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mds-in-the-family.blogspot.com

MDS in the family

Follows the fortunes of daughter and father who both have MDS myelodysplastic syndromes. Start with the oldest entry if you want to read the whole story

http://mds-in-the-family.blogspot.com/

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MDS in the family | mds-in-the-family.blogspot.com Reviews
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Follows the fortunes of daughter and father who both have MDS myelodysplastic syndromes. Start with the oldest entry if you want to read the whole story
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1 mds links
2 mds facebook site
3 macmillan cancer support
4 sad news
5 posted by
6 richard barker
7 no comments
8 email this
9 blogthis
10 share to twitter
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mds links,mds facebook site,macmillan cancer support,sad news,posted by,richard barker,no comments,email this,blogthis,share to twitter,share to facebook,share to pinterest,getting there slowly,1 comment,anyway,hoorah,ct scan results,intravenous ambisome
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MDS in the family | mds-in-the-family.blogspot.com Reviews

https://mds-in-the-family.blogspot.com

Follows the fortunes of daughter and father who both have MDS myelodysplastic syndromes. Start with the oldest entry if you want to read the whole story

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mds-in-the-family.blogspot.com mds-in-the-family.blogspot.com
1

MDS in the family: Gradually improving

http://mds-in-the-family.blogspot.com/2015/03/gradually-improving.html

MDS in the family. Follows the fortunes of daughter and father who both have MDS myelodysplastic syndromes. Start with the oldest entry if you want to read the whole story. MDS UK Support Group. Wednesday, 4 March 2015. I have another week of antibiotics to get rid of that persistent lung infection. Gradually starting to come off tablets and potions. One called Posaconazole is very expensive , so I have been told to keep it safe in case needed in the future. Subscribe to: Post Comments (Atom).

2

MDS in the family: Hopefully being discharged today

http://mds-in-the-family.blogspot.com/2015/05/hopefully-being-discharged-today.html

MDS in the family. Follows the fortunes of daughter and father who both have MDS myelodysplastic syndromes. Start with the oldest entry if you want to read the whole story. MDS UK Support Group. Monday, 18 May 2015. Hopefully being discharged today. Monday is a bad day for discharge, mainly to get the medication from the labs and through the paper work. I shall have to come in once a day for an hour or so for an IV drip. And blood tests I guess. Then I go back to being a day case patient. GVH in my gut.

3

MDS in the family: Two interesting procedures

http://mds-in-the-family.blogspot.com/2015/05/two-interesting-procedures.html

MDS in the family. Follows the fortunes of daughter and father who both have MDS myelodysplastic syndromes. Start with the oldest entry if you want to read the whole story. MDS UK Support Group. Tuesday, 12 May 2015. The first was a colonoscopy. Used to examine your large intestine (colon). Which basically did not find I had anything seriously wrong other than it is incredibly tender, probably caused by GVH. So no cancerous polyps or anything. Which is good. Subscribe to: Post Comments (Atom).

4

MDS in the family: Results have got better again

http://mds-in-the-family.blogspot.com/2014/12/results-have-got-better-again.html

MDS in the family. Follows the fortunes of daughter and father who both have MDS myelodysplastic syndromes. Start with the oldest entry if you want to read the whole story. MDS UK Support Group. Saturday, 27 December 2014. Results have got better again. My liver has improved improved. My liver counts have improved again, and the yellowness in the eyes decreased again. The ALT liver count has gone done to 936 - 20% or so down again (from the highest it got to a week ago of 2400). 28 December 2014 at 11:23.

5

MDS in the family: GVH in my gut

http://mds-in-the-family.blogspot.com/2015/05/gvh-in-my-gut.html

MDS in the family. Follows the fortunes of daughter and father who both have MDS myelodysplastic syndromes. Start with the oldest entry if you want to read the whole story. MDS UK Support Group. Friday, 1 May 2015. GVH in my gut. I have been suffering badly with Kidney and liver problems but they are just about OK now. The problem is GVH graft versus host desease which is giving me terrible diarrohia particularly overnight. But it's only a few days to put up with. Subscribe to: Post Comments (Atom).

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