Tag: Leukemia

  • IKEME ON RETIREMENT: I’ll forever have fond memories of Wolves

    After announcing his retirement on Friday, Carl Ikeme spoke at length on his exciting time with Wolves and the love and affection showered on him since his battle with leukemia

    In tough times, the Wolves family shows its strength, and the love former Nigeria number one goalkeeper, Carl Ikeme, has received over the past 12 months has left the goalkeeper filled with emotion for ‘his club’.

    The 32-year-old confirmed his retirement from football on Friday after a year-long battle with acute leukemia but is now looking towards the future with excitement both personally and at Molineux.

    Throughout his battle, Carl has received the love and backing from Wolves supporters through messages and fundraising events, and struggled to put into words the impact it made on him.

    “It’s moving because you never realise people like you,” he explained to wolves.co.uk. “When you’re playing you’re just in the mode of playing game after game, but when you’re in these circumstances you realise how people feel about you.

    “The support has been incredible, everyday someone has asked me how I am for a whole year. It’s incredible to think people actually care so much that they’ll do fundraisers in my name.”

    Now in remission, Carl on Friday made the tough decision to officially retire from football on medical advice but now has peace of mind that he can plan to the future and spend vital time with his young family.

    “I spoke with the doctor and he suggested I should retire, because of the toll the treatment has taken on my body. He thinks it’s what is best for me and I can’t really risk trying to come back, my health is the priority.

    “I want to be here for my children, family and friends. In the grand scheme of things with my life in danger, it’s the minimum price I have to pay to spend the rest of my time with my family.”

    Nevertheless, it was a decision Carl was never going to take lightly, after joining the club’s academy as a youngster and going on to make more than 200 appearances in a Wolves shirt.

    “It’s not really set in since speaking to the doctor. In time I can have a good look back, it’s been incredible for me personally to have been at Wolves from 14 to 31 – playing for just one club is something I’m proud of.

    “It’s nice to have been a one club man because it’s rare these days. I’m proud that I can always come back to Wolverhampton and always have friends here, and be loved, it’s incredible.”

    The longevity of his spell speaks volumes for Carl’s affection for the football club. He now plans to remain involved with Wolves in some capacity and return to watching the team play as a supporter.

    “This is my club. It’s been strange because this year I’ve enjoyed being a fan, watching the games. I’d be getting a bit heated on my own in my hospital room when nobody was about.

    “When I’m doing radio commentary it’s no different, I try to be professional but it spills out. This is my club and it always will be, now I’m not playing, I’m a fan and I’m looking forward to it. I’ll be coming to enjoy the games with the fans who’ve supported me in my whole career, through the hardest moments.”

    For now, Carl will rightly enjoy some much-needed family time and reflect on what has been a fine career as Wolves’ goalkeeper – but this isn’t the end of his Molineux journey.

    “It’s sad when you look back and think of the sacrifices you’ve made to be a footballer but I’m happy with what I achieved. If you’d have said I could have had this career at 11 I would have snapped your hands off.

    “I’ve still got friends in the academy and people working at Wolves who’ve helped me. I can’t thank Jeff, Kev and Laurie enough for how good they’ve been with me since the treatment.

    “Now I’m going to enjoy being around the club, experiencing the good and bad times, but I’ll definitely be in and around the club,” he said.

  • U.S. Scientists find new possible cure for leukemia

    U.S. Scientists find new possible cure for leukemia

    Group of American scientists have found a new possibility to cure leukemia, the results of a new study showed on Tuesday.

    Leukemia is a deadly disease that knocks down patients as young as only seven years old.

    In the study published in Journal Nature Medicine, the group of scientists from Stanford University and National Institute of Health (NIH) found that a molecule, called “CD22”, could serve as a potent target for the killer cells of acute lymphoblastic leukemia, a common childhood cancer.

    It came after the U.S. Food and Drug Administration approved last August a cell-based gene therapy, namely the “CAR T-cell” treatment.

    The CAR T-cell, is a therapy requires drawing blood from patients and separating out the T cells.

    It works by genetically modifying a patient’s own immune cells to seek out and attack leukemia cells that have a molecule called “CD19” on their surface.

    Such a therapy relies on the patient’s own T cells a type of immune cell that could become a powerful killing machine.

    Stanford oncologist Crystal Mackall and NIH’s pediatric hematologist Terry Fry discovered that a molecule called “CD22” can be a similar target.

    Scientists treated 21 patients with treatment-resistant B-cell leukemia who are aged seven to 30 to test the new “CD22-directed method.

    17 of them were previously treated with CD19-directed therapy and 15 of them had either relapsed or failed to respond.

    They found that at the lowest dose level, one in six patients achieved complete remission after treatment, and with an escalated dose, 11 of 15 patients entered remission.

    The new approach is helpful because the cancer cells of some patients who undergo CD19-directed therapy stop expressing the CD19 molecule on the cell surface.

    The relapse rate of CD22-directed therapy also proves high.

    The researchers hope that targeting “CD19 and CD22” simultaneously may produce an approach where cancer cells are unable to evade, thus leading to a new therapy for curing leukemia in the future.

    Read Also:  Breastfeeding may reduce risk of childhood leukemia -Study

  • Tips for leukemia, sickle cell disorder therapy

    When Seun Babalola called me about three weeks ago and asked for first aid therapy for a middle –age sickle cell man in deep crisis, I scribbled a note which formed the basis of today’s column.

    As a note, it cannot be comprehensive. But it should be useful for people who wish to avert a crisis or manage one.

    As I was scribbling the note, a young Mass Communications graduate of Moshood Abiola Polytechnic, Abeokuta, Miss Morayo Fadele, who was in my office, asked if I could broaden the tips to include a therapy for leukemia (blood cancer).  Her father bowed to this condition a few years ago. And, as she said, she would like to be of help to anyone challenged by it. I apologised that home or clinic therapies for leukemia would have to wait. But I made a few suggestions which included stinging Nettle, Yarrow, Blood root, Horsetail, wheatgrass, Chlorella etc.

    Leukemia is cancer of the blood. And the blood is the river of life flowing in our blood vessels. The blood has a specific composition. Anything outside this natural formula is at variance with healthy blood and can spell doom. This, constant recomposition of the blood to maintain the natural formula is crucial for averting blood disaster. But before we can recompose, we must clean out foreign elements from the bloodstream. This will lead us to detoxification.  All blood filters in the body must be at work and efficient. The liver, the kidneys, the lungs, the skin and the digestive tract are important for this purpose. Recomposition of the blood must recognise similarities in the green of Chlorophyll, “the blood of plants’’ and the red of hemoglobin, the red pigment of the human blood which transports oxygen the elixir of life. This, chlorophyII and hemoglobin are like two sides of a coin. The structure of cholrophyII is HYDROGEN – NITROGEN – CARBON and OXYGEN. Magnesium binds them together. The structure of hemoglobin is the same, except for iron, and not magnesium, which binds the structure together. The Nobel Prize was awarded to scientists who discovered this similarity. Thus, consuming greens as a salutary effect on the blood. As I always like to see it, taking greens is like recharging the blood as we recharge cell phone credit. The following herbs have been found to dramatically help leukemia cases: Garlic, Olive Leaf Extract, Milk thistle, Licorice, Aloe Vera, Raspberry, Curcumin, Green tea, Ginseng Citrus immature peel (which kills leukemia cells). Hedyotis diffusa- the Chinese remedy reported to be positively effective in killing cancer cell. Hungarian cancer therapist Alexander Ferenezi,in 1950, carried out a study with 22 patients whose cancers where advanced and inoperateable. He added Beet root to their diet for three to four months. All but one of them recovered dramatically. These herbs are set to clean and recompose the blood apart from helping the cancerous cell to commit suicide (apoptosis). The Hungarian study with Beet root, replicated in other countries encourages the use of herbs in leukemia and other cancers. The role of the spleen cannot be underplayed. It is a quality control centre for the blood. Blood cells which fail to pass the test are broken down by macrophages, special defense (immune cells) in the spleen. Thus, if leukemia cells roam free in the blood, the spleen deserve a query. It may be weakened, though, by infections and the generative liver conditions, among other problems.There will still be time for a more comprehensive discussion of leukemia therapies NOW. Seun Babalola, here comes the sickle cell note…

     

    Management of sickle cell anaemia condition

    Treating this condition the natural way involves, as in all health challenges, an understanding of the causes and effects, and consistent efforts to check them. I hope the following explanations and suggestions will help the conditions discussed.

     

    Explanations and suggestions

    • In sickle cell condition, the red blood cell is sickled, that is curved inwards from the edges or rumpled like rumpled, dry foliage.
    • A normal red blood cell, on the other hand, is flat like a coin.
    • In a rumpled state, the red blood does not enjoy maximum exposure to oxygen in the blood stream. Yet its job is to attract oxygen and take it to all cells for their metabolic and other living processes.

    Deprived of oxygen, the body’s growth is stunted, the immune system functions sub-optimally, microbes overgrow in population, attack and damaged healthy and unhealthy cells. As it is to be expected, the sickle cells cannot adequately defend themselves and, so, do not live beyond about half the lifespan of a normal cell.

    • When the red blood cells die prematurely, they create many health challenges.
    • Even the small amounts of oxygen they can absorb and transport diminished in quantum.That is why there is pain (or cry for oxygen) throughout the body.
    • The bone marrow where red blood cells are produced, comes under pressure to make more red blood cells. Yet it doesn’t have enough oxygen to do this extra job. That, again, is why bone pain is common among sickle cell challenged person, especially during a crisis.
    • A large quantum of sickle red blood cells dying prematurely soon breaks down, releasing a large amount of all their components, especially bilirubin, the yellow pigment.
    • The liver has a duty to conjugate this heavy bilirubin load which can become poisonous to the system, especially the brain, if not promptly transform (conjugated) into less harmful substances. It is this heavy congestion of bilirubin in the liver that makes the liver becomes inflamed and painful. The spleens, too, may become inflamed and painful, soft and purple, it is vascular and lies in the upper left region of the abdomen. As a filter for the blood, it removes all old or malformed or damaged red blood cells.
    • There may be other implications of this crises.

    SUGGESTIONS

    The suggestion addresses the symptoms.

    • Since the red blood cells cannot absorb the required amount of oxygen, this can be introduced through the diet by way of food and food supplements.

    Ready sources of oxygen in the food chain are chlorophyll rich foods. Chlorophyll is the green part of plants. It is now known as the ‘’blood’’ of the plant. As a matter of fact, four scientists won a Nobel Prize for showing that chlorophyll and the red of the human blood, the heamoglobin, have more–or–less the same structure, except for their central atoms.

    The chlorophyll structure is …Carbon, Hydrogen, Nitrogen and Oxygen.The structure is held together by Magnesium. The heamoglobin structure is Carbon, Hydrogen, Nitrogen and Oxygen. The structure is held together by Iron.

    Thus, when we consume deep green vegetables or their juices, the body will convert the chlorophyll plant blood to heamoglobin human blood by removing the magnesium central atom and replacing it with iron. The oxygen in this structure becomes available to oxygenate the human system short of oxygen. With this understanding, the health industry responded to sickle cell management by producing all sorts of green product for this purpose. I will mention only a few which includes:

    (1)Wheatgrass (2) Barley grass (3) Alfalfa (4) Spirulina (5) Kale (6) Chlorella and proprietary green products such as splina liquid chlorophyll. Nowadays oxygen tablet or liquid juice are also available.

     

    • VITAMIN E

    This vitamin helps the body to live on small oxygen supplies as if it has enough stock.

    That is why mountain climbers who take Vitamin E food supplements hardly experience oxygen- deficiency on mountains where oxygen levels are low. When the mineral selenium is taken with vitamin E, vitamin E performs better. The better it is if  grape seed extract is added to the list, being about 50 times more powerful than Vitamin E. When you purchase vitamin E, be sure to buy the natural (d-alpha) and not the cheaper dl-alpha which come from petroleum sources. Be sure, too that the d-alpha contains the full components of d-alphaTocopherols.

    Shark liver oil: One of the important components of this oil is SQULENE. It helps the shark to survive in the depths where oxygen is low. Squalence is produced in the human skin to protect it against ultraviolet radiation from the sun. But the quantum produced diminishes with age. Squalene should help humans beset with low oxygen situations.

    • Antioxidants: Magnessium, Zinc, and Manganese, ditto are many green plants. Grape seed extract, coral calcium, Alpha lipoic Acid, Bilberry, orange peel etc. are also. The list is too long to mention.
    • The liver: The liver is easily inflamed and hurt, if not damaged, by sickle cell crises. To boost its capacity to respond to these crises, many liver protective and toning (strengthening) herbs may be added to the diet. My favorites are: (1) Eclipta Alba (2) Milk Thistle (3) Carquega. My favourite proprietary formulas are: Liver Health, Liver Essentially and Liver Balance. They promote bile flow. And bile mops and excretes bilirubin through the stool.
    • The Bone Marrow: Bone pain can be eased with the forgoing suggestions. Comfrey Root Tea improves bone health and curbs the pain. So does Yarrow tea which has an affinity for the bone marrow. Beet Root is also good. Comfrey root powder can be mixed with shea butter and used as a massage cream on the painful bone.

    Diatom, also called Diatomaceous Health, is good too, especially as it is an alkaliniser and it has an affinity for the bone. As it strengthens connective tissue throughout the body, strengthening connective tissue in the bone marrow prevents the tearing which inflammation induces and of course, the pain which comes with tearing. The weapon in the hands of diatom is SILICA.

    Silica is present also in Horsetail and stinging Nettle. But it accounts for between 92 and 96 percent of Diatom. Recently I asked a throat cancer patient to try it. She had a terribly ulcerated stomach, and fed through a tube in her stomach. Whenever she passed liquefied food through this tube, her stomach was literally on fire, but when she ground two tablet of zinc to powder and passed it down with water, the pain eased as the zinc supported the healing process. And any time she felt the pain was about to come up and she fed Diatom to the stomach, the pain disappeared outright.

     

    • CLUMPING: Gumming (clumping) of cells or agglutination is one of the problems faced by a sickle cell challenged person. Clumping slows blood circulation, and, thus, delays oxygen and nutrient delivery to the cells as well as waste or poison evacuation from them. During clumping episodes, the cells are, thus, starved and malnourished and left to live in a mesh of poison. Natural blood thinners’ free them from this peril. Some naturals include Onion and Garlic. They should be present always in the diet.

    Kyolic garlic, a proprietary brand of garlic, is reported to be about 50 times more potent than natural garlic, having been specially aged for about 15 months. The proprietary product Curcumin 2000X is good for this condition.

    Curcumin is anti-inflamating and helps all the inflammation caused by this challenge. The Cayenne present in Curcumin 2000X is reported to make it 2000 times more active than when curcumin is taken alone. Cayenne is a blood thinner and drives the blood to every nook and cranny of the body. Cayenne may be used on its own where curcumin 2000X is not readily available. I add cayenne to my corn portage (pap) and herbal drinks. Serrapeptase is another good blood thinner which solves blockages in the system. In the cell or tissue salt category of food supplement, Ferrum phosphate disbands all congestions, oxygenates the blood.

     

    SUMMARY

    In conclusion, the therapy goals are the following:

    • Improvement of oxygen stock and delivery to the cells.
    • Decongesting an overworked liver, reversing its inflammation and healing its injury but, above all, preventing those discomfitures by ensuring liver herbs are part of the daily diet.
    • Protecting the bone marrow likewise.
    • Preventing cell agglutination or thinning the blood where it has occurred.
    • Elongating the lifespan of sickle red blood cells with the addition of antioxidants to the diet, as a way of preventing the occurrence of event and complication which form some of the scenarios of a sickle cell crises.
  • Breastfeeding may reduce risk of childhood leukemia -Study

    Breastfeeding may reduce risk of childhood leukemia -Study

    A new analysis of 18 studies suggested on Tuesday in Washington that children who are breastfed have lower risk of developing childhood leukemia.

    Leukemia is the most common childhood cancer, accounting for about 30 per cent of all childhood cancers, but little was known about its cause.

    Efrat Amitay and Lital Keinan-Boker of the University of Haifa, Israel, said they reviewed the evidence in 18 studies, researching the association between breastfeeding and childhood leukemia.

    They said the studies, published between 1960 and 2014, provided a total of 10,292 leukemia cases and 17,517 controlled individuals.

    They said the result showed that breastfeeding for six months or longer, was associated with a 19 per cent lower risk, compared with no breastfeeding or breastfeeding for a shorter period of time.

    The scientists said a separate analysis of 15 studies found that ever being breastfed, compared with never being breastfed, was associated with an 11 per cent lower risk of childhood leukemia.

    The researchers said several biological mechanisms of breast milk may explain the relationship, indicating that breast milk contains many immunologically active components and anti-inflammatory defence mechanisms that influence the development of infant’s immune system.

    Amitay and Keinan-Boker said that based on the current meta-analysis, 14 per cent to 19 per cent of all childhood leukemia cases may be prevented by breastfeeding for six months or more.

    They said the method was highly accessible and low-cost public health measure.

    The researchers said that because the primary goal of public health was basically prevention of morbidity, health care professionals should be taught the potential health benefits of breastfeeding and given tools to assist mothers.

  • Leukemia: 22 per cent of Nigerian youths are ignorant of symptoms – Expert

    Leukemia: 22 per cent of Nigerian youths are ignorant of symptoms – Expert

    Twenty two per cent of Nigeria’s adolescent population are ignorant of the early symptoms of leukemia (blood cancer), Dr Ayo Fayehun, Consultant, Family Health Department, University College Hospital (UCH) Ibadan, has said.

    Fayehun made the statement on Thursday in Ibadan on the side-line of an enlightenment programme on health for youths organised by Oluwapamilerin Oni Health Foundation.

    According to NAN, Fayehun expressed concern that several youths in Nigeria particularly males, were unaware of the early symptoms of leukemia, which he said, could be prevented or reduce if detected early.

    The consultant noted that the mortality rate of blood cancer was on the increase in Nigeria and stressed the need for stakeholders in the health sector to rise up to the challenge.

    He said that chronic lymphocytic leukemia is a slow growing cancerous cell that affects the development of B-lymphocytes also known as B–cells and specialised white blood cells.

    He said that though the cause of the disease was still unknown, “it is thought to result from damage to one or more of the genes that normally controls blood cell development.”

    The physician listed some symptoms of leukemia to include: swollen lymph glands in the neck, under the arms or in the groin due to collection of lymphocytes in these areas.

    He said the disease could be diagnosed through full blood count (FBC) or through examination of the bone marrow.

    He said that leukemia could be treated through chemotherapy or through administration of drugs orally or intravenously.

    In her remark at the occasion, Mrs. Omolara Oni, the Executive Director, Oluwapamilerin Oni Health Foundation urged mothers to be observant of changes in their children’s bodies and habits.

    She said she lost her son to leukemia due to late detection of the disease, adding that she was ignorant of the symptoms of the disease exhibited by her late son.

    She listed some of the symptoms to include anemia, malaria and swelling in the groin.

    Oni said the health awareness programme was organised by the foundation to sensitise the youths on the symptoms of the disease.

    Over 200 people including students, parents, the clergy, health workers, market women and men attended the programme.