Christmas is a time to gift the gift of love. If you are an ITP’er, or know one, here are a few ideas for Christmas. I have been the recipient of a few of the gifts below, and I can’t tell you how much they meant. Below are our highly recommended gifts for people with ITP this year.
Feature image from AMAZON
I have known about Louise Hay for a while. I thought everyone knew about her work, and her company Hay House. I was surprised to discover just how many people have not heard of Louise Hay, considering how widely successful and interesting she is.
Through Louise’s healing techniques and positive philosophy, millions have learned how to create more of what they want in their lives, including more wellness in their bodies, minds, and spirits. Louise was able to put her philosophies into practice when she was diagnosed with cancer. She considered the alternatives to surgery and drugs, and instead developed an intensive program of affirmations, visualization, nutritional cleansing, and psychotherapy. Within six months, she was completely healed of cancer. Louise Hay [dot] com
Louise Hay is a motivational speaker, alternative health practitioner, writer and public figure. She is also the founder of HAY HOUSE Publishing. Hay House Publishing begun as a small project run from her house, which grew into a hugely successful international publishing company. Hay House Publishing focus on self-help books and have all the big names on their list. Check them out. These guys are the ones that published Jess Ainscough’s book, MAKE PEACE WITH YOUR PLATE.
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Feature image from Bookmania.
If you are like me, then you have probably subscribed to a number of ITP blogs and websites; you may have even set a google alert to inform you of the latest ITP research and news. Maybe every now and again you do a random google search to see if there is anything new to read. Perhaps that is how you found this article? If you’re a parent or caregiver, you are probably finding yourself a tad obsessed, trying to keep up with everything that is going on with ITP. The more I read about ITP, the more I am sent round in circles; the more I search and scramble for answers, the more I have to read.
This morning I had a thought – I can’t read it all.
Today, with five different web tabs open, I stopped. I stopped researching, I stopped making lists of things I needed to read and I turned off my Google Alert. I can’t read it all, and even if I did, I wouldn’t know any more than I do now because the information is changing so rapidly. I can’t keep up. Every few days there is another newsletter in my inbox from PDSA, from Google, from Support Groups around the world, boasting the latest news – the latest research, latest everything! I am probably making the whole thing worse, by giving you one more thing about ITP to read. Sorry. Continue reading →
ITP is not often in the Media – But when it is, we know about it.
Check out all the latest Newspaper and online articles about ITP here.
Also, we have made a nice list of famous people who have ITP too.
How a TREATMENT GAMBLE Paid Off, 17 Feb 2015
The story of one patient’s decision to use the chemotherapy Rixtuxin, even though it is not currently approved as an ITP treatment. After a seven month battle with prednisone symptoms, side effect and withdrawal symptoms, the drug stopped working for Candace. ‘After my platelet levels plummeted down to 14, my doctors and I had to change the course of treatment.’
Rare Autoimmune Condition gives TEEN A NEW OUTLOOK ON LIFE, 15 Feb 2015
Initially diagnosed with a platelet count of 4, Lynn was given what all suspected ITP patients are given as a first line treatment, steroids. A story about how life changes for ITP patients who are still going to school, and how it does not all end up bad. Read more about this ITP patients life at school…
Angela, an occupational therapist for the forensic mental health service in Liverpool, is supporting a new campaign. Launched by The Haemophilia Society, the charity is encouraging everyone to get “Talking Red”, to make women more aware of the symptoms of a bleeding disorder. Angela has a platelet Pool disorder, which is not technically not ITP but still in our circle of friends.
When Azaria was 2 she had many bruises on her legs, arms, spine and a black bruise on her cheek, Wendy says. "She didn't remember getting any of them. Azaria was also tired and falling over a lot." She had X-rays, CT scans, a bone marrow biopsy, and up to four blood tests a week, as well as emergency hospital visits. "Azaria was diagnosed with ITP, which is not genetic and non-contagious," Wendy says. "It is likely a virus caused her disorder."
We have featured an article on ITP and Me on Azaria's Story which you can find here.
JACK MCINTYRE used to love judo. But the boy of eight from Cross Keys can't take part in his favourite pastime any longer - a condition developed two years ago means a knock to his head or abdomen could prove fatal.
His father, Mr McIntyre is now raising money for the ITP Support Association and will be running the Cardiff Half Marathon in October. Follow the link to donate here.
Meredith Prescott, Master's candidate of Fordham University, has written an insightful article for the Huffington Post, outlining what it is like to live with ITP and how we can raise awareness and support. After a very successful event, raising over $45,000, I decided to plan my second 5k walk/run this June with another fighter, Linda McGuirl, to find a cure and help rid this world of ITP. Linda and I were both diagnosed at 21, and although we are decades apart in age, we both take strong pride in raising awareness and taking control of ITP. Riding the roller coaster in the world of ITP is so much better when you're not riding alone...Read More.
The Storm flyer has received the green light from doctors, two years after Melbourne were warned he could bleed to death if he was exposed to heavy contact at training.
The 26-year-old will become Queensland's 179th Origin player if Billy Slater or Greg Inglis withdraw from Game Two on Wednesday night. Peter Badel for the Daily Telegraph Sydney.
Helena Woman does not let Auto Immune disorder keep her from traveling the world on her own, Oct 30 2013
In an article written by Peggy O'Neil for the Independent Record, Jamie Harwell speaks out about travelling the world with a platelet count of 30.
This year she will participate in the 31st annual El Tour de Tucson on November 23 where she will pedal 111 miles helping to raise money for ITP, idiopathic thrombocytopenia purpura, which she also has.
Phegley thrives after battling blood disease, Aug 26 2012
Charlotte Knights catcher Josh Phegley overcame a serious illness, itp in 2010. Today, Phegley is helping the Knights prepare for the International League playoffs, which begin next week...One day early in the season, a ball was fouled off his thigh, leaving a dark purple bruise. “Catchers get those kinds of nicks all the time,” Phegley said. “But I wondered about it because I don’t bruise easily.” The next day, the bruise had spread around to the back of his leg, growing to about 9 inches in diameter.
Rare blood disorder sidelines Chambers, Jun 7 2012
DESPITE feeling fantastic, Melbourne centre Will Chambers could have died from a rare blood-clotting disorder that has stalled his NRL career indefinitely.
Chambers will be sidelined until he recovers from the auto-immune disorder ITP (idiopathic thrombocytopenic purpura). The only symptoms were some red dot rashes that appeared in the 24 hours after the Storm's win against the Warriors on Sunday.
Australian Open 2013; Jamie Baker makes recovery, Jan 13 2013
After coming through qualifying, Baker wants to create his own fairytale here in Melbourne, and goodness knows he deserves a change of luck. So many of the difficulties he has experienced are connected to the horrific illness he contracted in March 2008, just as it seemed he was about to crack the top 200 for the first time. Coming back from a tournament in Mexico, Baker found that bruises were appearing all over his body for no apparent reason. Then, when he visited a hospital in Florida, he was diagnosed with ITP.
Actress Lisa Blount dead at 53 from blood disorder ITP
isa Blount, who co-starred in the 1982 drama An Officer and a Gentleman, died Oct. 25, 2010 at the age of 53 after battling the blood disorder Idiopathic Thrombocytopenic Purpura (ITP).
Not too sure what is happening in this article as the reporter likens ITP to the neurological illness like MS? 'Sources say the actress had complained of chronic back and neck pains, and her mother told police Blount had battled ITP, a neurological illness similar to multiple sclerosis for 17 years.'