It's been a while, a very long while actually. Ok catching up here, we've moved, to mid Michigan, I'm not as stressed out now, I'm still having issues.
So for those who don't know, I'm diabetic and I have a few other health issues other than my PPPP. I also have neuropathy and thyroid disease, not to mention I'm plum crazy too *grin* So, the decision was made recently that I am going on insulin. Pills and diet, or lack of diet have failed me so this is the best choice now. I hadn't had any huge flares or breakouts in so long but recently my feet have been giving me problems. Well neuropathy and PPPP is just a horrible combination. My feet are peeling, but its my toes that are taking the brunt of the blisters this time. mostly the tips of my toes. I saw something somewhere that said this is a dangerous and rare type of PPPP but I cant find where I read it at and my derm is a moron and doesn't care long as she gets paid. Anyways, I'm trying to do soaks and then massage in Neosporin on the places its cracked or peeling to the meat, then I massage in Vaseline on the rest of my feet. I have one problematic spot on my right big toe. Its very raw and red but it doesn't hurt really on that spot. However, its one of those spots you know right away you have to keep an eye on it, especially with me being a diabetic.
I'm hoping that when I actually start my insulin that my body will be more in balance and my feet will calm down. I still get spots on my hands but its nothing like it was previously thank God. I get dime size or less spots of blisters that I only notice once they start turning brown or start peeling.
The cover to my camera took a dive, nice design over the batteries, latch broke from the stress of the battery springs. Oh joy, or I would take a pic of my toe.
All in all I say I'm not doing too bad. I keep my spirits up, try to not feel too down and I don't let this control my life. Happy happy joy joy! I hope you are all doing well and that this isn't keeping you down either!
Showing posts with label peeling. Show all posts
Showing posts with label peeling. Show all posts
Thursday, September 9, 2010
Monday, August 31, 2009
Celexa
Well my hands are about the same, they aren't too bad, I do have some tender spots however and they are dry and peeling like crazy. Last Friday I went to the new PCP I have and she put me on Celexa because I haven't been sleeping and have been having panic attacks and mild depression. Well I didn't know at this point that Celexa has been known to cause psoriasis and to cause flare ups. *BIG SIGH* But since starting the Celexa I have been sleeping and I hadn't gotten more than an hour of sleep at a time for the two weeks prior so I am so thankful that the Celexa seems to have helped this problem. Its nice being able to sleep. When you get sleep its like seeing the world in color instead of black and white. Ill have to keep an eye on my PPPP very closely though. If I flare up Ill know it must be the Celexa doing it or at least it may be involved. If that happens then Ill have to go back to my PCP and ask her to change my antidepressant to something else and pray that doesn't also cause a flare. I have a spot on the bottom of my foot that has been extremely sore and if that doesn't get better Ill show her the spot. I am thinking of bringing up that my feet have been very very painful and ask if she can either check for arthritis or refer me to a rheumy. I hope I don't have PA.
Alright, I have things to do, hope you all have a wonderful P free day!
Monday, August 24, 2009
Gah Im in a flare!
Before I start, I didn't notice until today there was no "Subscribe to" button on my blog. You should be able to subscribe now and Ill subscribe back on you're as well.
Ok, so I don't think it was the chlorine in the pool. I'm thinking it is the fact that the doctor who prescribed me the Keflex was on vacation and I couldn't get a prescription refill until Friday. I have been off Keflex for two weeks. I'm on them again now though. I need to call my derm because I'm not sure that the topicals are doing any good at all. Maybe she will have me try another one, I don't know, I don't have much faith in her to begin with.
Ok so I took pictures the other day of the newest flare up. I think its going to be more mild this time, but here are the first ones.
Taken 8/22/09
And since I seem to have left my camera at my aunts house, those are the only ones I'm posting today lol I am using my topicals I did last night and the night before, I don't think I will have to use them tonight, but Ill decide closer to bedtime. My feet might get the topicals and not my hands because my feet are really bothering me. My right foot in particular is hurting pretty bad today.
So that's the update for now, I will try to get my camera and post more pictures tomorrow for you.
Hey can everyone tell me what you think has been the most beneficial thing you have done for yourself concerning your P.
Have a great day!
Ok, so I don't think it was the chlorine in the pool. I'm thinking it is the fact that the doctor who prescribed me the Keflex was on vacation and I couldn't get a prescription refill until Friday. I have been off Keflex for two weeks. I'm on them again now though. I need to call my derm because I'm not sure that the topicals are doing any good at all. Maybe she will have me try another one, I don't know, I don't have much faith in her to begin with.
Ok so I took pictures the other day of the newest flare up. I think its going to be more mild this time, but here are the first ones.
Taken 8/22/09
And since I seem to have left my camera at my aunts house, those are the only ones I'm posting today lol I am using my topicals I did last night and the night before, I don't think I will have to use them tonight, but Ill decide closer to bedtime. My feet might get the topicals and not my hands because my feet are really bothering me. My right foot in particular is hurting pretty bad today.
So that's the update for now, I will try to get my camera and post more pictures tomorrow for you.
Hey can everyone tell me what you think has been the most beneficial thing you have done for yourself concerning your P.
Have a great day!
Wednesday, August 12, 2009
In a nutshell
Ok, I'm going to try to put everything from the last 4 - 5 months into one post and catch up to today so that I can continue on from here :)
So you hopefully have read my P story which I previously posted. I haven't always had my camera to be able to take pictures so you wont see any from when it was severe. I have had some really rotten days even when my hands and feet looked mostly clear. Having something like psoriasis is not just physical, it's also a very hard emotionally and mentally. Its hard. It doesn't matter if you have pustular, palmoplantar, guttate, plague or any other type of psoriasis I haven't mentioned, this is a very hard skin disorder to have, no matter the severity.
So when I first started taking pictures I had like the very start of my first flare. I started getting the blisters and the pictures were taken the next night. They come up so fast you can almost watch them rise, literally. I only had pictures of my feet because at this point my hands hadn't really started doing anything yet. I had maybe 5 tiny blisters on the palm of one hand when the ones of my feet were taken.
A couple of days later my hands flared up and ugh, it was almost unbearable. I couldn't even dress myself, I couldn't walk, I couldn't use the restroom without assistance. I crawled around on my knees and elbows when I had to do anything. Thank God for my husband. I wouldn't have made it through that without him. It got really severe on the bottom center of my feet and my fingertips and hands.
These were taken about 2 weeks later.
At this point I only had one picture of one hand, its the one I use as my header for this blog. It was taken about 1 week after the previous feet pictures you see here.
All the skin ended up peeling off. The worse part of this has been the pain and not being able to live the way I want to. At one point it was so bad it was bleeding, the itching was driving me insane, it looked like my skin was rotting. I was crawling around the house on my knees and elbows because I couldn't walk.
So this is like one big roller coaster. You get better you get worse you get better again, you get worse. I did at one point clear up on my hands, my right hand completely but not my left. My left hand is always worse than my left which I am grateful for because I'm right handed.
Ill post some pics and date them so you can see how it gets better then worsens. Thank God its never been as bad as when it first started and I couldn't walk. Since that first flare, it's been much milder but as I said, it goes from mild to moderate then mild.
These were taken on 5/29/09 You can see I was doing great here. I had been on Presidone for a week and using Halobetasol Propianate Ointment 0.5% for 2 weeks at this point.
This was 5/30/09. Just a little bit of red spots and a tiny bit of peeling.
6/07/09 Check out my right hand, its beautiful! My left hand was getting a little rough though.
6/20/09 After using Halobetasol for a week prior to the pictures. I had to stop using it per doctors orders on this day.
6/22/09 Still not too bad I guess but what you can't see is the pain. The feeling like you have been playing with fiberglass.
6/23/09 The next day, you can really see how fast this stuff flares. My fingers were really hurting there. It didn't help that they were swelling up either.
6/24/09 Still about the same.
6/30/09 It looks a little bit angry here.
So, the 5th of July I got out of bed and my right heel hurt. It was a shock, put my foot down and OUCH! So I baby it all day and take it easy. Well the 6th comes and its worse. I really don't like going to the doctor. Besides it being about 15 miles away in the next town over, sometimes I just feel like its such a waste of time. So going against my husband telling me I need to go I stay home. Well when the 7th got here I could only limp around and I knew I needed to do something because it wasn't getting any better. I waited until I knew there wouldn't be a lot of people in urgent care and drove in. The doctor who was there that night is awesome. I really like her, she listens to what youre saying and doesn't just blow you off like a lot of doctors do. She determines that I have a skin infection from a small crack in my heel. Oh yay right? You bet your butt yay! lol She put me on Keflex. Well I had been trying for a while to get my dermatologist to put me on Keflex because one of the gals on the NPF forums says that it helped clear her up, so this is something I REALLY wanted to try. I was so happy. You couldn't slap the smile off my face. So I go on Keflex. At that point I was only taking baths with oatmeal and epsom salts and occasional Halobetasol. The next pictures were taken 3 days after I started the Keflex.
7/10/09
Next ones are taken 5 days later. Still kind of angry looking.
7/15/09
A very wise woman told me it takes time to heal, be patient. :)
Next ones were taken on the 18th, 10 days after starting Keflex.
7/18/09
Next ones you can really SEE the improvement. They're taken 23 days after starting on Keflex.
8/01/09
Wow huh? Yea WOW! To me this is a HUGE improvement! I did use my Halobetasol about 4 days during that time. If I wouldn't have I don't know it would have done so well.
Now, that pretty much brings you up to date. Right now I DO have some blisters coming up again. I'm using Halobetasol for a couple of days and then not for a couple days, on and off. I would be in trouble if it weren't for the Halobetasol I think.
So I have hard days and easy days and lately they have been more easy ones which is good. I have had days I hurt so much I couldn't open a bottle or hold a glass. Days I had to have help doing the most simple things.
I hope they find a cure one day. But until then Ill keep treating my psoriasis and doing the best I can while I try to help others. Ill try to keep posting updates on here, plus I have 3 other blogs so I'll most likely be going between them all on alternating days.
As for me Ill end this post for the night. Today is my 9th wedding anniversary and we have a drive planned to Lake Michigan to see lighthouses. Have a great day!
So you hopefully have read my P story which I previously posted. I haven't always had my camera to be able to take pictures so you wont see any from when it was severe. I have had some really rotten days even when my hands and feet looked mostly clear. Having something like psoriasis is not just physical, it's also a very hard emotionally and mentally. Its hard. It doesn't matter if you have pustular, palmoplantar, guttate, plague or any other type of psoriasis I haven't mentioned, this is a very hard skin disorder to have, no matter the severity.
So when I first started taking pictures I had like the very start of my first flare. I started getting the blisters and the pictures were taken the next night. They come up so fast you can almost watch them rise, literally. I only had pictures of my feet because at this point my hands hadn't really started doing anything yet. I had maybe 5 tiny blisters on the palm of one hand when the ones of my feet were taken.
A couple of days later my hands flared up and ugh, it was almost unbearable. I couldn't even dress myself, I couldn't walk, I couldn't use the restroom without assistance. I crawled around on my knees and elbows when I had to do anything. Thank God for my husband. I wouldn't have made it through that without him. It got really severe on the bottom center of my feet and my fingertips and hands.
These were taken about 2 weeks later.
At this point I only had one picture of one hand, its the one I use as my header for this blog. It was taken about 1 week after the previous feet pictures you see here.
All the skin ended up peeling off. The worse part of this has been the pain and not being able to live the way I want to. At one point it was so bad it was bleeding, the itching was driving me insane, it looked like my skin was rotting. I was crawling around the house on my knees and elbows because I couldn't walk.
So this is like one big roller coaster. You get better you get worse you get better again, you get worse. I did at one point clear up on my hands, my right hand completely but not my left. My left hand is always worse than my left which I am grateful for because I'm right handed.
Ill post some pics and date them so you can see how it gets better then worsens. Thank God its never been as bad as when it first started and I couldn't walk. Since that first flare, it's been much milder but as I said, it goes from mild to moderate then mild.
These were taken on 5/29/09 You can see I was doing great here. I had been on Presidone for a week and using Halobetasol Propianate Ointment 0.5% for 2 weeks at this point.
This was 5/30/09. Just a little bit of red spots and a tiny bit of peeling.
6/07/09 Check out my right hand, its beautiful! My left hand was getting a little rough though.
6/20/09 After using Halobetasol for a week prior to the pictures. I had to stop using it per doctors orders on this day.
6/22/09 Still not too bad I guess but what you can't see is the pain. The feeling like you have been playing with fiberglass.
6/23/09 The next day, you can really see how fast this stuff flares. My fingers were really hurting there. It didn't help that they were swelling up either.
6/24/09 Still about the same.
6/30/09 It looks a little bit angry here.
So, the 5th of July I got out of bed and my right heel hurt. It was a shock, put my foot down and OUCH! So I baby it all day and take it easy. Well the 6th comes and its worse. I really don't like going to the doctor. Besides it being about 15 miles away in the next town over, sometimes I just feel like its such a waste of time. So going against my husband telling me I need to go I stay home. Well when the 7th got here I could only limp around and I knew I needed to do something because it wasn't getting any better. I waited until I knew there wouldn't be a lot of people in urgent care and drove in. The doctor who was there that night is awesome. I really like her, she listens to what youre saying and doesn't just blow you off like a lot of doctors do. She determines that I have a skin infection from a small crack in my heel. Oh yay right? You bet your butt yay! lol She put me on Keflex. Well I had been trying for a while to get my dermatologist to put me on Keflex because one of the gals on the NPF forums says that it helped clear her up, so this is something I REALLY wanted to try. I was so happy. You couldn't slap the smile off my face. So I go on Keflex. At that point I was only taking baths with oatmeal and epsom salts and occasional Halobetasol. The next pictures were taken 3 days after I started the Keflex.
7/10/09
Next ones are taken 5 days later. Still kind of angry looking.
7/15/09
A very wise woman told me it takes time to heal, be patient. :)
Next ones were taken on the 18th, 10 days after starting Keflex.
7/18/09
Next ones you can really SEE the improvement. They're taken 23 days after starting on Keflex.
8/01/09
Wow huh? Yea WOW! To me this is a HUGE improvement! I did use my Halobetasol about 4 days during that time. If I wouldn't have I don't know it would have done so well.
Now, that pretty much brings you up to date. Right now I DO have some blisters coming up again. I'm using Halobetasol for a couple of days and then not for a couple days, on and off. I would be in trouble if it weren't for the Halobetasol I think.
So I have hard days and easy days and lately they have been more easy ones which is good. I have had days I hurt so much I couldn't open a bottle or hold a glass. Days I had to have help doing the most simple things.
I hope they find a cure one day. But until then Ill keep treating my psoriasis and doing the best I can while I try to help others. Ill try to keep posting updates on here, plus I have 3 other blogs so I'll most likely be going between them all on alternating days.
As for me Ill end this post for the night. Today is my 9th wedding anniversary and we have a drive planned to Lake Michigan to see lighthouses. Have a great day!
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