Make Your Vote Count Towards Migraine

Only a few days left…..

I have been nominated  for WEGO Health Awards. “The WEGO Health Awards program was created to recognize and honor those making a difference in the online health community. It provides the opportunity for community members to thank and support the Patient Leaders and patient-centric initiatives they admire.”

I need your help to endorse my nominations.  I’ve been nominated for

 

Please go to this link and click the orange thumbs up “endorse My Migraine Life” below my picture. You can endorse each category.

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I work so hard year round to advocate and increase migraine awareness.  Your endorsement is your way of participating and inspiring my efforts.

Don’t forget to share your endorsement on social media to encourage your followers to do the same.

Thank you!

 

 

 

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Puppy Alert….We’ve Added to Our Family

I have an announcement to make……..

We have added to our family!  After loosing my best friend, migraine warrior and therapy animal, Lucia, we decided to add some love to our home.  Remember Lucia and Sammy here

Meet Charlie……

 

Charlie Red is a Golden Retriever.  He has brought happiness and puppy energy  into our house.  He is our new normal and such a good boy.  He loves to play outside and eat mulch, dress up and cheer on his sister’s swim team efforts and fully supports my writing and blogging career.  He eats a lot, plays a lot, and sleeps a lot.

 

Thank you to everyone who has supported me during my greatest loss.  Many people remind me that he’s not a replacement.  My answer to that is, OF COURSE NOT.  Charlie is a different life time for all of us and there is no comparison.  It has been the most difficult summer of my life after loosing Lucia, 13, and Sammy, 20.  Charlie has made the house less quiet, less lonely and fills it with new memories.  His sweet face and curious eyes  makes us smile!

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Wet ears=happy puppy post walk and big drink

Charlie plans to make his Instagram debut  @mymigrainelife

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Don’t forget to endorse my nominations for WEGO AWARDS.  WEGO awards many bloggers from a variety a conditions.  Let’s let Migraine be represented and supported.  Thank you!

ENDORSE HERE

WEGO Health Awards Nominee for Advocating and Influencing the Migraine Community. Endorse Now

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I am excited to announce that I have been nominated for the 2018 WEGO Health Awards!!!!!!! I have been nominated for “best kept secret” “best in show Instagram” “best in show community” and “best in show facebook” WOW!!!!!!!!

WEGO Health is a mission-driven company connecting healthcare with the experience, skills, and insights of patient leaders. They are the world’s largest network of patient leaders, working across virtually all health conditions and topics.
The WEGO Health Awards were created to celebrate those who tirelessly support the mission of WEGO Health: to empower the patient voice. With 16 award categories, the WEGO Health Awards are the only awards across all conditions and platforms, that recognize the over 100 thousand inspiring Patient Leaders who raise awareness, share information, and support their communities – but often without recognition.
It is a huge honor to be part of such a great group of nominees!  Thank you SO much for your nominations!  Now, I need your help…..
I’m looking to my incredibly supportive network to help endorse me for these  awards. It is easy to endorse and only take seconds of your time!

Click here to be taken to my WEGO Health Awards profile where you can click “Endorse” under my nominee photo (thumbs up!)

ENDORSE HERE!!!!!!!!

If I have ever supported you, made you laugh, or inspired you to keep fighting – please consider endorsing me for this award.

Shades for Migraine World Solidarity Day, June 21st

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Tomorrow is Migraine Solidarity Day, June 21st.

“Shades For Migraine is a campaign to promote migraine awareness and create a viral buzz for a disease that affects over 1 billion people worldwide….

To participate, people will wear their sunglasses where they normally wouldn’t on Migraine Solidarity Day, June 21, even indoors when possible!  They prove it by posting photos on social media with the hashtag  #ShadesForMigraine. “

My Migraine Life is a proud participating blog and I hope you participate this year!

Watch for advocates outside the Today Show!

Here are some examples:

On left: I am wearing my Axon Optics indoor glasses.  I was working in the office with a skylight and needed protection from the computer glare and sunlight.  Check out my affiliate link to learn more

On right: I am wearing my Theraspecs indoor glasses and headed to a wedding.

For me, anytime is a good time to wear my #shadesformigraine

Any one can participate.  Last year, my best and favorite support jumped in on the fun.  She is missed every second of My Migraine Life.  Her support was priceless!

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Miles for Migraine Cincinnati Results 2018 race/walk

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This weekend, I was part of Miles for Migraine race in Cincinnati.  It was a beautiful and warm day filled with love, support and a group of people fighting stigma and raising money for Migraine and headache disorders.

 

 

The race raised $3,550

Team My Migraine Life raised $567.37.  Thank you to all those who donated.

We were the top team!!! I’m so proud of us 🙂

The day began with fighting a 3 day migraine that I had traveled with but had huge inspiration to make it to the event.  When I got there, I was surrounded with some migraine advocate powerhouses.
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Michelle Tracy, Migraine Warrior, represented the INVisible project with her smiling face and sharing her inspiring personal stories. She also spoke to the group about being a patient advocate and how we can all be one ourselves.

Not only is Michelle an amazing and strong advocate but she was brave enough to sing the National Anthem to begin our race.  She has a strong voice as a patient and as a singer!

Katie Golden, GoldenGraine, brought sparkle to all of our days.  She is the senior contributing writer to the INVisble Project and a fierce advocate.  I can’t possibly list all of the things she is doing for the migraine and pain community but check her out and follow along.  She was kind enough to run the race with my daughter and then touch up her sparkles…..because there is no such thing as too much glitter!

IMG_3555 I once again gave my patient perspective.  I was shaky and read my speech because I could not guarantee that I could string my words together and make sense.  I felt so proud that I stood up to the pain and was able to put a face on what migraine disease really looks like.

We also heard from Dr. Andrew Hershey, the chair and director of the division of neurology at Cincinnati Children’s. He is a professor of pediatrics and neurology.

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After that, we walked.  At the Miles for Migraine events you are welcome to run and be a fierce competitor, walk and enjoy your team or stay at the tents to mingle or relax.  It’s all about building community, moving how you can and raising funds so we all can live a healthier life.

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The best part of the day was being with the ones that I love.  Spending a morning for a good cause with good people is always a great way start to the day.  I woke up in pain, shaky, sick and not sure if I could make it.  Thanks to effective medication, endorphins and a bit of luck, I was able to enjoy the day.  I walked with some of our best friends, my husband and our mini me’s.  It was a day that we  plan on turning into a tradition.

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Wondering about the Brain Hat? The Brain Hat Society is for people with migraine, their caregivers, friends and family while recognizing  their heroic efforts.  If you raise $50 you can be a member.  Purple is for migraine sufferers and pink is for the caregivers and loved ones.

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Thank you to all that supported and continue to fight.  We are fighting not just for ourselves but for future generations.

IMG_3582Also, a BIG thank you to the sponsors and these hard working ladies!  Shirley Kessel is the Miles for Migraine president while Katie MacDonald oversees operations.  They work tirelessly on bringing these events to more cities and raising funds to benefit so many.

Check to see if Miles for Migraine is coming to your city and how you can participate virtually!

 

 

 

 

 

The Start to Migraine Awareness Month and Miles for Migraine walk/run in Cincinnati

Happy June!  Today marks the first day of Migraine Awareness Month!!!

I know a lot of you are thinking, “But how can I help?”  This month I will be sharing information and advocacy opportunities from a variety of migraine organizations that I am involved with and follow. I can’t wait for you to get involved also.

The simplest way to participate is sharing information, following on all social media and virtually “making some noise.”  Share with your followers how you suffer, important information and help break down the stigma.

To start the month out, I’d like to ask for your donation and participation with an organization that you’ve heard me talk about…..Miles for Migraine.

Miles for Migraine vision is ” to create some “big noise” in the migraine community and raise awareness that migraine and headache disorders are more than “a headache”. We are making great strides by growing our signature event, the Miles for Migraine 2-Mile walk, 5K/10K run; and by expanding our newer programs –  a day camp for adolescents who have  chronic migraine, and our adult seminar series”

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On June 10, the Cincinnati walk/run will be at Otto Armleder Memorial Park

How can you participate?

There are a few ways to support:

  1.  Join My Migraine Life Team.  If you live close enough to walk/run, please join my team!  I’d love to see you there.  Go here and join team C0F0B55B-F24F-4204-9928-E32EFED679D8.JPG
  2. If you’d like to donate and support my fundraising efforts but won’t be able to make the walk, go here and donate A9A554EE-1C69-463A-9846-ACD72F425E9D
  3. If you are unable to walk/run but want to participate.
    1. If you are local and want to participate but are unable to walk/run we’d love for you to come anyways!  Join my team and come to meet all the wonderful advocates and migraine supporters.  There will be a quiet tent to rest and you are not obligated to walk.  Your donation and presence is much appreciated!  We are all doing what we can do and any effort are spoons well spent. 30A7FB9F-D0E4-41D7-A0E1-9DA39E84FE15.JPG
    2. If you don’t live locally but would like to support.  Please donate to my page and participate virtually.  You can walk and raise money without being at an event.  Join the team and ask others to help raise funds.
    3. Ask a friend, co worker or loved one to help you raise money.  You’ll be surprised at how many are affected by migraine and are happy to help make a difference.
  4. If you want to donate but don’t have the funds.  I totally get it.  Between the price of medications and therapies and difficulty with keeping a job, it can be even harder to donate.  Remember that $10 makes a difference.  Each dollar goes a long way and any donation takes us a step closer to helping many!
  5. If none of these are an option, please share this post.  Sharing is caring and if you can’t support maybe a friend can.  It’s all about not being alone and spreading a message.  Everyone can share!

Please consider donating to My Migraine Life team and my personal fundraiser page.  Follow along on all social media and share, share, share this month.  Teaching your audience/social media followers how strong you are to be fighting migraine for yourself or for others will go really far.

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Miles for Migraine race/walk Cincinnati 2018 with My Migraine Life

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Please join us on June 10, 2018 for the inaugural Cincinnati Walk/Run

Date/Time: Sunday June 10, 2018 8:30 AM
Location: Otto Armleder Memorial Park
Distance: 2 Mile Walk / 5K Run / 10k Run

 

“Miles for Migraine is a registered 501(c)(3) Non-Profit with the mission of improving the lives of migraine patients and their families, raising public awareness about headache disorders, and helping find a cure for migraine. Miles for Migraine produces fun walk/run events, typically 2 mile walk and 5k and 10k race to raise money for migraine research. We also host youth camps for kids and teens impacted by migraine or other headache disorders.”

This years Cleveland’s race was such a success and I hope to make Cincinnati’s inaugural walk/run the same.  Here’s some highlights:

To sign up to the Cincinnati walk/run please follow these directions:

Follow this link

If you are donating:  click on  “donate to participant” on left side bar

  • Look up name: Sarah Rathsack and donate to my page 🙂

If you are registering: “view teams” on left side bar

  • Join team My Migraine Life

If you donate or register, in general, I will not get credit for my referral.  Miles for Migraine tracks their top fundraisers and referrals.  Please donate to my page or join team My Migraine Life to give our great community a voice and show how  united My Migraine Lifers can be.  Whether it’s for you, a family member, a friend or co workers.  You are fighting and walking to make a difference.  Your support is so appreciated!!!!!!

 

*Please notify me if you have donated or joined our team!  I would like to thank you personally and know that your donation has gone to my page and team.  I really am grateful for your consideration!!!

A9A554EE-1C69-463A-9846-ACD72F425E9DThank You