There is much to tell but today I am very tired, so I will only begin.
I saw my rabbi last week, thankfully. I wanted to be strong and in control but even on the way to meet him I was in tears. This recent downturn since the end of September has been hard though the increase in meds helps and I'm sleeping better and I've been through much, much harder. But it has kept me away from shul. Lately it has brought up too much pain, too much remembering of how it feels to be Unseen and not valued.
I know that my perspective is skewed at the moment, that the painful events feel closer and more painful than they do when I'm feeling strong and happy. I even said as much to him.
My rabbi said two things that really stuck with me. One was that he would do everything he could to prevent and help heal such painful experiences related to the shul, short of embarrassing me. I am glad and relieved that he wants to make this about the shul, not about me. I know that I am not the only one in the congregation battling depression and it would be grossly unfair for me to receive validation while others continue to remain Unseen.
The other was that he wants me to help him--and the shul by extension--learn how to help me and others like me. Already I had an idea. It is not unusual to train congregants on the mitzvah of bikkur cholim, visiting the sick. In my area it has been focused on hospital and nursing home visits. But why could we not expand it a bit to include people we see in shul, at work, friends, who are in pain?
The thing I hear most often here on the blog and in person conversations is that people don't know what to say, how to act, so they say and do nothing.
Why can we not teach people a range of things to say and do? The question or offer that helps me might not help another, but if there is a larger range to choose from, adaptable to the situation and the people involved, it would be a starting point. It would open a door that has remained closed for too long.
As if on some divine cue, I received today an invitation to join a committee at shul to study and make recommendations on inclusion. While inclusion is often used in terms of physical, developmental and learning disabilities, there is no reason it should not also include brain disorders such as depression, anxiety, bipolar, and others. Ours is often a hidden illness, but
by nature, these disorders make it hard--even impossible--for people going through an episode to reach out, get involved, or even to come to shul.
Shul should be a place that people can bring their confusion and fear and pain, a place that should be free of stigma for what we know is a biological medical brain illness, a place where those who are able can be there for those who are not, knowing that which end of the need spectrum we're on can change.
I went to another Jewish mental health conference, too. I wrote about last year's conference and I'm relieved that this year's was much, much better. I want to write more about that, too, but today I must take it slow and save my energy.
Showing posts with label Community: Education. Show all posts
Showing posts with label Community: Education. Show all posts
Tuesday, October 23, 2007
Friday, August 3, 2007
Who is the real expert on fringe Jews?
I have an appointment with my rabbi for next week.
I am scared.
The problem is that I can't trust what's in my head. I can't trust my emotions. My counselor has observed this, too, saying that I can't approach situations from a purely emotional stand. I have to go back to the facts, to what I know is real.
Sometimes, though, it is hard to differentiate between what is my interpretation of what I see around me and what is actually real. It is particularly hard when it concerns me.
There is a woman at my shul who has a child with a fairly severe disability. There is little hope for this child to successfully navigate any sort of shul-offered children's programming or bar mitzvah studies without individual and long-term assistance, such as a personal tutor. This woman has been an advocate for children with disabilities and their parents since her own child was diagnosed shortly after birth. Not one visible change has been made to the children's programming. No tutoring has been offered. This woman cannot enjoy Shabbos at shul because she is spending every moment assisting her child. She told me in tears that she is considering leaving the shul because it seems blind and deaf to her needs.
Not long after she told me this, another woman, a medical doctor who has children of her own but none with a diagnosed disability, spoke up at shul on behalf of children with disabilities and how to integrate them better within shul programming. Suddenly the board was interested. A committee was formed to study the issue.
When I discretely asked why no one was interested when the mother spoke but were after the doctor spoke, I was told that the disabled child's mother was seen as too close to the issue and as such, was too emotional to be trusted. Yet the doctor, being a doctor and not having any children with disabilities, was an impartial, trusted source. Now they could listen.
By this logic, I am too close to the issue of depression. I am too emotional to be trusted. Even though I know my depression inside and out and can usually find words to express what's going on. Even though I have perhaps identified some of the problems--lack of communication, insufficient community education--and proposed solutions that would accommodate a medium-sized shul with an overworked rabbi and a strapped budget.
Certainly, it would be nice to make a difference for me, to find the Jewish support I need. But that is not enough. There are far too many others, such as this woman with the child with the disability, such as Rabbi WAC's Fringe Jews, who are not finding support either. Someone needs to speak up for them. If that responsibility falls to me, I will accept it and do the best I can.
But how can I provide insight or guidance or be effective in any way if I can be written off as too close to the issue, too emotional, or worse yet, just another of the mentally ill?
It would seem to me that, having lived with this illness for most of my life, I would be something of an expert on it. Yet expertise is not something I can attribute to myself if it is not corroborated by others, is it? Can a teacher really call himself a teacher if he has no students?
And even if I could attribute expertise to myself, how does that have any impact on those many who will only listen if the speaker is objective, rational, and preferably has formal, post-graduate level training on the topic?
Or maybe my feeling ineffective and powerless is all coming from within, a product of the very illness I feel ineffective speaking about.
Too many questions for this erev Shabbos. I'm going to go braid the challah.
I am scared.
The problem is that I can't trust what's in my head. I can't trust my emotions. My counselor has observed this, too, saying that I can't approach situations from a purely emotional stand. I have to go back to the facts, to what I know is real.
Sometimes, though, it is hard to differentiate between what is my interpretation of what I see around me and what is actually real. It is particularly hard when it concerns me.
There is a woman at my shul who has a child with a fairly severe disability. There is little hope for this child to successfully navigate any sort of shul-offered children's programming or bar mitzvah studies without individual and long-term assistance, such as a personal tutor. This woman has been an advocate for children with disabilities and their parents since her own child was diagnosed shortly after birth. Not one visible change has been made to the children's programming. No tutoring has been offered. This woman cannot enjoy Shabbos at shul because she is spending every moment assisting her child. She told me in tears that she is considering leaving the shul because it seems blind and deaf to her needs.
Not long after she told me this, another woman, a medical doctor who has children of her own but none with a diagnosed disability, spoke up at shul on behalf of children with disabilities and how to integrate them better within shul programming. Suddenly the board was interested. A committee was formed to study the issue.
When I discretely asked why no one was interested when the mother spoke but were after the doctor spoke, I was told that the disabled child's mother was seen as too close to the issue and as such, was too emotional to be trusted. Yet the doctor, being a doctor and not having any children with disabilities, was an impartial, trusted source. Now they could listen.
By this logic, I am too close to the issue of depression. I am too emotional to be trusted. Even though I know my depression inside and out and can usually find words to express what's going on. Even though I have perhaps identified some of the problems--lack of communication, insufficient community education--and proposed solutions that would accommodate a medium-sized shul with an overworked rabbi and a strapped budget.
Certainly, it would be nice to make a difference for me, to find the Jewish support I need. But that is not enough. There are far too many others, such as this woman with the child with the disability, such as Rabbi WAC's Fringe Jews, who are not finding support either. Someone needs to speak up for them. If that responsibility falls to me, I will accept it and do the best I can.
But how can I provide insight or guidance or be effective in any way if I can be written off as too close to the issue, too emotional, or worse yet, just another of the mentally ill?
It would seem to me that, having lived with this illness for most of my life, I would be something of an expert on it. Yet expertise is not something I can attribute to myself if it is not corroborated by others, is it? Can a teacher really call himself a teacher if he has no students?
And even if I could attribute expertise to myself, how does that have any impact on those many who will only listen if the speaker is objective, rational, and preferably has formal, post-graduate level training on the topic?
Or maybe my feeling ineffective and powerless is all coming from within, a product of the very illness I feel ineffective speaking about.
Too many questions for this erev Shabbos. I'm going to go braid the challah.
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