Friday, April 11, 2014
Personal Fundraising Tips
Personal
Fundraising Tips
Many if not most people with Lyme Disease are, unfortunately, in debt. Even if you have disability benefits, the costs of Lyme Disease and all the adjunct therapies often FAR exceed the amount of money coming in from disability or in savings accounts. Personal fund-raising for medical bills is very commonplace nowadays, and something I did on a few occasions to help offset my huge medical debt. Since I also have a lot of experience with nonprofits and fundraising, as well as advising friends on personal medical fundraisers, I thought I would share some tips here.
Remember, there is no shame in asking for help. It is often the most courageous thing you can do.
Personal Fundraising Websites: these websites now make it very easy
for you to post your story, pictures, and a direct way to contribute to your
cause.
· Great
example on giveforward.com of a Lyme patient who raised almost $7,000: https://www.giveforward.com/fundraiser/tzq3/kate-s-return-to-wellness.
Fundrazr.com
- an easy way to
explain your story briefly, post on Facebook, and have it spread virally
through friends and friends of your friends. Have friends post something about
their connection to you, "this is my dear friend Sharon who…" on
their wall.
In-person
fundraiser - this
takes a lot of friends and work, but I did an event with a silent auction,
donated bar, etc. I had a dozen friends help me out with this, and we secured silent auction donations, as well as donated venue space and music. It takes some leg work but it is very possible (and really fun for those involved). If you are interested in this, let me know and I can give you
some advice. You can see the invite that was made by a co-worker of a friend below for my fundraiser, called "Monapalooza."
You might
want to make an easy blog page on blogger or wordpress. Simple, brief description, even pics
of you healthy or sick, whatever you want. A BRIEF story of why you need
financial help (people don't understand that Lyme treatments are hardly ever
covered). Then add a Paypal widget/button, and people can donate right there.
You can send this via email to friends and also have it on FB.
Remember, everyone has a different
comfort level with personal fundraisers. People with Lyme Disease are all in a boat where they should not be ashamed to
ask for HELP when it's needed. My advice is to make your personal fundraising page as it fits with how you
feel about asking for donations and spread the word!
This type of fundraising is commonplace in the
US now as so many people are ill and without medical coverage (or with it and
still in debt). Giveforward.com, for instance has raised $94 million for people
online for medical expenses (that is people self-fundraising for medical bills).
If people do not believe in Lyme Disease or do not support you emotionally, it is probably best not to send them the fundraiser information. However, you may be surprised how people you may not even know want to help you. In my case, for instance, my friends generously donated to my cause as well as many complete strangers (friends of friends or people who heard about my fundraiser by word of mouth). I was incredibly grateful and made sure to express this gratitude countless times. It was no easy feat to swallow my pride and ask for not just physical and emotional support, but financial support too.
*If you have not applied for Long Term Disability benefits (LTD) from your former employer or Social Security Disability Income (SSDI) from the government, you should do so as soon as possible. I am happy to give you some free advice on disability benefits via email, and also offer some other information about a system I designed myself with a colleague from law school while I was very disabled from Lyme Disease to help win my disability benefits quickly and easily.
Thursday, January 23, 2014
What got me better? The hidden power of thoughts and intent. Dr Emoto's Experiments on Thoughts and Health
A
lot of what I have alluded to in this blog are the actual treatments I did to
get better, supplements that helped me, adjunct holistic therapies, diet,
and detox tips. One thing I have touched on, only slightly, is the emotional
aspect of Lyme.
I
want to talk more about that. Many people ask me "what do you attribute to
you most getting better?" If I had to tell you ONE essential thing, I would say it
was…….
…….
the huge emotional shift I underwent during Lyme: the breaking down of my
old unhealthy patterns and relationships, the getting to the core of what got
me to being so sick that I was bedridden for more years than I care to
remember, the unresolved emotional blocks and traumas from childhood (my being a Type A
overachiever, always helping others before myself until my downfall, validating
my self-worth unknowingly on others' approval, among a variety of other
things!), the change in my MINDSET, AND the ability to see the
experience a blessing in disguise. Yes, I just said that last part.
Out loud.
Lyme transformed me more than I ever thought possible, because I allowed myself to experience the raw darkness, and then allowed myself to experience the great light that came from that. The transformation really changed my way of seeing the world, for the better.
REAL RAW UNPLEASANT FEELINGS
I
don't expect anyone to be jumping with joy going through the roller
coaster of emotional and physical pain related to Lyme Disease. I was
angry, depressed, horribly frightened, confused, hopeless, jealous, pissed off
for years when I was sick. Then, I slowly came to this new place - where I was able to HEAL
the unresolved emotional and spiritual blocks - while doing my antibiotics, my IVs, my holistic treatments, etc. Every day was not butterflies
and rainbows, but more and more moments I was able to see through the
darkness. More often than not, a 10 minute walk felt like I ran a triathlon. I was able to
APPRECIATE the small things in life - like stopping to stare at a flower (because I had nothing else to do with my time and couldn't really walk very far). And some moments DID seem like butterflies
and rainbows even in the midst of being disabled! Then, of course, anger, and sadness, and fear returned. But they did so in MUCH smaller doses.
I
worked with a therapist, of course, to help me just make sense of the fact that
my life was akin to a sedated vegetable. But, after a while, it did
not help to talk about my problems repeatedly. I was sick, VERY
sick. I could not function. I needed someone to spoon feed me at
times, and sometimes I crawled to the bathroom. My life as I knew it as a
20-something unraveled to pieces scattered SO far and SO wide that I couldn't
even see any resemblance of who I was. Talking about it over and over was not helping me, personally (I am not advocating for you to stop seeing a therapist if you are seeing one, only relaying my personal experience).
SLOW
BUT STEADY TRANSFORMATION and COMING OUT OF LYME
So
I stopped working with my therapist (who was amazing but whose help I no longer found useful), and I went INWARD. I had the help of another person (feel free to email me if
interested in his name). I read and listened all the spiritual books & CDs I could: Eckhart
Tolle, Wayne Dyer, Louise Hay, Bruce Lipton. I kept putting this information in
my brain even on days when I didn't feel any difference from it. Even on days when I wanted to put it off and go under the bed (if I could make it that far) and cry for hours. BUT,
over time, my subconscious brain PICKED UP the positive messages that I needed to
hear and see (I also had inspirational quotes ALL over my room). I listened to people like Bruce Lipton and others, who talked
about how much of our own beliefs about ourselves go into our health. I know we
all hear this, but do you know there is scientific proof of this?? Read below...
Dr.
EMOTO's EXPERIMENTS ON THOUGHTS AND HEALTH
Dr.
Masaru Emoto, a researcher and alternative healer from Japan, is
the author of the famous "Hidden Messages in Water"
book. This book has the potential to profoundly transform your world
view. Using high-speed photography, Dr. Masaru Emoto discovered that
crystals formed in frozen water reveal changes when specific, concentrated
thoughts are directed toward them. He found that water from clear springs and water
that has been exposed to LOVING WORDS shows brilliant, complex, and colorful
snowflake patterns. In contrast, water exposed to NEGATIVE thoughts,
forms incomplete, asymmetrical patterns with dull colors. The implications
of this research create a new awareness of how we can positively impact the
earth and our personal health. Given that humans are comprised of at
least 60% water, his discovery has far reaching implications on the impact of negative thoughts and words (not just from your own mind, but from anyone else as well). So, make sure you are surrounding yourself with the right kind of people.
Dr. Emoto showed the world a good deal of evidence of the magic of POSITIVE THINKING
again, below:
The rice
experiment is another famous Emoto demonstration of the power of
negative thinking (and conversely, the power of positive thinking.) Dr Emoto
placed portions of cooked rice into two containers. On one container he
wrote “thank you” and on the other “you fool.” He then instructed school
children to say the labels on the jars out loud everyday when they passed them
by. After 30 days, the rice in the container with positive thoughts had
barely changed, while the other was moldy and rotten. Check it out here.
I
am not here to tell you to ignore your painful feelings. Lyme is a traumatic
disease. In my opinion, it is the most traumatic disease on the planet. It is
incomprehensible. Experience your raw feelings, indeed the only way out of them is
through. Life will not be all rainbows and butterflies. But go within yourself and turn the negative energy that may be
lingering inside into something positive for YOURSELF, and slowly, over
time, you will notice a shift. By all means, ask for help (from friends,
family, religious or spiritual community, some of the authors above, meditation
class, email me if you need other ideas at monamorphosis at gmail dot com).
• I completely changed my
relationship to the outside world and my family (that latter relationships was
very toxic).
very toxic).
• I learned to say NO and
take care of myself first. Then, and only then, could I take care of
others.
• I expressed my anger, fear, sadness in the
proper outlets, or journaled about it, and then worked on
forgiveness, and other ways to clear through those emotions.
forgiveness, and other ways to clear through those emotions.
• I stopped blaming
circumstances or people for why I could not feel better or be happy. I was able to be
happy DESPITE feeling ill. It was a pretty cool thing to experience, actually. And once you are able to be happy despite the circumstances of your body through Lyme, you are pretty much able to handle anything.
• I started to do everything
possible to make sure I BELIEVED I could get better, with positive
thoughts and intentions surrounding me.
thoughts and intentions surrounding me.
"Suffice
It to say that whenever you want to improve anything in your life, there's only
one place to look: inside you. When you look, do it with love."
TIPS for implementing this in your life
1. Practice Gratitude on a
DAILY basis. Some
days I could think of nothing to be grateful for because I was
so miserable. Often I said easy things like: "I am grateful for having 2 legs to walk, a
roof over my head, my friends to support me." Anything to remind you of
what you DO have. I made a gratitude bowl and wrote on 5 little pieces
of paper what I was grateful for at the end of each day.
2. Put inspirational, positive
things and people around you. I printed up inspiring quotes and put them on my walls. I made a
collage (my mom helped me) of pictures of me when I was super healthy and happy
and I looked at it every day, to keep visualizing myself being that
healthy again. If you feel there are no inspirational people around you, keep
practicing gratitude for those who do provide to you, and more and more of
these people will show up in your life.
3. Work through emotional
blocks. Most
human beings have a lot to go through emotionally, but Lyme patients have
a whole added level of insane things to process. See a therapist, counselor, healer, talk to a friend, write a journal, do anything to make sure you have a way and place to
safely express your feelings.
4. Meditate. I cannot tell you how
much this has benefited me. If you are just starting, or feel reluctant to
start, try the free app called "HeadSpace." It guides you through
SIMPLE, easy 10 minute meditations for 10 days in a row.
5. Create joy with simple things! The easiest way to raise your vibration is to do anything, NO MATTER HOW small, that will make you feel better. Even if you have to cheat on your gluten-free, sugar-free, dairy-free, diet to sneak in a piece of chocolate pie (if it won't destroy your stomach), do it. Take a bubble bath with lavender oil. Watch a funny movie. Treat yourself to a massage or pedicure. Watch re-runs of your favorite show. Watch you tubes of puppies or orangutans or airplanes or whatever makes you SMILE. Invite a friend over that you know can make you laugh. Joy is so essential for human beings, and it is so rarely experienced by Lyme patients, so remind yourself you are doing an amazing job battling this disease, and give yourself something that soothes your senses.
Still
working on the ebooks and guides on my protocols, detox, diet, etc. if you want
to be on my mailing list, please send your email to monamorphosis at gmail dot com. I
will send updates there as to when the ebooks are done, and also migrate
content and information for Lyme patients over to private non-spam
newsletters.
Saturday, January 18, 2014
Why is the CDC Trying to Block an Accurate Lyme Disease Test?
Another disheartening article about how the CDC and mainstream medical community may be trying to block accurate testing and diagnosis of Lyme Disease. Shameful is an understatement.
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