Don’t Ever Give Up

Hello my friends!

I know it has been quite some time since I have written in this space.  I have been busy starting my art business, Zarit Glassworks (shameless plug, I know.) and trying to get my migraines under control.  I have also been hard at work with mental health advocacy.  I have never stopped that.  It has and always will be a passion of mine.  I may take a break from time to time as needed, but I always come back.

Well, today, I and a few others met with two of  Senator Murray’s staff members for two hours.  We were able to share our stories, our experiences, our concerns about mental health care reform, our concerns about current/future policies.  It was wonderful!  It was an incredible opportunity.  It was something I never thought would be possible on my own without the backing of a large organization.  I’ve never made it a secret that I parted ways with AFSP.  However, I harbor no ill feelings toward them at all.  We may have a difference of opinions, but without them I would not have the voice I have now nor the advocacy skills I possess.   In fact, I even advocated for their Centers of Excellence today because that is one of their lobbying points that I happen to agree with.  I still direct people to them for support and I even help people with fundraising for them.

Anyway, I’m not sure what the outcome will be of today’s meeting.  One thing I do know for sure, it felt great to have the ear of the highest ranking member of the senate.  Even if nothing comes of today’s meeting, I can rest easy now.  I know in my heart that I have truly done my best.  I can now get off my soap box about HR 2646.  I believe our HIPPA rights will be fine.  I know CIT for first responders is going to be alright.  I know Congress has been educated by people living with mental illness.  I know I have been heard.  What more could I ask for?

I can’t control what Congress will or won’t pass.  All I can do is try to educate people and hope it makes a difference.  For those of you that sent me your vignettes in the past, they made it to Congress.  They were read.  They would like more.  Please feel free to send me more.  I am happy to pass them along.  My email is bravelybipolar@gmail.com.  Just keep it to one page in length.

I will try to write more often.

Thank you for your support and thank you for reading.

Advocacy in Action

I blogged numerous times about my advocacy efforts.  I have complained about how hard it has been to go out on my own since leaving a national nonprofit.  Well, today I am here to tell you that it can be done!  One person can do it.  It takes a lot of time, patience (which I really do not have) and determination (I do have that).

If you will recall, I made several posts asking for you to send me your experiences living with mental illness so I share them with Congress.  I had a grand plan of having a round table discussion with a few members.  Well, the round table discussion did not happen.  What did happen was this.  I began calling each of my State members one by one for meetings.  I was only able to get one meeting, not even with my one Rep.  To be fair, that one was my fault.  I had already met with him personally and they wanted me to meet with a staffer.  I felt offended.  I have no idea why.  I’ll chalk that one up to Bipolar.  Any way, the one I met with really listened.  This has turned out to be a great working relationship with his local staffer. She has kept me informed on legislation and helped me get a meeting with one of my Senators…well the legislative aide.  And here is the rest of that story:

I had a meeting with my Senator’s legislative aide and it was absolutely wonderful. I told her of my concerns about Rep. Murphy’s bill (HR 2646). You know that fact that it will violate HIPAA laws and that of the 5 committees it forms, only one has a person with a mental illness on it. Oh, and that committee has NO power to do anything! Also, he’s getting rid of SAMSAH (I know the H is the wrong spot). I also talked to her about the partner bill in the senate (S.2680). The main problem with that one: HIPAA violations. She really didn’t think Sen. Murray would let anything pass with HIPAA violations. She also agreed with me that HIPAA violations would not prevent another Sandy Hook as Rep. Murphy is hoping. I felt so reassured. She actually agreed w/ me the correct statistic that people w/mental illness account for 1% of the violence nation-wide. Finally, someone who understands!

Anyway, as we left it, I will be asked to speak to committees and both of our Senators’ about living with mental illness. Now, will any of this change Murphy’s bill? I don’t know, but it might help change that senate bill. At least my voice, and others because I brought those stories I asked for months ago, were finally heard.

All in all, a good day. I even talked about the plight of Bullseye because art is a form of therapy. I gave her my letter that went to Oregon rep. as well. Not bad for being with a nation nonprofit anymore. I’m finally able to speak freely about what it is really important….preventing suicide and helping people like me, people living day in and day out with an illness of the brain

The moral of my story is this: Keep trying.  You will be heard.  My State senator is the highest ranking member of the senate and now our letters are firmly in her hands.  Our voices have been heard.  What will come of this?  I don’t know.  All I know is this:  I didn’t give up even when I so desperately wanted to.  So to all of you, please don’t give up either.  Keep writing your members of Congress.  I will help you if you need help. I will give you guidelines for writing an advocate letter, timeline for sending and re-sending letters and help with phone/in-person meetings.  Just don’t give up.  The more of us that do this, the louder our collective voice will be.

CALL TO ACTION

This is a modified letter I’m sending to all of Oregon’s congressional leaders and State leaders.  I would urge you to do something similar if any of you are glass artists or have a glass producer in your home state.  It’s too late for WA, but not for the others.  I won’t give up.  I’m doing everything I can and so are others to save an industry.  I hope you’ll join me.

I am the owner of Mind and Soul Art.  I am not an official business.  I create art for the sole purpose of raising funds for nonprofits. You see, I live with Bipolar Disorder and Anxiety Disorder.  Glass art is a way for me to manage my ongoing symptoms of my illnesses.  Sometimes it is the only way as modern medicine has not always worked for me.  Suicide rates continue to rise across the nation and I refuse to become another one of those statistics.  I am down to three medicines left that might work for me.  The only thing that has consistently worked is my glass art.

This is why I travel over 4 hours from Port Angeles, WA to Portland, OR for the classes that Bullseye provides.  I soak up their knowledge like a sponge.  While in Portland, I stay in a local hotel for several nights.  I eat in local restaurants.  I purchase from local shops.  I spend money in your state as do other people who come from out of State for Bullseye’s educational art classes.  Bullseye is not an island unto itself.  It is a vital part of Oregon.  It is also a vital part of my life.  Without their glass, their classes, their very kind and understanding employees, I wouldn’t be able to create.  If I can’t create, I wouldn’t have an outlet for the constant battles of a Bipolar mind.

Spectrum Glass will be closing its doors after 40 years because they simply can’t bear the unknown costs of what’s to come with the new EPA regulations.  Kokomo Glass is in trouble, as well, but they have the support of their local government.  Bullseye wants to do the right thing. and has done so voluntarily. Yet, unlike the government of Indiana, the government of Oregon seems to be making it very difficult for Bullseye to comply with the DEQ, by ordering Cease & Desist orders not once but twice.  This is not an accusatory statement against Oregon; this is a factual statement.

All I ask is for your help.  Please help Bullseye have a fair chance to do their part to comply with the standards that have been set forth.  Allow them to have a fair amount of time to fix the problem areas that need to be fixed.  I urge you to step in and do something to correct this situation because it is not only good for Bullseye as a local, small business, but it’s good for the Oregon economy as well.

It is not only Bullseye that stands to lose their business, but the thousands of others that rely on their products for their own small businesses. I believe, not long ago, the auto industry and the banking industry needed the government’s help and it was given to them.  Please consider helping Bullseye by giving them a fair and equal chance.

Thank you for your time. I know I can count on your support.

 

What will your mark on the world be?

 

To be one, to be united is a wonderful thing. But, to respect the right to be different and the rights of your fellow-man is even better.  We are here for a fleeting moment.  What will you do with your time?  For what do you want to be remembered?  What mark will you leave on the world?

I have always wanted to take on the world and help others when I could.  This has not always met with kindness.  Yet, I don’t give up.  Some have questioned my motives, thinking I do this to as a means to gain attention…not so; others think I do this for personal gain, not so.  I choose to help others because I want to.  Also, because when I was at my lowest point, someone was there for me to lend a hand.  Someone cared enough (without knowing who I was) to show me kindness, to tell me I was worth something and that I was somebody.  I know how that kindness feels and how that kindness can change a person.  I want others to feel that as well.   I see it as a gift I am allowed to give another human being.  It brings me great joy. I don’t see it as penance, for I have done nothing wrong.  I have a mental illness and I have those low times where I need help.

I don’t how much time I have left on this earth.  What I do know is that I want to make every moment count.  So I focus my time on my family and friends.  I also try to help as many people as I can.  The way I do that is through my art (stained and fused glass art).  As many of you know, it is my art that helps me control my Bipolar and Anxiety symptoms (yes, I do still take medications).  As many of you also know, sometimes medication isn’t enough.  My glass art has saved me so many times.

Now, the main supplier of my glass, Bullseye Glass (and the glass industry at large) is under attack (for lack of a better word).  I go to Bullseye for classes to learn new techniques and I absolutely love the employees there.  They are kind, knowledgeable and they put up with my craziness!  I remember the first time I went there for a class.  Oh my goodness!  I’m sure they had never met someone quite like me.  I just asked a ton of questions.  I think I was there for three hours and this was the day before the class!  I was picking out glass, asking questions about how to make projects,  questions about the sale in July, my goodness the questions from me seemed never to stop.  They were very kind to me.  Every time I call in, they seem to remember me.  I don’t know if they really do, but they play it off  well.  I’ll take it!  🙂  Anyway, I think you get my point.  They really care.  So, I won’t go into detail about what the State of Oregon is doing to them because I don’t have all of the facts and I don’t want to spread more rumors.  The one real fact is this:  Their business is threatened.  This effects not only Bullseye and it’s employees, but thousands of glass artists world-wide.

So, back to my original question: What mark do I want to leave on the world?  I’ve already established that I like helping others.  I know it goes beyond “like”.  I feel compelled to help others.  It’s become a part of who I am. Since this all happened with Bullseye, I’ve gone into full advocate mode sending out congressional contacts to concerned glass artists, working on a form letter (which must be cleared with Bullseye), fundraising mode to help them…  The mark I would like to leave on the world is this:  Whether I am remembered or not is immaterial.  What is important is the work I do.  If I have made the lives of people better, happier, easier, then I’ve made my mark.  The world doesn’t need to remember me, I will just feel better knowing that I’ve made some kind of difference.

I will leave will you with your own question and yes, I would really like to hear from you.

What mark would you like to leave on the world?

Embrace Bipolar

I’ve been writing this blog from the perspective of the positive side of Bipolar Disorder, at least that was my intention.  There were some times that it was difficult to do.  I feel I have grown  in the past year and a half since the start of this blog.  It hasn’t always been easy to see the advantage of having Bipolar Disorder especially when I’m in the middle of an episode.  I can assure you, though, there is…at least from my perspective, a definite advantage.

Let me start with a poem that my doctor read to me during our last session.  It’s called “The Guest House” by Rumi

This being human is a guest house.
Every morning a new arrival.

A joy, a depression, a meanness,
some momentary awareness comes
as an unexpected visitor.

Welcome and entertain them all!
Even if they are a crowd of sorrows,
who violently sweep your house
empty of its furniture,
still, treat each guest honorably.
He may be clearing you out
for some new delight.

The dark thought, the shame, the malice
meet them at the door laughing and invite them in.

Be grateful for whatever comes.
Because each has been sent
as a guide from beyond.

I found this poem so profound.  It really helped me put together all the work I’ve been doing to try to understand the different levels of mania and depression and how to function within them.  I have been working so hard to not only accept these states, but welcome them.  Now, let me explain that last part.  By welcoming the states, I am able to see the value and advantage in each state.  For instance, I’ll start with mania (that’s usually the easiest one).  When I’m in a manic state, but still in control (and not just in my head, others around can see the controlled state) I am able to be quite productive in work, house work, advocacy work, volunteer work, etc.  I, however, don’t stay in this state too long.  I am an ultra rapid cycler and if I don’t watch it, I can cycle out of control rather quickly.  When I’m in a depressive state, I tend to have more empathy for people.  I may not always be nice depending on the degree of depression, but this is when I tend to do more service oriented tasks.  By helping others, it helps to take my mind off of the depression.  This is when I will start more volunteer projects and usually just on my own…not with organizations.

I’m not saying these things to advocate that you should actively stay in either of your states.  I can just appreciate what I learn from each one.  I do learn something each time.  This goes right along with my “Live life with no regrets” motto.  If I learn from each state, how can I regret having been through it?  The advice my doctor gave me for the next time I’m in either mania or depression is to simply say “hello”.  Actually address it and welcome it.  By doing so, I take its power away and empower myself.  I like that.  The whole idea of the online course I’ve been taking (at least for me) is to empower myself.  To not live in fear of my illness.  To not be at the mercy of my illness.  I have by no means perfected the skills yet, but I practice every day. By practicing every day, I grow stronger every day.

This strength I gain means the world to me.  It spills over into other aspects of my life.  Once you can see the value and advantage in something that was once so scary and stigmatizing, it’s no longer stigmatizing to you.  Does that make sense?  For me, that is very empowering.

Medication, Reflection & Bipolar

I have written a few posts about what I call the “medication rollercoaster”.  For me, it has never been a question of whether to take medications or not.  It has been whether the medications are going to work and for how long.  I wouldn’t say I’m med resistant just yet, but I’m down to about 4 meds that I haven’t tried. It has just been extremely difficult and I know I’m not alone.

I had grown accustomed to a certain quality of care from my previous doctor.  When he retired, I went on a search for a new provider that took well over a year.  I quickly learned just how lucky I was to have the doctor I did have.  Dr. P. would take late night calls if I was in crisis.  He always made time for me if I needed a medication change or a quick therapy visit in between scheduled visits.  That is not the case now.  I don’t say this to complain about my current care.  I have a wonderful care team in place…now.  It took time and few bumps in the road, but it’s not quite the same.  It’s not bad.  It’s just different.

Now, I write all that because the new medication provider I have now seems to be quite good.  I’ve been with her a short time, but she understands my situation well. I’m finally back on a medication regime and, for the time being, it is working.  With caution, I have hope for the medication.  The doctor I see for therapy is just awesome and someone I can trust.  I really think I have a good team in place now.  It’s nice to be able to write that.  For once, I’m not writing about firing my med provider! Hahaha!

With my care in order, I’m able to think clearly and reflect back on this year.  I realize this is usually done at the end of December, but I’m gear up to check off a life goal from list.  It’s seems appropriate for me to do now.  I’ve always said that I live my life with no regrets.   Good or bad, whatever I’ve done, it’s all me.  There are some things I will do differently.  For instance, I think with this blog I might try to more of a conscious effort to improve it.  I think I let more of bad days creep in here than I would have liked.  I’d like to tone down trying to save the world.  Perhaps I’ll just take baby steps.  I’ll take on smaller projects and build up to the larger ones.

Question for the day:  If you were to write a book about your life, what would the title be?

~ Mine?  “If I Only Had A Brain”

Don’t get me wrong, I am quite smart.  I can just be so scatterbrained sometimes.  The title fits me.  🙂

The President “Responds”!

Okay, now I support the President, but I’m not a fan of everything he has done over his two terms.  What President has done everything perfectly well throughout their term?  Anyway, he has done tremendous things for mental health.  For instance, he finally fully enacted Patrick Kennedy’s Mental Health Parity Act of 2008.  So, kudos.  I decided to write him and ask for a meeting. Yes, I know I had a snowball’s chance in hell of actually getting that meeting.  If I didn’t ask, then I would never get it.  I knew this meeting was never going to happen, but in that letter I also let him know what it was like for those us living with mental illness. What it’s like navigating the mental health care system.  The stigma we face in the workplace, home, hospital, school…   I thanked him for what he had done so far.  I urged him to continue to do more.  I did explain that I was also an advocate.  How I have actively helped pass laws locally and nationally.  How I’ve worked with soldiers on and off military bases.  How I work with students.  This was the response…

Dear Susan:

Thank you for writing.  I have heard from many Americans whose lives have been affected by mental health problems, and I appreciate your taking the time to share your thoughts.

As you may be aware, in any given year one in five adults experiences a mental illness such as depression, anxiety, bipolar disorder, schizophrenia, or post-traumatic stress, and many others are troubled by significant emotional and psychological distress—especially in times of hardship or difficulty.  They are our family members, friends, and neighbors, and I believe there are things we must all do to help.  As a Nation, we can strive to eliminate the barriers that still keep people from accessing life-changing treatments.  We can also make sure every person struggling with psychological and emotional pain knows that asking for help is not a sign of weakness—taking action is a sign of strength.

My Administration has worked hard to help increase mental health services and improve access to care.  We are working with community health centers to expand the availability of behavioral and mental health services across the country, including in rural areas.  And thanks to the Affordable Care Act, over 60 million Americans now have expanded mental health and substance use disorder benefits and parity protections.  This law also prohibits insurers from denying coverage because of pre-existing conditions like a diagnosis of mental illness, and it requires most insurance plans to cover recommended preventive services without copays.  Additionally, as part of the BRAIN initiative, we are supporting innovative research that aims to revolutionize our understanding of how the brain works and uncover new ways to address conditions like depression.

We continue to support our troops and veterans.  I signed the Clay Hunt Suicide Prevention for American Veterans Act on February 12, 2015, which authorized additional steps to address mental health and prevent suicide.  The year before, I announced 19 Executive actions that make it easier for members of our Armed Forces and veterans to access the care they need, when they need it—including a new policy that will ensure the continuity of medication for mental health problems as service members transition to care at the Department of Veterans Affairs (VA).  The VA has also worked to increase mental health staffing, enhance community partnerships, and expand the capacity of the Veterans Crisis Line.

To learn more about mental health assistance and health care reform, please visit www.MentalHealth.gov or www.HealthCare.gov.  Calling 1-800-662-HELP is also a free, confidential way to receive a treatment referral or further information. 

Again, thank you for writing.  Michelle and I—like so many Americans—have known people who have experienced mental health problems, and we understand the effects these illnesses have on their lives and on their families.  We must continue to work toward better prevention and treatment, and as caring individuals, we must do what we can to ensure those with mental health issues get the care and support they need and deserve.

Sincerely,

Barack Obama

I do realize that the President did not write this email to me.  I also realize that the person who did, obviously did not read a word of the letter I sent.  Yes, I snail mailed a letter…the old fashioned way.  Although I did expect this, I am a bit saddened by it.  As an advocate, I am well aware of all the stats.  I certainly don’t need to learn to go the .gov sites.  I didn’t expect the President to actually read the letter, but at least a staffer would have been nice.  I know I’m no one important.  I don’t have that much of an inflated ego.  It’s just interesting.  Imagine if we all wrote letters and sent them on the same day.  I wonder if we would all get the same response or if someone would actually take notice.  Hmmm.

*Please do not make any negative political comments.  I know not everyone is a fan of the President.

Losing Our HIPAA Rights

I’m reposting this in light of recent events in Oregon because Rep. Murphy is using the campus shooting as an excuse to promote his bill. Again I say, we are not the ones to be feared. Gun control is what we need. Not a bill restricting the rights of those that account for only 1% of the violence nationwide. Get facts straight Murphy! We all want the mental health care system to be improved, but don’t attack us, don’t shackle us and don’t single us out. Work with us, for we have so much say that is important, valid and worth listening to!  Congress should not make laws based on irrational fear.

That is if Rep. Tim Murphy has his way. Yes, he’s at it again. He has re-introduced his oh so lovely “Helping Families in Mental Health Crisis Act”. Oh my goodness will that man ever stop?! And please, Mr. Murphy, stop calling yourself a psychologist! When was the last time you actually practiced? If it were recently, he would not make these horrendous changes to HIPAA that he is proposing in Sec 401 pages 115 through 120 (look them up people!). I can’t believe that anyone who does or has treated mental health patients would allow a “caregiver” such access to our records. If he ever truly did treat patients, he would know that our privacy is all that we have. This HIPAA situation is exactly what I wanted to speak with him about, but, nope he wasn’t going to listen to me. You may say it’s because of “rants” like this one. But I don’t “rant” until I have exhausted all options in a respectful manner. Yes, I was respectful…well up until the very last email (which I did post for all of you to see). There is the added bonus that I highly doubt Mr. Murphy reads any of my posts. After all, he wouldn’t even take a phone call!

So, we have an already failing “mental health care” system that is over loaded, under staffed, uncaring, uneducated… For those of us that do finally make that gut wrenching decision to get help, we are treated like criminals and/or children that couldn’t possibly understand what is happening to us. Is Murphy’s bill going to fix that? NO!

I understand that family members of adult children would like to have more of a say in the care of their loved one. The fact of the matter is, their loved one is an adult. Whether that adult, in the opinion of the “caregiver”, is capable of making decisions for themselves…as an adult they are. As an adult, if they don’t want to seek treatment or aren’t ready to seek treatment, that is their choice. It may not be the best choice, but it is their choice to make. Allowing people to have information from private sessions with a mental health professional is not the answer. The way HIPPA works now is just fine…I’ll use myself as an example.

My husband can call my doctor and give him all the information that he wants. My doctor will say thank you and that is all. It is a one way road of information, none of my information goes out. Now I have nothing to hide from my husband, but knowing that I have this safe haven to turn to at any time is comforting. If Murphy’s bill goes through, that one way road becomes a two-way road. My safe haven is destroyed. Not just mine, but millions of others. You may as well chain me up now because this bill restricts what I can and can’t say in my sessions…if I even choose to continue to go. Millions of people will be facing this same dilemma. So, if Murphy’s bill goes through, he will have single-handedly made a broken system much worse.

You may feel differently than I do about this and that is fine. Everyone is entitled to their opinion. I feel very strongly about this.

What is a Mental Health Advocate?

Well, by definition the word advocate is a verb…an action word.  It means “to speak or write in favor of; support or urge by  argument; recommend publicly”.  It goes on further to describe a person who says they are an advocate.  It says “a person who speaks or writes in support or defense of a person, cause, etc”.  Yes, I realize my teacher side just came out, but it had to.  When you call yourself an advocate of a cause, like mental illness and suicide prevention, you can’t just sit back and regurgitate some pre-written email or letter that an organization wants you send to your representatives.  It needs to come from you.  It needs to come from the heart.  It needs to be original.

I’m not condemning anyone who chooses this route.  I did it myself, but I also used it as a learning experience for when I stepped out on my own.  Some of you may have read my last blog about HR3717.  It has some good points in it, but it is very detrimental to the mental health community.  I’ve seen many people speaking out against it on some of the boards I belong to.  Yet, when I ask for help, you could hear a pin drop.  So that brings up the question of “What is a Mental Health Advocate?”.

Is it someone who blogs about it?  Well, some might argue yes.  I would say maybe.  It depends on who that blog is reaching and how effective it is at raising awareness and advocate support.  My blog? I would say not really advocacy.  I try sometimes, but people don’t want to read those.  Why am I posing this question now?  Because I’m fed up!  I’m fed up about hearing people complain about the system and then not striking when they are given the chance to do something about it.  It’s like complaining about the president when you didn’t vote in the election.

Is it someone who shares their story?  Well, that depends as well.  I’ve shared my story within the mental health and suicide prevention community to thousands of people.  I wouldn’t call this advocacy.  I’d call it more giving insight and (hopefully) giving hope.  I’ve shared my story with over 100 members of Congress.  I call this advocacy.  This is putting a real face to a real illness for legislators that previously had no clue.  It’s opening eyes.  Will it do any good?  I don’t know, but I have to try.

Is it someone who’s goes into their community and tries to educate?  I would say yes, that is advocating.  This ties into the previous description.  Sharing your story and being open about mental illness with people who don’t know is HUGE.  It’s scary sometimes, but can be so rewarding.

I’m no expert and I figure I’ll probably lose a few (if not more) readers over this, but we can’t sit back and let Congress make and pass laws about mental illness when they are truly not informed.  We are the only ones that can do that.  If HR3717 passes, I  will be very worried for the state of mental health care in our country.  It’s not that I’m trying to defeat it.  I just want to help them change it so that it doesn’t alienate us so much.  So this is my last plea.  If you would like to join with me and help, please let me know.  I have the bill summary (as the original is about 100 pages long) and a list of emails.  It’s time to make a stand and make a difference.

Thank you for reading…I hope you will continue to do so.  🙂

Murphy’s Rotten Bill

To give you some background, I was in the process of getting a phone meeting with Rep. Murphy.  His scheduler then decided he was fully booked…Really? Too busy for a 10-15 minute conversation?  So I’ve been passed off to his Senior Legislative Aide, not even his Chief of Staff that deals with policies.  This aide assures me that he will put what I write on Murphy’s desk. Murphy gets plenty put on his desk, do you really think he’s going to see this let alone respond to it.  If he is too much of a coward to speak with someone who has a mental illness in person, then why would he respond to my letter?  Oh, ya…I am also sending it to all 108 co-sponsors as well.  I told them that all I wanted to do was bring both sides to the table. Apparently this is a sticking point.  Below is a summary of the bill (the original is about 100 pages) and in bold are my ideas.  I’d love to get your opinion.

Helping Families in Mental Health Crisis Act of 2013 – Creates in the Department of Health and Human Services (HHS) an Assistant Secretary for Mental Health and Substance Use Disorders, who shall supervise and direct the Administrator of the Substance Abuse and Mental Health Services Administration (SAMHSA).

Why mess around with SAMHSA? It’s running fine on it’s own. By implementing your agenda, you are endangering wonderful programs such as The Trevor Project that rely on SAMHSA.

Directs the Assistant Secretary to establish a National Mental Health Policy Laboratory to: (1) identify and implement policy changes and other trends likely to have the most significant impact on mental health services; (2) collect information from grantees; and (3) evaluate and disseminate to such grantees evidence-based practices and services delivery models, using the best available science shown to reduce program expenditures while enhancing the quality of care furnished to individuals by other such grantees.

This National Mental Health Policy Laboratory is NOT necessary. What we need is accountability for those already working in the field. This will vastly increase the quality care that patients receive. We also need to provide access to residency positions for new psychiatrists. If we can do this, it would greatly improve the amount of psychiatrists available to treat people and it would force those already practicing to improve how they practice.

Amends the Public Health Service Act (PHSA) to require the Assistant Secretary to establish: (1) an Interagency Serious Mental Illness Coordinating Committee; and (2) a four-year pilot program to award up to 50 grants each year to counties, cities, mental health systems, mental health courts, and any other entities with authority under state law to implement, monitor, and oversee assisted outpatient treatment programs.

Who decides what is a “serious mental illness”? As a person with Bipolar Disorder and Anxiety Disorder, I would consider these to be serious mental illnesses. They are quite debilitating. Every mental illness has the potential to become extremely serious. The wording needs to be changed to just say “mental illness”. As a psychologist, you should know not to exclude anyone; this only adds to the stigma we are trying so hard to fight.

Directs the Assistant Secretary to establish a program of tele-psychiatry and primary care physician training grants to states to promote the use of qualified telehealth technology for the identification, diagnosis, mitigation, or treatment of a mental health disorder.

Tele-psychiatry is already in use.

Directs the HHS Secretary (Secretary), in coordination with the Assistant Secretary, to award planning grants to enable up to 10 states to carry out 5-year demonstration programs to improve the provision of behavioral health services by federally qualified community behavioral health clinics.

Why only 10 states when it is the entire nation that is in desperate need of a complete overhaul of the community mental health system Also, How are these states chosen? What happens after the 5 years? Are programs abandoned or are they then implemented throughout the US?

Requires the Assistant Secretary to certify federally qualified community behavioral health clinics that meet specified criteria.

This sounds good, but what are those criteria. For instance, my local county behavioral health clinic is in desperate need of intervention. They treat their clients like numbers. They don’t listen to them. You can hear staff talking about them. These are the experiences of friends and students that are forced to go there because they don’t have private insurance.

Requires the caregiver of an individual with a serious mental illness to be treated as the individual’s personal representative with respect to protected health information, even though the individual has not consented to disclosure of such information to the caregiver, when the individual’s service provider reasonably believes it is necessary for protected health information to be made available to the caregiver in order to protect the individual’s health, safety, or welfare or the safety of one or more other individuals.

I cannot say enough about what a mistake this would be to allow this to remain in the bill. I understand why it’s there, but our privacy in our sessions is sometimes all we have. Please do NOT give away our right to privacy. This will cause people to either leave treatment or not go in the first place. If they choose to remain in treatment, they will not be as forth coming with information and this will severely hinder their treatment and thus any hope of recovery. We’re not treated very well in ER’s. We face stigma on a daily basis, sometimes from our own family. Even in treatment centers, we’re not treated as human beings. So, our private conversations in our sessions are sometimes all we have.

Amends the General Education Provisions Act to allow an educational agency or institution to disclose to such a caregiver the individual’s education record in certain related circumstances.

Same as I just stated above.

Amends the Omnibus Crime Control and Safe Streets Act of 1968 to make available: (1) Edward Byrne Memorial Justice Assistance Grants for mental health programs and operations by law enforcement or corrections officers, and (2) public safety and community policing grants to provide specialized training to law enforcement officers to recognize and intervene properly with individuals who have mental illness.

This is excellent. We have CIT training in my town and it has greatly reduced the number of deaths by suicide. It’s nice to have an officer meet with someone with a mental illness and they “pick each others brains” so to say. They can let each other know what will and won’t work in mental health situations. This is what I’m trying to do with you.

Reauthorizes and revises requirements for the Mentally Ill Offender Treatment and Crime Reduction Act of 2004.

I would just like some clarification on what they are.

Authorizes the Attorney General to award grants to: (1) establish or expand veterans treatment court programs; and (2) enhance the capabilities of a correctional facility to identify, screen, and treat inmates with a mental illness, as well as develop and implement post-release transition plans for them.

This seems good to me.

Requires any data prepared by or submitted to the Attorney General or the Director of the Federal Bureau of Investigation (FBI) with respect to homicides, law enforcement officers killed and assaulted, or individuals killed by law enforcement officers to include data about the involvement of mental illness in such incidences, if any.

I’m not too sure about this one. This paints us in a very violent light and we really aren’t that. We are more likely to be the victim of a crime than a perpetrator. We only account for about 1% of all the violent deaths nationwide. To more accurately get a picture, we need NVDRS in every state. That would give you the information you’re looking for.

Directs the Comptroller General (GAO) to detail the cost of federal. state, or local imprisonment for persons who have serious mental illness.

Amends title XIX (Medicaid) of the Social Security Act (SSA) to prohibit a state medical assistance plan from prohibiting payment for a same-day qualifying mental health service or primary care service furnished to an individual at a federally qualified community behavioral health center or a federally qualified health center on the same day as the other kind of service.

Allows states the option to provide medical assistance for inpatient psychiatric hospital services and psychiatric residential treatment facility services for individuals age 21-65.

Amends both SSA titles XIX and XVIII (Medicare) to cover prescription drugs used to treat mental health disorders.

Amends the PHSA to increase funding for the brain initiative at the National Institute of Mental Health.

Transfers responsibility for the administration of community mental health block grants to the Assistant Secretary from the Director of the Center for Mental Health Services (CMHS).

Revises requirements for the funding agreement under a formula block grant to a state for community mental health services to prescribe the general standard under state law for court ordered inpatient or outpatient mental health treatment as well as assisted outpatient treatment.

This is another sticking point for me. Forced treatment rarely, if ever, has a lasting effect. The decision to be treated has to made by the patient. I know this was put in for family members of adult children with mental illness, but I’ve spoken with so many people across this country that agree with me. They’ve forced their loved ones into treatment only to have them relapse very soon after release. That decision for treatment is tough because we (those with mental illness) know that it is something we must do for life. The meds are for life. The therapy is for life. The constant use of coping skills is for life…. The list goes on. These are life long illnesses and we have to have some control, some say in it because we have no control over the illness itself.

Requires the Assistant Secretary to evaluate the combined paperwork burden of certain community mental health centers as well as of certified federally qualified community mental health clinics.

Directs the Secretary of Education, along with the Assistant Secretary, to organize a national awareness campaign to assist secondary school students and postsecondary students in: (1) reducing the stigma associated with serious mental illness; (2) understanding how to assist an individual demonstrating signs of a serious mental illness; and (3) understanding the importance of seeking treatment from a physician, clinical psychologist, or licensed mental health professional when a student believes the student may be suffering from a serious mental illness or behavioral health disorder.

Amends the PHSA to include as health care providers any behavioral and mental health professionals, substance abuse professionals, psychiatric hospitals, certain community mental health centers (including one operated by a county behavioral health agency), and residential or outpatient mental health or substance abuse treatment facilities.

Amends SSA title XVIII (Medicare), with respect to incentives for meaningful use of certified electronic health records (EHR) technology under the pay schedule for physician’s services, to include as additional eligible professionals clinical psychologists providing qualified psychologist services and clinical social workers. Subjects any additional eligible professionals, including those under a MedicareAdvantage (MA) plan, to reductions in incentive payments after a certain date for failure to be a meaningful EHR user.

Amends SSA title XIX (Medicaid) to treat as Medicaid providers the following additional Medicaid providers: (1) public and certain private hospitals that are principally psychiatric hospitals, (2) certain community mental health centers, and (3) certain residential or outpatient mental health or substance abuse treatment facilities.

Just an FYI here: Medicaid will pay for an ambulance if you are involuntarily committed. If you are seeking help and want to voluntarily commit yourself, they won’t cover the ambulance ride. I think this needs to be changed.

Makes eligible Medicaid professionals certain clinical psychologists providing qualified psychologist services and certain clinical social workers.

Amends the PHSA to accord health care professional volunteers at community mental health centers and federally qualified community behavioral health clinics the liability protections of Public Health Service employees.

Requires the Assistant Secretary to transfer all functions and responsibilities of the Center for Behavioral Health Statistics and Quality to the National Mental Health Policy Laboratory.

Revises the duties of the CMHS Director.

Reauthorizes the Secretary’s authority to address priority mental health needs of regional and national significance.

Amends the PHSA to reauthorize and revise requirements for a youth interagency research, training, and technical assistance center to prevent suicides (the Suicide Prevention Technical Assistance Center). Expands the program’s focus from youth suicides to suicides among all ages, particularly among groups that are at high risk for suicide. Repeals authority for grants to establish research, training, and technical assistance centers related to mental health, substance abuse and the justice system.

Reauthorizes a program of grants for the development of state or tribal youth suicide early intervention and prevention strategies.

Reauthorizes and revises a grant program to enhance services for students with mental health or substance use disorders at institutions of higher education. Requires the Secretary (who currently is merely authorized), acting through the CMHS Director, to award grants to enhance such services and to develop best practices for the delivery of such services. Permits grant funds to be used for the provision of such services to students and to employ appropriately trained staff. Requires the Secretary to give special consideration to applications for grants that describe programs that demonstrate the greatest need for new or additional mental and substance use disorder services and the greatest potential for replication.

Requires the Assistant Secretary, before making a grant to a public entity for comprehensive community mental health services to children with a serious emotional disturbance, to consult with the Director of the National Institutes of Health (NIH) to ensure that the grant recipient will use evidence-based practices. Reauthorizes funding for such grants.

Repeals current authority of the Secretary to carry out directly or through grants, contracts or cooperative agreements with public entities a program to assist local communities in developing ways to assist children in dealing with violence.

Reauthorizes the National Child Traumatic Stress Network. Amends the Protection and Advocacy for Individuals with Mental Illness Act to reduce corresponding funding for protection and advocacy systems for mentally ill individuals.

Prohibits lobbying by any such systems accepting federal funds to protect and advocate the rights of individuals with mental illness.

Does this mean Congress will do the same for all other organizations whose lobbyists receive federal funding? I think you ought to take a look at that.

Prohibits the SAMHSA Administrator from hosting or sponsoring any conference that will not be primarily administered by SAMHSA without giving at least 90 days prior notice to specified congressional committees.

Prohibits the SAMHSA Administrator also from establishing (and the Secretary from delegating to the Administrator responsibility for) any program or project not explicitly authorized or required by statute. Terminates by the end of FY2014 any SAMHSA program or project not so explicitly authorized or required.