Benzo Withdrawal

Many people believe that playing video games rots people’s brains. But what if playing video games – in moderation – can also help people to heal from brain injuries?

When I was going through physical withdrawal after coming off of clonazepam, I was so impaired that for many years, I could not read or write.

For a time, I couldn’t bear to look at any electronic screens. There was something about those blue screens that I just couldn’t tolerate. If you’ve ever watched a TV show on a broken television screen, that’s kind of how I experienced screens: the picture appeared pixilated and it was just too stressful for my poor, injured brain to handle.

At some point, someone suggested I start trying to “retrain my brain” to handle stress by playing simple video games. They suggested that I would be able to measure my distress tolerance by seeing how long I could play, that it would be a fun way to chart my healing process.

The game seemed easy enough to play: you simply try to get three or four or five of a one color candy in a row and try to blow up a certain number of translucent gels or collect nuts and cherries. No one was being shot at or injured, and – for some reason – the colors and shapes didn’t bother my eyes.

And while I’ve never been particularly interested in video games, I downloaded the app.

At first, I could barely play for even a minute. It was impossible for me to tolerate all the action on the screen; my eyes watered and I found my pulse rate would increase to the point of discomfort.

Instead of quitting though, I decided I would challenge myself to play every day for as long as I could.

I mean, if someone said playing video games helped him to heal, well… I was willing to give it a try.

After a while, I found I could last for one full life. Then two lives. Eventually, I was able to play long enough that I actually ran out of lives and had to wait to play another day.

Strange as it sounds, this is how I began to measure progress.

As I became more successful at the game – I could play longer with better results and less physical distress – I found a little place inside myself that reasoned that I was actually healing and that I could apply the same principle with everything.

There is something about the immediate and concrete feedback in video games (e.g., through points, coins, dead ends in puzzles) that served to reward my continual effort. In fact, research has shown that the extent to which individuals endorse an incremental versus entity theory of intelligence reliably predicts whether individuals in challenging circumstances will persist or give up, respectively (Dweck & Molden, 2005). These implicit theories of intelligence have implications for how failure is processed and dealt with.

Being immersed in Candy Crush taught me an essential basic lesson: persistence in the face of failure reaps rewards.

And my experiences of failure did not lead to anger, frustration, or sadness; instead, I responded to failures with excitement and interest and a motivation to improve my performance. When faced with failure, I was motivated to return to the task of winning, and I felt optimistic about reaching my goals.

Shortly after I started playing Candy Crush, I started painting.

At first my paintings were primitive – simple hearts and words. Over time, I tackled imaginary monsters, portraits of pets & people.

Six years later, my brain is nearly healed.

I still have some trouble with long-term planning and some memory loss between August 2013 and September 2015.

But I’m reading again.

Teaching again.

I’m painting & participating in art festivals.

I have friends again.

A social life.

Rituals.

And I still play Candy Crush every day.

(PS: I’m on Level 1197, in case anyone was wondering.)

What weird thing do you believe helped you to heal when going thru difficult circumstances?

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Last year at this time, I was nervously preparing to show my artwork at my very first art festival.

The event was to take place in The South Wedge, a funky/artsy neighborhood here in Rochester, New York.

I had no idea what my booth would look like or how my display was going to work.

I had no idea what I was doing.

Fast forward twelve months.

Today, I’m calmly preparing for the same show in the South Wedge this Saturday.

So it’s a mile marker, an anniversary of sorts, and – as such – it’s an opportunity to reflect.

When I started painting in 2014, the paintings were for myself.

When I was sick and mostly homebound, it NEVER occurred to me that the affirmations I used to get through benzodiazepine withdrawal would one day become a business, a way for me to connect with and help people who are going through their own invisible struggles.

Now that I have a little space from all of that, I see I was experiencing what Carl Jung refers to as the ‘Dark Night of the Soul’ – a period of spiritual desolation suffered during which time all sense of consolation is removed.

It has taken me over five years to get to where I am now.

Those of you who’ve been with me for a long time can probably see the changes better than even I can. I never knew I possessed the kind of strength necessary to get thru the kinds of crises I faced, and I can honestly say I am a stronger, a more empathetic person on the other side of this mess.

I’d like to take this opportunity to express my gratitude to everyone who has believed in me, supported me personally, financially, intellectually, and spiritually.

I want you know that in a real way, YOU helped save my life. When you bought my work, or shared it, you showed me you believed in me. You saw something in me that I didn’t see in myself.

To me, this is nothing short of a miracle.

And now it’s the holiday season.

The Season of Miracles.

Everyone is rushing around, furiously shopping for gifts to show their friends and family members how much they are loved.

And that’s awesome because presents are fun and fabulous and obviously I’m selling my work, which is weird and wonderful and I love everything about the festivity of the season.

And yet.

It’s important to remember it’s not about the stuff.

The greatest gift you can ever give to someone is your time & attention.

Check in with the people around you. Really check in.

Not via text message, but with a phone call. A meal.  A walk.

Sit down with your most cherished people and tell them you love them, you need them, and you support them.

Many of us feel we have to hide the fragile parts of ourselves, the places where we are insecure.

Ask questions.

Get curious about what people are really feeling, what they’re really going thru but not sharing.

It’s healthy.

It’s necessary.

And we’re not doing enough of it these days.

Just because someone looks at you and says ‘I’m fine,’ it doesn’t mean they’re fine.

XOXORASJ

I’ve always seen and heard things that other people didn’t. Early on, I could feel other people’s energy and emotions and see people with superimposed color trails ― white, blue, red, orange ― around them. Often, I heard people’s thoughts as clearly as if they’d said them out loud, which, in many cases, I believed they had. As a child, hearing people “say” things and then being told they had not said them was extremely confusing, and I was often accused of making up stories or telling fibs.

To be honest, it was scary to experience reality in a profoundly different way than everyone around me, and over time, I learned to be quiet about my visual and auditory “hallucinations” due to the negative feedback I received.

On August 14, 1999, during the traumatic delivery of my son, I had a near-death experience (NDE). I remember feeling myself levitate from the table. Hovering above my body, I looked down at myself — and the entire room — from about eight feet above. I remember seeing the top of the surgeon’s flowered paper bonnet, and peering down into one of those pink, plastic hospital-order basins. That’s a lot of blood, I thought to myself. I wonder whose blood that is. I also remember feeling like I was being pulled away from the scene below, almost as if I was on some kind of a conveyor belt. I didn’t experience a white light or the feeling of overwhelming love and connection the way many people do. Instead, I felt something malevolent tugging at me. It was scary, and I didn’t like it.

The next thing I knew, I was back inside my body, lying on my back in a room lit only by a dull blue light.

“Am I dead?” I said aloud, to no one in particular.

A nurse reassured me I was not dead at all, and then she left me, ostensibly to locate my husband who was somewhere in the hospital.

Lying in my hospital bed, I found I could hear and connect with the consciousness of others whose physical bodies had died in that space. I felt these agitated spirits swirling around me. Many were angry about being trapped in that room, and they shouted at me to listen to them.

From that moment on, the voices followed me everywhere. It was hard to focus on nursing my newborn son with angry spirits shouting at me. And it was scary not to have anyone to talk to about what I was experiencing. The only way I could deal with the voices was to ignore them, and that is what I did.

Or what I tried to do, anyway.

I stopped talking about what I was hearing, and I tried to exist on one level of consciousness, the way everyone around me expected me to exist.

That’s when the insomnia started.

It was awful.

At night, I’d get out of bed and press my ear against the brick chimney in the bedroom I shared with my husband. “Do you hear that?” I’d ask him night after night. “Do you hear people talking?” But Mark never heard anything and, after a while, he got upset with me for waking him up so frequently.

The rest is a story that many of you have heard.

Busy with a newborn all day and tormented by voices all night, I wound up in a psychiatrist’s office, where I was poly-drugged, first with SSRIs – Celexa, Zoloft, Prozac; then with the anticonvulsant, Lamictal. Eventually, I was given Klonopin, a powerful anti-seizure medication. After seven years of dutifully listening to “experts” and taking the medication exactly as prescribed, I learned Klonopin is not supposed to be taken long-term, that it has many dangerous side effects, and I slowly weaned off of it with the assistance of a specialist. Unfortunately, this wean was a disaster. I endured an horrifying iatrogenic injury which left me disabled and debilitated for many years.

While healing from that trauma, my world blew open again. The voices returned, and this time I could see things, too. 

It’s taken me a long time to figure out what brought me to meds in the first place & I’m finally crystal clear on it.

Today, I own all of it.

I’m an artist and a writer and a teacher and a mother.

I’ve survived rape and withdrawal.

And yes, I’m a psychic medium.

Instead of being afraid of the visions and the voices, I now embrace them. Being a medium is like being a translator, decoding a universal emotional language into English ― and at times, hearing words and phrases, feeling impressions of things or watching little movie clips. It is a receiving of information rather than a retrieving of it.

Last weekend, I had the opportunity to work with a modern-day healer who did a SIX-HOUR cleaning with me, during which time he sealed up a portal through which malevolent energy was being transmitted. He confirmed that I am plugged into something powerful. (Not that I needed his validation.)

Working with CD was transformative. All my broken soul-pieces have been integrated. I no longer hear angry voices. I’m alert & aware & whole & so very grateful.

Three months short of five years, I am here.

I am healed.

And I have a new understanding about myself and the world.

Western culture teaches us to seek medical help when we are sick, to visit the dentist to get our teeth un-mucked, and we think nothing of hiring specialists to assist us with personal hygiene, legal, financial and medical matters. We hire handymen to help us with things that break in our homes, landscapers to weed our gardens and plumbers to unclog our drains.

And yet, somehow we remain resistant to the idea that things can get clogged up in our heads, too. Old emotional pain can build up in just the same way that a drain can become clogged. We aren’t always great about working these things through on our own – and, in fact, sometimes we need professional help. For some people, talk therapy is enough. For others of us, with more complex trauma, we need to call in the big guns.

And guess what? There are talented practitioners who know how to unclog gunked up emotional pipes, too.

Clearing my emotional mess has allowed me to see my psychic abilities as a blessing rather than a curse. Doing this work requires a willingness to deconstruct one’s life & figure out where you got off your path. It is possible to put yourself back together, but only YOU can do it. As painful as it may be, looking at your life is an opportunity to rebuild.

If you’re interested in learning more about my experience and/or would like to meet with this amazing healer, feel free to contact me and I’ll put you in touch.

Do you believe there there’s another dimension beyond the one we see with our eyes? Or is this waaaay too woo-woo for you? Leave a comment!

I’ve been consulting with people in benzodiazepine withdrawal for nearly a year now. It’s something I do quietly, privately. Right now, I have four or five people who call me regularly for emotional support. Each of them shares a similar story.

They were going through a difficult time in their lives – usually involving profound loss or grief – when they started to experience somatic symptoms. Rather than being sent to therapy to discuss their life experiences, these individuals were sent down the psychiatry route.

After a short meeting with a psychiatrist, their behavior was determined to be pathological or disordered, and they were told to take was medication which would help alleviate their symptoms.

In each case, they were prescribed benzodiazepines which, they were assured, would work for them like magic. And for a time, they did. However, just like any drug, these drugs lose their efficacy and individuals find themselves needing to take more to achieve the same results. Some people become tolerant more quickly than others, for whom reaching tolerance may take years.

It doesn’t matter.

The end result is the same.

Once you hit tolerance, you’re in trouble because you can’t stay on the drug, but you cannot get off without scads of horrifying side effects.

Today, I received this message via email (shared with permission):

I had a severe seizure in the late afternoon yesterday. My eyes spasmed and blinked uncontrollably. My mouth twisted and stuck in a contorted position. As my jaw moved with violent force from left to right, my bottom lip moved up and down up and down. I felt dizzy and sick. My eyebrows went up and down, my neck convulsed, along with my lips. My teeth chattered nonstop. I feel violated by my own brain and body.

This has been going on since for over a year!

I am hopeless and in despair.

My primary doctor has destroyed my life and murdered me.

I am suicidal & asked for a closed casket.

I don’t think I will make it. The stress is slowly killing me.

I don’t know what to do.

If you are having an adverse reaction to a drug that can’t be stopped, how do you get off of it? How?

This woman is a warrior.

Her brain is zapping her; her body is betraying her. She cannot walk or talk or watch television or listen to music. She cannot enjoy a casual lunch with a girlfriend or go to the beach. She’s homebound and isolated, having to endure thousands of horrifying symptoms.

The fact that people are continuing to suffer is unacceptable.

Pharmaceutical companies have known about the dangers of benzodiazepines since the 1970s and ill-informed physicians continue to prescribe benzodiazepines longterm without understanding their efficacy, and patients continue to be harmed.

Up until now, I’ve used my art work and my blog as vehicles to bring attention to this travesty.

Moving forward, I’m offering education and individual case consulting for medical personnel.

I’d like to visit medical schools and speak to future doctors about my experience and the experience of so many people who have been harmed by psychiatrists who have mistakenly deemed certain drugs as “safe” and “tried and true.”

For more information on how I can help you better help you, your loved ones, or your patients, please contact me HERE.

Last night, I shared with a new friend how someone hurt my heart this weekend.

I explained how I’d been dancing on the beach, basking in the sunrise, grateful for the opportunity to plant my feet firmly in the sand and be so close to the ocean. “I selected the spot carefully,” I said. “Off to the left of the only sunbather on the beach.”

I told him how I’d popped in my headphones, so I could tune out the world and tune into my body.

Fifty months ago, in the throes of acute benzodiazepine withdrawal, my body was in continuous pain. Unable to walk or talk, or take care of any of my most basic needs, I was confined indoors (mostly) for over a year.

I never thought I’d heal.

So there I am, quietly expressing gratitude to the Universe when this woman ~ this stranger ~ tells me to move myself down the beach. She tells me I’m distracting her.

“Your ass is in my face,” she says.

Obviously, she didn’t know about what I’d been through ~ but it felt terrible to be shamed for feeling being myself, for expressing my joy.

“Aw babe,” my friend said. “Don’t cry. All that’s over now.”

The rabbis teach that to truly know another person, we must not know only their pleasures and their successes but also the sorrows they bear.

Burying my face in my friend’s shoulder, he stroked my back. “If you need to cry, it’s okay,” he said. “Cry long and hard.”

The moment he gave me permission to share my sadness, my burden was cut in half, and I didn’t feel like crying any more.

I don’t know if he realizes the gift he gave me, but I do know these tiny interactions are what life is all about.

And I believe it is our charge to remember to do that for someone else every day.

Be on the lookout for someone to help today.

Who/what helps you feel better when you’re feeling low? 

Four years ago, after weaning off a powerful anti-anxiety medication, I had a seizure in my kitchen.

Lying on my back, I stared up at the ceiling, baffled by what was happening to me.

For months, I suffered hundreds of physical and emotional symptoms that kept me locked in a state of constant terror.

No one knew how to help me.

In February of 2014, I flew out to Arizona, to The Meadows of Wickenburg, a rehabilitation facility where I watched shattered people heal…while I remained terribly ill.

No matter what I did, my brain remained scrambled.

I had absolutely no evidence that I’d ever heal.

While in rehab, I spent a lot of time in the art room. I painted a tree and a house and a bird. A boy told me my picture was pretty, so I gave it to him.

Back in Rochester, I kept painting: hearts & animals, monsters & sad-faced girls.

My paintings got bigger and bigger. I created The State of Undress Project and connected with dozens of people, exchanging life stories and forging friendships.

Three years have passed, and I just had my very first art opening. People I’d previously only “known” online showed up and introduce themselves in person. A childhood friend I hadn’t seen in over 30 years drove over an hour to be there. My parents were there, old friends and new, and I felt loved and supported by everyone who was in attendance.

Sitting here this morning, I received payment for a commissioned painting I have not yet painted. People are buying my work. They tell me they like my goofy videos. I have travel plans to look forward to. Work plans. Artist friends who generously answer my newbie questions. Patrons who are actively collecting my paintings, if you can believe it. And yesterday, a new artist friend asked me for advice.

Recently, after completing a whimsical painting of a funny looking critter, my cousin commented that he reminded her of The Velveteen Rabbit, a book I’d many years before. Upon revisiting it, I see what she means. The book offers many lovely themes, but the one that had the most resonance for me is its reminder that It’s Important to be Real.

(Rabbit doesn’t need the garden rabbits to tell him he’s Real, and he doesn’t need the Boy to keep loving him in order to stay that way. Once he recognizes his own Realness, the Rabbit has the confidence to be his own person.)

It sounds like it’s easy, this ‘being real’ business.

But it isn’t.

And I see it now, how I’d fallen off my path.

How I’d stopped creating, stopped loving, stopped trusting the voices that guide me.

How I was surviving but not thriving.

How I was spending my days living the way others wanted me to live.

A way that wasn’t my way.

At all.

How I’d stopped being real.

The Velveteen Rabbit also reminded me to remember the people who have helped me.

(Even after he’s Real and living with the garden rabbits, the Rabbit still comes back to visit the Boy whose love gave him life. He could have easily forgotten the Boy, living in Rabbit-land, but he doesn’t. The Velveteen Rabbit teaches us to never forget the people who made us who we are, even when we’re living in two different worlds.

So I’m thanking all of you: my parents, my family, my friends ~ new and old ~ my patrons, my followers… (Even those of you who have hurt me ~ and you know who you are ~ you taught me something. I may be a slow learner, but I’ve definitely learned from you. Better late than never, eh?

It’s time to stop focusing on the past.

Why? Because it’s happening.

I’m becoming real: a full-time creative who gets to express herself in color and words.

It’s a dream come true.

Tweet me at @rasjacobson and follow me on Facebook at rasjacobson originals.

Here is the official press release which I’m sending out to anyone and everyone here in Rochester. If anyone has contacts at the New York Times, the LA Times, or the Chicago Tribune, I sure would like to get some national exposure. This is not about selling paintings. It’s about raising awareness about the dangers of psychiatric drugs. So many people are suffering in silence right this very moment, their voices unheard. I’m grateful to be able to use my art as a vehicle to share my story, which is the story for so many of us.

• • •

ARTIST TO DISPLAY WORKS IN “THE STATE OF UNDRESS” PROJECT AT WHITMAN WORKS COMPANY OPENING SEPTEMBER 16, 2017

Renée Schuls-Jacobson’s Art Represents her Healing Journey

Toward Mental Wellness & the Struggle of Others With Invisible Challenges

 August 1, 2017 – Rochester, NY – Whitman Works Company in Penfield, New York is pleased to present “THE STATE OF UNDRESS PROJECT: THE HEALING OF RASJACOBSON”. The exhibit’s opening will take place September 16^th with a reception from 6:00-9:00 p.m. at 1826 Penfield Road, Penfield, NY. This exhibit represents Renée Schuls-Jacobson’s on-going healing journey after becoming disabled as a result of improper treatment and withdrawal from a powerful anti-anxiety medication.

During her illness, Jacobson realized there was a profound disconnection between how she looked and how she felt. While speaking with others who were willing to admit that they, too, were struggling to overcome invisible obstacles of their own, she became interested in the tension between outward appearance and internal reality, creating impressionistic portraits based on the stories people shared.

As a result, Jacobson’s art reflects this duality, and her colorful crowd of characters is enigmatic. Despite her use of a cheerful color palette, her subjects often appear deep in thought, even a little sad.

Jacobson hopes her artwork (and the accompanying non-fiction narratives) will allow people to speak more freely about their own insecurities and invisible disabilities which are, to some degree, present in all of us. She also seeks to educate the public about the dangers associated with psychotropic drugs, like the one she was prescribed.

The artist will be in residence for the opening of the exhibit on September 16, 2017 from 6 PM to 9 PM. The show will continue in the Whitman Works Company Gallery through October 7th. Regular gallery hours are Tuesday through Saturday, 11 AM – 6 PM. For additional information please visit the gallery shop in person at the address above or online at www.whitmanworks.com.

 

 

I’m going to be one of those artists who actually gets some love while I’m still ALIVE!

The opening is set for Saturday, September 16, 2017 between 6-9PM. at Whitman Works Gallery in Penfield, New York.

A small reception will be held, and – if I know me – there will be much weeping and hugging.

My greatest wish is that every person who is currently suffering the debilitating effects of benzodiazepeine withdrawal will see this and continue to hold on with the understanding that, eventually, the suffering ends. It ends. Healing is real, and it is proof that the Universe is truly looking out for each and every one of us.

I’m sharing the formal press release information here, in hopes that you will save the date on your calendars. I hope you will schedule me into your fall plans.

I am truly grateful for your support as I continue to rebuild my life.

•••

Whitman Works Company in Penfield, New York is pleased to present “THE STATE OF UNDRESS: THE HEALING OF RASJACOBSON”. This exhibit represents Renée Schuls-Jacobson’s on-going journey to mental health after becoming disabled as a result of improper treatment and withdrawal from a powerful anti-anxiety medication.

During her illness, Renée realized there was a profound disconnection between how she looked and how she felt. In speaking with others who admitted that they, too, were struggling to overcome invisible obstacles of their own, she became interested in the tension between outward appearance and internal reality, creating impressionistic portraits based on the stories people shared.

Renee’s art reflects the duality between appearance and reality. Her colorful crowd of characters is enigmatic. Despite her use of a cheerful color palette, her subjects often appear to be deep in thought, even a little sad. For the full story, read her bio at https://www.rasjacobson.store.

The artist will be in residence for the opening of the exhibit on September 16, 2017 from 6 PM to 9 PM. The show will continue in the Whitman Works Company Gallery through October 7th.

Regular gallery hours are Tuesday through Saturday, 11 AM – 6 PM. For additional information please visit the gallery shop in person or online.

More information about the paintings is being made available on My Patreon Page where, for a minimum of $1 per month, you can read my entire story, as I write it, and receive special content that no one else can see.

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

The first night in my apartment building, the upstairs’ neighbor’s toilet clogged and overflowed. Bilgy water rained down from the ceiling, soaking my new bathroom mat. I’m not a squeamish person. I can touch spiders and snakes. I don’t mind getting dirty. But I was completely unprepared for brown water dripping on my head. I didn’t know what to do or who to call.

At the time, I didn’t even own a mop.

That night, I stayed up very late with a dear friend who’d come over to help me unpack. Together, Sara and I furiously unboxed my housewares, strategically placing what few pots and pans we could find all over the bathroom.

After Sara went home, I climbed into bed and wept.

For hours.

The next day, I packed until dinnertime. After I’d washed the dishes, I decided to hang up some artwork. It was early, and, outside my windows, the sky was still light. If I had to guess, I’d say I hung up three paintings.

So maybe 15 whacks with a hammer.

Maybe 20.

The next morning, I found a handwritten note that someone had slid under my door.

“Too loud!!!” the note read in cursive. “Do not make noise after 5PM!!!”

I stewed for a little while, wondering which neighbor had left me the note. Eventually, I tossed the note in the trash and decided to venture out. The wait for the elevator took forever. When the doors opened, I stepped into the lobby area. It’s a formal space, and even after two years, it feels more like a hotel than anywhere I’d ever call home.

The doorman pointed at me. “You’re the new girl everyone is complaining about,” he said. “The loud one.” 

It. Was. Awesome.

(And by awesome, I mean it sucked.)

It took me a year to get brave enough to buy a stereo speaker and actually play some music. Because, seriously, screw them. I’m not going to bed at 8PM.

Since my first day, I’ve received more notes. Apparently, I don’t empty the lint trap in the dryer well enough. And while I enjoy having a diverse group of friends, it seems some folks don’t like “the colored girls” coming round.

Another year has passed, and I’m still rebuilding. Apartment living for me is a lot like solitary confinement. The nature of the work I do (writing and painting) is isolating. I spend a lot of time in other people’s backyards, gardening, helping to decorate their patios. I’m still looking for a house, a community, people with whom to share a heart connection. I have Sara, thank goodness, and my parents, and the reality is that very few people check in on me with any regularity. When I need a ride to the airport, I call a taxi.

What does my life look like now? I get up, shower, make my bed, eat a little breakfast, lunch and dinner. Somewhere in there, I paint, write, do some yoga. I take long walks and learn something new every single day. (Thank goodness for NPR podcasts.) I help one person in benzo withdrawal every day. I clean, do my laundry, and try to connect with another human being in real life.

Weekends are hard.

I spend time going to garage sales in search of abandoned picture frames and Mason jars. I never had a thing for glass before I moved into an apartment, but I especially like the ones with rusty metal lids. I relate to their weatheredness, their fragility.

So here I am. It’s early, and I’ve run thru my entire bag of tricks. I’ve painted and shopped. Walked and cleaned. Visited with friends. Got a carwash. Made dinner.

I don’t cry every night anymore, but I’m still not smiling as much as I’d like.

I’m on mission to find a new home. My son will graduate from high school next Saturday. He’s ready to fly, and I’m so excited for him. Unlike my son, I don’t feel quite ready to launch. I need to do a bit more research, poke around and decide where I want to start the next chapter of my life.

A triangular girl, all I know is that living in a rectangle is not for me.

If you were starting over, where would you go and why? Got any suggestions?

 

 

This photo was taken on July 30, 2013.

I was in Florida with my (then) husband.

We were out to dinner with his cousin when the world tipped sideways.

This is not an exaggeration.

The world suddenly shifted, and it would not be right again for 36 months….

• • •

So many people have been reaching out to me, asking for help. They want to know what my life was like before benzos, how much I was taking, for how long, how I weaned, how fast, what my withdrawal was like, how long the symptoms lasted, and what my life is like now.

I can only speak to so many people a day, and it’s never enough.

And that is why I decided do something completely different.

I’m sharing the full story of my battle with benzodiazepines at Patreon.

And you get to read the story as I’m writing it.

It’s taken me nearly 4 years to kick benzos’ ass!

You will too!

• • •

If you’d like to read more, contribute to MY PATREON PAGE at https://www.patreon.com/rasjacobson. For $1 per month, you can read all about my story. I will post relevant art, writing & videos at least 4 times a month.

Please help me share my story!

XOXO