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Posts tagged Fibromyalgia

Physical Therapy

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Lizze has physical therapy this morning.  She had a really rough day yesterday so I hope she does ok with this today.

The physical therapy is for her migraines I believe.  It’s kind of a last ditch effort to help prevent them. I could be totally wrong on this one though. 

Everything kinda blends together after awhile.  Maybe it’s for the fibromyalgia? 

Either way,  I think it’s a great way to start the week,  albeit,  a painful one. I’m really proud of her for not giving up and continuing to push through the pain.  

Awesome job honey,  what a fine example you are setting for the boys :-)

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Prayers and good thoughts are needed

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Please say a prayer for Lizze.  She went into the emergency room a little bit ago.  Her migraine is so bad that she has become unsteady on her feet and sick every time she eats.  It’s also been 3 days since she has been able to sleep.

I had to sorta strong arm her in order to get her to go.  She is very reluctant to go to the hospital because of the approach many doctors take to patients suffering with fibromyalgia.

In our experience,  there are quite a few doctors that don’t buy into this disorder and subsequently treat those seeking relief as drug seekers. While there are people out there looking for their next fix,  people with fibromyalgia, live every single day in almost constant pain.

Wanting relief from the pain isn’t wrong or weak.  I can’t imagine what my wife goes through on a daily basis.

Her mother came and picked Lizze up and took her.  It was the quickest and easiest way to get her there.  I’m staying with the boys until my mother comes and picks up Emmett.  

Please say a prayer for Lizze.  You can follow her at @fibromamaby3

Thank you all..

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They come in three’s

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We all know the old saying, “they come in three’s”. Well, we were hit, smack dab in the face with that today. Typically, this saying refers to death but thankfully, that doesn’t apply in this case. What I’m talking about is more along the lines of just bad things happening. For whatever reason, my family seems to be just like a magnet for bad things. We have, over the years, adopted the notion that anything that can happen, will happen.

I know that not the best attitude to have but it’s the reality we find ourselves in, more often than not.

Today was just one of those days where both of these sayings applied.

 

Number 1

Lizze, in desperation, was seeking additional help from a Rheumatologist to help manage her fibromyalgia. She was basically denied access. She was informed that once she started pain management (which she did a few years ago) that Rheumatology would be a step backwards and that no one would touch her. This was pretty much a kick in the gut for her. She is in really bad shape and this was something she had been clinging to, as a possible light at the end of the tunnel.

As it turns out, once again, that light was a train, not hope, speeding towards her.  

 

 

Number 2

My littlest minion, Emmett John, has hit yet another fever cycle. It started on the way to OT today. His cheeks were beat red but he hadn’t yet spiked the fever. We were going to just take him home but he was very insistent that he stay and finish. he did really well but we took it easy. He has been struggling though since this afternoon. He has the beginnings of the cold sores already. His fever right now is not very high but sitting around 100 oF. History dictates that this is only the beginning of a hellashish 10 days.

Emmett is already a handful and this will just make him all that more challenging. Plus, there’s very little we can do to make this time more bearable for him.

 

Number 3

We met with Dr. Reynolds this afternoon. Dr. Reynolds is Gavin’s primary Psychiatrist. We spent some time going over everything that is now or has been going on with Gavin.. Dr. Reynolds is still concerned about Childhood Disintegrative Disorder or CDD. I don’t really know what to think anymore. Dr. Reynolds did point something out that I hadn’t thought about, and I can’t for the life of me, explain why this hadn’t occurred to me yet.

We know that Gavin has some type of degenerative neurological disorder, whether or not it’s CDD or something else remains to be seen. However, Dr. Reynolds pointed out that not only are we seeing neurological degeneration, but also muscular degeneration as well. It hadn’t clicked with me that Gavin no longer being able to move his tongue in an upwards direction, is a muscular issue as well.  While this knowledge doesn’t fundamentally change anything, it absolutely knocked the wind out of me.

It’s just one more thing to worry about.

These are the three things that really weighed heavy today. It’s worth mentioning that I’m still sick and getting worse instead of better. I’m falling ever more behind now.

Sigh….it’s time for the wonderfully disgusting elixir that is called NyQuil. Hopefully, the 30 ml’s of green liquid magic, will carry me off to a restful sleep tonight. Here’s hoping anyway :-)

**Thanks for reading**

       -Lost and Tired

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Overcoming the stigma of chronic pain and medicaid

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image

Lizze is waiting to be seen by the doctor. We have to overcome the stigma of chronic pain and medicaid. There are judgements and assumptions made about people with chronic pain like Fibromyalgia and people on assistance. It’s wrong but it happens. I worked in the emergancy medical field a very long time and I saw it happen quite often. Not everyone is abusing the system not everyone is a drug seeker. Sometimes life is just to much and you need help. Some times you have 3 special needs boys that require tremendous sacrifice and public assistance is one of the pills you have to swallow in order to help your children.

Relief from pain shouldn’t be based on your economic status. Hopefully, they will see past all that and look at the situation for it actually is….. I’m praying Lizze finds relief tonight….:

Autism, Fibromyalgia and IMPOSSIBLE decisions..

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`~Special needs parenting of children with Autism is a very challenging task. However, when one parent has major health issues those challenges exponentially increase. Sometimes these situations require choices to be made that are far from easy~

 

I’ve been pretty overwhelmed all week. Well, let’s be honest, I’m overwhelmed pretty much ALL the time. Parenting 3 boys with Autism will have that affect. I have so many thoughts in my head that I want to get out but I can’t seem to organize them enough to string two of them together coherently.  Friday was a really challenging day. The Lost and Tired family made some progress but also suffered some pretty major setbacks. Today isn’t any better as Lizze can’t physically get out of bed today.

Friday was full of “to-do”s” for me to try to accomplish. I managed to get Emmett’s speech therapies back on track. Beginning next week Emmett will receive speech therapy twice a week. As you may remember Emmett was being seen once a week but that wasn’t meeting his needs as he is “mod-severely” speech and language impaired. He needs at least twice a week (which ONLY equates to 1 hour/wk) in order to continue making progress. Originally the increase had been denied but there had been some miscommunication. After speaking with insurance and Concorde Kids I got things straightened out….at least for now. Progress.

I also spent the better part of the afternoon on the phone with the Cleveland Clinic. I was trying to get Lizze into the Neurology and Rheumatology departments. Lizze is in desperate need of help and the Cleveland Clinic is basically the BEST hospital in the US. I had everything set up and she was registered but when I went make the appointment I was informed that they don’t take her insurance. I asked about self-pay or hardship programs and I was told that Lizze would have to drop her insurance coverage in order to qualify. If she did that then she would lose her other doctors. The other option is to change carriers but then the kids would lose their doctors. How do you make that choice. Good doctors that accommodate kids with Autism are not easy to find but at the same time someone that can help Lizze has been IMPOSSIBLE to find. How do you choose? Who takes priority?

I had to sell my phone on eBay this week. I needed to money to try to get the van fixed…again. This means I had to shut down my Android development/Autism Awareness projects as I no longer have a platform to develop on (ie Samsung Epic). While I was VERY happy to be able to do this, developing was my only outlet aside from this blog. Hopefully I’ll be able to get another phone in the near future so I can get back to it.

"The Tube"

I also spent some time on Friday looking into getting the van fixed. There is NO POSSIBLE way for me to do this myself as I believe the front axle has to be dropped in order to gain access to the water pump. There is a part called “the tube” (and yes that’s the official name….seriously) that runs off the top of the water pump and it ruptured. “The tube” is a separate serviceable item from the water pump. I called around and the repair runs about $300. The problem is that sometimes “the tube” can’t be removed from the water pump and so the water pump will need to be replaced as well. This is a VERY big game changer as the price of the repair more then doubles. So basically the
repair will cost $300-$800. The really crappy part is that they won’t know if the water pump needs replaced until they get started. The problem is that once they get started there is NO going back. I spoke with Waterloo Transmission made an appointment for Monday morning. I bought the part at the dealership (dealer only part) so there won’t be a delay. I’ll drop the van with the part off on Monday. Not only are they cheaper but they are Autism Aware and have worked with us in the past. They have agreed to look at it and if it appears to be a problem then they will abort the repair as I just can’t afford to replace both. So I’m crossing my fingers that everything goes smoothly so we can get the van back up and running.

~When you have to choose between your children with Autism and your spouse with health problems~

As I said earlier, today is a really bad day, especially for Lizze. She physically can’t get out of bed. I tried to help her but the pain is just to much. I don’t know how to help her. I want to just lay there with her but the kids need me as well and I can’t leave them alone. Being a special needs parent is hard enough but when your spouse is disabled words can’t describe how challenging it becomes. I just realized that I used the word “disabled” to describe Lizze. While her and I have used that word in private I haven’t said anything like that here. The truth is that Lizze is disabled. Her health has declined to such a point that she can no longer even walk without assistance. While it shouldn’t be about me, I can’t help but feel torn. I have to be there for the kids AT ALL TIMES but Lizze is my best friend, my wife and the mother of my kids. How can I not be there for her. I feel like I have to choose who gets my help and that SUCKS… Life shouldn’t require these types of choices.

If your family is happy and healthy PLEASE don’t EVER take that for granted. If you take one thing away from this post I hope it’s that.

Autism can touch ANY family in MANY ways. Never forget that. Every day is Autism Awareness day.

**Thanks for reading**

       -Lost and Tired

MyFreeCopyright.com Registered & Protected

Facing new challenges ahead

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Yesterday Lizze received her cane. It’s difficult for Lizze to be physically reduced to needing assistance to walk. I won’t speak for her as she will be sharing her own feeling soon enough. For me though, it’s heartbreaking to watch her struggle with so much pain.

I will be taking Lizze to the Cleveland Clinic to a  rheumatologist for a second opinion. Not really a second opinion more like a re-evaluation. The doctor that have diagnosed her with Fibromyalgia is a top 50 doctor in that field in the US so we’re pretty confident with his diagnosis. The concern right now is that she is unresponsive to medications. It could VERY easily be the stress we are experiencing each day or she has the wrong diagnosis. We will be seeking help at the Cleveland Clinic to once again rule out MS. I say once again because it was ruled out 6 years ago when she was diagnosed with Fibromyalgia instead.

The concern is that it may have been to early to detect MS 6 years ago. Since then things may have progressed to a point that it’s now detectable.The symptoms of both are very similar and she’s losing more and more mobility each day. The odds of someone at her age having all of these things going on is extremely unlikely, according to some of the doctors. It’s so uncommon that it’s becoming more and more likely that something was missed. That something could very likely be MS, as it fits quite well into her plethora of symptoms.

The other thing we are looking into at the same time is that Lizze is VERY likely an adult with Aspergers. It makes a great deal of sence.  Big picture, it really doesn’t really matter that much. In reality she wants to know and I agree. It would give her a better understanding of herself and help me to better communicate as that is typically a struggle for us. Lizze is adopted and so we have no reliable medical history. It’s important to her because it will also help to explain having 3 kids on the spectrum as there is a genetic link. This is however, a much lower priority then the rest of her medical issues but it’s still important none-the-less.

Lizze is on day 20 (I believe) of her migraine. As I said before she will be having a procedure called headache infusion done. This will hopefully finally break the migraine. Today, however, we were told she can’t have the procedure done until May 25th. That means she has almost another month to try and deal with this crippling migraine. Nothing so far has helped and she is long past the end of her rope.

I’m auctioning off my phone so that I can get the van fixed. I can’t get Lizze or Emmett to Cleveland without it. Hopefully we can get some new information from the Cleveland Clinic that sheds light on to her situation. Hopefully…..hopefully….it’s the stress that is making everything untreatable and not something more sinister.

Please pray that she finds some relief from her pain ASAP.

**Thanks for reading**

       -Lost and Tired

MyFreeCopyright.com Registered & Protected
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