As I mentioned before, Systemic Mastocytosis runs in my family. My dad has SM and I am being closely watched for it. I don’t remember exactly when my dad was diagnosed but I remember him being rally sick. However, I do remember I was in 3rd grade when he had to go through chemo, which means I was about 9 years old. So of course I had no idea what was going on when I was 9. I just remember that I had to stay with a family friend’s house, which happened to be my sister’s best friend’s family. My dad’s doctor wanted to try chemo, they were not sure if it would work. Thankfully it did and my dad came home, and of course because of the chemo it made him weak and not look too good. I also just recently found out that my dad has a tumor in his stomach, no one in my family knew about it. …show more content…
Most doctor do not know much about Systemic Mastocytosis and if they do it is only a little bit. After a while the doctors wanted to keep a close eye on me and my siblings. My brother and I only showed signs of the disease. However, my brother was growing out of the disease and signs of the disease like most kids, who show signs of SM. I on the other hand was not. I have one major sign of SM, which is Dermatographia. Dermatographia is a condition in which lightly scratching your skin causes raised, red lines where you’ve scratches, which is basically hives. But this is not limited to scratches. You could be scratched, hit, or, this has happened to me before, I sat a really cold hold and developed hives. The hives to go way by the time 30 minutes past. Although I do show signs of SM I have not be officially diagnosed. My dog just so happened to have a tumor in her leg. When the vet sent it in to be tested, they found that it was mast cells. My dog has staged two cancer and the same disease as my dad, what is the
Arch Dermatol. 2007;143(1):124–125. Puchenkova, S. G. (1996). "
Barone, Eugene J., Judson C. Jones, and Joann E. Schaefer. "Hidradenitis Suppurativa." Skin Disorders. Philadelphia: Lippincott Williams & Wilkins, 2000. 21-25. Print.
If having dry skin isn’t bad enough, witnessing it in front of you get into clumps and morphing into a patch of dry skin most be the worst. Ichtyosis Vulgaris (or also called fish scale disease) is a skin disorder that is passed down the family line that leads to dry, scaly skin. Ichtyosis Vulgaris is one type of skin disorder that is very common. You are born with this skin disease which it is inherited in an autosomal dominant pattern. This type of skin disease is not life threating at all but there really isn’t a way to cure it at you just have to go on living with it. They symptoms of Ichtyosis Vulgaris are: dry skin, scaly skin, mild itching of the skin, and maybe some skin thickening. With time the dry skin can actually begin to bunch up together and start to create patches on your skin covering large areas of your body such as the back, arms, and legs. Unless spotted at a young age most cases of Ichtyosis Vulgaris go undiagnosed due people thinking that it is only “dry skin”
Most animals are susceptible to the development of cancer at some stage of their life. Among all types of cancer, squamous cell carcinoma is one of the skin cancer that commonly affects domestic animals. Cutaneous squamous cell carcinoma is a type of cancer caused by neoplasms arising from the squamous epithelium of an animal regardless of species. However, this essay will only focus on this condition among felines since my chosen species is a white cat called Rosie. There are several forms of cutaneous squamous cell carcinoma among felines, which are known as solar keratosis and multicentric squamous cell carcinoma in situ, sometimes known as Bowen’s-like disease, but in this case, Rosie is diagnosed with
The incidence of mastitis is associated with impaired PMN function (Cai et al., 1994) since the resolution of the disease is dependent on the ability of PMN for recognition of the pathogen, migration to the site of infection, phagocytic ability and its elimination (Vangroenweghe et al., 2005), and dependable of the generation of ROS by PMN (Heyneman et al., 1990).
It has been 9 months since my diagnosis, and I am still learning coping mechanisms and pain management. Not everything is 100% though. In a perfect world it would be, but also in a perfect world there would be no disease or sickness. I can only hope for the best and continue living life as I have been for the last 28 years. There may be many changes in my life, some are worse than others, and instead of viewing them as disadvantages I will see them as a metamorphosis. At the end of this journey, I will emerge a stronger person who can withstand fire and brimstone, so to speak. For now I will continue to smile and walk through live with my head held high, even though my body is a battlefield filled with constant aches and pains.
It seemed like it would make her die, just speaking it. So I didn't tell anyone, not even my best friends. At school I would slip into a fantastical dreamland, nobody there knew that I should be troubled, pensive. I put on my best front and paraded around the school halls with some sort of smile plastered on my face. At lunchtime I'd stare at my food thinking that my friends should know. I thought of a million different ways to tell them. Each time that I came close to telling them, I would think about their potential reactions. There would be the normal lunchtime banter going on, complaints about the ranch dressing, and I would blurt out, "Hey guys, my mom has breast cancer." The whole cafeteria would turn silent and the plastic forks would drop from their hands, making a sad little clinking noise. Then I would stare at my food mentally kicking myself for having opened my mouth. I chose to say nothing. I remember very clearly the day that I went to go sit with her while she got her chemotherapy. I only did this once because it was too hard for me. I walked down an overly-lit sterile hallway trailing behind my dad. When we reached her room I wished that I could just keep walking, pretend I hadn't seen her. I went in and sat down. Her shirt was partially unbuttoned so that the IV could be inserted into the porto-cath surgically implanted under her collarbone. She was hooked up to three different kinds of poisons, and one normal IV. There were some knitting things spread across her lap and the ever present bag of lemon drops was faithfully at her side. Her head was laid back in the chair, she was tired. She and my dad tried to involve me in some nice chit-chat, I met and shook hands with the doctors and nurses, "It's nice to meet you Dr. McCoy." Yeah right. They complimented her on what a beautiful daughter she had. I blushed, smiled politely then excused myself to the bathroom. I wiped away my forming tears and gave myself a mental pep talk to be cheery. As long as I didn't look at her tired eyes I was OK. Half an hour later, she was done and we got to go home.
I chose to discuss a chronic illness that has actually affected my family, rather than an illness that could affect a patient of mine. My mother-in-law has been diagnosed with cancer multiple times. The first time, was when my husband was 16 years old. She was diagnosed with a rare liver cancer. She was put on a waiting list
“Basal cell carcinoma is an uncontrolled, abnormal growths or lesions that arise in the skins basal cells, which line the deepest layer of the epidermis.” (Phillip, 2011) Basal cell carcinoma often times resembles open sores, red patches, shiny bumps or scars. Majority of basal cell carcinoma cases occur on parts of the body such as the face, ears, neck, scalp, shoulders and back that are excessively exposed to the sun.
Throughout the duration of research paper, the researcher was able to receive first-hand testimony from a breast cancer survivor via email. The interview included questions such as: (1) the year and stage the breast cancer was diagnosed; (2) the level of awareness prior to diagnosis; (3) treatments used to combat cancer (chemotherapy, radiation or a combination of both); (4) the present condition of the breast cancer; and (5) the treatment, prevention, or examinations used to keep breast cancer in remission. The interviewee (remains nameless) was diagnosed on July 5, 2002 at Jefferson Hospital from a yearly mammogram. Her breast cancer was diagnosed in stage I, less than 1 mm in diameter (Office of Women’s Health n.d). She exclaimed she was very aware of the heredity risk in her family because of previous family members diagnosed with breast cancer. She received two lumpectomies, following a port was placed in her arm for easier access to her vein during chemotherapy. She received four rounds of chemotherapy, each spaced out by three weeks; she also underwent six weeks of r...
She’s been struggling everyday of her life for the past 10 years; battling and fighting this horrible disease has made it hard on her and her family. The cancer has now metastasized, making it difficult for her to take care of everyday responsibilities and participate in daily activities. Her 13-year-old daughter is watching as her mother suffers and becomes brittle and weak.
Imagine having to wake up each day wondering if that day will be the last time you see or speak to your father. Individuals should really find a way to recognize that nothing in life is guaranteed and that they should live every day like it could be there last. This is the story of my father’s battle with cancer and the toll it took on himself and everyone close to him. My father was very young when he was first diagnosed with cancer. Lately, his current health situation is much different than what it was just a few months ago. Nobody was ready for what was about to happen to my dad, and I was not ready to take on so many new responsibilities at such an adolescent age. I quickly learned to look at life much differently than I had. Your roles change when you have a parent who is sick. You suddenly become the caregiver to them, not the other way around.
The symptoms of psoriasis differ from type to type, although inflamed, scaly lesions are present in all five types. The most common form of the disease, plaque psoriasis, is identified by small bumps that begin to grow and become scaly. These lesions flake easily, but removing these patches can cause the tender skin below to bleed. In the Guttate type, small, individual, red drops form. This type does not have as much scaling as plaque psoriasis. The drops usually clear up on their own, but may also reappear as a different form of psoriasis, usually plaque. Inverse psoriasis usually occurs in places where the skin folds, such as the genitals, breasts, armpits or the backs of knees. This type will appear red, yet it will be smooth and dry. Also, no scaling will occur. Pustular psoriasis is a type that's significantly more rare. It is also more painful. In this type, blisters filled with non-infectious pus appear within a few hours and then dry up and peel within another two days. Severe medical risks exist for those who have this particular form of psoriasis, due to its side effects; exhaustion, anemia, weight loss, fever, chills, rapid pulse rate, severe itching and muscle weakness. Even less common than pustular psoriasis is erythrodermic psoriasis. This type is...
The lymphatic system is a link of tissues and organs that help clear the poisonous toxins, waste and further unwanted elements that are inside the human body. The key function of the lymphatic system is to transport lymph which is a watery fluid substance holding infection that are fighting white blood cells, all over the human body.
...e the cancer and look for the positives in the prognosis and treatment find encouragement for the future. There are various models and theories such as health belief model that are used to explain ones belief on risks and associated risks of a chronic illness and then there are theories such as Crisis theory when dealing with shock when diagnosed with a chronic illness and gate control theory when looking at pain and the psychological issues around dealing with pain. However even with various theories and models trying to explain crisis, pain and compliance to treatment the outcome and understanding and ultimately the way an individual deals with a chronic illness such a breast cancer falls very much down to self-efficacy and the belief the individual holds towards the illness itself the attitude and perception in the outcome of the illness, treatment and beyond.