fingers. She took the top of the silver chain with her right hand and drew it up taut, so that the peridot just rested on her palm. â€Å"Concentrate,† she said. â€Å"Earth and Air, help us see what we need to see. Show the traces of the dark energy to us. Everybody concentrate on the crystal.† Earth and Air, wind and tree, show us what we need to see, Cassie thought, her mind automatically setting the simple concept in a rhyme. The wood of the wall, the air outside; those were what they needed to help them. She found herself murmuring the words under her breath and quickly stopped, but Diana’s green eyes flashed at her. â€Å"Go on,† Diana said tensely in a low voice, and Cassie started up again, feeling self-conscious. Diana removed the hand that was supporting the crystal. It spun on the chain, twirling until the chain was kinked tightly, and then twirling the other way. Cassie watched the pale green blur, murmuring the couplet faster and faster. Earth and Air†¦ no, it was useless. The peridot was just spinning madly like a top gone wild. Suddenly, with broad, sweeping strokes, the crystal began swinging back and forth. Someone’s breath hissed on the other side of the circle. The peridot had straightened out; it was no longer twirling, but swinging steadily and hard. Like a pendulum, Cassie realized. Diana wasn’t doing it; the hand that held the chain remained steady. But the peridot was swinging hard, back toward the center of the chalk circle on the floor, and forward toward the burned place on the wall. â€Å"Bingo,† Adam said softly. â€Å"We’ve got it,† Melanie whispered. â€Å"All right, now you’re going to have to move it out of alignment to get outside. Walk-carefully- to the door, and then try to come back to this exact place on the other side of the wall.† Diana wet her lips and nodded, then, holding the silver chain always at the same distance from her body, she turned smoothly and did as Melanie said. The coven broke up to give her room and regrouped around her outside. Finding the right place wasn’t hard; there was another burned circle on the outer wall, somewhat fainter than the one inside. As Diana brought the crystal into alignment once more, it began to swing again. Straight toward the burned place, straight out. Down Crowhaven Road, toward the town. A shudder went up Cassie’s spine. Everyone looked at everyone else. Holding the crystal away from her, Diana followed the direction of the swinging. They all fell in behind her, although Cassie noticed that Faye’s group kept to the rear. Cassie herself was still fighting every second to not watch Adam. Trees rustled overhead. Red maple, beech, slippery elm-Cassie could identify many of them now. But she tried to keep her eyes on the rapid swish of the pendulum. They walked and walked, following the curve of Crowhaven Road down toward the water. Now grasses and hedges grew poorly in the sandy soil. The pale green stone was swinging at an angle, and Diana turned to follow it. You read "The Secret Circle: The Captive Chapter Two" in category "Essay examples" They were heading west now, along a deeply rutted dirt road. Cassie had never been this way before, but the other members of the Circle obviously had-they were exchanging guarded glances. Cassie saw a chain-link fence ahead, and then an irregular line of headstones. â€Å"Oh, great,† Laurel muttered from beside Cassie, and from somewhere in back Suzan said, â€Å"I don’t believe this. First we have to walk for miles, and now†¦Ã¢â‚¬  â€Å"What’s the problem? Just gonna visit some of our ancestors underground,† Doug Henderson said, his blue-green eyes glittering oddly. â€Å"Shut up,† Adam said. Cassie didn’t want to go inside. She’d seen many cemeteries in New England-it seemed there was one on every other street in Massachusetts, and she’d been to Kori’s funeral down in the town. This one didn’t look any different from the others: it was a small, square plot of land cluttered with modest gravestones, many of them worn almost completely smooth with time. But Cassie could hardly make herself follow the others onto the sparse, browning grass between the graves. Diana led them straight down the middle of the cemetery. Most of the stones were small, scarcely reaching higher than Cassie’s knees. They were shaped like arches, with two smaller arches on either side. â€Å"Whoever carved these had a gruesome sense of humor,† she breathed. Many of the stones were etched with crude skulls, some of them winged, others in front of crossbones. One had an entire skeleton, holding a sun and moon in its hands. â€Å"Death’s victory,† Faye said softly, so close that Cassie felt warmth on the nape of her neck. Cassie jumped, but refused to look back. â€Å"Oh, terrific,† said Laurel as Diana slowed. The light was dying from the sky. They were in the center of the graveyard, and a cool breeze blew over the stunted grass, bringing a faint tang of salt with it. The hairs on the back of Cassie’s neck were tingling. You’re a witch, she reminded herself. You should love cemeteries. They’re probably your natural habitat. The thought didn’t really make her feel less frightened, but now her fear was mingled with something else-a sort of strange excitement. The darkness gathering in the sky and in the corners of the graveyard seemed closer. She was part of it, part of a whole new world of shadows and power. Diana stopped. The silver chain was a thin line in the gloom, with a pale blob below it. But Cassie could see that the peridot was no longer swinging like a pendulum. Instead it was moving erratically, round and round in circles. It would swing a few times one way, then slow and swing back the other way. Cassie looked at it, then up at Diana’s face. Diana was frowning. Everyone was watching the circling stone in dead silence. Cassie couldn’t stand the suspense any longer. â€Å"What does it mean?† she hissed to Laurel, who just shook her head. Diana, though, looked up. â€Å"Something’s wrong with it. It led here- and then it just stopped. But if we’ve found the place, it shouldn’t be moving at all. The stone should just sort of point and quiver-right, Melanie?† â€Å"Like a good hound dog,† Doug said, with his wild grin. Melanie ignored him. â€Å"That’s the theory,† she said. â€Å"But we’ve never really tried this before. Maybe it means†¦Ã¢â‚¬  Her voice trailed off as she looked around the graveyard, then she shrugged. â€Å"I don’t know what it means.† The tingling at the back of Cassie’s neck was getting stronger. The dark energy had come here-and done what? Disappeared? Dissipated? Or †¦ Laurel was breathing quickly, her elfin face unusually tense. Cassie instinctively moved a little closer to her. She and Laurel and Sean were the juniors, the youngest members of the Circle, and witch or not, Cassie’s arms had broken out in gooseflesh. â€Å"What if it’s still here, somewhere†¦ waiting?† she said. â€Å"I doubt it,† Melanie said, her voice as level and uninflected as usual. â€Å"It couldn’t hang around without being stored somehow; it would just evaporate. It either came here and did something, or-† Again, though, she could only finish her sentence with a shrug. â€Å"But what could it do here? I don’t see any signs of damage, and I feel†¦Ã¢â‚¬  Still frowning, Diana caught the circling peridot in her left hand and held it. â€Å"This place feels confused- strange-but I don’t sense any harm the dark energy has done. Cassie?† Cassie tried to search her own feelings. Confusion-as Diana said. And she felt dread and anger and all sorts of churned-up emotions-but maybe that was just her. She was in no state to get a clear reading on anything. â€Å"I don’t know,† she had to say to Diana. â€Å"I don’t like it here.† â€Å"Maybe, but that’s not the point. The point is that we don’t see any burns the dark energy could have left, or sense anything it’s destroyed or hurt,† Diana said. Deborah’s voice was impatient. â€Å"Why are you asking her, anyway?† she said with a jerk of her dark head toward Cassie. â€Å"She’s hardly even one of us-â€Å" â€Å"Cassie’s as much a part of the Circle as you are,† Adam interrupted, unusually curt. Cassie saw the arch, amused glance Faye threw him and wanted to intervene, but Diana was agreeing heatedly with Adam, and Deborah was bridling, glaring at both of them. It looked as if an argument would break out. â€Å"Be quiet!† Laurel said sharply. â€Å"Listen!† Cassie heard it as soon as the voices died down; the quiet crunch of gravel at the roadside. It was noticeable only against the deathly quiet of the autumn twilight. â€Å"Somebody’s coming,† Chris Henderson said. He and Doug were poised for a fight. They were all hideously on edge, Cassie realized. The crunch of footsteps sounded as loud as firecrackers now, grating against her taut nerves. She saw a dim shape beside the road, and then saw Adam move forward, so that he was in front of both Diana and her. I’m going to have to talk to him about that, she thought irrelevantly. There was a pause in the footsteps, and the dim shape came toward them. Adam and the Henderson brothers looked ready to rush it. Quarrel forgotten, Deborah looked ready too. Sean was cowering behind Faye. Cassie’s heart began to pound. Then she noticed a spot of red like a tiny burning coal floating near the figure, and she heard a familiar voice. â€Å"If you want me, you got me. Four against one ought to be about fair.† With a whoop, Chris Henderson rushed forward. â€Å"Nick!† Doug grinned, while still managing to look as if he might jump the approaching figure. Adam relaxed and stepped back. â€Å"You sure, Adam? We can settle this right here,† Nick said as he reached the group, the end of his cigarette glowing as he inhaled. Adam’s eyes narrowed, and then Cassie saw the daredevil smile he’d worn at Cape Cod, when four guys with a gun had been chasing him. What was wrong with him, what was wrong with everybody tonight? she wondered. They were all acting crazy. Diana put a restraining hand on Adam’s arm. â€Å"No fighting,† she said quietly. Nick looked at her, then shrugged. â€Å"Kind of nervous, aren’t you?† he said, surveying the group. Sean emerged from behind Faye. â€Å"I’m just high-strung.† â€Å"Yes, you ought to be-from a tree,† Faye said contemptuously. Nick didn’t smile, but then Nick never smiled. As always, his face was handsome but cold. â€Å"Well, maybe you have a reason to be nervous-at least some of you,† he said. â€Å"What’s that supposed to mean? We came here looking for the dark energy that escaped last night,† said Adam. Nick went still, as if struck by a new idea, then his cigarette glowed again. â€Å"Maybe you’re looking in the wrong place,† he said expressionlessly. Diana’s voice was quiet. â€Å"Nick, will you please just tell us what you mean?† Nick looked around at them all. â€Å"I mean,† he said deliberately, â€Å"that while you’ve been scurrying around here, a crew’s been up at Devil’s Cove, pulling rocks off old Fogle.† Fogle? Cassie couldn’t place the name. And then suddenly she saw it in her mind’s eye-on a brass plate in a wood-paneled office. â€Å"Our principal?† she gasped. â€Å"You got it. They say he got caught in an avalanche.† â€Å"An avalanche?† demanded Laurel in disbelief. â€Å"Around here?† â€Å"How else do you explain the two-ton chunk of granite that was on top of him? Not to mention all the smaller stuff.† There was a moment of shocked silence. â€Å"Is he†¦Ã¢â‚¬  Cassie couldn’t finish the question. â€Å"He wasn’t looking too good when they got that chunk off him,† Nick said, and then, with less sarcasm, â€Å"He’s been dead since last night.† â€Å"Oh, God,† Laurel whispered. There was another silence, just as shocked and even longer this time. Cassie knew they were all seeing the same thing: A crystal skull surrounded by a protective ring of candles- and one of the candles going out. â€Å"It was Faye’s fault,† Sean began in a whine, but Faye interrupted without looking at him. â€Å"It was his fault.† â€Å"Wait, wait,† said Diana. â€Å"We don’t know the dark energy had anything to do with it. How could it have, when we know it came here and then stopped?† â€Å"I don’t think that’s much comfort,† Melanie said in a low voice. â€Å"Because if it wasn’t the dark energy, who was it?† There was a sort of strange shifting in the group, as if everyone was standing back and looking at all the others. Cassie felt a void in the pit of her stomach again. The principal was-had been-an outsider, who hated witches. And that meant they all had a motive-especially anybody who blamed the outsiders for Kori Henderson’s death. Cassie looked at Deborah, and then at Chris and Doug. Most of the rest of the coven was doing the same. Doug glared back, then gave a wild, defiant grin. â€Å"Maybe we did do it,† he said, eyes glittering. â€Å"Did we?† said Chris, looking confused. Deborah just looked scornful. There was another silence, then Suzan spoke in a petulant voice. â€Å"Look, it’s too bad about Fogle, but do we have to stand here forever? My feet are killing me.† Adam seemed to shake himself. â€Å"She’s right; we should get out of this place. There’s nothing we can do here.† He put an arm around Diana, and gestured everybody else ahead. Cassie lingered. There was something she wanted to say to Diana. But Diana was moving now, and Cassie didn’t have a chance. With the Henderson brothers in the lead, the group was taking a different route than the one they had taken in, cutting toward the northeast corner of the cemetery. As they approached the road, Cassie noticed the ground sloped up. There was a strange mound of grassy earth near the chain-link fence on this side; she almost tripped when she reached it. But even stranger was what she saw when they had passed it and she looked back. The front of the mound was faced with stone slabs, and there was an iron door, maybe two feet square, set between them. The door had an iron hinge and a padlock on it, but it couldn’t have opened anyway. Pushed right up against it was a large, irregular hunk of cement. Grass was growing up around the cement, showing it had been there a while. Cassie’s hands were icy cold, her heart was thudding, and she was dizzy. She tried to think, noticing with only part of her mind that she was passing by newer gravestones now, marble slabs with writing not worn smooth by time. She was trying to figure out what was wrong with her-was it just reaction to all the events of the past day and night? Was that why she was shaking? â€Å"Cassie, are you okay?† Diana and Adam had turned around. Cassie was grateful for the growing darkness as she faced both of them and tried to get her mind clear. â€Å"Yeah. I just-felt weird for a minute. But wait, Diana.† Cassie remembered what she had wanted to say. â€Å"You know how you were asking me about my feelings before†¦ well, I have a feeling about Mr. Fogle. I think the dark energy did have something to do with it, somehow. But†¦Ã¢â‚¬  She stopped. â€Å"But I don’t know. There’s something else strange going on.† â€Å"You can say that again,† Adam said, and he reached for her arm to get her moving once more. Cassie evaded him and shot him a reproachful glance while Diana was staring into the distance. He looked at his own hand, startled. There was something strange going on, something stranger than any of them realized, Cassie thought. â€Å"What is that thing back there, with the iron door?† she asked. â€Å"It’s been there for as long as I can remember,† Diana said absently. â€Å"Something to do with storage, I think.† Cassie glanced back, but by now the mound was lost in darkness. She hugged herself, tucking her hands under her clasping arms to warm them. Her heart was still thudding. I’ll ask Grandma Howard about it, she decided. Whatever it was, it wasn’t a storage shed, she knew that. Then she noticed that Diana was toying with something around her neck as she walked lost in thought. It was a fine golden chain, and at the end of it dangled a key. How to cite The Secret Circle: The Captive Chapter Two, Essay examples

Research Paper on Zionism Essay Example

Research Paper on Zionism Essay Zionism is a political movement aimed at reunification and revival of Jewish people in their historic homeland, Israel, as well as an ideological concept fundamental for the movement. The ideology of Zionism unites various movement different in their trends, from the left socialites to orthodox religious groups. Before the World War II, Zionism was one of the largest Jewish political movements (along with working-class movement the Bund, which struggled for the culture autonomy). Those college writers who are about to write an interesting and argumentative research paper on the topic have to understand that the word â€Å"Zionism† is derivative from the toponym Zion (from Hebr. ), in addition, Israel is often named as â€Å"Zion’s daughter,† and Jew people as â€Å"Zion’s sons.† Since the Babylonian captivity, Zion has become for the Jewish diaspora a symbol of the lost homeland. In this meaning it is often encountered in religious scripts and secular press. We will write a custom essay sample on Research Paper on Zionism specifically for you for only $16.38 $13.9/page Order now We will write a custom essay sample on Research Paper on Zionism specifically for you FOR ONLY $16.38 $13.9/page Hire Writer We will write a custom essay sample on Research Paper on Zionism specifically for you FOR ONLY $16.38 $13.9/page Hire Writer In the second half of the 19th century the toponym semantic was used for the name of a pro-Palestine movement Hovevei Zion. The term itself was coined by one of the earliest Zionism theoretics, the leader of the Ortodox Judaism movement Agudat Yisrael and Yiddishisme Nathan Birnbaum. It was first used in 1890 in the publications of his magazine Selbstemancipacion as a name of the party, which stood for the the return of Jews to Israel though the political activity, as opposed to the purely practical immigration policy by Hovevei Zion. Nevertheless, up to the end of the 19th century, Zionism primarily meant practical activity aimed at the organization of agricultural communities in Israel. The same meaning has been put in the word by Theodor Herzl until The First Zionist Congress, which adopted the so-called Basel program joining political and practical aspects of the movement with the establishment of the World Zionist Organization, which consolidated most Hoveveis of Zion, whet the term received its today meaning. In some sources, Zionism is regarded as a movement of Jewish people national liberation in the context te European national liberation movements of the 19th century. At the same time, the critics of Zionism regard it as a form of racism and racial discrimination. Often the term is mistakenly used for the definition of any Jewish movement of the national trends, for example, the demand for the establishment of the national-cultural autonomy in Crimea, the right for immigration in other countries beside Israel, and even any struggle for the equality of rights for Jews. The term â€Å"Zionism† is also often used by the proponents of the Judeo-Masonic conspiracy theory having antisemitism nature. Zionism as well should not be confused with territorialism, which means the intention of part of Jewish people to establish the state on any territory, while Zionism is an intention to reconstitute the state exactly in Israel. Using free sample research papers on Zionism you may learn a great deal of relevant data on the topic. At EssayLib.com writing service you can get a high-quality custom research paper on Zionism topics. Your research paper will be written from scratch. We hire top-rated Ph.D. and Master’s writers only to provide students with professional research paper assistance at affordable rates. Each customer will get a non-plagiarized paper with timely delivery. Just visit our website and fill in the order form with all paper details: Enjoy professional research paper writing service!

Pain Management and Quality of Life for Sickle Cell Disease Patients Essays

Pain Management and Quality of Life for Sickle Cell Disease Patients Essays Pain Management and Quality of Life for Sickle Cell Disease Patients Essay Pain Management and Quality of Life for Sickle Cell Disease Patients Essay Pain Management and Quality of Life for Sickle Cell Disease Patients Cynthia Evans Mississippi College Pain Management and Quality of Life for Sickle Cell Disease Patients This is a review of literature examining how frequent recurring episodes of pain affect the quality of life in the sickle cell disease patients. Several studies conducted concerning pain management and quality of life for sickle cell disease patients indicate additional studies needed. Identifying additional effective complementary alternate therapies is vital for a more improved quality of life. This will be necessary in order to reduce the number of painful episodes experienced by the sickle cell patient. Sickle cell disease is a genetic disorder of the red blood cells and further characterized by painful acute vaso-occlusive episodes where the sickle cell is stuck in the blood vessels, blocking the blood flow. This is one of the most common reasons leading up to hospitalization, the vaso-occlusive episodes. These episodes can lead to ischemia and infarctions over the entire body region with painful recurring, unpredictable, intense, and relentless episodes, lasting approximately 3-14 days (Yaster, Kost-Byerly, Maxwell, 2000). According to Granados and Jacob (2009), the purpose of their study was to examine pain experienced and the effectiveness of analgesics for hospitalized adults with sickle cell disease. The literature review indicates a variety of reasons why inadequate pain management is ongoing in the adult (SCD) patients admitted with vaso-occlusive episodes. The focus is mainly on factors that affect the management of pain, including methods of analgesic administration, and non-pharmacologic regimens, therefore the perception of the provider is important in regards to treating sickle cell pain as identified in the study by (Shapiro, Benjamin, Payne Heidrich, 1997; Steinberg, 1999; Yale et al. , 2000). Little attention in the way of research studies has been examined in relation to the pain experience of the sickle cell adults. Ballas and Lusardi (2005) evaluated the sequence of hospital admissions of patients with sickle cell disease, reviewing the causes of recurring admissions, and the importance of the patient’s outcome of illness. All readmissions examined specifically within seven to thirty days from the initial admission discharge assessing for the rationale of the recurrence of hospital admission and relation to the prognosis of the sickle cell disease patient. The researchers evaluated the pain by a descriptive underlying research design knowledgeable by the sickle cell disease patients for intensity, location, and quality of pain. Fifty percent of patients admitted for intense painful episodes were readmitted within one month after discharge, and another estimated 16% were readmitted within one week after discharge. Severe pain is described as a degree of pain greater than six on a zero to ten numerical rating scales. A mean score of seven or greater indicates prematurity in discharging the sickle cell disease patients from the hospital. In conclusion, the patients admitted to the hospital with high pain scores were more likely to have lengthy hospitalizations, and to be discharged home with equally higher pain scores. The pain intensity scores from the previous discharge examined by the researchers indicated 71 readmission, in which 52 patients were readmitted for vaso-occlusive episodes, (Ballas Lusardi, 2005). The pain score of study participants indicated a high pain intensity score, and the scores did not change consequently during prolonged episodes. Even higher pain intensity more so on days seven and eight were indicated for increase pain significance. Researchers further indicated that the main reason for hospital readmissions were early discharge to home settings, signs and symptoms of medication/drug withdrawal, that brought about the intense reoccurring episodes of vaso-occlusive illnesses. It was noted that readmissions to the hospital for the adult sickle cell disease patient is more common and researchers recommended future studies for improvement in pain management in the hospital and at home. In future studies, researchers will need to use a larger sample size to evaluate patterns of pain management, effectiveness and influence on quality of life in the sickle cell disease patient. Although, no evidence was identified where upward titration of analgesics was done it is recommended that development of algorithms be encouraged to help carefully plan decisions regarding titration of medications in adult patients with sickle cell disease during hospitalizations. Jiles and Morris, (2008) made known in their descriptive study of 62 patients (18 years of age and older) using Burckhardt and Anderson’s 16 item self-report and a demographic uestionnaire used for data collection. The purpose of the study was to investigate the quality of life in adults with sickle cell anemia, hemoglobin SC, or Hemoglobin S beta thalassemia. The results revealed that the healthy populations average scores for quality of life scale is 90 and in this study the overall mean QOL score was 83. 6 ( SD=13. 2) lower than those of the overall general population. The outcome of this study indicated additional research is necessary to advance the understanding of the factors that greatly affect quality of life in the management of sickle cell disease in order for patients to enjoy normal activities of life. A cross sectional descriptive study conducted by Yoon and Black (2006) researched both pharmacologic and complementary therapies used for pain management by caregivers of children with sickle cell disease (SCD). They further studied the prevalence and types of complementary therapies used for pain management by caregivers of children with SCD and made inquiries of caregivers’ concerning their interests in using complementary therapies in the future. Since there was no obtainable questionnaire to meet the principle of the study, a questionnaire was created by the chief researcher. Items included on the questionnaire was age of child, age of caregiver, use of analgesic, annual income estimate, caregivers educational level, and type of health insurance their child had available. Divisions were randomly ordered and included massage, chiropractic, acupuncture, energy healing, relaxation techniques, imagery, meditation, hypnosis, biofeedback, self-prayer, spiritual healing by others, music therapy, herbal or fold remedies, megavitiamins, yoga, tai chi and other body works, and transcutaneous electrical nerve stimulation. The prospective patients were identified, approached, and invited to participate in the study by the clinical coordinator of the sickle cell disease clinic. The study was explained and potential participants were provided an informed consent letter. All subjects were provided a room for privacy and questionnaires were completed either by the caregivers of the participants or by the research assistance. The research assistant was nearby in either case to answer any questions that might arise by the caregivers when completing his/her form. The instructions provided to the caregivers indicated the questionnaires listing of the sixteen complementary therapies. The caregivers were to indicate any usage of them within the last six months and were asked would they be interested in using any of the listed complementary therapies in the future. Statistical analyses was used including how often an event repeats itself over a set amount of time and expected values with standard deviations, were used to compare demographic variables, research use of pharmacological therapies for pain management between age groups, and evaluate pharmacologic/analgesic and complementary therapy use. Chi-square tests were done in the beginning of the study and carried through to completion comparing the demographic variables, scrutinized use of pharmacologic therapies for pain management between age groups, and compared use of pharmacologic and complementary therapies. The results of the most frequently used pain medication for children revealed a mean age of 9 years. The results indicated children using pain medications most frequently identified was ibuprofen (37. 5%), acetaminophen with codeine (32. 1%), and acetaminophen with oxycodone (14. 5%). Complementary and alternative medicine use among children as well as adults has increased in the last ten years. In the study, caregivers with a mean age of 33 years was 70% of the 63 caregivers identified as using some form of complementary therapy. African American mothers made up 79% of the predominant race of caregivers and (56. 9%) indicated an annual income less than $20,000. Sixty percent of caregivers had twelve years of education or less, and twenty-four percent reported at least 2 years of college education. Medicaid (76%) was the major source of coverage for the children, although 24% had private or other identifying insurance. Future studies should include investigating the safety and effectiveness of the most commonly used complementary therapies reported in this study as well as recognizing possible ways complementary and alternative medicine (CAM) may be used effectively with pharmacologic therapies for pain management in children with Sickle cell disease in order to offer greater longevity and overall improved quality of life. Yoon and Black (2006), Jiles and Morris (2008) and Granados and Jacob (2009) all indicate the need for future studies in management of pain in the sickle cell disease patients. All studies indicate that the genetic disorder most commonly found in the African- American affects approximately 70,000 in the United States. This genetic disorder affects the red blood cells causing a stasis of sickle shaped erythrocytes, in which occlusion of the cells microcirculation, causing ischemia, and infarction. These recurring, unpredictable, intensified, and persistent painful episodes prevent stability and overall quality of life in the sickle cell disease patient and all authors indicate the need for future studies. The purpose of this review of literature is to identify all of the effective therapies of pain management for sickle cell disease patients. Whether the therapies used are complementary or alternative therapies vs. analgesic regimens. There must be future studies to seek out the answers for improved methods of pain treatment in order to improve the quality of life for the patients with sickle cell disease to exceed living past the age of forty-two with an increased zest and quality of life. References Granados, R. , Jacob, E. , (2009, May/June). Pain Experience in Hospitalized Adults with Sickle Cell Disease. Medsurg Nursing, 18 (3), 161-167,182. Jiles, V. M. , Morris, D. L. , (2009). Quality of Life of adult patients with sickle cell disease. Journal of the American Academy of Nurse Practitioners, Volume 21, 340-349. doi: 10. 1111/j. 1745-7599. 2009. 00416x Yoon, S. L. , Black, S. , (2006) Comprehensive, Integrative Management of Pain for Patients with Sickle-Cell Disease. The Journal of Alternative and Complementary Medicine, Volume 12, Number 10, pp. 995-1001.

Pain Management and Quality of Life for Sickle Cell Disease Patients Essays

Pain Management and Quality of Life for Sickle Cell Disease Patients Essays Pain Management and Quality of Life for Sickle Cell Disease Patients Essay Pain Management and Quality of Life for Sickle Cell Disease Patients Essay Pain Management and Quality of Life for Sickle Cell Disease Patients Cynthia Evans Mississippi College Pain Management and Quality of Life for Sickle Cell Disease Patients This is a review of literature examining how frequent recurring episodes of pain affect the quality of life in the sickle cell disease patients. Several studies conducted concerning pain management and quality of life for sickle cell disease patients indicate additional studies needed. Identifying additional effective complementary alternate therapies is vital for a more improved quality of life. This will be necessary in order to reduce the number of painful episodes experienced by the sickle cell patient. Sickle cell disease is a genetic disorder of the red blood cells and further characterized by painful acute vaso-occlusive episodes where the sickle cell is stuck in the blood vessels, blocking the blood flow. This is one of the most common reasons leading up to hospitalization, the vaso-occlusive episodes. These episodes can lead to ischemia and infarctions over the entire body region with painful recurring, unpredictable, intense, and relentless episodes, lasting approximately 3-14 days (Yaster, Kost-Byerly, Maxwell, 2000). According to Granados and Jacob (2009), the purpose of their study was to examine pain experienced and the effectiveness of analgesics for hospitalized adults with sickle cell disease. The literature review indicates a variety of reasons why inadequate pain management is ongoing in the adult (SCD) patients admitted with vaso-occlusive episodes. The focus is mainly on factors that affect the management of pain, including methods of analgesic administration, and non-pharmacologic regimens, therefore the perception of the provider is important in regards to treating sickle cell pain as identified in the study by (Shapiro, Benjamin, Payne Heidrich, 1997; Steinberg, 1999; Yale et al. , 2000). Little attention in the way of research studies has been examined in relation to the pain experience of the sickle cell adults. Ballas and Lusardi (2005) evaluated the sequence of hospital admissions of patients with sickle cell disease, reviewing the causes of recurring admissions, and the importance of the patient’s outcome of illness. All readmissions examined specifically within seven to thirty days from the initial admission discharge assessing for the rationale of the recurrence of hospital admission and relation to the prognosis of the sickle cell disease patient. The researchers evaluated the pain by a descriptive underlying research design knowledgeable by the sickle cell disease patients for intensity, location, and quality of pain. Fifty percent of patients admitted for intense painful episodes were readmitted within one month after discharge, and another estimated 16% were readmitted within one week after discharge. Severe pain is described as a degree of pain greater than six on a zero to ten numerical rating scales. A mean score of seven or greater indicates prematurity in discharging the sickle cell disease patients from the hospital. In conclusion, the patients admitted to the hospital with high pain scores were more likely to have lengthy hospitalizations, and to be discharged home with equally higher pain scores. The pain intensity scores from the previous discharge examined by the researchers indicated 71 readmission, in which 52 patients were readmitted for vaso-occlusive episodes, (Ballas Lusardi, 2005). The pain score of study participants indicated a high pain intensity score, and the scores did not change consequently during prolonged episodes. Even higher pain intensity more so on days seven and eight were indicated for increase pain significance. Researchers further indicated that the main reason for hospital readmissions were early discharge to home settings, signs and symptoms of medication/drug withdrawal, that brought about the intense reoccurring episodes of vaso-occlusive illnesses. It was noted that readmissions to the hospital for the adult sickle cell disease patient is more common and researchers recommended future studies for improvement in pain management in the hospital and at home. In future studies, researchers will need to use a larger sample size to evaluate patterns of pain management, effectiveness and influence on quality of life in the sickle cell disease patient. Although, no evidence was identified where upward titration of analgesics was done it is recommended that development of algorithms be encouraged to help carefully plan decisions regarding titration of medications in adult patients with sickle cell disease during hospitalizations. Jiles and Morris, (2008) made known in their descriptive study of 62 patients (18 years of age and older) using Burckhardt and Anderson’s 16 item self-report and a demographic uestionnaire used for data collection. The purpose of the study was to investigate the quality of life in adults with sickle cell anemia, hemoglobin SC, or Hemoglobin S beta thalassemia. The results revealed that the healthy populations average scores for quality of life scale is 90 and in this study the overall mean QOL score was 83. 6 ( SD=13. 2) lower than those of the overall general population. The outcome of this study indicated additional research is necessary to advance the understanding of the factors that greatly affect quality of life in the management of sickle cell disease in order for patients to enjoy normal activities of life. A cross sectional descriptive study conducted by Yoon and Black (2006) researched both pharmacologic and complementary therapies used for pain management by caregivers of children with sickle cell disease (SCD). They further studied the prevalence and types of complementary therapies used for pain management by caregivers of children with SCD and made inquiries of caregivers’ concerning their interests in using complementary therapies in the future. Since there was no obtainable questionnaire to meet the principle of the study, a questionnaire was created by the chief researcher. Items included on the questionnaire was age of child, age of caregiver, use of analgesic, annual income estimate, caregivers educational level, and type of health insurance their child had available. Divisions were randomly ordered and included massage, chiropractic, acupuncture, energy healing, relaxation techniques, imagery, meditation, hypnosis, biofeedback, self-prayer, spiritual healing by others, music therapy, herbal or fold remedies, megavitiamins, yoga, tai chi and other body works, and transcutaneous electrical nerve stimulation. The prospective patients were identified, approached, and invited to participate in the study by the clinical coordinator of the sickle cell disease clinic. The study was explained and potential participants were provided an informed consent letter. All subjects were provided a room for privacy and questionnaires were completed either by the caregivers of the participants or by the research assistance. The research assistant was nearby in either case to answer any questions that might arise by the caregivers when completing his/her form. The instructions provided to the caregivers indicated the questionnaires listing of the sixteen complementary therapies. The caregivers were to indicate any usage of them within the last six months and were asked would they be interested in using any of the listed complementary therapies in the future. Statistical analyses was used including how often an event repeats itself over a set amount of time and expected values with standard deviations, were used to compare demographic variables, research use of pharmacological therapies for pain management between age groups, and evaluate pharmacologic/analgesic and complementary therapy use. Chi-square tests were done in the beginning of the study and carried through to completion comparing the demographic variables, scrutinized use of pharmacologic therapies for pain management between age groups, and compared use of pharmacologic and complementary therapies. The results of the most frequently used pain medication for children revealed a mean age of 9 years. The results indicated children using pain medications most frequently identified was ibuprofen (37. 5%), acetaminophen with codeine (32. 1%), and acetaminophen with oxycodone (14. 5%). Complementary and alternative medicine use among children as well as adults has increased in the last ten years. In the study, caregivers with a mean age of 33 years was 70% of the 63 caregivers identified as using some form of complementary therapy. African American mothers made up 79% of the predominant race of caregivers and (56. 9%) indicated an annual income less than $20,000. Sixty percent of caregivers had twelve years of education or less, and twenty-four percent reported at least 2 years of college education. Medicaid (76%) was the major source of coverage for the children, although 24% had private or other identifying insurance. Future studies should include investigating the safety and effectiveness of the most commonly used complementary therapies reported in this study as well as recognizing possible ways complementary and alternative medicine (CAM) may be used effectively with pharmacologic therapies for pain management in children with Sickle cell disease in order to offer greater longevity and overall improved quality of life. Yoon and Black (2006), Jiles and Morris (2008) and Granados and Jacob (2009) all indicate the need for future studies in management of pain in the sickle cell disease patients. All studies indicate that the genetic disorder most commonly found in the African- American affects approximately 70,000 in the United States. This genetic disorder affects the red blood cells causing a stasis of sickle shaped erythrocytes, in which occlusion of the cells microcirculation, causing ischemia, and infarction. These recurring, unpredictable, intensified, and persistent painful episodes prevent stability and overall quality of life in the sickle cell disease patient and all authors indicate the need for future studies. The purpose of this review of literature is to identify all of the effective therapies of pain management for sickle cell disease patients. Whether the therapies used are complementary or alternative therapies vs. analgesic regimens. There must be future studies to seek out the answers for improved methods of pain treatment in order to improve the quality of life for the patients with sickle cell disease to exceed living past the age of forty-two with an increased zest and quality of life. References Granados, R. , Jacob, E. , (2009, May/June). Pain Experience in Hospitalized Adults with Sickle Cell Disease. Medsurg Nursing, 18 (3), 161-167,182. Jiles, V. M. , Morris, D. L. , (2009). Quality of Life of adult patients with sickle cell disease. Journal of the American Academy of Nurse Practitioners, Volume 21, 340-349. doi: 10. 1111/j. 1745-7599. 2009. 00416x Yoon, S. L. , Black, S. , (2006) Comprehensive, Integrative Management of Pain for Patients with Sickle-Cell Disease. The Journal of Alternative and Complementary Medicine, Volume 12, Number 10, pp. 995-1001.

Pain Management and Quality of Life for Sickle Cell Disease Patients Essays

Pain Management and Quality of Life for Sickle Cell Disease Patients Essays Pain Management and Quality of Life for Sickle Cell Disease Patients Essay Pain Management and Quality of Life for Sickle Cell Disease Patients Essay Pain Management and Quality of Life for Sickle Cell Disease Patients Cynthia Evans Mississippi College Pain Management and Quality of Life for Sickle Cell Disease Patients This is a review of literature examining how frequent recurring episodes of pain affect the quality of life in the sickle cell disease patients. Several studies conducted concerning pain management and quality of life for sickle cell disease patients indicate additional studies needed. Identifying additional effective complementary alternate therapies is vital for a more improved quality of life. This will be necessary in order to reduce the number of painful episodes experienced by the sickle cell patient. Sickle cell disease is a genetic disorder of the red blood cells and further characterized by painful acute vaso-occlusive episodes where the sickle cell is stuck in the blood vessels, blocking the blood flow. This is one of the most common reasons leading up to hospitalization, the vaso-occlusive episodes. These episodes can lead to ischemia and infarctions over the entire body region with painful recurring, unpredictable, intense, and relentless episodes, lasting approximately 3-14 days (Yaster, Kost-Byerly, Maxwell, 2000). According to Granados and Jacob (2009), the purpose of their study was to examine pain experienced and the effectiveness of analgesics for hospitalized adults with sickle cell disease. The literature review indicates a variety of reasons why inadequate pain management is ongoing in the adult (SCD) patients admitted with vaso-occlusive episodes. The focus is mainly on factors that affect the management of pain, including methods of analgesic administration, and non-pharmacologic regimens, therefore the perception of the provider is important in regards to treating sickle cell pain as identified in the study by (Shapiro, Benjamin, Payne Heidrich, 1997; Steinberg, 1999; Yale et al. , 2000). Little attention in the way of research studies has been examined in relation to the pain experience of the sickle cell adults. Ballas and Lusardi (2005) evaluated the sequence of hospital admissions of patients with sickle cell disease, reviewing the causes of recurring admissions, and the importance of the patient’s outcome of illness. All readmissions examined specifically within seven to thirty days from the initial admission discharge assessing for the rationale of the recurrence of hospital admission and relation to the prognosis of the sickle cell disease patient. The researchers evaluated the pain by a descriptive underlying research design knowledgeable by the sickle cell disease patients for intensity, location, and quality of pain. Fifty percent of patients admitted for intense painful episodes were readmitted within one month after discharge, and another estimated 16% were readmitted within one week after discharge. Severe pain is described as a degree of pain greater than six on a zero to ten numerical rating scales. A mean score of seven or greater indicates prematurity in discharging the sickle cell disease patients from the hospital. In conclusion, the patients admitted to the hospital with high pain scores were more likely to have lengthy hospitalizations, and to be discharged home with equally higher pain scores. The pain intensity scores from the previous discharge examined by the researchers indicated 71 readmission, in which 52 patients were readmitted for vaso-occlusive episodes, (Ballas Lusardi, 2005). The pain score of study participants indicated a high pain intensity score, and the scores did not change consequently during prolonged episodes. Even higher pain intensity more so on days seven and eight were indicated for increase pain significance. Researchers further indicated that the main reason for hospital readmissions were early discharge to home settings, signs and symptoms of medication/drug withdrawal, that brought about the intense reoccurring episodes of vaso-occlusive illnesses. It was noted that readmissions to the hospital for the adult sickle cell disease patient is more common and researchers recommended future studies for improvement in pain management in the hospital and at home. In future studies, researchers will need to use a larger sample size to evaluate patterns of pain management, effectiveness and influence on quality of life in the sickle cell disease patient. Although, no evidence was identified where upward titration of analgesics was done it is recommended that development of algorithms be encouraged to help carefully plan decisions regarding titration of medications in adult patients with sickle cell disease during hospitalizations. Jiles and Morris, (2008) made known in their descriptive study of 62 patients (18 years of age and older) using Burckhardt and Anderson’s 16 item self-report and a demographic uestionnaire used for data collection. The purpose of the study was to investigate the quality of life in adults with sickle cell anemia, hemoglobin SC, or Hemoglobin S beta thalassemia. The results revealed that the healthy populations average scores for quality of life scale is 90 and in this study the overall mean QOL score was 83. 6 ( SD=13. 2) lower than those of the overall general population. The outcome of this study indicated additional research is necessary to advance the understanding of the factors that greatly affect quality of life in the management of sickle cell disease in order for patients to enjoy normal activities of life. A cross sectional descriptive study conducted by Yoon and Black (2006) researched both pharmacologic and complementary therapies used for pain management by caregivers of children with sickle cell disease (SCD). They further studied the prevalence and types of complementary therapies used for pain management by caregivers of children with SCD and made inquiries of caregivers’ concerning their interests in using complementary therapies in the future. Since there was no obtainable questionnaire to meet the principle of the study, a questionnaire was created by the chief researcher. Items included on the questionnaire was age of child, age of caregiver, use of analgesic, annual income estimate, caregivers educational level, and type of health insurance their child had available. Divisions were randomly ordered and included massage, chiropractic, acupuncture, energy healing, relaxation techniques, imagery, meditation, hypnosis, biofeedback, self-prayer, spiritual healing by others, music therapy, herbal or fold remedies, megavitiamins, yoga, tai chi and other body works, and transcutaneous electrical nerve stimulation. The prospective patients were identified, approached, and invited to participate in the study by the clinical coordinator of the sickle cell disease clinic. The study was explained and potential participants were provided an informed consent letter. All subjects were provided a room for privacy and questionnaires were completed either by the caregivers of the participants or by the research assistance. The research assistant was nearby in either case to answer any questions that might arise by the caregivers when completing his/her form. The instructions provided to the caregivers indicated the questionnaires listing of the sixteen complementary therapies. The caregivers were to indicate any usage of them within the last six months and were asked would they be interested in using any of the listed complementary therapies in the future. Statistical analyses was used including how often an event repeats itself over a set amount of time and expected values with standard deviations, were used to compare demographic variables, research use of pharmacological therapies for pain management between age groups, and evaluate pharmacologic/analgesic and complementary therapy use. Chi-square tests were done in the beginning of the study and carried through to completion comparing the demographic variables, scrutinized use of pharmacologic therapies for pain management between age groups, and compared use of pharmacologic and complementary therapies. The results of the most frequently used pain medication for children revealed a mean age of 9 years. The results indicated children using pain medications most frequently identified was ibuprofen (37. 5%), acetaminophen with codeine (32. 1%), and acetaminophen with oxycodone (14. 5%). Complementary and alternative medicine use among children as well as adults has increased in the last ten years. In the study, caregivers with a mean age of 33 years was 70% of the 63 caregivers identified as using some form of complementary therapy. African American mothers made up 79% of the predominant race of caregivers and (56. 9%) indicated an annual income less than $20,000. Sixty percent of caregivers had twelve years of education or less, and twenty-four percent reported at least 2 years of college education. Medicaid (76%) was the major source of coverage for the children, although 24% had private or other identifying insurance. Future studies should include investigating the safety and effectiveness of the most commonly used complementary therapies reported in this study as well as recognizing possible ways complementary and alternative medicine (CAM) may be used effectively with pharmacologic therapies for pain management in children with Sickle cell disease in order to offer greater longevity and overall improved quality of life. Yoon and Black (2006), Jiles and Morris (2008) and Granados and Jacob (2009) all indicate the need for future studies in management of pain in the sickle cell disease patients. All studies indicate that the genetic disorder most commonly found in the African- American affects approximately 70,000 in the United States. This genetic disorder affects the red blood cells causing a stasis of sickle shaped erythrocytes, in which occlusion of the cells microcirculation, causing ischemia, and infarction. These recurring, unpredictable, intensified, and persistent painful episodes prevent stability and overall quality of life in the sickle cell disease patient and all authors indicate the need for future studies. The purpose of this review of literature is to identify all of the effective therapies of pain management for sickle cell disease patients. Whether the therapies used are complementary or alternative therapies vs. analgesic regimens. There must be future studies to seek out the answers for improved methods of pain treatment in order to improve the quality of life for the patients with sickle cell disease to exceed living past the age of forty-two with an increased zest and quality of life. References Granados, R. , Jacob, E. , (2009, May/June). Pain Experience in Hospitalized Adults with Sickle Cell Disease. Medsurg Nursing, 18 (3), 161-167,182. Jiles, V. M. , Morris, D. L. , (2009). Quality of Life of adult patients with sickle cell disease. Journal of the American Academy of Nurse Practitioners, Volume 21, 340-349. doi: 10. 1111/j. 1745-7599. 2009. 00416x Yoon, S. L. , Black, S. , (2006) Comprehensive, Integrative Management of Pain for Patients with Sickle-Cell Disease. The Journal of Alternative and Complementary Medicine, Volume 12, Number 10, pp. 995-1001.

WEBER Surname Meaning and Family History

WEBER Surname Meaning and Family History Weber is an occupational surname given to one skilled in the ancient craft of weaving, from the from the Middle High German word wà «ber,  a derivative of weben, meaning to weave.  The Weber surname is sometimes Anglicized as Webber or Weaver. Weber is the 6th most common German surname. It is also frequently found as a  Czech, Hungarian, Polish or  Slovenian surname.  WEBB and  WEAVER are English variants of the name. Surname Origin: German Alternate Surname Spellings:  WEEBER, WEBBER, WEBERE, WEBERER, WAEBER, WEYBER, WEBERN, VON WEBER, VON WEBBER Famous People with the WEBER  Surname Max Weber  -  19th-century German sociologist and one of the founders of modern sociologyCarl Maria von Webber -  German composer, conductor, pianist and  guitaristConstanze Weber - wife of Wolfgang Amadeus MozartAlfred Weber - German economist, geographer and sociologistJohn Henry Weber - American fur trader and explorerJoseph Weber - American physicistLudwig Weber -  German Protestant pastor and social reformer- German-born physician, best known for first describing the brain condition which carries his name (Webers syndrome) Where is the WEBER Surname Most Common? According to surname distribution from Forebears, WEBER is the 3rd most common surname in Germany. It is also very common in Switzerland, where it ranks 7th, and Austria, where it is the 19th most prevalent last name. While Weber is common throughout Germany, WorldNames PublicProfiler indicates it is most frequent in southwestern Germany, in the regions of Rheinland-Pfalz, Saarland and Hessen. Weber is also a very common surname in Gussing, Austria.   Genealogy Resources for the Surname WEBER Meanings of Common German SurnamesUncover the meaning of your German last name with this free guide to the meanings and origins of common German surnames. Weber  Family Crest - Its Not What You ThinkContrary to what you may hear, there is no such thing as a Weber  family crest or coat of arms for the Weber surname.  Coats of arms are granted to individuals, not families, and may rightfully be used only by the uninterrupted male line descendants of the person to whom the coat of arms was originally granted. Weber Y-Chromosome DNA  Surname ProjectWEBERs from all over the world are participating in this group DNA project in an attempt to learn more about Weber family origins. The website includes information on the project, the research done to date, and instructions on how to participate. WEBER  Family Genealogy ForumFree message board is focused on descendants of Weber  ancestors around the world. FamilySearch - WEBER  GenealogyExplore over 5 million results from digitized  historical records and lineage-linked family trees related to the Weber  surname on this free website hosted by the Church of Jesus Christ of Latter-day Saints. WEBER  Surname Mailing ListFree mailing list for researchers of the Weber  surname and its variations includes subscription details and a searchable archives of past messages. DistantCousin.com - WEBER  Genealogy Family HistoryExplore free databases and genealogy links for the last name Weber. GeneaNet - Weber  RecordsGeneaNet includes archival records, family trees, and other resources for individuals with the Weber  surname, with a concentration on records and families from France and other European countries. The Weber Genealogy and Family Tree PageBrowse genealogy records and links to genealogical and historical records for individuals with the Weber  surname from the website of Genealogy Today. - References: Surname Meanings Origins Cottle, Basil.  Penguin Dictionary of Surnames. Baltimore, MD: Penguin Books, 1967. Dorward, David.  Scottish Surnames. Collins Celtic (Pocket edition), 1998. Fucilla, Joseph.  Our Italian Surnames. Genealogical Publishing Company, 2003. Hanks, Patrick and Flavia Hodges.  A Dictionary of Surnames. Oxford University Press, 1989. Hanks, Patrick.  Dictionary of American Family Names. Oxford University Press, 2003. Reaney, P.H.  A Dictionary of English Surnames. Oxford University Press, 1997. Smith, Elsdon C.  American Surnames. Genealogical Publishing Company, 1997. Back to  Glossary of Surname Meanings Origins