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A Fierce Fight against CIDP

A Fierce Fight against CIDP. Tuesday, August 9, 2016. Day 365: One crazy (and wonderful) year. Aug 3rd was my 1 year post transplant birthday. I spent it in Chicago for my one year checkup and have been reflecting on my improvements since March 2015 when I came for evaluation. Miles of myelin repairing. I still have challenges with: fatigue, fine motor skills in hands, numb hands and feet (I cannot operate a zipper without looking), occasional balance issue and strength. However the improvements outw...

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A Fierce Fight against CIDP | stephsfiercefight.blogspot.com Reviews
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A Fierce Fight against CIDP. Tuesday, August 9, 2016. Day 365: One crazy (and wonderful) year. Aug 3rd was my 1 year post transplant birthday. I spent it in Chicago for my one year checkup and have been reflecting on my improvements since March 2015 when I came for evaluation. Miles of myelin repairing. I still have challenges with: fatigue, fine motor skills in hands, numb hands and feet (I cannot operate a zipper without looking), occasional balance issue and strength. However the improvements outw...
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A Fierce Fight against CIDP | stephsfiercefight.blogspot.com Reviews

https://stephsfiercefight.blogspot.com

A Fierce Fight against CIDP. Tuesday, August 9, 2016. Day 365: One crazy (and wonderful) year. Aug 3rd was my 1 year post transplant birthday. I spent it in Chicago for my one year checkup and have been reflecting on my improvements since March 2015 when I came for evaluation. Miles of myelin repairing. I still have challenges with: fatigue, fine motor skills in hands, numb hands and feet (I cannot operate a zipper without looking), occasional balance issue and strength. However the improvements outw...

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stephsfiercefight.blogspot.com stephsfiercefight.blogspot.com
1

A Fierce Fight against CIDP: December 2015

http://stephsfiercefight.blogspot.com/2015_12_01_archive.html

A Fierce Fight against CIDP. Friday, December 18, 2015. Day 137: Prepare to re-enter the Matrix. The days and nights are quite colder, there are twinkle lights everywhere I turn. Holiday music plays at every gas station and photo cards with friendly faces are pouring in. What a season to be healthy and thankful. I missed my hair. Nerves have a mind of their own. Happy Holidays and New Year. Whatever you celebrate, whomever you celebrate with and wherever you may be celebrating: have a wonderful Holiday S...

2

A Fierce Fight against CIDP: October 2015

http://stephsfiercefight.blogspot.com/2015_10_01_archive.html

A Fierce Fight against CIDP. Monday, October 19, 2015. Day 77: Status Quo and Hand Puddy. The changes week to week aren't as significant as they were in the beginning.The blog updates may spread out to every two or three weeks. I think there is a way to "follow" the blog so you get emailed when there are changes, but I'm not sure how. The beau took me on a drive to Half Moon Bay Saturday and we decided to stop by the Art and Pumpkin Festival. Free admission and handicapped parking! I'm becoming a crock p...

3

A Fierce Fight against CIDP: Day 365: One crazy (and wonderful) year

http://stephsfiercefight.blogspot.com/2016/08/day-365-one-crazy-and-wonderful-year.html

A Fierce Fight against CIDP. Tuesday, August 9, 2016. Day 365: One crazy (and wonderful) year. Aug 3rd was my 1 year post transplant birthday. I spent it in Chicago for my one year checkup and have been reflecting on my improvements since March 2015 when I came for evaluation. Miles of myelin repairing. I still have challenges with: fatigue, fine motor skills in hands, numb hands and feet (I cannot operate a zipper without looking), occasional balance issue and strength. However the improvements outw...

4

A Fierce Fight against CIDP: January 2016

http://stephsfiercefight.blogspot.com/2016_01_01_archive.html

A Fierce Fight against CIDP. Monday, January 25, 2016. Day 174: Back into the groove. Fast approaching is my 6 month immune sytem birthday (Feb. 3rd). I have been back to work since January 8th, this is my third week back. My brain is beyond happy to be of good use again. Physically it is quite a challenge. My back and neck are taking the brunt of the adjustment, which is why I see both a massuese and a chiroprator once a week. I am starting to notice more of the pre-CIDP traits in me: craving physical a...

5

A Fierce Fight against CIDP: September 2015

http://stephsfiercefight.blogspot.com/2015_09_01_archive.html

A Fierce Fight against CIDP. Tuesday, September 29, 2015. Day 56: where did 60 days go? Days I've been back home:45. It blows my mind a that its been almost two months since transplant. While nerve pain is still present, I am gaining stamina. Meaning, I can stand/walk for longer duration over this last week. Depending on the activity I might have an extra 5-10 min. on my feet in a day, which doesn't seem like a lot. But to someone with nerve pain, it's monumental. I will let you be the judge of which is ...

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Facebook Groups, Post-HSCT Patient Blogs: What Happens Next

https://www.the-irf.org/post-hsct-patients/patient-blogs.aspx

Your Best Advocate Is You. Blogs of Post-HSCT Patients. The cure for multiple sclerosis. An End To Autoimmune Disease Progression. Brian Tilaro's Multiple Sclerosis Homepage At ALLYOUMED.COM. A Fierce Fight against CIDP. Chrome can translate to English). Chrome can translate to English). Hematopioetic Stem Cell Transplant - MS and Autoimmune Diseases. Http:/ www.facebook.com/groups/149103351840242/. No Chemo, No Cure - HSCT in India. Https:/ www.facebook.com/groups/113034538879355/.

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A Fierce Fight against CIDP

A Fierce Fight against CIDP. Tuesday, August 9, 2016. Day 365: One crazy (and wonderful) year. Aug 3rd was my 1 year post transplant birthday. I spent it in Chicago for my one year checkup and have been reflecting on my improvements since March 2015 when I came for evaluation. Miles of myelin repairing. I still have challenges with: fatigue, fine motor skills in hands, numb hands and feet (I cannot operate a zipper without looking), occasional balance issue and strength. However the improvements outw...

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