Sunday, December 27, 2009
11th Day of Vacation - DR. GRAYSON!
Saturday, December 19, 2009
32/32
- Basic Nutrition
- Physiology III
- Pathology II
- Professional Development
- Philosophy IV
- Orthopedics II
- Diversified Technique III
- Basic Technique II
- Neuromusculoskeletal Diagnosis
- Fundamentals of Diagnostic Imaging
- only 3 labs - the finals for labs are usually while we still are in class full time - can be stressful.
- Hwy 40 is OPEN - that means about 45 minutes or so less per DAY of time spent in my car - close to 5 extra hours a week!!!
- only 31 hours of class per week - a savings of 3 hours per week over tri-3
Thursday, December 17, 2009
Tri-3, Wk15, Day 200! Thursday - 16/16
2:30 a.m. - less than 6 hours before this Trimester is over -
Tuesday, December 15, 2009
Tri-3, Wk15, Day 199 - Wednesday - 15/15
Tri-3, Wk15, Day 198 - Tuesday
Monday, December 14, 2009
Tri-3, Wk15, Day 197+, Monday (cont) 5/5
Public Health & Basic Technique I are in the book and give me a total of 5 credit hours earned out the the 32 credit hours attempted. So far - 5/5.
Tri-3, Wk15, Day 197, Monday
Definitely a time crunch w/ school. I slept in until 4:30 this morning. Our first final isn't until 9 a.m. and a little extra sleep probably isn't a bad way to start the last week of Tri-3. I woke up wondering what I could have done differently to allocate my time but I don't think there's much different I could have done except w/ Sat night. Cutting back to two hours w/ family or maybe getting things pushed off a week it about it. Once I get through this trimester I'll work at doing more to make Tri-4 more productive. That's pretty much an imperative.
Sunday, December 13, 2009
Sunday Studies ...
Saturday Studying, Mon will be day 197
Saturday was a pretty good study day up until about 5:30 p.m. I finished my micro lab paper by noon then made up flashcards and went through test for both Diversified and Pathology.
Friday, December 11, 2009
Tri-3, Wk14, Day 196+ Two Offensive Blows!
Tri-3, Wk14, Day 196, Friday
Went to bed around 10 last night and got up a little before 1 a.m. It was good to get a little shuteye.
Thursday, December 10, 2009
Tri-3, Wk14, Day 195, Thursday
Wednesday, December 9, 2009
Tri-3, Wk14, Day 194, Wednesday
did pretty well on today's micro test. I went to the first half of philosophy this morning but wasn't able to study sufficiently so I left for the second half. I also opted out of my Basic class and was able to get in an extra 3 hours of studying that way. I'm close to an A in philosophy and close to not passing in Micro so I thought it was a good move and having seen my grade for the test today in micro it was the right decision.
Tri-3, Wk 14, Day 193, Tuesday
Monday, December 7, 2009
Tri-3, Wk14, Day 192, Monday Rocked Path Exam!
- Diversified - if i put in the effort tonight - good chance i can pull it out
- Micro - the lab paper is supposed to help our grade - maybe not much sleep tomorrow night while I prep for Micro lab final.
- Ortho - I'll have to learn a ton for this exam/practical. We have this class tomorrow so I'll learn more then.
- Public Health & Basic - these two are kind of easy, I'll just be up all night Thursday studying for them
Sunday, December 6, 2009
Sunday Evening Post...
9 days left of Tri-3. Our last day of finals will coincide with our 200th class day at Logan.
Friday, December 4, 2009
Tri-3, Wk13, Day 191, Friday, Little Blue Dots
Today was pretty fascinating overall. We started in on Chapter 6 in Pathology which covers Neoplasia which most people might refer to as cancer. A lot of words aren't meaning what they used to. Terms and phrases which used to be part of my everyday lexicon now seem vague and without meaning or don't make much sense anymore. Take the notion of a heart attack for instance. That doesn't really mean anything in a medical sense and I see more comfort in thinking of it in terms of infarction, ischemia and necrosis. I think terminology change first happened in gross anatomy when I started to wonder what an ankle was. I'm familiar with a lateral and medial malleolus but am no longer sure exactly what an ankle refers to, in particular, which side of the leg, medial or lateral?
Thursday, December 3, 2009
Tri-3, Wk13, Days 189 & 190, Wed & Thur
My attitude has been rather lackluster lately. For most of today I've just been thinking I want to get off this Merry-go-round. I want it to stop, I want this to be over. Normally, I don't think I'd blog such despair but I also realize that one reason I wanted to complete the program at Logan and become a DC was that such completion would necessarily force me to become a better person and I have learned throughout my life that it usually works best if I am in a situation where I'm forced to improve and that's certainly where I find myself now... forced to improve.
- XLA, Brunton's dz - the XLA stands for X-linked agammaglobulinemia which seems like a mouthful until you break it down a bit - recall the 'a' stands for "without" so, we're without gamma globulin in the blood - the emia part always seems to refer to blood. The disease makes a bit more sense w/ a picture (guess I'm a visual type learner) but, the B cells never quite make it out of the bone marrow with this disease which is why you don't find much of their consequences out in the blood.
- CVI - (or CVID) - Common Variable Immunodeficiency dz - with this dz the B cells make it out of the bone marrow but not much further. Instead of agammaglobulinemia we have hypogammaglobulinemia. which is to say instead of without that stuff, we have hypo or low gamma globulin in the blood.
- Isolated IgA Deficiency - this is the most common of the immunological deficiency diseases and occurs in about 1 out of 600 people and it's asymptomatic - ...there's that letter 'a' at the beginning of the word again so, it literally means "without symptoms".
- DiGeorge or Thymic hypoplasia - this is a defect in the thymus gland itself and that's where T cells grow up to become adult T cells.
- SCIDS - Severe Combined Immunodeficiency - This is really bad. Do you remember that show, the Boy in the Bubble? I think John Travolta may have played that little kid in the bubble. With this dz, the stem cells with the potential to be either B or T cells is thwarted at the very beginning.
Tuesday, December 1, 2009
Tri-3, Wk13, Day 188 - Tuesday
Tri-3, Wk13, Day 187 - Monday
- 12/01 Tue - Irene Gold NBCE prep $ due
- 12/03 Thur - Pathology review @ 4
- 12/04 Fri - Pathology Exam 4
- 12/05 Sat - Physio Final review at Logan
- 12/06 Sun - Volunteer w/ BJC at St. Louis Science Center
- 12/07 Mon - Physio Exam 5 and Diversified Practical and physio final review at Double Tree
- 12/08 Tue -
- 12/09 Wed - Microbiology Lab Exam
- 12/10 Thur - Orthopedics Final Practical
- 12/11 Fri - Basic I Final & Public Health Final and NBCE application due
- 12/14 Mon - Diversified Final and Pathology Final
- 12/15 Tue - Philosophy Final and Microbiology Final
- 12/16 Wed - Physiology II Final & Embryo Final
- 12/17 Thur - Orthopedics Final
Sunday, November 29, 2009
Pathology I: Immune System
I've got another picture from the book helping me out and will post it as today's pic of the day. The analogy I gave yesterday about the inner workings of the General Motors plant being messed with has more to do with a viral infection, when a virus overtakes the inner workings of a cell. This is known as Cellular Immunity, sometimes referred to as cell-mediated immunity.
Saturday, November 28, 2009
Pathology I: Immune System
ADCC, Antibody-Dependent Cell-Mediated Cytotoxicity. It's enough to make you cry after countless hours trying to study something only vaguely familiar however, the picture on slide 106 of our pathology power point presentation shows a picture of ADCC and a few elements of confused gases swirling around in my brain have begun to form into something that makes sense based on that picture. I'll post the picture as today's pic of the day.
Thursday, November 26, 2009
Tri-3, Wk12, Days 185 & 186, Tue & Wed - Survival
Mon 11/30
Tue 12/1 Path Exam
Wed 12/2
Thur 12/3 Diversified Practical (B)
Fri 12/4
Mon 12/7 Diversified Practical (C)
Tue 12/8 Diversified Practical (A)
Wed 12/9 Microbiology Lab Exam at 11
Thur 12/10 Orthopedics Final Practical
Friday 12/11 Basic Final, Public Health Final
Mon 12/14 Diversified Final @ 9 a.m. 156B
Pathology Final @ 2 p.m. Purser
Tue 12/15 Philosophy Final @ 7 a..m.
Microbiology Final @ 11
Wed 12/16 Physiology II Final @ ? a.m.
Embryology Final @ ? a.m. in ?
Thur 12/17 Orthopedics Final @ 7?
Tuesday, November 24, 2009
Tri-3, Wk12, Day 184, Monday
We have two test scheduled for Tuesday; one in Embryo & one in Physio. We also have two fellow classmates who act as educational coordinators (EC's) for our class and I learned earlier that at least one of those EC's was able to take the embryo test on Monday. I can't help wondering if that person will be gone today or just got the embryo test knocked out so they could wholly focus on physio for Tuesday. I can't help thinking that would have been a fantastic option for everybody because we could have totally focused on studying embryo Sunday night then devote all of our attention to studying physio on Monday night.
Sunday, November 22, 2009
Pathology I: Immune System (Simple Outline)
What Happens When An Enemy Invades Your Body?
- THE IMMUNE SYSTEM
- The purpose of the Immune System is defense and protection through a system of surveillance
- This surveillance operates on the simple principal of distinguishing "self" from "non-self"
- The purpose of the Immune System is defense and protection through a system of surveillance
Outline Contents:
Effectors of the Immune System
Histocompatibility Genes
Immune Mechanisms
Autoimmune Disorders
Immunodeficiency Diseases
- EFFECTORS OF THE IMMUNE SYSTEM
- Cells & Cytokins
- T Lymphocytes
- B Lymphocytes
- Macrophages
- Dendrtitic & Langerhans Cells
- Natural Killer Cells
- Cells & Cytokins
- T Lymphocytes
- In the blood, T cells constitute 60 to 70% of peripheral lymphocytes
- In the blood, T cells constitute 60 to 70% of peripheral lymphocytes
- B Lymphocytes
- B lymphocytes constitute 10 to 20% of the circulating peripheral lymphocyte population
- B lymphocytes constitute 10 to 20% of the circulating peripheral lymphocyte population
- MACROPHAGES
- Macrophages play a major role in inflammation, but also have many activities in the immune response. (s28)
- Macrophages play a major role in inflammation, but also have many activities in the immune response. (s28)
- Dendric & Langerhan's Cells
- Dendritic cells are widely distributed. They are found in lymphoid tissue and in the interstitium of many nonlymphoid organs, such as the heart and lungs. Similar cells within the epidermis have been called Langerhans' cells (S31)
- Dendritic cells are widely distributed. They are found in lymphoid tissue and in the interstitium of many nonlymphoid organs, such as the heart and lungs. Similar cells within the epidermis have been called Langerhans' cells (S31)
- Natural Killer (NK) Cells
- Approximately 10 to 15% of the peripheral blood lymphocytes do not bear TCR or cell-surface immunoglobulins.
- Approximately 10 to 15% of the peripheral blood lymphocytes do not bear TCR or cell-surface immunoglobulins.
- HISTOCOMPATIBILITY GENES /Molecules
- Originally identified as antigens that evoke rejection of transplanted organs, histocompatibility molecules are now extremely important for the induction and regulation of the immune response and for certain nonimmunologic functions (s39)
- Originally identified as antigens that evoke rejection of transplanted organs, histocompatibility molecules are now extremely important for the induction and regulation of the immune response and for certain nonimmunologic functions (s39)
- Cytokines
- The induction and regulation of the multiple immune responses involve multiple interactions among lymphocytes, monocytes, inflammatory cells (neutrophils) and endothelial cells.
- The induction and regulation of the multiple immune responses involve multiple interactions among lymphocytes, monocytes, inflammatory cells (neutrophils) and endothelial cells.
- IMMUNE MECHANISM
(S66)
- Contact with antigen leads not only to induction of a protective immune response, but also to reactions that can be damaging to tissues
- An antigen is a substance that can be specifically recognized by the immune system and cause a response
- Contact with antigen leads not only to induction of a protective immune response, but also to reactions that can be damaging to tissues
- Tissue Damage (Hypersenstivity) (s76)
- Tissue-damaging immune reactions may be evoked not only by exogenous antigens, but also by those that are intrinsic to the body (endogenous) (s76)
- Tissue-damaging immune reactions may be evoked not only by exogenous antigens, but also by those that are intrinsic to the body (endogenous) (s76)
- Type I Hypersensitivity (Anaphylactic Type)
- A rapidly developing immunologic reaction occurring within minutes after the combination of an antigen with antibody bound to mast cells or basophils in individuals previously sensitized to the antigen.
- A rapidly developing immunologic reaction occurring within minutes after the combination of an antigen with antibody bound to mast cells or basophils in individuals previously sensitized to the antigen.
- Type II Hypersensitivity (Antibody Dependent)
- This type is mediated by antibodies directed toward antigens present on the surface of cells or other tissue components.
- This type is mediated by antibodies directed toward antigens present on the surface of cells or other tissue components.
- Complement-Dependent Reactions
- #1 – Antibody (IgM or IgG) reacts with an antigen present on the surface of the cell, causing activation of the complement system and resulting in the assembly of the membrane attack complex that disrupts membrane integrity by "drilling holes" through the lipid bilayer (s100)
- #2 – Cells become susceptible to phagocytosis by fixation of antibody or C3b fragment to the cell surface (opsonization). (s101)
- #1 – Antibody (IgM or IgG) reacts with an antigen present on the surface of the cell, causing activation of the complement system and resulting in the assembly of the membrane attack complex that disrupts membrane integrity by "drilling holes" through the lipid bilayer (s100)
- Antibody-Dependent Cell-Mediated Cytotoxicity
- This form of antibody-mediated cell injury does not involve fixation of complement but instead requires the cooperation of leukocytes.
- This form of antibody-mediated cell injury does not involve fixation of complement but instead requires the cooperation of leukocytes.
- Antibody-Mediated Cellular Dysfunction
- In some cases, antibodies directed against cell surface receptors impair or dysregulate function without causing cell injury or inflammation. (s107)
- In some cases, antibodies directed against cell surface receptors impair or dysregulate function without causing cell injury or inflammation. (s107)
- Graves' disease
- Graves' disease is the most common cause of hyperthyroidism
- Graves' disease is the most common cause of hyperthyroidism
- Type III Hypersensitivity (Immune Complex–mediated)
- These reaction are induced by antigen-antibody complexes that produce tissue damage as a result of their capacity to activate a variety of serum mediators, principally the complement system. (s114)
- These reaction are induced by antigen-antibody complexes that produce tissue damage as a result of their capacity to activate a variety of serum mediators, principally the complement system. (s114)
- Local Immune Complex Disease (Arthus Reaction)
- The Arthus reaction is a localized area of tissue necrosis resulting from acute immune complex vasculitis, usually elicited in the skin 128
- The Arthus reaction is a localized area of tissue necrosis resulting from acute immune complex vasculitis, usually elicited in the skin 128
- Type IV Hypersensitivity (Cell-Mediated)
- This type of hypersensitivity is initiated by specifically sensitized T lymphocytes, rather than by antibodies
- This type of hypersensitivity is initiated by specifically sensitized T lymphocytes, rather than by antibodies
- Summary of Immune Mechanisms
- Graft-versus-Host (GVH) Disease
- GVH disease occurs when immunologically competent cells are transplanted into immunologically crippled recipients. GVH disease occurs most commonly in the setting of allogeneic bone marrow transplantation but may also follow transplantation of solid organs rich in lymphoid cells (e.g., the liver) or following transfusion of unirradiated blood 139
- GVH disease occurs when immunologically competent cells are transplanted into immunologically crippled recipients. GVH disease occurs most commonly in the setting of allogeneic bone marrow transplantation but may also follow transplantation of solid organs rich in lymphoid cells (e.g., the liver) or following transfusion of unirradiated blood 139
- AUTOIMMUNE DISEASES
- Three requirements for autoimmunity:
- Three requirements for autoimmunity:
- Immunologic Tolerance
- Immunologic tolerance is a state in which the individual is incapable of developing an immune response to a specific antigen
- Immunologic tolerance is a state in which the individual is incapable of developing an immune response to a specific antigen
- Clonal Deletion
- This refers to loss of self-reactive T and B lymphocytes during their maturation
- This refers to loss of self-reactive T and B lymphocytes during their maturation
- Clonal Anergy
- This refers to prolonged or irreversible functional inactivation of lymphocytes, induced by encounter with antigens under certain conditions 144
- This refers to prolonged or irreversible functional inactivation of lymphocytes, induced by encounter with antigens under certain conditions 144
- Peripheral suppression by T cells
- Many factors, both cellular and humoral, that can actively suppress autoreactive lymphocytes have been described.
- Many factors, both cellular and humoral, that can actively suppress autoreactive lymphocytes have been described.
- Mechanisms of Autoimmune Diseases
- The pathogenesis of autoimmunity appears to involve immunologic, genetic, and viral factors interacting through complicated mechanisms that are poorly understood 147
- The pathogenesis of autoimmunity appears to involve immunologic, genetic, and viral factors interacting through complicated mechanisms that are poorly understood 147
- Bypass of Helper T Cell Tolerance
- Tolerance may be broken if the need for helper T cells is bypassed
- Tolerance may be broken if the need for helper T cells is bypassed
- Molecular Mimicry
- Several infectious agents cross-react with human tissues through their haptenic determinants (B-cell epitopes)
- Several infectious agents cross-react with human tissues through their haptenic determinants (B-cell epitopes)
- Polyclonal Lymphocyte Activation
- Autoimmunity may occur if such self-reactive but anergic clones are stimulated by antigen-independent mechanisms 151
- Autoimmunity may occur if such self-reactive but anergic clones are stimulated by antigen-independent mechanisms 151
- Imbalance of Suppressor-Helper T-Cell Function
- Any loss of suppressor T-cell function will contribute to autoimmunity, and, conversely, excessive T-cell help may drive B cells to extremely high levels of autoantibody production 152
- Any loss of suppressor T-cell function will contribute to autoimmunity, and, conversely, excessive T-cell help may drive B cells to extremely high levels of autoantibody production 152
- Emergence of a Sequestered Antigen
- Any self-antigen that is completely sequestered during development is likely to be viewed as foreign if introduced into the circulation, and an immune response will develop.
- Any self-antigen that is completely sequestered during development is likely to be viewed as foreign if introduced into the circulation, and an immune response will develop.
- Consequences of the loss of self-tolerance: autoimmune diseases
- Autoimmune diseases range from those in which the target is a single tissue, such as the autoimmune hemolytic anemias and thyroiditis, to those in which a host of self-antigens evoke a constellation of reactions against many organs and systems 154
- Autoimmune diseases range from those in which the target is a single tissue, such as the autoimmune hemolytic anemias and thyroiditis, to those in which a host of self-antigens evoke a constellation of reactions against many organs and systems 154
- Systemic Lupus Erythematosus (SLE) 155
- SLE is the a multisystem disease of autoimmune origin, characterized by a many autoantibodies, particularly antinuclear antibodies (ANAs).
- SLE is the a multisystem disease of autoimmune origin, characterized by a many autoantibodies, particularly antinuclear antibodies (ANAs).
- Sjögren's Syndrome
- Sjögren's syndrome is characterized by dry eyes (keratoconjunctivitis sicca) and dry mouth (xerostomia) resulting from immunologically mediated destruction of the lacrimal and salivary glands. 159
- Sjögren's syndrome is characterized by dry eyes (keratoconjunctivitis sicca) and dry mouth (xerostomia) resulting from immunologically mediated destruction of the lacrimal and salivary glands. 159
- Systemic Sclerosis (Scleroderma)
- Characterized by excessive fibrosis throughout the body. The skin is most commonly affected, but the gastrointestinal tract, kidneys, heart, muscles, and lungs also are frequently involved 162
- Characterized by excessive fibrosis throughout the body. The skin is most commonly affected, but the gastrointestinal tract, kidneys, heart, muscles, and lungs also are frequently involved 162
- IMMUNOLOGIC DEFICIENCY SYNDROMES
- Traditionally, immunodeficiency disorders are considered according to the primary component or components involved (i.e., the B cell, the T cell, the undifferentiated stem cell, or complement); however, in view of the extensive cell interactions between T and B lymphocytes and macrophages, these distinctions are not always clear-cut 167
- Traditionally, immunodeficiency disorders are considered according to the primary component or components involved (i.e., the B cell, the T cell, the undifferentiated stem cell, or complement); however, in view of the extensive cell interactions between T and B lymphocytes and macrophages, these distinctions are not always clear-cut 167
- Expansion of Immunologic Deficiency Syndromes