Emily's Mental Health Resources

This is Emily’s second day with us as the Mental Health Blogger of the Week.  If you have not check out her wonderful site Surviving Limbo, you really should.

I really got a lot out of what Emily shared with us on Monday.  The reasons for our diagnosises  may be different, however, it appears she and I share similar manifestations of symptoms. Not only that, but I discovered we live in the same state.  It is comforting for me to get to know someone that I already have so much in common with.

Today, Emily shares her favorite mental health resources with us.  Please take the time to check out at least a few of the sites she has listed.  There are some real gems.

1.  Untypically Jia –  I think you know her.  She has OCD.  She’s so wonderfully quirky.  She will make you smile no matter how bad you feel.
2. No Points For Style –  Mother of a child with mental illness.  She gives a different perspective about how mental illness affects the entire family.  She also uses humor a great deal.
3.  A Daring Adventure – Free life coaching.  I love the cartoonish pictures and his very “daring” or brutally honest look at different topics.
4.  Depressions and Confessions – alexis had PPD as well as at least one major depressive episode.  her writing style is unique.  she reminds me of e e cummings
5.  Dr. Deb – A professional psychologist whose posts often surprise me such as her latest about Therapy Service Dogs.  I didn’t know such existed.
6.  Violence Unsilenced – Survivor stories.  Very emotional.  Very disturbing.  But it’s the truth.
7. Psychology Today – This site has a variety of blogs, all of which I have found useful.  They’ve got it covered.
8.  PsychCentral – Like Psychology Today, they have multiple resources.
9.  NAMI (National Alliance for Mental Illness) – Mental health advocates, and another source of information.
10. Sugar Filled Emotions – I’m not always as vocal as I should be, but Melissa is a fellow Georgian with similar illnesses to mine.  She works very hard at educating people through her blog and a Twitter newspaper.

Circle Of Death

When I saw the counselor on Thursday, she had a suggestion – homework – for me.  It has to do with setting boundaries and finding ways for my family – husband and daughter – to remember to not cross them. This is going to sound absolutely crazy – no pun intended – but she suggested I do something silly and create a Circle Of Death.

She knows I like to try and use some humor when I set boundaries, it makes it easier for the family to accept them. She is also aware that when I am feeling like I am now, I do not want to be touched, or even like people in my personal space. I feel as if I am being smothered when I am having personal space issues and people insist on entering it. Her rather unusual homework was for me to take some duct tape and create a circle around me. Include where I am sitting to do my writing – the couch.

After I create my circle, I am to let my family know that as long as I am in it they cannot talk to me, or touch me or do anything that compromises my personal space. I am also to tell them that the Circle of Death is for their own protection.  It is a way for me to be with them, while at the same time separating myself from them just enough so that I do not yell at them or hurt their feelings, given my extreme irritability and agitation right now.

Creating the Circle of Death will give them a fair verbal warning and also a physical reminder that there is a zone they should not enter. This will eliminate any confusion – on their part – about where my boundary begins, and what the consequences will be if they choose to cross it. If they choose to ignore the boundary then they are responsible for the consequences – taking their lives in their own hands, so to speak.

I will let you know how it goes!

Depression And Cooking

Due to how popular my first Depression and Cooking post has been, I decided that I would try and have a post about Depression and Cooking at least a couple of Fridays a month.

When my depression is active, I feel like being extremely inactive. That includes feeding my family. However, since I do not want my depression to control my life, any place I can claim victory over it is a good thing. Sometimes that victory takes the form of preparing my family a tasty and nutritious meal. The key is, the meal needs to be simple. Something I can accomplish with very little effort, or something I can help my family prepare.

When I was visiting my parents, my mother prepared several meals for us. One in particular I enjoyed. I enjoyed it so much because it was something that she had served for supper when I was a kid, and it was very simple. It was our version of a Mexican Salad and cheese quesadillas.

One of the reasons I like the Mexican Salad is that she and I fix it differently and both versions are good. The other reason I like the salad is that it is extremely simple and I usually have at least some of the ingredients around the house. The quesadilla is even more simple and involves two ingredients.

Here is a rough idea of what the recipe is for the Mexican Salad:

Lettuce (salad in a bag works good for this. No prep involved)
ground meat (beef, turkey, chicken, even tofu crumbles)
taco seasoning (I buy it in a pack. All that requires is me dumping it on the meat)
shredded cheese (You can buy cheese already shredded. I buy fairly large packs so I usually have some in the fridge)
canned Kideny beans, drained (I almost always have these in the cabinet. Store brands are cheap, so I buy more than one can at a time)
Russian Salad dressing (This can be a hard type of salad dressing to find, Catalina is a good substitute_
Frito corn chips (crushed) or tortilla chips (broken into bits)

Brown the ground meat, once browned stir in taco seasoning. Put in salad bowl with remaining ingredients. Toss with dressing.

I often serve this same salad with green onions and no ground meat. Instead I will bake a piece of salmon to have with it.

Cheese Quesadillas are great for many reasons.  I have a thing for grilled cheese sandwiches, unfortunately the carbs in the bread are not good for my diabetes.  Using tortillas instead of bread, especially the veggie tortillas reduces the amount of carbs I ingest. Little kids seem to enjoy these as well.

You will need shredded cheese (your choice of the type)

Tortillas (your choice of the type)

Heat olive oil in a pan large enough to hold tortilla. When heated place one tortilla in pan, cover in cheese (the amount of cheese is up to you).  Place second tortilla on top of cheese.  Cook until you think the first tortilla is browning, then flip.  You cheese should be melting.  Once you think the second side has cooked enough.  Remove from heat.  I like to slice the quesadilla up into triangles and then serve.

Let me know if you try these simple recipes out, and what you thought about them!

Maybe, Possibly, Might Be…

The appointment with my psychiatrist this week was interesting and eye opening at the same time. She has not officially changed my diagnosis from Major Depression to Bi-polar disorder. However, I think she brought it up because she is seriously considering it. She seems like a good doctor, so I believe she would not have said it out loud to me if there had not been a significantly good chance of her doing it. I wonder if her purpose for bringing it up was to get me used to the idea of having a diffiernt diagnosis.

The doctor used the word decompansating in reference to me.  As in, she thinks I am decompansating rather quickly.  In other words she thinks I am rapidly heading toward a Major Depressive Episode due to having no anti-depressant in my system.  I also tend to worry psychiatrists.  You see, even when I have no suicidal thoughts, I have a suicide plan. Proper etiquette will not allow me to divulge my suicide plan here, so there is no chance that someone reading this will get inspired by it and use it for themselves.  What I can say is that it involves the many medications – including insulin – that I have at my disposal.  Since the core of my plan is in my face everyday, the plan is always there.   The best I can answer when I am asked if I have a plan, is to say I have no plans to act on my plan.

We had a decent discussion about possible medications.  My previous psychiatrist had made a list of some that he felt might work on me, as we were trying to figure out what really did work.  Many of those included the type of medications used to treat bi-polar disorder.  I did not think it was all that significant because I know that in many cases, Major Depression is treated with those same types of drugs, especially when the patient is at a high risk for suicide. It is frustrating to try and find a mental health medication that I can take.  Most affect a person’s blood sugar, so in a diabetic that presents a significant problem.  They also happen to affect the same chemicals in the brain that cause Restless Leg Syndrome – making it worse.  She has decided to try me on Celexa because she has had many patients similar to me do very well on it. However, because of the possible change in diagnosis, she has some concerns that it might flip me into, at the very least, a state of hypmania.

A possible bi-polar diagnosis scares me.  It really does.  It scares me because I know society is less accepting of someone with a bi-polar.  It scares me to think that as easy I have had it over all these months, people find depression more acceptable – it could change because my diagnosis has changed.  It scares me because I know my depression, I am familiar with it and I do not know Bi-polar. I am happy with my depression.  It has become like an old friend.

However, I do know a great many people – on the internet – who either have bi-polar or have a family member who does.  If my diagnosis changes I know I can count on them to lead me through the process of getting to know it as well.

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The Joys Of Withdrawal

Happiness often sneaks in through a door you didn’t know you left open.  ~John Barrymore

Whine. Whine. Tears. Scared. More Whine – with a little bit of cheese. I cannot do this.  I do not want to do this.

Those are just a few of the words that could be used to describe how I felt when I found out that I was going to have to stop taking Effexor.  The way I felt the first few days of the withdrawal process reinforced those feelings.  At one point, I was so miserable that all I wanted was to check into a hospital so I could be miserable all by myself. Maybe I physically felt as bad as I did because of my state of mind, maybe not.

What I do know is that so far some of the physical problems that the Effexor was causing seem to be be getting better.  My blood sugar is coming down, and so is my blood pressure.  As those have come down, I have felt so much better.

Most experts agree that exercise is good for depression, and is extremely beneficial for people with Type II Diabetes.  I have felt such guilt and self condemnation at the fact that I almost never exercised.  People who did not know what I felt like on a daily basis may have thought that I was lazy, and unmotivated.  Or they may have thought that I did not care about my physical and mental well being. The reality is that everyday of raging high blood sugar was like a day “walking through jello”.  I was so darn tired ALL OF THE TIME. The extreme high blood pressure also made me feel rotten.  Quite simply, I did not have the energy or strength to do much of anything.

The change in how I feel is so remarkable.  The amount of  change that has taken place in such a short time is a miracle.  Stopping the Effexor was the best possible choice for me.  I am not saying that I do not need to go back on an anti-depressant, because I most definitely do.  What I am saying is that I can see now that although Effexor helped my brain, it was so bad for me physically.

One of the most joyous things that has happened since I have begun to physically feet better has been the fact that I have walked miles in just a matter of a few days. Those walks were so wonderful because it was something my daughter and I could do together.  Sometimes when we walked, we talked about silly things, other times we engaged in serious discussions, and there were times when neither one of us said a word. No matter what type of conversation we engaged in or did not engage in, it has been a real bonding experience for us.

Laughter Makes Me Feel Good!

It is hard to joke around and laugh when you feel yucky.  However, in the last few days I have felt more like joking around with Anna than I have in a long while. I even had a great opportunity to embarrass her in public yesterday. I did not realize how much I had been missing a good long and loud belly laugh shared with my daughter.  I cannot explain to you how wonderful it has been to be able to tease her and have her tease me for the first time in a long while.

Giving Back

I have been using a local free clinic for my medical needs for over a year now.  I have probably received better health care there than I have at most of the doctors I have ever had to pay to see.  I have been wanting a way to repay them for all the kindness they have shown me.  I have tried to volunteer there, but every time I am set up to do that, I end up getting sick with something – usually an asthma flare up.  The last few months I have simply not been physically able to even consider volunteering there. However, my withdrawal from Effexor afforded me an opportunity to give something back.

One thing the volunteers at the clinic have been able to help me with is obtaining free medications from the drug manufacturers.  One of those they helped me get was a year’s worth of Effexor, sent to me – via the clinic – three months at a time.  Today I had to go pick up some of my medications from them.  One of those items was my three month supply of Effexor.  Obviously, I can no longer make use of it, and I did not want that medication to go to waste.  So today, when I was at the clinic’s pharmacy I asked them if there was any possible way I could donate the unopened supply of Effexor to the clinic.  To my surprise and delight, they said yes.

The pharmacist explained to me that Effexor was one of those medications that they could not keep on hand as much as they would like to because of its expense.  I should be receiving at least two more refills of it from the drug manufacturer and we went ahead and made plans for the pharmacy to take those as well. She also said that my little donation would help many patients. It really did make me feel good to be able to give back to the place that has helped me so much.

All this joy from something I did not want to happen.  I love it when things work out that way.


Are You The Victim or Victor?


“If it’s never our fault, we can’t take responsibility for it. If we can’t take responsibility for it, we’ll always be its victim.” – Richard Bach

Are you choosing to be the Victim of your mental health issue/mental illness? Or are you choosing to be the Victor?

I know what some of you might be thinking…Did she really just ask if I am choosing to be a victim of my mental illness?

Ummmm, yeah, I really did just ask that.

Now before you decide that I am yet another one of those self help guru’s who has never had their own mental health challenge, and that I have no basis in reality to ask that question, I urge you to read a little bit more of this blog post.

I have spent the last three to four years facing my own mental health challenges. For a good portion of that time, I chose to be the victim. I made that choice because:

  • I was scared
  • I thought my family would not understand
  • I was embarrassed
  • Making choices was hard, especially given how I felt. It required more effort on my part than I desired to put into anything.

I allowed my mental illness – depression – to become so strong that eventually any choices that I might have made were taken out of my hands. The disease itself took away my choice to live or die. My thoughts were so irrational that other people – family and medical personnel – had to make life choices for me.

Once I began to reach a bit of clarity in my thinking – this came after a two suicide attempts and a psychiatric hospitalization – I realized that I had choices to make. I could choose to continue being the victim of my mental illness or I could choose to become victorious over it.

In the past, when I thought of someone being victorious over something, the mental image I had was of glittering confetti falling down, golden streamers flowing from their hair, and crowds in the street cheering for them. There was no doubt that there had been a victory of some kind and there was no doubt who the victor was. I think that this type of imagery is common for most people, which is why I believe it is hard for most of us to visualize any type of victory over a mental health issue/mental illness. We want clear cut answers. We want to see hard evidence that we have defeated something. It is hard to get that clear cut, “I won” answer when we talk in terms of defeating something as intangible as a mental illness.

However, we can live in victory over our mental health issue. I am not talking about a cure. I am not talking about no longer having to take any medications we are on. I am not even talking about stopping any type of therapy we might be engaging in. I am talking about changing our attitudes when it comes to our own mental health “label”

I am talking about Personal Responsibility.

Give me a minute….I need to check and see if I actually wrote those words. Oh..I. Did. Is it possible to irritate yourself with your own “wise words”?

I have been thinking a lot this week about Personal Responsibility in reference to mental health issues/mental illnesses. I have been thinking about the role Personal Responsibility plays in regards to a disease – an organic process – that takes place in someone’s brain.

Nine months ago if I saw or heard someone use the words Personal Responsibility in reference to my depression diagnosis, my reaction would have been one of polite disdain. I probably would have rolled my eyes, and politely listened to what they had to say – if they were in front of me – and privately ranted about how that person had no idea what they were talking about. Or I would have skimmed through what they had written so at least I could truthfully say, “What a thought provoking read”, while keeping what thoughts they had actually inspired to myself. It is possible that seeing or hearing the words Personal Responsibility even four weeks ago might have inspired me to call the person who used them a few not nice names – only in my head of course.

The reality is that we do have some personal responsibility when it comes to our mental health. Even in the times when we are barely holding on, we still have choices. Granted, the choices could be yucky ones, but we do have choices. To the outside world, those choices may seem silly or inconsequential but they are still our choices.

We have to do the best we can. This is our sacred human responsibility. – Albert Einstein

I believe that Personal Responsibility is doing the best YOU can in your set of circumstances. Not what your Aunt Fay thinks is your best, or what your Mom believes you should be doing, or even what someone else who has the same diagnosis as you is currently able to do. It is doing the best that YOU are capable of at that point in your life. Having been there, done that, and have the hospital bracelet to prove it, I can whole heartedly say that for some of us, the best we can do is simply to put food on our forks and then into our mouths. As long as we are doing the best that we can, even if it only involves making the simplest of choices, we are living in victory over our mental health issue/mental illness. It is a victory born out of Personal Responsibility.

Personal Responsibility means that we STOP using our mental illness as an excuse for why we cannot do something. It means that we STOP blaming that disease for why our life is not going the way we want it to. Dare I use this phrase? Yes, I think I will. Personal Responsibility means we are going to have to COWBOY UP,and get about the business of living our lives the best we can. It also means that we must do what we can to manage our own mental health. For some of us that will mean making sure that someone else is in charge of giving us our medications, because either we cannot remember to take them, or the temptation to take too much at one time is harder than we can presently handle. For others, taking Personal Responsibility over our own mental health means that we need to push our comfort zones more. Sometimes taking Personal Responsibility for our own mental health means we have to take a step back in our treatment process in order to relearn how to use a particular “tool”.

When we take Personal Responsibility for our mental health, our attitude about our particular mental health challenge changes. The way we feel about ourselves changes. Very often we are surprised to find ourselves rising to challenges that we might not have even considered attempting to conquer before all the business in our brains got started. I believe taking Personal Responsibility for our mental health has the potential to make us happier. We have more to be proud of, and that increases our own sense of self worth.

Personal Responsibility:

  • Gives Us Choices – there is never any choice that is too small or too silly when it comes to Personal Responsibility.
  • Is doing the best you can in your set of circumstances. – If the best we can do on a particular day is making the choice to live for that day then we are doing the best we can in the set of circumstances that exists for us at that time.
  • Gives us a sense of pride – When we can truthfully say, “I did the best I could today”, no matter how big or small what we did may seem to the rest of the world, we can feel good that we did the best that we could. The more things we have to be proud about, the more our self worth grows.
  • Means we are choosing to be the Victor and not the Victim. By choosing Personal Responsibility, we are choosing to no longer allow our disease to dictate our life circumstances – we no longer choose to be the victim.  We are choosing to do the best we can, no matter what the circumstances are, which means we WIN – we are living in victory over our mental illness.

This post was written as part of The Blog Gang. A circle of bloggers who write about the same topic, each from their own point of view. This month’s topic was personal responsibility.

Thankful Five

I love going places with my mom.  It is always an adventure of some kind.  It is not because she does anything particularly exciting, it is you have no idea how many places you may end up before you reach the final destination. Today, our four hour trip from Talking Rock, Georgia to Augusta Georgia took us about six hours.  We had some great stops though.

Our first stop was at the Animal Clinic where my brother practices veterinary medicine.  From there we spent an hour and a half in Costco.  We had great fun there, we picked out a couple cute little baby outfits for my granddaughter who is due in February.  Right after Costco was a quick visit to Steak and Shake.  I skipped the shake and watched with envy as my mother and daughter drank theirs.  On the South side of Atlanta, on I-20, we stopped at an official rest area, traveled a bit more and made it all the way to the Flying J. At the Flying J I bought myself a special $.50 souvenir key chain.  It has a section where the words “Love Jesus” flash, and it is completely solar powered.

When we finally made it to my parents house, I managed to stay awake 30 to 45 minutes, then I needed to get some sleep.  I am enjoying all this extra sleep.  It has been years since I have spent so much time in bed.

Time for this week’s Thankful Five

  1. I am thankful for being able to go to the family reunion on Sunday.
  2. I am thankful that I am being given the opportunity to relearn the importance of having a positive attitude.
  3. I am thankful that I am able to spend some time at my mother’s, and take some pressure off of my husband.
  4. I am thankful for some newly inspired ideas that are running around in my head.
  5. I am thankful for the interesting and varied things my mother and I talked about today.

Back To Basics

Happiness is an attitude. We either make ourselves miserable, or happy and strong. The amount of work is the same. ~Francesca Reigler

I have decided that I need to return to the basics. You know, that basic homework my counselor had me use to create a more positive thought process in my head. It is a fairly simple bit of homework, all I have to do is look for at least three positive things out of every situation. Okay, well maybe it sounds simpler then it really is.

I thought I had gotten extremely skilled at doing this. I suppose in comparison to how I used to think – glass is always half empty, life sucks and the world is out to get me – I was getting fairly adept at it. However, this whole withdrawal process has shown me, that I am still a long way from being as skilled at positive thinking as I want to be.

“Would I like some cheese with my Whine?”

Instead of focusing on the positive parts of withdrawing from Effexor, I have spent a lot of time thinking about how rotten I have been feeling. The headaches, the muscle aches, the constant need to sleep, and even the nausea have been what I have been concentrating on. Thinking so much about how my body feels has done me no good. In fact, I have allowed it to create a negative mental attitude in me. I do not know about the rest of you, but when I have a negative attitude it also affects how I feel physically.

It is time to practice what I preach!

I talk often about being positive.  I tell other people that thinking positive will help them/us get through the trials that depression and other mental health issues throw at us.  I say that I practice positive thinking everyday.  Yet, when I am faced with my biggest personal trial since I began depression treatment I revert, to some extent, to old patterns of behavior.

I believe that I had become complacent. Taking it for granted that I would always pick a positive attitude and/or thought process.  At the same time, I had not really paid attention to the fact that it has been months since I have had to face any real difficulties in my life and depression treatment. This withdrawal process has turned into a much needed reminder that when it comes to my mental health, I can not take anything for granted.

Beginning again

1.  Withdrawing from the Effexor is allowing me to sleep more than I have in years and years.

2.  The constant feeling of wanting/needing to cry is a great reminder that I still need to be on an anti-depressant.

3.  At least during the time that I am not having to take any anti-depressant my sex life will be better than it has been in about four years (3 years of untreated depression and about 1 year of being on Effexor)


Looking Fear In The Face

You gain strength, courage and confidence by every experience in which you stop to look fear in the face. You are able to say to yourself, “I can take the next thing that comes along. -Eleanor Roosevelt

Sometimes I think I am like the Cowardly Lion in The Wizard of Oz.  The one thing he most wanted in the world was courage.  He wanted it so much he was willing to face the scary, powerful Wizard to obtain it.  Little did he realize that he had courage all along, facing the Wizard proved it.   Silly Lion, facing the fear is a mark of courage!

One of my biggest fears since a medication was found that worked on my depression has been anyone or anything getting in the way of me being able to take it.  That includes when I have been in the hospital for asthma, and the timing of when I was to take the depression medication was changed.  I have had such a fear of it that my previous psychiatrist was able to detect severe anxiety in me even when I just thought about my depression medications being changed in some way.

I have been so afraid that a medication change would happen, that I actually deluded myself into believing that it could never happen. Now, what I have feared has become a reality.  Not only has changing depression medications become a reality, I am having to stop taking the one I have been on cold turkey. I cried when I received the news.  I cried mostly because I was afraid.

I admit it.  I am afraid. I am afraid that I will lose all or at least most of what I have gained over the last year and a half.  I am afraid that I will lose my sanity.  I am afraid of feeling as sick in my head and body as I used to.  I am more afraid of these things than of death.

I have realized something over these last few, very hard days – thanks in part to my mother.  Being afraid is okay. Being afraid is normal. Mentally Ill or not, anyone in a similar set of circumstances would probably be afraid.

So here I am on my third day of withdrawing from Effexor.  I feel rotten.  I have the worst headache I have ever had in my life. I am constantly thirsty.  I get hungry, eat, then I want to throw up.  My body aches from head to toe.  I have no idea how long it will be before I can start on a new anti-depressant. I am still afraid. However, the fear that I have now feels different than it did.  It is hard to explain but the fear I have now feels as if it is empowering.  Like I looked that fear I had of depression medication changes in the face and said, “I know you now.  You still scare me, but you cannot defeat me.”

Now I know what it feels like for other people when they have medication changes. I can sympathize and empathize with what they are going through. I can be of better help to them.  I also know that the next time I have to go through something like this – I am sure there will be a next time – I am strong enough to handle it.

To myself I say, “Silly Melissa, facing the fear is a mark of courage!  You Win!”

Depression, Diabetes And Autumn…A New Beginning?

I like Autumn. I like the smells, sounds and the feel of Autumn. I have always looked at Autumn as a time of new beginnings. It gives me a sense of renewal. I think it is because it heralds the end of Summer, and welcomes in the cooler, crisper temperatures.

This year, in particular, I have really been looking forward to Autumn.  Summer has been really hard on me.  Diabetes makes my internal thermometer a little off on a good day, throw in Effexorantidepressant – and I spent most of this Summer sweating.  I do not mean a slight glistening of my brow.  I am talking about a full on sweat pouring off my face and body almost constantly.  Once I got heated up that way, even if I went into a cold room, it took hours and hours for me to feel cool again.  I was changing clothes a minimum of three times a day, and my hair never seemed to get dry.

This is the Summer that I had my first fainting spell, which ended in a face plant on the road in front of my parent’s house. It is also the Summer that I was treated for dehydration for the first time in my life. This has just been a miserable summer.

It is now officially Autumn.  I have been able to detect a slight cooling of the air at night and it is not nearly as humid during the day as it has been.  From here on out, it will quickly become cooler, leaving a refreshed feeling in me and in the environment around me.

Just as it is time for the Seasons to change, it is a time for my depression treatment to change.  A new beginning.  It was this time last year that an appropriate drug mix was found for my depression.  It is at this time a new drug mix needs to be found.

I have really enjoyed being able to think clearly, and for my brain to feel and function better.  That is what Effexor has done for me.  Unfortunately, the side effects of Effexor have done many things to me.

From the beginning of my relationship with Effexor there have been struggles.  At first it caused me to have a flat affect – my face did/could not express the emotion I felt and my emotional response was dampened internally. The next thing that it affected was my sex life.  My already low libido basically went away. Then it began to raise my blood sugar.  That was hard to identify in the beginning, because of two asthma attacks – one in December and one in February – that required me to be on steroids. Steroids drastically increase blood sugar levels. Then Effexor started messing with my blood pressure, raising it to extremely high levels.   As I previously mentioned, my body’s ability to control its own temperature was also affected by it.

After looking at my blood test results yesterday, my Psychiatrist was extremely concerned.  She said she was, “sorry, but you absolutely cannot take Effexor another day.” She also said “I do not even know how you are functioning right now”

Which leads me to a confession.  There have been days that I have barely been able to function.  Those are the days when I tell people, I am not feeling well, because I do not want to tell anyone just how awful I feel.  High blood sugar makes you feel so completely horrible.

Withdrawing from Effexor could be be bad, or it might not be.  Right now, I feel extremely, horribly fatigued. No matter how difficult or easy the withdrawal turns out to be, it is something I must go through.  As my mother pointed out “Being happy does not do you any good if you are dead”.  As dire as her statement sounds, that is where my physical health is heading due to the side effects that I am experiencing because of the Effexor.

This new beginning, this new Season in my life, will offer me a chance, once again, to be healthier.  New beginnings are not alway meant to be easy.  I believe if they are easy, then people do not get as much benefit out of the process. One thing I will do, is keep trying to get through each day as best as I can, and only take it one day at a time. I will also keep in mind, that no matter how rotten I feel now, it will not last forever, and once I get through the process I will probably feel better than I did before it began.