Showing posts with label awards. Show all posts
Showing posts with label awards. Show all posts

Thursday, July 29, 2021

News From Our House: Awards, Vaccines & Treatments


It's been about two months since my last personal update, so I have a lot to share with you, mostly good news!

Award Nominations for Me and this Blog

 
I have now been nominated for 6 WEGO Health Awards!! I was stunned by this, as the nominations kept rolling in the past few weeks. I've been nominated for one at a time before, in 2003 and 2007, but I've been really touched by this outpouring of support. These are the awards I'm nominated for:

  • Healthcare Collaborator
  • Patient Leader Hero
  • Advocating for Another
  • Best in Show: Blog
  • Best in Show: Twitter
  • Best in Show: YouTube

Wow! I was really surprised by the YouTube nomination, since my YouTube channel is so new (here's my Chronic Illness playlist).

THANK YOU to whoever nominated me for these awards - it means a lot for all my hard work (14 years with the blog now!) to be recognized and appreciated.

Please take a quick moment to endorse me for these awards. Just click this link, click on "Endorse this patient leader" under the list of awards, then you can click on whichever award(s) you think I deserve. The endorsement period ends Saturday, July 31, and I would love to make it to the finals, so thanks for your endorsement(s) ... and any comments are appreciated, too!



COVID Vaccines & Recovery

As of my last update, my son and I had each had our first shots, of the Moderna vaccine, after months of research and preparation. I wrote three blog posts about the vaccines, covering general info, patient experience, and recommended preparation, to share what I'd learned and how we came to decide it was OK for us to get them, which one to choose, and how we prepared.


Since that last update, we are now both fully vaccinated, with both Moderna shots. As is typical for us, we both reacted pretty similarly. After the first shot, we each experienced mainly just a mildly sore arm, though we each had some mild extra on-and-off fatigue during the next couple of weeks, which may or may not have been from the vaccine.

After the second shot, we again reacted pretty much the same, feeling fine for the first 24 hours and then awful for the next 24 hours (pain all over, exhaustion, moderate flu-like symptoms). After that, I thought I'd returned to baseline. In hindsight, though, I realized I was a bit more fatigued than usual for the next week (still functioning but a little more worn out than is typical for me). For about a month after, I noticed that I was fine and at my normal baseline most days but about once or twice a week, I would wake up totally exhausted and need to rest all day. Again, pretty mild reaction compared to some, but it was unusual for me and the timing points to the vaccine as cause. Since about the 1-month mark post-vaccine, I have been pretty much back to my normal baseline.

My son was at the end of that awful 24 hours, 2 days after his second shot, when we made a trip to visit his Lyme specialist and functional medicine practitioner. They are located out in the country, about 45 minutes from here, and my son was still pretty wiped out that morning, not yet quite through his 24 hours of feeling bad. He slept in the backseat on the way there. BUT, while there, he got the IVs he usually gets when he visits them (Myer's cocktail, a mix of vitamins and minerals, and a bag of glutathione). Like magic, he came back to life! By the time we left, he was feeling great, had plenty of energy, and he stayed that way, with no further reaction to the vaccine! I suspect it was mainly the glutathione that did the trick, since it directly affects the immune system and helps with detox. You might try it yourself, both before and after your vaccine. There are lots of ways to increase glutathione, as explained in this blog post. He and I use glutathione nasal spray every day, but his glutathione IV seems to have given him a big extra boost.

 

Continued Treatments and Improvements 

As I reported in my last update, I've been trying lots of new treatments since the start of the year, including increased treatments for immune dysfunction and for Lyme disease. I am still keeping up with all of those, as described in that last post. The only change since then was coming up to my full dose (30 drops twice a day) of Crypto-Plus for Lyme disease. I didn't experience any Herx reaction at all from this new addition, so I am hoping my Lyme is mostly treated at this point. We'll see what the Lyme specialist has to say at my next appointment and whether there's anything else she wants me to try.

My son and I both decided to continue the liposomal vitamin C that we started as vaccine preparation because it seemed to help us both overall, and it's great for the immune system.

My son continues to make lots of changes to his own regimen, mostly based on the advice of the functional medicine specialist and extensive testing she's done. He has lots of GI issues, but he is hugely better in the past two years, after treating lots of pathogens discovered in his GI tract, treating other issues found through testing, and zeroing in on some food issues (like severe gluten intolerance). In 2019, he had lost 40 pounds, was severely nauseous and vomiting every day, and had a burning pain in his stomach. All of those symptoms have cleared up now, and he's back at a healthy weight.

In fact, our son is really doing well. He has a summer internship, related to his college degree! He's working 20-30 hours each week, usually 6-8 hours at a time. There is some flexibility, with assignments lasting 2-4 days and breaks in between. Sometimes, he doesn't have to be there until 5 pm (which he loves!), but other days, he needs to show up at 7 am ... and he's managing that! This would have been absolutely impossible two years ago. The job has periods of physical activity interspersed with periods of downtime, and he's handling it really well, feeling good, and thrilled to be out in the world working! It's thrilling for all of us, to see him able to take this step forward.

 

What We're Watching and Reading

We've seen two movies since my last update and both were very good (my reviews plus trailers at the links below). 

We watched Leave No Trace on streaming. It's a quiet but powerful movie, based on the real-life story of a father and daughter living off the grid. It's set in the stunning forests of the Pacific Northwest, so it is gorgeous to watch and also a very moving story. If you prefer quieter movies, without a lot of suspense (there is some mild suspense), this is a great option for you. My husband and I both enjoyed it very much.

And ... drumroll, please! ... we went back to the theater! With me now fully vaccinated, and our area quite safe with very high vaccination rates, we went to the movie theater for the first time since early March 2020! We put our feet up in a lovely recliner theater, shared a bucket of popcorn, and enjoyed watching A Quiet Place II. We loved the first movie, which was completely unique and unlike any other movie, ever. The sequel continues the story of the family in this post-apocalyptic world where making a single sound could get you killed. If you haven't seen it yet, you should! The double-feature is still showing in some theaters (or just the sequel), and both movies are now on streaming, too. We saw a matinee, so there was only one other couple in the entire theater! A good situation for dipping our toes back into movie-going.


As for TV, I posted an overview of TV Shows in Summer 2021. This is a collection of shows on various streaming services, cable, and networks that we are currently enjoying this summer. It includes some returning old favorites of ours, some new favorites, and a few airing in August that we are looking forward to trying. Please take a look and let me know what YOU are watching this summer: we can always use some new ideas!


In my reading world, I am fully immersed in my annual Big Book Summer Reading Challenge, enjoying books and audio books with 400 or more pages and getting through some of the chunksters that have been piling up on my bookcase! You can hear about some of them in my June Reading Wrap-Up on YouTube and hear me gush about my favorites.

I just finished two more Big Books in July that were both outstanding! Blackout (my review at the link) by Connie Willis is a part of her Oxford Time Travel  series and features a bunch of Historians (Oxford grad students) in the near future using time travel technology to travel back to various times and places in World War II England so that they can observe events first-hand, like the Blitz, the evacuation of children to the country, VE Day, and the ordinary citizens who helped to evacuate soldiers from Dunkirk to Dover with their boats. But problems start to occur with the technology, and these time-traveling Historians might not be able to get home. It's a gripping novel, filled with fascinating historical detail ... but be forewarned that it is part 1 of a 2-book series.

The other one I really enjoyed in July was The Air You Breathe by Frances de Ponte Peebles, a historical novel. It's about the intense friendship between two very different women from opposite backgrounds, beginning in 1930's Brazil. Their friendship--and the story--centers around music, and the novel was wonderful, beautifully written, and engrossing. I enjoyed learning more about Brazil and its music.

 

 

How have YOU been? And what have YOU been watching and reading lately? Please share your thoughts and recommendations in the comments below!

Thursday, July 15, 2021

Nominated for Awards - Please Endorse Me!


Hi, all!

Just a quick stop by the blog to share some wonderful news with you:

I've been nominated in the 10th Annual WEGO Health Awards for a Healthcare Collaborator award! This is in recognition of my 14 years of work in writing this blog, sharing information on social media, starting and participating in support groups, and advocacy efforts.

It's my 3rd nomination for a WEGO Health award in the last 10 years, and I am honored.

Now I need your help to become a finalist!

Just take a moment to endorse me at this link. The website is a bit wonky and not all that clear, but just click on Endorse This Patient Leader, under the award name. A box will pop up saying "Healthcare Collaborator" that looks grayed out, but just click on it to endorse me. Super easy and only takes a few moments.

Thank you for your endorsement ... and for many years of interacting on the blog, on social media, and in real life to help build a supportive patient community for all of us!

UPDATE ON JULY 17: Wow, I have now been nominated for 4 WEGO Health awards:

  • Healthcare Collaborator
  • Patient Leader Hero
  • Best in Show: Blog
  • Advocating for Another
I am honored and very touched by the endorsements and comments left by people. Thank you for your support. If you already endorsed me, thank you and please consider clicking the link again to endorse me for the other 3 awards, and if you haven't visited the WEGO awards yet, please consider endorsing me for whichever awards you like, if you have gained any value from my work on this blog, in groups, on social media, and in advocacy. THANK YOU!!

Wednesday, July 11, 2018

I've Been Nominated for a Patient Leader Award!

I look forward to the WEGO Health Awards every year because it is a wonderful way to recognize some of the people who have done so much for our patient community! Last year, Jennie Spotila was nominated for a Best in Show Blog award for her excellent Occupy M.E. blog and Tom Kindlan was nominated for a Best in Show: Twitter award (and was a finalist). Both are tireless patient advocates for ME/CFS.

So, I am thrilled to be in such good company, with my nomination this year for a Patient Leader Hero Award!

This blog was nominated several years ago for a Best in Show Blog Award. This year's award nomination means a lot to me because I now spend so much of my time helping other patients, through this blog but also through both local and online support groups. I run groups for Delaware ME/CFS, Teens & Young People with ME/CFS and Related Illnesses, and Parents of Kids, Teens & Young Adults with ME/CFS and Related Illnesses (and participate in other groups). I also spend a lot of time helping patients through e-mail, Twitter, and Facebook and am working on a book on ME/CFS Treatments, based on our own experiences. Helping others has become a huge part of my life, so this award nomination means a lot to me - a big thanks to whoever nominated me!!

Now comes the fun part, where YOU can impact the outcome!
Just visit my WEGO profile and click on the "Endorse Sue Jackson" button to add your endorsement - you just have to enter your name and e-mail address, so it only takes a few seconds to complete. The nominees in each category with the most endorsements will be Finalists. Endorsements are only open until August 17, so click over now! While you're there, you can also stop by to endorse Tom Kindlan, who has again been nominated, this time for a Lifetime Achievement Award, which is well-deserved!
Good luck to all the award nominees in all the categories!

Tuesday, February 04, 2014

WEGO Health Activist Award Nomination





I was very honored to hear last month that this blog had been nominated for a WEGO Health Activist Best in Show Award! Unfortunately, between my own challenges and my sons' medical problems, I haven't had time to even tell anyone about it until now.


Anyway, the award nominations are open for voting now, so if you have found my blog useful, you can vote for me at this link.

And thank you for eight years of kindness, encouragement, and support!


Thursday, August 26, 2010

Top Chronic Illness Blog Award

Medical Assistant Schools
Presented by: Medical Assistant Schools



When I returned from our Catskills trip this week, I had a pleasant surprise waiting in my e-mail inbox - a notice that my blog is one of the Top 35 Chronic Illness Blogs, according to a recent survey by Medical Assistant Schools! 

They told me the winners were chosen based on votes by blog readers, so this post is really for all of you...THANK YOU!!! 

I really appreciate your support and acknowledgment.  I feel like I get at least as much back from this blog as I put into it.

Check out the full list of winners - I noticed quite a few favorite CFS blogs among the top 35 - congratulations to all!  (I would include links right here, but I'm just too wiped out - the link above takes you to the full list of 35 winners with links to each one.)

Tuesday, March 16, 2010

The Happiness Award


I was very pleased this weekend when Forgetful Girl gave me The Happiness Award (check out her excellent blog and its list of other Happiness Award winners)! This award is right up my alley because I'm usually a pretty happy person, and I've made a special effort, since my CFS diagnosis, to recognize and appreciate the joys in my life - the things that make me happy.

So, thank you, Forgetful Girl! Now, I'm supposed to list 10 things that make me happy and pass the award on.

Ten Things That Make Me Happy

  • Sunshine! It was shining brightly today and making everything seem better.
  • Music - listening to lively, feel-good music and, of course, singing along!
  • My husband and kids. I love our little family of four.
  • Being outdoors. I wrote a blog post about The Joy of the Outdoors.
  • Good food. Especially with so many of life's little's splurges now unavailable, I love to enjoy really good food (and prepare it for my loved ones when I'm able).
  • Springtime! The sight of the first snowdrops blooming today made me smile.
  • Good friends - both in-person and virtual! I wrote previously about The Joy of Friendship.
  • Losing myself in a really great book.
  • Watching a wonderful, uplifting movie that makes me laugh and cry.
  • Travel. Oh, I love to travel!! I'm currently planning our spring break road trip to Louisiana and am so excited I can hardly wait.
Just making this list made me happy!

So, it's time to pass on The Happiness Award to a few others. As with the last award, this one comes from me with no strings attached. If you feel up to passing the award along, great! If not, no problem. You might want to try listing 10 Things That Make You Happy, though - just making the list will cheer you up!

I'd like to recognize the following bloggers who have shared their happiness with me and inspired me with their upbeat spirits and focus on joy:

Please stop by their wonderful blogs to share in their happiness!

Friday, February 19, 2010

A Long Week...and An Award!


Sorry I've been so silent since Tuesday. This week turned out to be packed full and pretty exhausting. Besides the busy start to the week with Mardi Gras, Ken and I had somewhere to go every single evening - I'm used to lying low in the evenings. I also started and finished our taxes in record time by working on them all day Monday and Tuesday (I was motivated to get our refund back fast). And after a whole week of snow days last week, Jamie was home sick - badly crashed - all this week. Poor kid was flat on his back all week (still is). He and Craig both had stomach cramps for about 24 hours, so it was probably a virus that triggered this crash.

So, I've been pretty wiped out the second part of this week. I haven't gotten any work done, and I haven't had even 5 minutes with enough energy to read blogs (sorry!). Jamie and I have been watching old Lost reruns on DVD every day!

And, finally, I have been remiss in recognizing a blog award, The Sugar Doll Award, that Dominique at 4 Walls and a View gave me earlier this week! I'm not sure of the exact meaning of the Sugar Doll Award, but it sounds nice, and I appreciate it! I'm supposed to tell you 10 things about myself, then nominate some other deserving bloggers. It's too bad Dominique already received this award herself because I've really been enjoying her new very well-written CFS blog this past month!

So, I've been thinking of what 10 things to tell you. This is a bit of a challenge because, after 4 years of writing this blog, I've already told you an awful lot! I've been pretty open here, so you already know all kinds of facts about me - how I love reading, camping and the outdoors, and travel, that I'm from Rochester and used to live in New Orleans, etc. So, I've had to dig deep (and in some cases way back!) to try to come up with some things you might not know about me:
  1. When I was 13, I decided I wanted to be called Sue (it sounded more mature, I thought), but most of my family still calls me Suzie to this day! I use Suzan for my writing, just because Sue Jackson seemed way too generic, but no one who knows me actually calls me Suzan...which is why I used Sue for this blog.
  2. I have a sister who is 6 years younger than I am.
  3. I went to England and France with my high school French Club when I was 16. I've been to England several times since then but haven't gotten back to France yet. I'm dying to take my kids to Europe.
  4. I took dancing lessons from age 5 to 16, then a few classes in college - tap, ballet, and jazz. I still have the purple spandex one-shouldered jumpsuit I wore to dance to "Fame" when I was a teenager (don't ask me why I've saved it all these years!)
  5. I drive a 1992 VW Cabriolet convertible - red with a black roof - affectionately known in our house as "the little red car." I expect it to last forever and put my fingers in my ears whenever Ken suggests otherwise.
  6. Ken and I met at work, at the DuPont plant in Louisiana where we both worked. He was assigned to be my mentor when I started there!
  7. I love to play games of all kinds. My best friend, Michelle, and I used to play marathon board games - Monopoly games that lasted for days, 30 games of Clue in a row, etc. My kids love games, too (I wouldn't have it any other way!), and my mom and I love to play Scrabble together.
  8. I kind of like the vivid dreams that come with CFS. I enjoy dreaming and remembering my dreams, especially dreams of flying (but I don't like chase dreams or pee dreams).
  9. I have a degree in chemical engineering from Clarkson University, a small engineering school in remote northern NY, near the Canadian border. My years as an engineer seem like a different lifetime.
  10. I love to cook tasty, healthy meals for my family. I really hate when I'm too sick to cook. Cooking Light is my favorite source of recipes.
And I better get cooking now or we'll be eating dinner at midnight tonight!

Thanks for the award, Dominique! I nominate:
What's After 29? isn't a CFS blog, but it's written by Lori, who many of you know for her blog, Living Chronically, about her daughter's struggles with CFS and celiac disease. This blog is just for fun, and Lori has a wonderful sense of humor! I hope you enjoy visiting all three of these excellent blogs.

(By the way, I know from my book blog that awards can sometimes be a bit of a burden if you're not feeling well - having to pass it along and include links, etc. in a blog post - so if you would prefer to just accept it graciously and not pass it along, I understand completely! No problem.)

OK, I am SO ready for the weekend...

(P.S. Moments after I clicked on the Publish button, I found out I was also nominated for the Sugar Doll Award from Robyn at "How Are you?" and Other Dumb Questions. Check out Robyn's awesome blog, written from the perspective of a young woman with CFS. Thanks, Robyn!)