Dear 12-Year-Old Me

December 14, 2011

This is a wonderful letter written by Alisa Lipscombe who is Fellow Advocate,and RSD Angel.

Dear twelve-year-old me,

Right now, life is pretty good for you. You've just started High School. You're the Form Captain for your class. You got into the audition-only choir at school. You're in concert band and orchestra playing tenor saxophone, and you were just selected to be the solo singer at the School Easter service. If I remember rightly, your favorite show is The O.C currently and every morning you head to the gym with Mum before walking up to school. Every day is hectic - you're running around from one rehearsal to the next, texting your friends frantically as you hurry around the school. Yeah, right now, life is great.


But on April 15th that's about to change. You're going to fall over at the school bus stop and hurt your ankle. Yep, in front of EVERYBODY. But don't be embarrassed. Everyone is really nice to you and they look after you as you wait for the ambulance. The next few months are going to be pretty tough. You'll go to lots of appointments, where most doctors aren't going to believe you when you say how much pain you are in. But the pain is real. So don't let anybody tell you otherwise. You will be diagnosed with CRPS (Complex Regional Pain Syndrome) 8 months later, which is an incurable nerve condition that leaves you in excruciating pain 24/7.


From now on you're going to rely on crutches and a wheelchair to get around. At first, it will be hard because everyone stares at you, but keep your chin up - people stop staring so much after awhile. School stops being as fun as it was at the beginning. Your friends are going to leave you now that you're "weird" and sick. But next year, you're going to meet some amazing people who will still be your friends for years to come. I know it's cliche to say "it gets better" but it truly does. So please, don't give up hope. Just keep studying and never stop singing. Music will save your life countless times in the coming years.


In 2007, you're going to fall into a coma and nearly die. It's going to be one of the scariest experiences for you and your family, but don't worry. You're going to wake up and you'll be ok. From here on in, you're going to spend a lot of time in hospital, and you'll get to know the nurses really well. Make the most of it - befriend the other patients, and try your hardest to bring a smile to someone Else's face every day. You can't change where you are, but you can change how you deal with the situation. You'll be sick of hospital food by your 6th week as an inpatient, but Eryn will come in and swap "real" food for your hospital meals. Remember to thank her. Rehab is going to suck. You're going to hate the phrase "No pain, no gain" and want to scream every time a physio or doctor says it to you. Please don't get too mad. They are just trying to help.


When your CRPS starts to spread, you're going to be scared. That's ok. You're allowed to be scared, and crying is not a sign of weakness. It's a sign that you've been strong for too long. So cry. Let it out. And remember you're not alone. You're going to meet some of the most amazing people because of this disease. You'll make friends with other patients here in New Zealand, as well as those living in California, New Jersey, Canada, Israel, Australia, to name but a few. These people are going to help you survive each day. They understand what you're going through and when it feels like nobody else "gets" this pain, they do. So never forget that.


If I had any advice for you, it's enjoy these last few months of normality. Enjoy playing your saxophone. In 2008 when you stop being able to play it, you're going to miss it more than words can say. Appreciate every step you take without pain, and please try to remember this feeling. I can't. Every time you see something beautiful, stop and soak it up. In 2009 when your CRPS moves into your eyes and you start to lose your vision, you'll miss not seeing the ocean sparkle or your cat rolling about in the sun. When you get that Merit next year in your exams, don't cry. Hold onto the fact that you got 25 other Excellence's. Remember that it's OK to say you're not OK. So ask for help when you need it.

 

When you're diagnosed it's going to seem like the end of your life. But it's not. It's just the start of a new life you didn't imagine you'd be living. But trust in God, trust yourself and your own strength, and keep on keeping on. You'll be ok. Trust me.


Love,

Your Future Self.

 

~*IMPORTANT*~ ALL RSD ANGELS PLEASE READ!~

November 15, 2011

My dearest of RSD Angels.

 

It has come to our attention that yet again there is an abundance of argument, slander, gossip, and general hate against each other within the RSD Angel Community.

We wrote a note similar to this one back in Feb. of 2010 and again a couple years later we are having to write the same exact thing.

 When we made this Awareness Group and Fan Page we never would have believed we would hear that our wonderful Angels were fighting among themselves.

We deal with horrific p...


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Living unwell in a well world - Coming to terms with RSD - By Kylee Black

November 9, 2011
RSD spreads in up to 80 percent of cases with only 8 percent of these cases being full body or systemic. (Lucky me being in the 8% huh?? Jokes!)

I've been working and pondering over this for a while now...Well, it was more just thought, but I thought I'd share it none the less since I say I'm all about being real and honest and since this is my space for chatting and getting my thoughts and pondering's out I thought I would....... Hopefully it makes sense..

See this is a strange jou...
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"Excuse me? Can you Move?" A Hilarious List of Answers from a Disabled Person

November 8, 2011

So a while back my mom and I went to see a movie! This was a big deal for me and caused a great deal of pain. We found good seats in the first row with the railing in front so i could prop up my leg and I have an extra seat so I can stretch my leg out when it spasms. My mother was on my bad side a seat over and I had left a seat open and I put my RSD Leg up on it so it doesn't get hit. This man came in late and wanted mom to move over so he and his wife could sit down. I perked u...


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A Letter To Those That Don't Believe

November 8, 2011

Some members have asked me to re-post this.

I wrote this for a member and friend of mine because someone was harassing them because they didn't believe in RSD/CRPS.

You can use this and take out my experience and add in your own. Never let someone make your feel bad for something that you cannot help. Do not hate yourself just because you have RSD/CRPS, you are a wonderful person and deserve love.

If you need to talk to someone or feel lonely, and like no one understands please email us at...


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Review of "Choosing to Choose" by Dr. Tony Robbins

November 6, 2011
We do not usually do reviews on non-RSD/CRPS related books but this is one exception I could not pass up.

This book moved me to write a review and also tie it into RSD/CRPS as well. So please bear with me.

The title of the book is Choosing to Choose by Dr. Tony Robbins.
Everything we do boils down to choice. We choose to be happy, sad, angry, and everything in between. In fact in the Declaration of Independence it is mentioned twice.
The pursuit of happiness. People give up so much just so they ...
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RSD/CRPS Awareness Month

October 31, 2011

Hello RSD Angels!

Tuesday November 1st is the beginning of RSD/CRPS Awareness Month.

 

This month is very important.

 

You may be asking yourself why is it important and why does it matter?

Remember back when you first found out you had RSD?

For a lot of you it it probably went a little like this:

Doctor/Medical Professional: "You have RSD...."

You: RSD? What is the World is that?"

 

Imagine if just by spreading awareness this wouldn't happen to someone in the future. Imagine if they had found out day...


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SSD/SSI

July 9, 2011
Hi to all of you as I am going to do my best in giving you information on various insurance help and information.  Please feel free to ask questions and I will do my best to answer them and/or research it for you.  I worked many years as a Medical Insurance Specialist and for a variety of doctors including Pain Management which became my specialty as I was diagnosed with RSD in 1995.  I will start with some clarifications of different insurance and money help for the various companies....

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Glial Cells & Pain

May 25, 2011
What are Glial cells?

According to About.com "Glial cells are non-neural cells that perform "housekeeper" functions such as clearing out debris and excess materials. Glial cells support neurons by providing support and nutrition. There are several different types of glial cells: astrocytes, oligodendrocytes, microglia, ependymal cells, radial glial, satellite cells and schwann cells. It is estimated that there are 10 to 50 times more glial cells than there are neurons in the brain."

Ac...
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Calmare Treatments Questions Answered Straight from the Doctor's Mouth.

December 2, 2010
Recently we had the honor of meeting a doctor who is currently doing Calmare. Dr. Robert Chalmers was kind enough to take his time and answer some questions we had about the Treatment so we could make an educated decision on trying it.

We hope you enjoy!

Dr.Robert Chalmers

Q-First off, Other then the Spinal Cord Stimulator, what medical devices are incompatible with Calmare?
Any other implantable electric device such as Heart Pacemakers/Defibrillators or Interstim Device.
Q-How do you do Calmar...

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