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Living with Scleroderma | this is nothing but a curve ball

this is nothing but a curve ball (by kcmunda)

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Living with Scleroderma | this is nothing but a curve ball | myscleroderma.wordpress.com Reviews
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this is nothing but a curve ball (by kcmunda)
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Living with Scleroderma | this is nothing but a curve ball | myscleroderma.wordpress.com Reviews

https://myscleroderma.wordpress.com

this is nothing but a curve ball (by kcmunda)

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October | 2014 | Living with Scleroderma

https://myscleroderma.wordpress.com/2014/10

This is nothing but a curve ball. Chemo #6 and Rituxan again. Sorry I’ve been so MIA lately I haven’t updated the blog. After my 6th chemo, my rheumatologist said my skin has gotten so much softer, yay! He even brought in an intern to feel my skin and told her that unlike the other patients, my skin isn’t as thick and puffy as theirs. Just for precautionary measures, i was prescribed another 2 rounds of rituxan. It’s hard for me to admit that I’ve been having a hard time more everyday with th...God&#8217...

2

Team Kristine Promo Video | Living with Scleroderma

https://myscleroderma.wordpress.com/2014/05/09/team-kristine-promo-video

This is nothing but a curve ball. Laquo; It’s been a tough week. Follow up from my May 3rd post. Team Kristine Promo Video. On May 9, 2014. It’s that time of the year again when we walk to support the Scleroderma Foundation. They have been great at providing patient support, research funds, and caregiver information. Please go to: http:/ www.scleroderma.org/goto/teamkristine. To join or donate. Leave a Reply Cancel reply. Enter your comment here. Fill in your details below or click an icon to log in:.

3

News Coverage | Living with Scleroderma

https://myscleroderma.wordpress.com/2014/06/23/news-coverage

This is nothing but a curve ball. Laquo; Follow up from my May 3rd post. On June 23, 2014. My story on the news. Leave a Reply Cancel reply. Enter your comment here. Fill in your details below or click an icon to log in:. Address never made public). You are commenting using your WordPress.com account. ( Log Out. You are commenting using your Twitter account. ( Log Out. You are commenting using your Facebook account. ( Log Out. You are commenting using your Google account. ( Log Out. Almost a year later.

4

Scleroderma Links | Living with Scleroderma

https://myscleroderma.wordpress.com/scleroderma-links

This is nothing but a curve ball. Scleroderma Foundation So Cal Chapter. Leave a Reply Cancel reply. Enter your comment here. Fill in your details below or click an icon to log in:. Address never made public). You are commenting using your WordPress.com account. ( Log Out. You are commenting using your Twitter account. ( Log Out. You are commenting using your Facebook account. ( Log Out. You are commenting using your Google account. ( Log Out. Notify me of new comments via email. Almost a year later.

5

It’s been a tough week | Living with Scleroderma

https://myscleroderma.wordpress.com/2014/05/03/its-been-a-tough-week

This is nothing but a curve ball. Laquo; Cytoxan #2 update. Team Kristine Promo Video. It’s been a tough week. On May 3, 2014. Even though most of my symptoms from the chemo was pretty much nausea in the first few days, I started feeling a lot of fatigue. Not that waking up in the middle of the night 3-4 times from coughing was helping either. I’m trying to get my fibro under control by thinking about pleasant things and doing things that make me happy. This morning when I woke up, I didn’t feel so...

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Memes | A happy mommy's Weblog

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A happy mommy’s Weblog. Just another WordPress.com weblog. Here are a few Blog carnivals/memes I enjoy. They help blogging much easier. Hosted by Ann Kroeker. Make and take Mondays. Hosted by The 6 o’clock Stitch. Hosted by Katie from A Listmaker’s Life. Hosted by 5 Minutes for Mom. What Works for Me Wednesdays. Hosted by Kristen from We are that Family. Hosted by 5 Minutes for Mom. Hosted by Iris from Grace Alone. Hosted by Crystal from Biblical Womanhood. Hosted by Sarah from I Blame my Mother.

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kcmunda | A happy mommy's Weblog

https://ahappymommy.wordpress.com/author/toddlertimes

A happy mommy’s Weblog. Just another WordPress.com weblog. Posts by KC :. June 22, 2013. San Francisco Trip 2013. June 19, 2013. Elle Graduates from Pre K. June 19, 2013. Mother’s Day 2013. June 19, 2013. June 19, 2013. Elle’s 5th Flower Birthday. May 29, 2013. Say No to Chuck E Cheese. February 19, 2013. Kids Bento Lunch Menu Idea. Older Posts ». San Francisco Trip 2013. Elle Graduates from Pre K. Mother’s Day 2013. Elle’s 5th Flower Birthday. Works for me wednesdays. 5 Minutes for Mom.

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June 2014 ~ Sclero-what?

http://sclero-what.blogspot.com/2014_06_01_archive.html

Experiences of a 30-year old living with a rare auto-immune disease called Scleroderma. Sunday, June 29, 2014. Scleroderma Awareness Day 2014. June has been Scleroderma Awareness month, and I did a poor job of spreading the word, but today is World Scleroderma Awareness Day, so I'm making it a priority to not only "rock teal" (the color for Scleroderma), but to also spread awareness via facebook, instagram, and through my blog. My strength. I am a wuss. I have a hard time lifting my purse, or a g...My jo...

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May 2014 ~ Sclero-what?

http://sclero-what.blogspot.com/2014_05_01_archive.html

Experiences of a 30-year old living with a rare auto-immune disease called Scleroderma. Friday, May 16, 2014. Looking back over the past few months can be a bit overwhelming when I consider all the random acts of kindness that I have received. I mean, really over the last two years it's been quite amazing to me, but for some reason the past two months it seemed like one thing right after another. I haven't been feeling overly stressed, everything is good, so why now? It was hard, because I like to think ...

sclero-what.blogspot.com sclero-what.blogspot.com

July 2014 ~ Sclero-what?

http://sclero-what.blogspot.com/2014_07_01_archive.html

Experiences of a 30-year old living with a rare auto-immune disease called Scleroderma. Thursday, July 31, 2014. PAH and Right Heart Cath. So, Monday morning finally rolled around, and my rheumy called me first thing in the morning. He told me that my echo hadn't changed much from last year, but there was still a bit of high pressure in one of my arteries. Because pulmonary arterial hypertension. Saturday, July 26, 2014. Because Scleroderma, and especially the form that I have, can affect the internals, ...

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A "Typical" Wednesday ~ Sclero-what?

http://sclero-what.blogspot.com/2015/06/a-typical-wednesday.html

Experiences of a 30-year old living with a rare auto-immune disease called Scleroderma. Thursday, June 11, 2015. My stomach does not handle large breakfasts very, and using silverware I'm not used to can be hard, really uncomfortable, and hurt my fingers. Not to mention, eating sitting straight up is really hard. Then there's the fear of spilling on myself. I can't just run home and change quickly. It's not that easy for me. What will be easy to cut into small pieces and fit in my mouth? Questions most p...

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Writing With Hand Pain | Diary of a Mad Nanoer

https://crazynovelingmonth.wordpress.com/2015/04/21/writing-with-hand-pain

Diary of a Mad Nanoer. Ten Ways to Tighten Your Writing and Hook the Reader. My Characters Are Weird →. April 21, 2015 · 11:35 pm. Writing With Hand Pain. Yesterday was the first day to validate. Did you validate? In fact, I have done very little writing the last few days. I printed out my manuscript, then punched holes in it, so that I could put it in a notebook to see it better. Unfortunately, I strained my thumb. Have you ever tried to write with an injured thumb? Let me tell you, it isn’t fun. One th...

sclero-what.blogspot.com sclero-what.blogspot.com

February 2014 ~ Sclero-what?

http://sclero-what.blogspot.com/2014_02_01_archive.html

Experiences of a 30-year old living with a rare auto-immune disease called Scleroderma. Monday, February 24, 2014. Says about immunosuppressive therapy,. And cyclophosphamide. A recent study suggested that methotrexate did not significantly alter the skin score (a measure of skin thickening) compared with placebo (no treatment). Cyclosporine is not completely studied due to reports of renal toxicity. The most promising drugs are mycophenolate mofetil. With Dr. Garg. It was scheduled for Monday, t...I'm g...

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Scleroderma Foundation Video ~ Sclero-what?

http://sclero-what.blogspot.com/2014/03/scleroderma-foundation-video.html

Experiences of a 30-year old living with a rare auto-immune disease called Scleroderma. Monday, March 3, 2014. I have been so lucky to meet people who suffer with Scleroderma, Raynaud's, and other various Auto-immune diseases through Instagram. Totally random, right? And her facebook page here: https:/ www.facebook.com/kcmcreations? Scleroderma Foundation Michigan Chapter. Kind of neat right? Contact Me: bre11414@hotmail.com. To the Dentist I Go. Comfortable In My Thick Skin. Daily Ramblings of Bre.

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April 2014 ~ Sclero-what?

http://sclero-what.blogspot.com/2014_04_01_archive.html

Experiences of a 30-year old living with a rare auto-immune disease called Scleroderma. Tuesday, April 29, 2014. The same week I got shingles, I actually had my next appointment with Dr. Walker. By then I was feeling much better compared to the beginning of the week. When he walked in he said, "Really? I should have told him that I blamed him, but I didn't. We just talked for a little, then he had me hop up on that bed thing (seriously, is there a name for that thing? Sunday, April 20, 2014. Monday came ...

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Living with Scleroderma | this is nothing but a curve ball

This is nothing but a curve ball. Chemo #6 and Rituxan again. Sorry I’ve been so MIA lately I haven’t updated the blog. After my 6th chemo, my rheumatologist said my skin has gotten so much softer, yay! He even brought in an intern to feel my skin and told her that unlike the other patients, my skin isn’t as thick and puffy as theirs. Just for precautionary measures, i was prescribed another 2 rounds of rituxan. It’s hard for me to admit that I’ve been having a hard time more everyday with th...God&#8217...

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My Scleroderma Life

A way to Cope, Journal, and have Hope! Thursday, March 19, 2015. Not going down without a fight! Today I feel amazing! At this time I've decided to continue being med free.like Dr. Call said to me on Tuesday, "with Scleroderma we treat the symptoms that come along. If you feel great then let's not change that by making any drastic changes and ride it out." XOXO Brittany. Sunday, November 30, 2014. If "Plan A" Didn't Work. I can only wash and blow dry my hair twice a week or I'm afraid it would really be ...

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