{"id":58535,"date":"2014-09-16T17:09:15","date_gmt":"2014-09-16T21:09:15","guid":{"rendered":"https:\/\/rarediseases.org\/living-with-blood-cancer\/"},"modified":"2014-09-16T17:09:15","modified_gmt":"2014-09-16T21:09:15","slug":"living-with-blood-cancer","status":"publish","type":"post","link":"https:\/\/rarediseases.org\/es\/living-with-blood-cancer\/","title":{"rendered":"Living with Blood Cancer"},"content":{"rendered":"

Editor’s note: The following blog is being published to highlight Blood Cancer Awareness Month and MPN Awareness Day. \u00a0<\/em><\/p>\n

I was diagnosed with essential thrombocythemia (ET) at age 16 after collapsing in my high school cafeteria. At that time, lab results showed I had a platelet count of over 1 million and my world was forever changed. During the last 18 years, I have traveled along the highs and lows of platelet counts, treatments, and the emotions of this blood cancer. ET has created some of the worst fears I’ve had in my life, but has also given me more purpose than I could have hoped for at a young age. One of the most difficult aspects of dealing with this diagnosis was the feeling of isolation I encountered with having an “orphan disease.” When ET entered my life, there was limited funding and attention towards myeloproliferative neoplasms (MPNs). As a board member of the MPN Research Foundation<\/strong><\/a>, I am very proud of the research and patient support that the foundation has made possible over the years. The research and knowledge has come a long way since I was diagnosed and our work continues in order to further understand and develop a cure for MPNs.<\/p>\n

After several years of treatment with Anagralide and Interferon and their associated side effects, I’m quite lucky to be currently maintaining my platelet counts without any treatment. I’ve been able to accomplish things I feared I would not have been able to because of ET. I have grown up with the challenges of ET and have learned so much about myself through all of the experiences. It is interesting how a diagnosis given to me 18 years ago continues to have an effect on my daily choices and perceptions. Because of the hardships and bad days I have had in the past related to essential thrombocythemia, I strive to find the good in each new day I am given, with as much laughter and appreciation as possible. I do admit it is easier to accomplish this on some days compared to others.<\/p>\n

What have you learned about yourself through your experience of diagnosis, symptoms, and treatments? Have you found your inspirations have changed?<\/p>\n

Watch this YouTube\u00a0video<\/a> to learn more about the MPN Research Foundation’s impact on research.<\/em><\/p>\n

<\/h1>\n","protected":false},"excerpt":{"rendered":"

Editor’s note: The following blog is being published to highlight Blood Cancer Awareness Month and MPN Awareness Day. \u00a0 I was diagnosed with essential thrombocythemia (ET) at age 16 after … <\/p>\n

Continue reading “Living with Blood Cancer”<\/span><\/a><\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"_relevanssi_hide_post":"","_relevanssi_hide_content":"","_relevanssi_pin_for_all":"","_relevanssi_pin_keywords":"","_relevanssi_unpin_keywords":"","_relevanssi_related_keywords":"","_relevanssi_related_include_ids":"","_relevanssi_related_exclude_ids":"","_relevanssi_related_no_append":"","_relevanssi_related_not_related":"","_relevanssi_related_posts":"","_relevanssi_noindex_reason":"","_price":"","_stock":"","_tribe_ticket_header":"","_tribe_default_ticket_provider":"","_tribe_ticket_capacity":"","_ticket_start_date":"","_ticket_end_date":"","_tribe_ticket_show_description":"","_tribe_ticket_show_not_going":false,"_tribe_ticket_use_global_stock":"","_tribe_ticket_global_stock_level":"","_global_stock_mode":"","_global_stock_cap":"","_tribe_rsvp_for_event":"","_tribe_ticket_going_count":"","_tribe_ticket_not_going_count":"","_tribe_tickets_list":"[]","_tribe_ticket_has_attendee_info_fields":false,"footnotes":""},"categories":[232,190,210,191,192,193],"tags":[459,460,408,461,462,422,463,411,464,465,466],"class_list":["post-58535","post","type-post","status-publish","format-standard","hentry","category-advocacy","category-featured-news","category-industry","category-medical","category-patients-members","category-research","tag-anagralide","tag-blood-cancer","tag-essential-thrombocythemia","tag-et","tag-interferon","tag-mpn-research-foundation","tag-mpns","tag-myeloproliferative-neoplasms","tag-orphan-disease","tag-platelet","tag-stephanie-cindric"],"acf":[],"_links":{"self":[{"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/posts\/58535","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/comments?post=58535"}],"version-history":[{"count":0,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/posts\/58535\/revisions"}],"wp:attachment":[{"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/media?parent=58535"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/categories?post=58535"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/tags?post=58535"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}