Jump to content
Sclero Forums

Biopsy Results In ~ Morphea

Recommended Posts

My biopsy results came back as morphea. I'm a bit bummed today as well, because I think I see 2 or 3 new spots coming up. No, not a bit. I'm bummed.


Anyway, I had already (due to some wise advice) my appt with the rheumatologist set up and will see him on Tuesday.


I was at the Gastro today who sent me for the following tests.






CDT CLOSTER. DIFFICILLE TOXIN (know this one too well)




I have IBS (hoping that doesn't mean something in regard to systemic!) and it has been acting up due to recent antibiotic treatment for a tragus piercing gone bad...thus the c diff test.


The rheumatologist has asked me to wait for tests until I saw him, why get poked twice, but yesterday I was at the gyno for a vulva biopsy...and my friends, after you've had that...one more needle poke is small taters. My gastro knows me well, and knows the ability for me to go to the rheumatologist doctor with some information makes me feel a little ahead of the curve.


He is also sending me to a therapist, as my anxiety level is through the roof.


What do I take to the rheumatologist doctor?


I was told a list of any and everything I could think of that may pertain to health issues he should be aware of:


Raynauds for 15 years...


Itching all over consecutively for two months each Spring




I can't think of any others right now but will continue with the list.


Plus a list of questions with space below to write answers.




Is there anything else I should take?


Specifics I should ask?




I so want to do this right, and be my best advocate...proactive, and as much as I can...one step ahead.


Also...I am breathing...but my last question for the night, is it normal to freak out and be so scared? I heard localized scleroderma and thought ok...til I began to read of systemic, and read the list of uh ohs and saw I had several.


How do you deal with the wave of overwhelming, oxygen stealing angst that sneaks up on you occasionally?


I really do appreciate any thoughts, guidance, or shove in the right direction.



Share this post

Link to post
Share on other sites



I freaked out at first, then my kids split (I believe due to my illness) and haven't heard from them since June.


I went back to a therapist I began seeing when I was getting divorced. That helped with both recent slaps to my head.


My rheumatologist suggested I attend a sclero group at a well known hospital in order to get a handle on the disease. As I explained to him, too much information is as bad as too little information. I know what it is, I know what it does, I know there is no cure, I know I will deal with symptoms as they arise. In other words, Karen, stop exploring too much; in general the "worst" is always generated in articles and stories.


Stop reading up on it for now, and keep your appointments, accept and get your head together before exploring. Then, you will be able to keep all information in perspective. It's like the warning information on prescription drugs; they have to tell you if one out of seven million had a reaction (even if on a placebo), although it may be as safe as a mother's arms. It's the law to report that one, even if it's not a reality. Same applies with a lot of reading material. Better they report the worst case scenario, probably for the same reasons.


Hope I have allayed your apprehension a little this evening.


PS: The spots that keep showing up, I've learned to live with it, just as one would liver spots. If that's the worst at this time, that's the least. I was never one into perfection, so I'm not that upset over those things.

Share this post

Link to post
Share on other sites

Hi Karen,


Oh I have so been there done that with the freaking out. The thing that calmed me the most was communicating with all the wonderful people here and learning what life is like for others with diffuse systemic. Not to mention learning how long some have been living with it. That sounds bad....the key words there are long and living.


I'ts good to have yourself prepared intellectually and emotionally. It's hard to prepare for the worst without freaking out. I am the same way, I want to know worst case scenario and then be pleasantly surprised that I don't have to deal with that. And if I DO have to deal with that then at least I was prepared emotionally and I won't be shocked.


But the hardest part is not letting your emotions run away with you and trying to keep from stressing out. I wish I had a magic answer but there isn't any. For me it just took time and coming here to talk to others in my same boat and learn about the treatments that have worked (or not worked) for them.


As far as dealing with the overwhelming oxygen stealing angst: Just go with it. Let yourself feel it. Find a private place or a broad shoulder and cry. Let it all out. Don't keep it in thinking that you're being strong. In the long run keeping it in will only make you weaker.


It is a learning experience. You are doing fine. Better than fine. You have armed yourself with information and are getting to the right doctors and coming here for support and advice. So here is a pat on the back for you: pat-pat-pat :D


(((((((((((((((((((And a big cyber hug for strength)))))))))))))))))))))))))))


Keep us posted.



Share this post

Link to post
Share on other sites

Hi Karen,


If it's any help at all, as I understand it, it is very common for people with morphea to have one or two symptoms besides just the skin involvement. However, it is exceedingly rare for morphea to occur in overlap with systemic scleroderma, with most studies putting the odds at 0% to 2%. There is more elaboration on this in our last book, Voices of Scleroderma Volume 3, which has articles by world experts in scleroderma as well as an entire chapter of stories from people who have morphea and, occasionally, other symptoms as well.


Morphea is known to sometimes occur in overlap with lichen sclerosus, which it sounds like you are also being tested for. There are treatments available for both lichen sclerosus and morphea. Small morphea lesions tend to fade or go away on their own, even without any treatment, in 3 to 5 years. If you have more than a few or they are spreading, then prompt treatments can be helpful in preventing the spread.


Within Sclero Forums, look for the "Search sclero.org main site" in the left sidebar of each page. Use it to find more info on morphea and lichen sclerosus, too.


Odds are you'll feel much better when the diagnostic process is complete!

Share this post

Link to post
Share on other sites

Hi Karen,


I do not have Morphea, so I can't speak to that. However, I do know the angst that can come about while waiting ... in limbo.


Once I knew what I "HAD", my anxieties really eased.


Keep posting.... that's a good thing, because there are very experinced folks here who are a great comfort and support to us all.


Soft Hugs,


Share this post

Link to post
Share on other sites

You know, I knew it was morphea. The dermatologist (actually the PA...you know, if you pay for a doctor, you ought to get a doctor *stumbles off minor soapbox moment*) had pretty much AVOWED it was prior to biopsy being back, and when I went to my gastro yesterday he got a gander and said the same thing...


I guess kind of *knowing* it and then being told...there is a difference.


It broke my heart, and I don't understand why. I am emotion driven, we'll leave it at that.


Truman, while I know that if all it is is spots, it's the least...they are still on my body, and I don't know, I guess I worry about is that it? I'm trying to stop reading, but as barefut has noted, some of us cannot help ourselves. We're all different, I suppose, and what a good thing that is or what a dull old world this would be (although at this time...a little dull, I could do with!)


I'm so sorry to read of your children. There is nothing more I can say than, that stinks...and I'm so sorry. When you need them most, they leave.


You always allay my fears, and any bit of peace anyone can give me is so very appreciated. Tomorrow I get blood work back...may be another bad afternoon for me. I'm not looking forward to it, and yet need to know. What a double edged sword, it stinks. You are so right on the worse always seeming to be represented, and even when you are freaking out, those are the ones that scream at you, aren't they?


Thank you.



A girl after my own heart! My sister in the over think and overload of information in trying to be informed, and be prepared department! :P Hubby said to me that the spots are more white today than yesterday...*wonders if that is from the severe stress overload from yesterday, or not*. He took the day off and we went out warm glove, hat and electric blanket shopping for me. Also to see the movie with Dwayne, The Rock, Johnson in it...the movie was not so good, but the actor warmed my blood and that's a good thing. lol :unsure:


Thank you for the pats on the back. I'm still frightened. I took an atarax last night because, to be truthful, I thought I'd lose my mind (had some I was given for itching two years ago...they sure didn't seem to lose their potency any!) I won't do that tonight, I don't like how they make me feel.


My finger tips feel all tingly today, all day...probably stress. I have moments of greatness...Thank you for the pats on the back...you were just trying to feel my morphea spots...I know it. LOL That may not make you laugh but it does me. ;)


Thank you too!




Are we allowed to cyber squish hug each other. I'll make it a gentle one! That first paragraph...I actually felt a breath, and a full breath at that, after reading that. First one in days.


Excuse the newbie, but...how does one come across the book mentioned? Is it for sale, where and how do you go about getting one?


I go to the dermatologist on Monday (and actually see the doctor this time...woo hoo) and he is to begin treatment of the spots. One of the smallest looks like it is going away, or maybe fading?


I hope I like the dermatologist doctor better than I did the PA.


Close your eyes Tru....I think I will go look at the search sclero.org main site stuff for morphea here in a bit. Thank you for the heads up onthat.


Other than my bowel complaint (pipings been awful (no pun intended) for 25+ years), the itching (which I have not had in many months, and only two episodes of), and the morphea...I feel fine.


OH...yes, that lichen sclerosis...my gyno did it as a precaution as I had some irritation and this diagnosis caused some concern. She says if it is that, it is likely one of the earliest caught cases of all time! :D THAT BIOPSY...well, let me tell you, OUCHIE!


Thank you so very much.




How very wonderful of you to check in and share part of yourself and your thoughts with me. Thank you...I think you are right...once I know what is going on, I'll find a way to peace.



Thank you all, so much. I'm so glad I found this site.



Share this post

Link to post
Share on other sites



I forgot to tell you another thing I did to help me through my "freak out" period. I bit the financial bullet and went to counseling. My counselor really didn't DO or SAY much but it was helpful to me to have an ear, albiet an expensive ear.


Anyway, It was easier for me than to go to a friend or family member because I was (still am) in the middle of a divorce so I didn't have a spouse to go to and I didn't want to "burden" my busy friends and family with my new problem.


My insurance did pay for 1/2 of each visit, so it wasn't too bad. I would recommend counseling. I think it might help you to get through this rough patch.


Take Care,



Share this post

Link to post
Share on other sites

Hi Karen -


I just wanna give you a big hug. First of all, I freaked out big time when I was diagnosed, I pretty much started digging my own grave. That was almost 8 years ago and I have not progressed much since then.


As far as what to take with you to the rheumatologist - you really seem to already know that. Remember he deals with this all the time and he'll know what to ask you. Although, I am a full believer in being your own advocate, so anything that pops into your head, write it down, don't worry about having too long of a list, remember you are paying for this appt. Make him work for you.


I think right now what you need to hear from him is what good news there is today in terms of you living a long good life. I'm going to give you a link to our emotional adjustment page - hoping it will help you tonight.


Much love,

Share this post

Link to post
Share on other sites

Hi Karen:


Just a follow up to my recent adventures this week. As I've posted here in the past, I've been fighting an extremely painful ulcer on my big toe. general practitioner and rheumatologist have been treating me nearly every week now for months, and I have been on temporary disability for four weeks due to this.


I finally dragged myself to the wound care unit close to my town on Monday. The doctor was shocked that my general practitioner had not sent me sooner. I told him he had not sent me at all, and I came on my own.


Long story short, he numbed my foot and laying down, I turned my head away. When I got direction on soaking and dressing changes, I left. SHOCK when I took the bandages off. The top and both sides of my toe are gone, in addition to my toe nail. The doctor at the center had to remove gangrene that had developed. I asked my general practitioner several times if the blackness was gangrene and he assured me no. Well lo and behold........I'm not angry that it came to this, I'm not angry that a good portion of my toe is gone........I'm relieved this doctor is taking care of the situation. I have to go once a week until it is healed. He tells me I should be able to wear a shoe by December. He has informed me that if I get so much as a pimple in the future, I am to have them check it immediately. Heavy expense as this center is out of network with my insurance.


All this has also landed me a longer stint of temporary disability.........my dogs love it!

Share this post

Link to post
Share on other sites

I'm calling the therapist today. I just found out my insurance pays 100% for 20 visits! What a great thing.



I was glad to read it the counselor helped you. I think one of the things that will help me most is getting my blood results back. My Monday dermatologist appt and learning how they plan to treat the lesions, and the Tuesday rheumatologist appt to cry all over him and unburden all my fears, see what he has to say about them, besides...'good grief woman, I'm going to have to charge you extra for those three boxes of tissue!!!".


Thank you, sweet lady!




Apropos name! I will look at the link. Thank you for it.


I believe what has helped me most is what everyone (and especially Shelley) wrote. I feel so good, yet am so scared. I think it is the scare of what happened with our neighbor lady. As soon as the word 'scleroderma' was said...my head and heart went to her case. I too began digging a grave.


I have a list of all my past ills, in order of concern! I plan to take that. I have no questions yet until I get my blood panel reports today and then I am sure I will have plenty.


When I called for this appt with the rheumatologist, his nurse informed me he made his appts what you needed them to be, so not to expect a quick in and out (ala the dermatologist, I soooo need to find a new one)...but is more the ilk that wants you to understand and make sure you go home, not a mess...but informed. YAHOO.


I will be switching insurances in January, so that I can get to the University of Michigan (I live an hour away). The local chapter of the Sclero group in my area is Ann Arbor and the wonderful woman I spoke to from there is really encouraging me in this.


Thank you for your kind words...your encouragement, and your help.






Oh sweetheart, your poor toe!!!! How did it get that bad. I know nothing about gangrene! Methinks you need a new general practitioner!!! You go find a new one of those, and I'll go find a new dermatologist!!!! How could he have missed that? It seems to me that would be fairly obvious. I'm so very sorry to hear this.


I can't see your av as I type this, but what type of dogs do you have? I think it is a cocker in the av, if I remember right.


I have Cavalier King Charles spaniels. I love those little furballs...they are a menace, but so cute.


I hope you begin feeling better and better. You know I wish you only good things.






Thank you for the link. I actually ordered it through the library I used to work at, and it is on it's way!


I am anxious for it to get here...thank you for the link.


Today I wait for blood results. The next step on this road. Shelley's post has me feeling so much hope, I am afraid of it! LOL How silly that is.


It was very helpful to read that logically and statistically I should be in the 98%, not the 0-2%.


I got a sclero sticker for my car in the mail today...I plan to put it on. I'm considering attending the Piston basketball game with the Michigan group and meeting everyone. Everyone seems so nice, and dang it...accepting and wonderful...why wouldn't I want to meet them.


Thank you all again...so very much. I can't even begin to tell you the peace you have given me.



Share this post

Link to post
Share on other sites

Hello karen,

I wanted to welcome you to the forums! I am a little late in the game, but none the less, am so glad that we found you. As you can see, there is so much support to be had here, and tons of great and encouraging info on the ISN. It sounds like you have a good team of doctors and that is esential!


Gentle hugs &

Share this post

Link to post
Share on other sites

Truman, I am so sorry to hear about your toe...its hard to believe that your doctor missed gangrene! However, you caught it before it spread too far. Take extra special care of those toes...and try to enjoy this time with your pups!

Share this post

Link to post
Share on other sites



Thank you for the kind welcome.


I just heard from the gastro.


All my results are in, and all good. Nothing showing in any blood tests that would indicate systemic.


I feel MUCH relief in this. I'm glad the gastro had me go have them, so I'd not fret through the weekend.


So it looks it may only be the morphea for me....and I'll stay on that, and do what I have to to make that better.


Also will be seeing the rheumatologist to be doubly sure I am doing as I should.


Hugs all around, and let us all now form a circle (or are you all line dancers?) and do the happy dance!



Share this post

Link to post
Share on other sites

Hi Karen:


My dogs are cocker spaniels and I love them to death. I absolutely adore Cavalier King Charles spaniels.. That is hopefully, going to be the next addition to my family. They are just the cutest little sweeties.


Share this post

Link to post
Share on other sites

Join the conversation

You can post now and register later. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.

Reply to this topic...

×   Pasted as rich text.   Paste as plain text instead

  Only 75 emoji are allowed.

×   Your link has been automatically embedded.   Display as a link instead

×   Your previous content has been restored.   Clear editor

×   You cannot paste images directly. Upload or insert images from URL.

  • Create New...