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Things have gone south so fast I literally can't keep up anymore. My fate is sealed.

Vanquished

Well-Known Member
#1
I just turned 53 a few days ago, and yet so much of what my body is experiencing is usually reserved for those in their elderly years - if at all. What's even stranger is that for years, I'm talking decades, I never knew anything was up with me. I always saw myself as a relatively healthy person, but little did I know what was brewing and awaited me. Exactly ten years ago my life, my health began to change, and it's been rolling downhill ever since - much to my dismay. I've done my best to take it in stride, even though I've had to walk this road entirely alone. I can't even really say I've only had Dr's. I mean I've had them, and they expressed interest in taking me on then after a year or two they would drop me. During the early years of the first major condition without the proper care I was unaware of what lie ahead although I did know none of it would be good. As of last year (8yrs into the first major condition) I finally was connected to the proper doc for it, and he assured me that he is definitely not going to drop me.

What I didn't expect was to be hit with multiple more major issues in just the span of a year. Six of them have come in just the last month. The most recent was just yesterday. I now have three more issues I need to find yet another new doc for. It just doesn't end. I don't even know if I dare talk about my issues cuz I already know most won't even know what any of it is (except maybe a few), and I totally get it. I didn't know what any of this stuff was either - until I found myself face to face with it.

It's so crazy. I sit here in tears thinking about what I just shared, and reflecting on just how isolating my life has truly been. I came into this world alone (I was abadoned at birth). I grew up alone (no family). I guess it would seem only fitting that I would endure such rare conditions alone, too. I mean, it's not like I have relateable, common issues. Some things I have are common, but the ones that have been plaguing me the longest aren't. I don't have things people can understand. I often try to educate people, and thankfully the vast majority are open to learning. This helps me feel not quite so alone, but the issues just keep piling on.

Just last month I was diagnosed with something that I need infusions for, but before those could begin I had another two issues arise, a couple complications, with one of my rare conditions, that's going to require two surgeries. I wasn't going to beat my immune system down before those. I feel like I need every fighting chance I can get, and that Dr agrees I should hold off on it for now. One of the surgeries is particularly risky given it involves my abdominal aorta. I was waiting for my annual CT scan last week to make sure there was nothing else I was contending with (and that nothing else would need to be done with this aorta), and now I found out I have other problems that are going to make doing the surgeries even more risky. So now I need to address this first before I can feel safe enough to schedule the surgeries which are desperately needed. I don't have a doc I can sit down and discuss all these things with, but I do know this - my days are numbered no matter what. To say my health is bad would be an understatement. It's just so crazy that at 53 I would have the body of an 80yr old, and even then I've known plenty of 80yr olds who were and are better off than I am.

I feel so beat down and defeated sometimes. It's so surreal that so much would come up so fast, and trying to figure out what's best for me is no easy task. Drs all have their say, but it's all with their respective specialty. Unfortunately, I don't have that one Dr that I can sit down and discuss it all with. I need to figure out where to put my time and energies especially with so much going on. With so many things going on I get overwhelmed, and then things turn out even more poorly which is why I need to keep things as simple and as efficient as possible. Drs want to get on everything right now, and while I appreciate that, surgery is what began me down one of my roads in the first place. So I have to trust they'll forgive me while I do what I can to give myself a fighting chance, especially when I realize, more fully than they do, just how much the odds are stacked against me. I had a feeling I was going to end up with more issues from this CT scan which is why I waited. I was bummed to find out what they were, but I'm glad I know now at the same time. All the surgeries are going to do is buy me some more time. My fate is already sealed. The one surgery could bring that fate about faster, too. So many decisions, so much to weigh.

The issues I deal with are:

1) Type B Aortic Dissection (Most dissections are Type A, and most dissections are very tiny in nature and are almost always spontaneous. Mine was not spontaneous, and is considered very large as it goes from the top of my right leg all the way up to my heart. In the abdominal area it branches into the left side a little bit as well.)
2) Coronary artery calcification (still mild at this point, but this is known as the widow maker)
3) Congestive heart failure (milder phase atm last I knew)
4) Artificial mitral valve
5) Axial Spondyloarthritis (This is the one I have to wait for treatment.)
6) May-Thurner Syndrome (one of the surgeries)
7) Partially collapsed lung
8) Emphysema
9) Nodule on the lung
10) Degenerative disc disease
11) I'm prone to strokes. I've already had a TIA, and have had several mild strokes despite being on an anti-coagulant aka blood thinner. I had pre-eclampsia during my 3rd pregnancy which automatically made me prone to these.
12) Ischemic small vessel disease (in the brain)
13) Raynauds phenomenon without gangrene
14) Hypothyroidism
15) Mixed hyperlipidemia
 

Vanquished

Well-Known Member
#2
I guess I say all that cuz I’m at a loss. I don’t even know how to fight anymore. Everything I did over this past year was clearly for nothing as my health plummeted downhill anyway. Sometimes I find myself resolved to simply accepting my fate and not fighting anything anymore. No trying to do any treatments that will only buy me time although undoubtedly I’m sure my kids would love it if I did, and yet at the same time I’m not entirely sure they’d blame me if I didn’t.

They’re old enough I should probably talk with them about it. Thankfully we have such a relationship that we can have the tough conversations. We’ve already been through this because two of my three kids already lost their dad. His was unexpected. He died 25 days after being diagnosed with Non-Hodgkins Lymphoma. He waited much too long to be seen out of denial and fear. We had to have a lot of tough talks during that time, and with my health being as it is I’ve always been open to them saying whatever is on their hearts and minds. It’s deepened our relationships. This is so much, even on them. It’s just natural to them now that of course I’m going to get diagnosed with more and more things. How sad is that? They just expect it now, and who can blame them? At literally any time I can go (die), and I live day by day knowing that. And when more and more gets piled on me like this well….

I’ve been tackling and facing my issues head on from the beginning, and I’m not going to lie. I’m exhausted! I’m burnt out!
This doesn’t even include the regular life’s stressors I’ve been dealing with. Although in all fairness some aren’t regular for me, and are just other forms of being burned.

I’m not one to give up, but how do I keep fighting? I’m exhausted.
 
#4
I just turned 53 a few days ago, and yet so much of what my body is experiencing is usually reserved for those in their elderly years - if at all. What's even stranger is that for years, I'm talking decades, I never knew anything was up with me. I always saw myself as a relatively healthy person, but little did I know what was brewing and awaited me. Exactly ten years ago my life, my health began to change, and it's been rolling downhill ever since - much to my dismay. I've done my best to take it in stride, even though I've had to walk this road entirely alone. I can't even really say I've only had Dr's. I mean I've had them, and they expressed interest in taking me on then after a year or two they would drop me. During the early years of the first major condition without the proper care I was unaware of what lie ahead although I did know none of it would be good. As of last year (8yrs into the first major condition) I finally was connected to the proper doc for it, and he assured me that he is definitely not going to drop me.

What I didn't expect was to be hit with multiple more major issues in just the span of a year. Six of them have come in just the last month. The most recent was just yesterday. I now have three more issues I need to find yet another new doc for. It just doesn't end. I don't even know if I dare talk about my issues cuz I already know most won't even know what any of it is (except maybe a few), and I totally get it. I didn't know what any of this stuff was either - until I found myself face to face with it.

It's so crazy. I sit here in tears thinking about what I just shared, and reflecting on just how isolating my life has truly been. I came into this world alone (I was abadoned at birth). I grew up alone (no family). I guess it would seem only fitting that I would endure such rare conditions alone, too. I mean, it's not like I have relateable, common issues. Some things I have are common, but the ones that have been plaguing me the longest aren't. I don't have things people can understand. I often try to educate people, and thankfully the vast majority are open to learning. This helps me feel not quite so alone, but the issues just keep piling on.

Just last month I was diagnosed with something that I need infusions for, but before those could begin I had another two issues arise, a couple complications, with one of my rare conditions, that's going to require two surgeries. I wasn't going to beat my immune system down before those. I feel like I need every fighting chance I can get, and that Dr agrees I should hold off on it for now. One of the surgeries is particularly risky given it involves my abdominal aorta. I was waiting for my annual CT scan last week to make sure there was nothing else I was contending with (and that nothing else would need to be done with this aorta), and now I found out I have other problems that are going to make doing the surgeries even more risky. So now I need to address this first before I can feel safe enough to schedule the surgeries which are desperately needed. I don't have a doc I can sit down and discuss all these things with, but I do know this - my days are numbered no matter what. To say my health is bad would be an understatement. It's just so crazy that at 53 I would have the body of an 80yr old, and even then I've known plenty of 80yr olds who were and are better off than I am.

I feel so beat down and defeated sometimes. It's so surreal that so much would come up so fast, and trying to figure out what's best for me is no easy task. Drs all have their say, but it's all with their respective specialty. Unfortunately, I don't have that one Dr that I can sit down and discuss it all with. I need to figure out where to put my time and energies especially with so much going on. With so many things going on I get overwhelmed, and then things turn out even more poorly which is why I need to keep things as simple and as efficient as possible. Drs want to get on everything right now, and while I appreciate that, surgery is what began me down one of my roads in the first place. So I have to trust they'll forgive me while I do what I can to give myself a fighting chance, especially when I realize, more fully than they do, just how much the odds are stacked against me. I had a feeling I was going to end up with more issues from this CT scan which is why I waited. I was bummed to find out what they were, but I'm glad I know now at the same time. All the surgeries are going to do is buy me some more time. My fate is already sealed. The one surgery could bring that fate about faster, too. So many decisions, so much to weigh.

The issues I deal with are:

1) Type B Aortic Dissection (Most dissections are Type A, and most dissections are very tiny in nature and are almost always spontaneous. Mine was not spontaneous, and is considered very large as it goes from the top of my right leg all the way up to my heart. In the abdominal area it branches into the left side a little bit as well.)
2) Coronary artery calcification (still mild at this point, but this is known as the widow maker)
3) Congestive heart failure (milder phase atm last I knew)
4) Artificial mitral valve
5) Axial Spondyloarthritis (This is the one I have to wait for treatment.)
6) May-Thurner Syndrome (one of the surgeries)
7) Partially collapsed lung
8) Emphysema
9) Nodule on the lung
10) Degenerative disc disease
11) I'm prone to strokes. I've already had a TIA, and have had several mild strokes despite being on an anti-coagulant aka blood thinner. I had pre-eclampsia during my 3rd pregnancy which automatically made me prone to these.
12) Ischemic small vessel disease (in the brain)
13) Raynauds phenomenon without gangrene
14) Hypothyroidism
15) Mixed hyperlipidemia
Oh mam..I'm so sorry things have been hard for you.. I'll pray for you..
 
#6

Livelife

SF Supporter
#7
That definitely is a full plate, having all these diagnoses and the challenges that come with them. I understand them all, except for the May Thurner syndrome and I'll look that up after I close here.
I have a bit of question....in reference to your comment ".......I was going to end up with more issues from this CT scan.....", Are you saying the CT would show more issues or create more issues?
I'll put you in my prayers....I saw your desire for added discernment now....and also some help for being lifted from an exhausted state and also finding good doctors if you are needing additional ones......
*brohug
 

Vanquished

Well-Known Member
#8
That definitely is a full plate, having all these diagnoses and the challenges that come with them. I understand them all, except for the May Thurner syndrome and I'll look that up after I close here.
I have a bit of question....in reference to your comment ".......I was going to end up with more issues from this CT scan.....", Are you saying the CT would show more issues or create more issues?
I'll put you in my prayers....I saw your desire for added discernment now....and also some help for being lifted from an exhausted state and also finding good doctors if you are needing additional ones......
*brohug
I had a feeling the CT scan would reveal more issues. I just wasn’t sure what it would reveal. However, I’ve had a few scans recently so that in itself poses its own risks. I was trying to avoid so many scans, but I have been throwing clots in my legs from the May-Thurner syndrome and not sure why I had one in my right foot, but it may be because I have severe stenosis at the point where the dissection began at the top of my right leg. (That’s the other surgery they want to do. They want to put a stent in the dissected artery which I’m extremely nervous about. He said this surgery will be a bit trickier but possible.) The stenosis he said will begin to cause my leg to give way only when I try to use it. It did that for the first time last week when I woke up in the middle of the night. It hasn’t happened since, but it’s clearly coming my

This CT scan revealed the lung issues, so today I was referred to a pulmonologist. Hopefully I can get seen quickly because I need the peace of mind that my lungs are gonna be able to handle doing the surgeries as well as my heart given the lung situation.

I have some of the best Drs in the state now, so I’m grateful for that. But it’s hard to overcome having been treated so crappy for so many years too. I feel like I’m the only one who actually has my own best interest at heart now. Drs don’t even tend to go over everything in the scans. I already know this for a fact.

My aorta dissected during my valve replacement surgery. It’s an exceedingly rare complication, and definitely not one they warn you about. The surgeon who did the surgery had done over 2,000 surgeries by the time he had done mine, and I was the first dissection to have ever happened on his operating table. If that gives you an idea of its rarity. So they don’t tend to warn you about everything. I just want to go into this as prepared as I can - in every way possible cuz with my luck I just never know.
 

Vanquished

Well-Known Member
#10
I had to go to the ER yesterday due to an acute pain on the inside of my upper right thigh. Because I'm sick of seeing Drs and/or going into the ER I tried doing a few things to tend to it before going in like taking a nice long hot shower; took a mile and a half walk with my dog (to stretch my leg out), and put a heating pad on it for about a half hour with no effect. Given all my issues, I had to go in to make sure there wasn't a clot in it. After numerous tests I was thankful to learn there wasn't one (although we didn't learn what is causing the pain), but I did learn thru their notes that my aortic dissection is in fact worsening (their exact words). It's impacting my right kidney.

I've been noticing over the last few years that my kidneys have been slowly getting smaller and smaller, and while I realize that they can get smaller as we age my gut told me this was not norm. I had a sneaky suspicion that the dissection was causing this, but of course no Dr was going to come out and say it. I still believe this, and still no Dr has said it. Dissections have everything to do with blood flow. It diverts and impacts blood flow. That's it's MO. It also weakens the artery it hits. I also have heart issues which, at times, can also impact that blood flow.

The dissection directly impacts my kidneys. The walls (there are a few) of the artery are referred to as the lumen. For me, because they're dissected (have come apart from one another), mine are referred to as the true lumen (the original wall), and the false lumen (the walls that came apart). The true lumen feeds my left kidney. While the blood that passes thru the false lumen feeds my right kidney. I have partial thrombosis (blockage) of the false lumen and my right kidney is suffering for it. From what little I know about this it would be better if it were fully blocked or not blocked at all - even as crazy as that sounds. The prognosis is actually worse for those with the partial thrombosis.

I am more than well aware that I can live with one kidney. My daughter was born with only one, so I'm definitely no stranger to it. That's not the issue. It's the fact that in my case they have to deal with a freyed artery to remove it. Most people don't have to worry about that when having to remove one, so that's the added risk involved in my case.

I already have my annual visit with the aortic doc scheduled for this Wed, so I will be learning more specifically about this and what will be happening from here. This dissection happened nine years ago the end of May. I always knew this time was coming. Guess I just wish it were a out a bit further, but then again, not sure I'll ever be ready for this - although I am trying.
 

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