Livedoid vasculopathy
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.
And something I forgot:Livedoid vasculopathy as far as I know is vasculopathy and not vasculitis!
Sorry I'm not a doctor, The doctors have called it vasculopathy but for some time we been calling it vasculitis .. my bad.
As far as the diagnosis, There has been lots of blood and other samples sent to the lab and my Rheumatologist and a Dermatologist have examined me as well as those at the hospital wound care.
You don't have to say sorry! In this discussion we try to help each other!Have you discussed with your doctors any other treatment options in case the therapy doesn't help;
Hello @gtalan,
Welcome to Connect; I see that you have some excellent support from @patientrea...thank you so much patientrea!
We have some incredible discussions about LV here on Connect. I encourage you to read them here:
– LIvedo Vasculopathy or Livedo Reticularis (whole body face white) http://mayocl.in/2qoA4jr
– Treatment options for Lividoid Vasculopathy (LV) http://mayocl.in/2cH8jhA
– Livedoid vasculopathy http://mayocl.in/2dd7pKa
@spence, @prairiesmoke @mlemieux @angelasmom @vickieb @zenk @gonefishinmt @grandmaabby @srusti @canderson12 @marlene64, would you join in to share your experiences and insights about livedoid vasculopathy?
@gtalan, have you discussed other treatment options (blood thinners, Doxycycline Therapy) with your doctor, or perhaps thought of getting a second opinion regarding getting relief?
Pain relief is the biggest obstacle in my opinion... I have tried everything to no avail.
Hello @swing1929,
It’s great to see you back on Connect, and although I'm so sorry to hear that you haven't found any relief, I'm really glad that you chose to join this discussion.
Would you share some of your insights and experiences with the members in this group? Sometimes, what may not work for one, may be of great help to another!
Welcome back, Jenn.
Thank you, it's nice to see that there is more info about LV, The doctors haven't put me on blood thinners yet other then aspirin 325mg (was 81mg). I have been getting treatment from my PCP, my Rheumatologist that's been treating me for Fibromyalgia, a Dermatologist that treated me 14 years ago for LV and those at the Hospital Wound Care. I do have pain most of the time but not all from LV, I have been taking Prednisone and about 4 different antibiotics 2 to 3 weeks at a time for the last 6 months. For the wound treatment I was using a wound vacuum (lots of fun) I was so happy when they told me I could stop using it. but it helped, now I have a 3 layer compression sock. I think I'll be asking about some other treatments, some of the meds are not so good for long term use.
Hello again!Courage!!!I was started on acetylsalicylic acid plus dipyridamole.Some improvement at the beginning,but not pain relief and wound healing.And all of the sudden I read zenk's post about xarelto.Complete healing!!I have to admit that a therapy that helps some people might not help others.TRY!!!!Talk with your doctor about other treatment options.Best of luck!Be in touch!
@zenk thanks a lot!!I owe you
Hello @swing1929!Can you please tell us all the therapies you have tried;