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Our Fight With C.F

Our Fight With C.F. Tuesday, 26 June 2012. Alan had clinic today. He is very productive of sputum at the moment so his physio session this morning before we went got a very good sample to sent to the lab, hopefully the results will be back on Thursday. We have to go back on Friday as alan needs to go into the lung Lab every month now as his Lung function has been down by over 10% and we don't know why. Monday, 25 June 2012. He has the cf clinic tomorrow so. Will update tomorrow x. Sunday, 10 June 2012.

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Our Fight With C.F | jewels1311.blogspot.com Reviews

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Our Fight With C.F. Tuesday, 26 June 2012. Alan had clinic today. He is very productive of sputum at the moment so his physio session this morning before we went got a very good sample to sent to the lab, hopefully the results will be back on Thursday. We have to go back on Friday as alan needs to go into the lung Lab every month now as his Lung function has been down by over 10% and we don't know why. Monday, 25 June 2012. He has the cf clinic tomorrow so. Will update tomorrow x. Sunday, 10 June 2012.

<META> KEYWORDS

1 cf clinic

2 posted by

3 julie

4 1 comment

5 mri scan

6 alan

7 no comments

8 clinic visit

9 first day back

10 happy new year

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Our Fight With C.F | jewels1311.blogspot.com Reviews

https://jewels1311.blogspot.com

Our Fight With C.F. Tuesday, 26 June 2012. Alan had clinic today. He is very productive of sputum at the moment so his physio session this morning before we went got a very good sample to sent to the lab, hopefully the results will be back on Thursday. We have to go back on Friday as alan needs to go into the lung Lab every month now as his Lung function has been down by over 10% and we don't know why. Monday, 25 June 2012. He has the cf clinic tomorrow so. Will update tomorrow x. Sunday, 10 June 2012.

INTERNAL PAGES

jewels1311.blogspot.com

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Our Fight With C.F: July 2011

http://jewels1311.blogspot.com/2011_07_01_archive.html

Our Fight With C.F. Sunday, 31 July 2011. Another day the same. Saturday, 30 July 2011. Thursday, 28 July 2011. Sunday, 17 July 2011. If you have time to check out my own blog only about me, please feel free xxx. Subscribe to: Posts (Atom). View my complete profile. I've been married to Alan for 21 years, he is my soul mate and he gets me through my darkest days he is my rock. This is Nikki my Eldest Daughter who is 20, She is at college at the moment and is hoping to go to uni this year to do midwifery.

2

Our Fight With C.F: December 2011

http://jewels1311.blogspot.com/2011_12_01_archive.html

Our Fight With C.F. Monday, 26 December 2011. Subscribe to: Posts (Atom). View my complete profile. I've been married to Alan for 21 years, he is my soul mate and he gets me through my darkest days he is my rock. This is Nikki my Eldest Daughter who is 20, She is at college at the moment and is hoping to go to uni this year to do midwifery. This is Amy who is 16 she is doing really well at school, she plays the clarinet and keyboard. Thankyou Carrrie for the Award. Free Guestbook by UltraGuest.com.

3

Our Fight With C.F: MRI scan

http://jewels1311.blogspot.com/2012/06/mri-scan.html

Our Fight With C.F. Monday, 25 June 2012. Alan had a MRI scan on Saturday of which we get the results of on the 30th july. He was very brave and lay very still, it took about a hour to scan his head and neck. After the clinic we went to the kelvingrove museum to have a look around and to have a bite of lunch. We saw a dinosaur footprint. He also has started insulin at lunch time too, it's 5 injections a day and 10 finger pricks. He's my very brave special boy . He has the cf clinic tomorrow so. 2016 CF W...

4

Our Fight With C.F: February 2011

http://jewels1311.blogspot.com/2011_02_01_archive.html

Our Fight With C.F. Friday, 11 February 2011. I don't know what has happened but Alan is really struggling doing his insulin again, after months of doing it no problem he is now finding it impossible to do the injections. He gets very tearful and upset, saying he wants to do it but cant. Any tips would be gratefully received :-). Subscribe to: Posts (Atom). View my complete profile. I've been married to Alan for 21 years, he is my soul mate and he gets me through my darkest days he is my rock.

5

Our Fight With C.F: Cf clinic

http://jewels1311.blogspot.com/2012/06/cf-clinic.html

Our Fight With C.F. Tuesday, 26 June 2012. Alan had clinic today. He is very productive of sputum at the moment so his physio session this morning before we went got a very good sample to sent to the lab, hopefully the results will be back on Thursday. We have to go back on Friday as alan needs to go into the lung Lab every month now as his Lung function has been down by over 10% and we don't know why. 19 August 2012 at 15:38. Hi My Name is Jenna. You are a brave courageous fighter, and an inspiration.

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SOS Мucoviscidose (Cystic Fibrosis): Май 2013

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SOS Мucoviscidose (Cystic Fibrosis). Снегът продължава да вали в моята душа :-( Направихме семинар за муковисцидоза. Много лекари не дойдоха, много пациенти над 18години дойдоха. До сега познавах няколко от тях, вече познавам още толкова, но всички имат спешна нужда от качествена терапия. Тъжно е и боли! Всички имат право на достоен живот! 17 май, 2013. Муковисцидоза - 14.05.2013 OnlineDCTV. 15 май, 2013. Муковисцидоза - да добавим живот. 8221;Акция Сиси”. Изработването на картичките ще бъде на 16.05...

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SOS Мucoviscidose (Cystic Fibrosis): Да добавим живот +1

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SOS Мucoviscidose (Cystic Fibrosis). Снегът продължава да вали в моята душа :-( Направихме семинар за муковисцидоза. Много лекари не дойдоха, много пациенти над 18години дойдоха. До сега познавах няколко от тях, вече познавам още толкова, но всички имат спешна нужда от качествена терапия. Тъжно е и боли! Всички имат право на достоен живот! 14 септември, 2014. Да добавим живот 1. Абонамент за: Коментари за публикацията (Atom). Живота на нашите деца с муковисцидоза. Дари кръв, спаси живот! Сайт на болните ...

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SOS Мucoviscidose (Cystic Fibrosis). Снегът продължава да вали в моята душа :-( Направихме семинар за муковисцидоза. Много лекари не дойдоха, много пациенти над 18години дойдоха. До сега познавах няколко от тях, вече познавам още толкова, но всички имат спешна нужда от качествена терапия. Тъжно е и боли! Всички имат право на достоен живот! 29 юни, 2013. ПОКАНА за Годишна среща на Асоциация „Муковисцидоза“. Устав “Асоциация муковисцидоза”. Годишна среща на Асоциация „Муковисцидоза“. Светлана Атанасова &#8...

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SOS Мucoviscidose (Cystic Fibrosis): Септември 2014

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SOS Мucoviscidose (Cystic Fibrosis). Снегът продължава да вали в моята душа :-( Направихме семинар за муковисцидоза. Много лекари не дойдоха, много пациенти над 18години дойдоха. До сега познавах няколко от тях, вече познавам още толкова, но всички имат спешна нужда от качествена терапия. Тъжно е и боли! Всички имат право на достоен живот! 14 септември, 2014. Да добавим живот 1. Физиотерапевтични упражнения с Володя Матвеев. Рехабилитация на пациенти с муковисцидоза с д-р Радостина Симеонова, упр. Направ...

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SOS Мucoviscidose (Cystic Fibrosis): Ноември 2012

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SOS Мucoviscidose (Cystic Fibrosis). Снегът продължава да вали в моята душа :-( Направихме семинар за муковисцидоза. Много лекари не дойдоха, много пациенти над 18години дойдоха. До сега познавах няколко от тях, вече познавам още толкова, но всички имат спешна нужда от качествена терапия. Тъжно е и боли! Всички имат право на достоен живот! 26 ноември, 2012. Доклад за инициативите по повод Международния ден на болните от муковисцидоза 21.11.2012г. Http:/ www.lifewithcf.org/index.php? В сега съществуващите...

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SOS Мucoviscidose (Cystic Fibrosis): Декември 2013

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SOS Мucoviscidose (Cystic Fibrosis). Снегът продължава да вали в моята душа :-( Направихме семинар за муковисцидоза. Много лекари не дойдоха, много пациенти над 18години дойдоха. До сега познавах няколко от тях, вече познавам още толкова, но всички имат спешна нужда от качествена терапия. Тъжно е и боли! Всички имат право на достоен живот! 04 декември, 2013. Пустота / Иван Вазов. Пустота в обществото, в главите,. Редом царствува сън или мраз,. Пустота във словата, в душите,. Пустота пълни всичко у нас,.

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SOS Мucoviscidose (Cystic Fibrosis): Декември 2012

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SOS Мucoviscidose (Cystic Fibrosis). Снегът продължава да вали в моята душа :-( Направихме семинар за муковисцидоза. Много лекари не дойдоха, много пациенти над 18години дойдоха. До сега познавах няколко от тях, вече познавам още толкова, но всички имат спешна нужда от качествена терапия. Тъжно е и боли! Всички имат право на достоен живот! 04 декември, 2012. Благотворителен концерт за болните от муковисцидоза в град София. Благотворителен концерт за болните от муковисцидоза. В Дом на културата "Средец".

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SOS Мucoviscidose (Cystic Fibrosis): ДЕН НА РЕДКИТЕ БОЛЕСТИ - 28.02.2015г.

http://srazmah.blogspot.com/2015/02/28022015.html

SOS Мucoviscidose (Cystic Fibrosis). Снегът продължава да вали в моята душа :-( Направихме семинар за муковисцидоза. Много лекари не дойдоха, много пациенти над 18години дойдоха. До сега познавах няколко от тях, вече познавам още толкова, но всички имат спешна нужда от качествена терапия. Тъжно е и боли! Всички имат право на достоен живот! 27 февруари, 2015. ДЕН НА РЕДКИТЕ БОЛЕСТИ - 28.02.2015г. НАЦИОНАЛЕН АЛИАНС НА ХОРАТА С РЕДКИ БОЛЕСТИ:. Абонамент за: Коментари за публикацията (Atom). Направихме семин...

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SOS Мucoviscidose (Cystic Fibrosis): Май 2012

http://srazmah.blogspot.com/2012_05_01_archive.html

SOS Мucoviscidose (Cystic Fibrosis). Снегът продължава да вали в моята душа :-( Направихме семинар за муковисцидоза. Много лекари не дойдоха, много пациенти над 18години дойдоха. До сега познавах няколко от тях, вече познавам още толкова, но всички имат спешна нужда от качествена терапия. Тъжно е и боли! Всички имат право на достоен живот! 30 май, 2012. ЧУВСТВАМ, ЧЕ ИМАМЕ МНОГО ПОДКРЕПА И НАДЕЖДА ЗА БЪДЕЩЕТО. ВСЕКИ ДЕН Е МНОГО ВАЖЕН, ЗАЩОТО ДОКАЗВА, ЧЕ ТРЯБВА ДА СЕ БОРИМ И ИМАМЕ ШАНС. В град Варна -.

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SOS Мucoviscidose (Cystic Fibrosis): КЛИНИЧНА ПЪТЕКА МВ - 950лв. ЦЕНА - 6 ГОДИНИ БОРБА

http://srazmah.blogspot.com/2015/02/15-httplifewithcf.html

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Our Fight With C.F

Our Fight With C.F. Tuesday, 26 June 2012. Alan had clinic today. He is very productive of sputum at the moment so his physio session this morning before we went got a very good sample to sent to the lab, hopefully the results will be back on Thursday. We have to go back on Friday as alan needs to go into the lung Lab every month now as his Lung function has been down by over 10% and we don't know why. Monday, 25 June 2012. He has the cf clinic tomorrow so. Will update tomorrow x. Sunday, 10 June 2012.

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