Livedoid vasculopathy

Posted by angelasmom @angelasmom, Aug 3, 2011

Looking for people with the rare blood clot and leg and foot ulcer disease of Livedoid Vasculopathy. Mayo seems to be experienced at treating this disease so I thought I would find you here, I have it.

Interested in more discussions like this? Go to the Blood Cancers & Disorders Support Group.

@robingayle

Is anyone still monitoring this group? I have LV and I am in desperate condition. Mostly, it is the chronic, excruciating pain for the last 5 years that has me profoundly depressed, exhausted and feeling as if the quality of my life has reached the point of diminishing return. I get flares 4 to 7 times per day that feel like a torch is being held to my feet. I have had the same open ulcers for 5 years. one on the top of each foot. I had 2 other ulcers that took 3 years to heal. I feel as if I am being tortured. Thank you for letting me vent.

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I don't know if anyone is monitoring or not. I asked a question over 6 months ago and got no reply. I have had an LV ulcer on my ankle for 25 years. It has not healed in the last 4-5 years, and the pain, which seems to hit without warning, is like boiling water being poured on the ulcer. I take aspirin in the morning and Alleve at bedtime for pain. It dulls pain somewhat. When my ankle hurts I put my feet up and try to concentrate on something else (TV, games, book, etc) until the pain goes away. If I wake up and the pain starts I try to lie so that nothing touches the ulcer, and relax my muscles. I can not stand in one place for very long, as this aggravates the ulcer, and I can not walk or work moving around for more than a half hour at a time or I pay for it later in the day. It is depressing at times. Hang in there, you are not alone!

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@robingayle

Is anyone still monitoring this group? I have LV and I am in desperate condition. Mostly, it is the chronic, excruciating pain for the last 5 years that has me profoundly depressed, exhausted and feeling as if the quality of my life has reached the point of diminishing return. I get flares 4 to 7 times per day that feel like a torch is being held to my feet. I have had the same open ulcers for 5 years. one on the top of each foot. I had 2 other ulcers that took 3 years to heal. I feel as if I am being tortured. Thank you for letting me vent.

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Hi,you're not alone!!Are you taking any medications?

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Hi @robingayle and @prairiesmoke thank you for sharing your stories. Connect is a place where you can always vent and share your stories with people like you.

I want to thank @patientrea for responding to your post and I also wanted to tag @zenk as they may be able to offer you support.

To repeat @patientrea's questions, what medications are you on right now?

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@patientrea

Hi,you're not alone!!Are you taking any medications?

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Hi Sheila and all, Are you taking any blood thinner? Xarelto or other blood thinners are the best way to treat the ulcer because it will allow for more oxygenated blood to get to the wounds. You probably need somebody in wound care to talk with, and maybe get more pain control. Zenk

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@zenk

Hi Sheila and all, Are you taking any blood thinner? Xarelto or other blood thinners are the best way to treat the ulcer because it will allow for more oxygenated blood to get to the wounds. You probably need somebody in wound care to talk with, and maybe get more pain control. Zenk

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I am taking 2 regular aspirin a day for blood thinning. I have been on warfarin in the past for blood clots in legs and lung. I have been leery of trying stronger pain meds. I am in a test study now with a new grafting material made from placental tissue. It has worked somewhat, but it is a slow process. I talked to my regular Dr. about Xarelto, but she seemed to think I was ok with aspirin as a blood thinner. I also have factor V Leiden, which aggravates the blood clotting. Sheila

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@ethanmcconkey

Hi @robingayle and @prairiesmoke thank you for sharing your stories. Connect is a place where you can always vent and share your stories with people like you.

I want to thank @patientrea for responding to your post and I also wanted to tag @zenk as they may be able to offer you support.

To repeat @patientrea's questions, what medications are you on right now?

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I take 2 regular aspirin a day for clotting control, and Aleve for pain control in the evening.

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Hi Shiela, Just wondering if you would benefit from a more potent blood thinner. Aspirin is not enough to get oxygen to the wound. Maybe just a trial on something like Xarelto would be a thought. Also, some wound care studies have suggested the an eye drop called Timolol Maleate , your doctor would know what it is, placed on the ulcer a few times a day has been shown to improve blood flow to the wound. The drops are a prescription but are not expensive.
Wishing you better treatment, Zenk

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@zenk

Hi Shiela, Just wondering if you would benefit from a more potent blood thinner. Aspirin is not enough to get oxygen to the wound. Maybe just a trial on something like Xarelto would be a thought. Also, some wound care studies have suggested the an eye drop called Timolol Maleate , your doctor would know what it is, placed on the ulcer a few times a day has been shown to improve blood flow to the wound. The drops are a prescription but are not expensive.
Wishing you better treatment, Zenk

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Thanks for the info on the eye drops! I will see about the timolol Maleate. If I try it I will have to test it on my skin first to see if I have a reaction to it. I have a number of allergies which complicates things.

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@steph1567

Not sure if this is still an active blog.
I'm 23 years old and was diagnosed with this a few years ago.
I'm wondering if anyone has the ulcers that itch extremely bad? Or if they have ever had a rash that spreads to their thighs, forearms, buttox, back and stomach from this condition?
Also, how bad is the risk for clots?
I am trying to be on birth control with estrogen for PCOS but I am apparently at too high of a risk because of this condition even while taking aspirin.
Thank you!
Stephanie

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Hi Steph! I have not been diagnosed with LV but I have been struggling with symptoms identical to what has been described in this chain for the last 10 years. I am 29 years old. I got a blood clot and was diagnosed with activated protein C resistance at the age of 19. At the age of 23, a previously very painful chronic ulcer on my right ankle went through a phase of being extremely itchy. In fact, the itchiness spread across my whole leg and got so bad I struggled to sleep. This was treated successfully with cortisone cream and by wearing a compression sock. I was treated in Switzerland. It took several months to heal but the good news was that the scar on my ankle got less painful than before the itchiness. I don’t know why. With regards to birth control, I used a copper IUD for five years since I cannot use hormones. Hoping that you will get rid of the itchiness soon, if you haven’t already!

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@prairiesmoke

I am taking 2 regular aspirin a day for blood thinning. I have been on warfarin in the past for blood clots in legs and lung. I have been leery of trying stronger pain meds. I am in a test study now with a new grafting material made from placental tissue. It has worked somewhat, but it is a slow process. I talked to my regular Dr. about Xarelto, but she seemed to think I was ok with aspirin as a blood thinner. I also have factor V Leiden, which aggravates the blood clotting. Sheila

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My Dermo yesterday changed my meds from 300 mg Aspirin a day to Xarelto. I hope it makes a difference. I am also doing a full AIP Auto Immune Protocol food regime to try and knock this thing on the head

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