DFSP Friends.
Comments
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Hi Jo thanks for your answerOntario48 said:How Are You Feeling?
Hello Lone...I put a few posts on the other thread Dermofibrosarcoma Protuberans (DFSP), I had a hard time finding some of the threads there so I first searched it in "content" and then linked from there and was able to see all the pages...go to page five (Nat our DFSP hostess helped me with that ").
I haven't read much about the immune system and cancer. I do know in general that a strong immune system helps in the fight against cancer and many other diseases. There was a recent study a friend found that scientists had found receptors that pin point how cancer cells speak to normal cells and infiltrate them. The idea is to come up with something that changes the messaging to promote healthy cells to remain healthy. Pretty cool.
In regards to mets, I've only found a couple reports of those who had mets. The most common spot is in the lungs, this is true for most sarcomas. Some doctors do a chest CT or MRI to screen for this. Some to do not. Even though the numbers are very low most of those who have mets to the lungs have the FS-DFSP variant, a higher grade malignancy. Standard DFSP mets to the lungs is even rarer. Looks like a lot of patients in the USA have an MRI or CT as standard routine. My doc didn't do it (skin cancer specialist-dermatologist). He said only for recurrence or FS variant. I will be seeing a sarcoma specialist for my follow up and management (I rant about that on the other thread). I will discuss this with her and get her opinion. For piece of mind I would like a chest screen as part of my baseline moving forward. Adult soft tissue sarcomas represent 1% of all adult cancers. DFSP is a smaller precentage within that and of those 2-5 percent get mets to the lungs. So if they don't test them how do they know. The cases I read they got it later in life (5 - 15 years later). No regrowths just distal cancer in the lungs, confirmed to be DFSP. So for me it would be nice to know if I get a clear chest screen so if something should happen down the road we have a benchmark.
Push for it, cry if you have to LOL!
Take care...Jo
Hi Jo thanks for your answer and thanks for clearing some things for me.
My surgeon told that giving me an MRI would present a greater danger to my health than the DFSP would have for spreading. He did have x-rays of my lungs and they came back clear. In Denmark the checkup program for all cancers is 5 years, after that you're on your own. Maybe I should demand a new x-rays of the lungs in 5 years time, just to make sure.
I trying to keep busy reading about how to strengthen my immune system and what to in general to minimize the risk of ever getting cancer again. Don't know what else to do.
Btw it was me who send you a freind request nd I got one from Nat that i too get errors reviewing.
take care too.
lone
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Lungs are clear...GREAT!Lone111 said:Hi Jo thanks for your answer
Hi Jo thanks for your answer and thanks for clearing some things for me.
My surgeon told that giving me an MRI would present a greater danger to my health than the DFSP would have for spreading. He did have x-rays of my lungs and they came back clear. In Denmark the checkup program for all cancers is 5 years, after that you're on your own. Maybe I should demand a new x-rays of the lungs in 5 years time, just to make sure.
I trying to keep busy reading about how to strengthen my immune system and what to in general to minimize the risk of ever getting cancer again. Don't know what else to do.
Btw it was me who send you a freind request nd I got one from Nat that i too get errors reviewing.
take care too.
lone
Hi Lone, this system is a bit quirky for sure.
Glad you had the chest cleared. I am not sure, from what I've been reading about his type of cancer, if your immune system would have made a difference. I know some cancers they can show a direct correalation. Soft tissue sarcomas come from "translocation" of genes and this occurs after birth so not hereditery. Obvisoulsy the healthier you are the better your immune system is. I know there is a lot of focus on keeping the immune system healthy while you are going through treatments (radiation/chemo etc) and there are foods/supplements that you can take that contribute to that.
Most people ask the question, why me, what could I have done to avoid this, how did I get it. I don't think there is a clear cut answer for this. Obvisously if you live a certain kind of life style (drugs/alcohol/chemical exposure etc) that would contribute to getting some cancers. I read somewhere that most people who have cancer fear it's recurrence for about a year and then it starts to fade and it's not prevalent in their lives any longer.
That old saying...time heals everything! Or we get old and forget
, lol!! My saying is..."it is what it is". Life throws us meany things. It doesn't matter how much I think I know about DFSP, it doesn't matter how much the experts say, it doesn't matter if I do all the right thinks, if it comes back...it comes back and I deal with it. No matter what, we keep on going. It's our human spirit. So enjoy your life to the fullest. I had a friend die in our early 20's. She was one of the healthiest people I knew. It was cancer, it was sudden and she went quickly. At that point I made a decision that I would always tell those around me how much I loved them. A quick "love ya" at the end of phone call, love you and a kiss as they left from a visit, end a letter or email with "XO Love you". You just never know what life with bring you. But you deal with it and it makes your stronger.
Hope the hip is healing well...Jo
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tricky subjectsOntario48 said:Lungs are clear...GREAT!
Hi Lone, this system is a bit quirky for sure.
Glad you had the chest cleared. I am not sure, from what I've been reading about his type of cancer, if your immune system would have made a difference. I know some cancers they can show a direct correalation. Soft tissue sarcomas come from "translocation" of genes and this occurs after birth so not hereditery. Obvisoulsy the healthier you are the better your immune system is. I know there is a lot of focus on keeping the immune system healthy while you are going through treatments (radiation/chemo etc) and there are foods/supplements that you can take that contribute to that.
Most people ask the question, why me, what could I have done to avoid this, how did I get it. I don't think there is a clear cut answer for this. Obvisously if you live a certain kind of life style (drugs/alcohol/chemical exposure etc) that would contribute to getting some cancers. I read somewhere that most people who have cancer fear it's recurrence for about a year and then it starts to fade and it's not prevalent in their lives any longer.
That old saying...time heals everything! Or we get old and forget
, lol!! My saying is..."it is what it is". Life throws us meany things. It doesn't matter how much I think I know about DFSP, it doesn't matter how much the experts say, it doesn't matter if I do all the right thinks, if it comes back...it comes back and I deal with it. No matter what, we keep on going. It's our human spirit. So enjoy your life to the fullest. I had a friend die in our early 20's. She was one of the healthiest people I knew. It was cancer, it was sudden and she went quickly. At that point I made a decision that I would always tell those around me how much I loved them. A quick "love ya" at the end of phone call, love you and a kiss as they left from a visit, end a letter or email with "XO Love you". You just never know what life with bring you. But you deal with it and it makes your stronger.
Hope the hip is healing well...Jo
Hi lone, Isn't our.friend Joanne doing a.great job wth all the.new info she is posting. Firstly lone I don't understand how you Dr can say MRI can increase cancer recurrence and no t xrays. Before all my DFSP issues (3yrs ago). I found out I have a brain tumor, its inoperable due to its location but luckily it's benign. But the neurosurgeon told me never to have xrays of my head only MRIs as xrays mess with your cells and increase the risk of cancer( that's why the radiology staff run and hide before they push the button). A few xrays over.many yrs obviously don't seem to make any difference but if there was need in the future for repeated testing any where on.my body I will be requesting MRIs. But in saying that let's not borrow trouble from the future. As Jo says, " it is what it is" and we can only deal with what is in the here and now. Sure we can try and keep are selves as healthy as possible, but sometimes we just don't have control over what happens. My Dr also said what Jo wrote that there is no predicting DFSP its not hereditary and there was mo way I could have been tested or prevented its occurence as they now can do with so many other conditions not just cancers. In regards to the immune issue, I personally like to eat lots of fresh green and red fruits and veggies as they are the highest in antioxidants and have been proven to reduse the chance of certain cancers. And I take vitamin supplements to cover the times Im to busy for th the real food. So you must be almost ready to have your stitches out. That should make things feel better, well at least until the itching starts lol. But you're through it now please don't dwell on the "what ifs" .. We have all done our home work on this subject . But except for watching our scars(for changes) having our regular checkups( Jo I promise I make that appointment today) there really isn't anything we can do. Take care ladies Ps. Get those hugs and.kisses while you can specialy from your children, unfortunately my boys all did the "mum stop it Im not a.little boy anymore" but now I have a cuddly little granddaughter so that makes up for it. :-)
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They are always your little boys.natmcg said:tricky subjects
Hi lone, Isn't our.friend Joanne doing a.great job wth all the.new info she is posting. Firstly lone I don't understand how you Dr can say MRI can increase cancer recurrence and no t xrays. Before all my DFSP issues (3yrs ago). I found out I have a brain tumor, its inoperable due to its location but luckily it's benign. But the neurosurgeon told me never to have xrays of my head only MRIs as xrays mess with your cells and increase the risk of cancer( that's why the radiology staff run and hide before they push the button). A few xrays over.many yrs obviously don't seem to make any difference but if there was need in the future for repeated testing any where on.my body I will be requesting MRIs. But in saying that let's not borrow trouble from the future. As Jo says, " it is what it is" and we can only deal with what is in the here and now. Sure we can try and keep are selves as healthy as possible, but sometimes we just don't have control over what happens. My Dr also said what Jo wrote that there is no predicting DFSP its not hereditary and there was mo way I could have been tested or prevented its occurence as they now can do with so many other conditions not just cancers. In regards to the immune issue, I personally like to eat lots of fresh green and red fruits and veggies as they are the highest in antioxidants and have been proven to reduse the chance of certain cancers. And I take vitamin supplements to cover the times Im to busy for th the real food. So you must be almost ready to have your stitches out. That should make things feel better, well at least until the itching starts lol. But you're through it now please don't dwell on the "what ifs" .. We have all done our home work on this subject . But except for watching our scars(for changes) having our regular checkups( Jo I promise I make that appointment today) there really isn't anything we can do. Take care ladies Ps. Get those hugs and.kisses while you can specialy from your children, unfortunately my boys all did the "mum stop it Im not a.little boy anymore" but now I have a cuddly little granddaughter so that makes up for it. :-)
Grab them and hug them and kiss them. They love it!!! They are just being coolieo's. Mine is in the prime of I'm too cool for mom. But tonight, when hes' tired, his leg hurts because he bailed on a jump and he's just done!, I grab him and squeeze and he totally gives in for just that one moment. Mom's know what that feels like...you know you rock in there world. No words exchanged. He's too cool.
Mom's rule the world!!!
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Wise words Jo and Nat I hear youOntario48 said:They are always your little boys.
Grab them and hug them and kiss them. They love it!!! They are just being coolieo's. Mine is in the prime of I'm too cool for mom. But tonight, when hes' tired, his leg hurts because he bailed on a jump and he's just done!, I grab him and squeeze and he totally gives in for just that one moment. Mom's know what that feels like...you know you rock in there world. No words exchanged. He's too cool.
Mom's rule the world!!!
Thanks ofcourse you're both right, i probably just have too much time on my hand while waiting for my surgeon to call or waiting to get get ready to go to work again. I have 11 metal stiches and they have to stay in for 14 days so a week more of waiting, doctors orders I can't even drive a car for 14 days.
I think the reason my said it was better with an x-ray is maybe because it is less expensive...and if I'm not confusing it with something else isn't MRI a scan of the whole body? i'm not sure but I will ask him. I had a friend who had 4 small tumors from breast cancer removed followed by chemo and radiation, she was never offered an MRI either with the same excuse of the radition thread being greater than the risk of metastation.
And like you I too give my kids lots of hugs and kisses, that is when I can catch them of course :-)
I have read some very interesting things about alkalized food preventing cancer from spreading. It is good idea to keep eating those veggies
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MRIs yes very expensive.Lone111 said:Wise words Jo and Nat I hear you
Thanks ofcourse you're both right, i probably just have too much time on my hand while waiting for my surgeon to call or waiting to get get ready to go to work again. I have 11 metal stiches and they have to stay in for 14 days so a week more of waiting, doctors orders I can't even drive a car for 14 days.
I think the reason my said it was better with an x-ray is maybe because it is less expensive...and if I'm not confusing it with something else isn't MRI a scan of the whole body? i'm not sure but I will ask him. I had a friend who had 4 small tumors from breast cancer removed followed by chemo and radiation, she was never offered an MRI either with the same excuse of the radition thread being greater than the risk of metastation.
And like you I too give my kids lots of hugs and kisses, that is when I can catch them of course :-)
I have read some very interesting things about alkalized food preventing cancer from spreading. It is good idea to keep eating those veggies
Hi lone, I was intending to just have a little check then saw you had posted so had to respond. MRI can be done on all or specific parts of the body. They are not xrays they work from sound waves, Its quite noisy(they give you ear plugs) and you do have to stay in a tunnel device for quite a long time. Some people have to be mildly sedated as they can't handle it otherwise. I have no choice when it comes time for checking my brain tumor so I just grin and bear it. Iv been talking to my husband about the chest xray issues we have been discussing with Jo and he.seems to think that a chest xray would be ok, but that I should check with the Dr.and if it's risky then have the MRI instead Im lucky enough that a can afford it even though we are not in a private health insurance fund. ( Ill just get him to work more ovettime lol.
I have my checkup appointment booked for the 27th March. I know they will take photos and they give me copies so it makes it easier for me to notice if ant changes occur.
Jo and I had internal dissolving stitches and external ones which were taken out after 10-12 days, so I just assumed that you had similar. We call what you have staples . Any way as long as your not doing to much Im sure it will all heal wonderfully.
Oh you asked about my family. My dad came to Australia as a displaced person after WW2. He was 28 .Left all his family behind in Ukrainian( at that particular time he had lost contact with most of them). My mum arrived about 12mths later with her patents,an older sister(married with a son) and three brothers. Mum was 19. They met and married in 1951. I grow up speaking Ukrainian( and English).
Take care.
Natalie0 -
Chest Xraynatmcg said:MRIs yes very expensive.
Hi lone, I was intending to just have a little check then saw you had posted so had to respond. MRI can be done on all or specific parts of the body. They are not xrays they work from sound waves, Its quite noisy(they give you ear plugs) and you do have to stay in a tunnel device for quite a long time. Some people have to be mildly sedated as they can't handle it otherwise. I have no choice when it comes time for checking my brain tumor so I just grin and bear it. Iv been talking to my husband about the chest xray issues we have been discussing with Jo and he.seems to think that a chest xray would be ok, but that I should check with the Dr.and if it's risky then have the MRI instead Im lucky enough that a can afford it even though we are not in a private health insurance fund. ( Ill just get him to work more ovettime lol.
I have my checkup appointment booked for the 27th March. I know they will take photos and they give me copies so it makes it easier for me to notice if ant changes occur.
Jo and I had internal dissolving stitches and external ones which were taken out after 10-12 days, so I just assumed that you had similar. We call what you have staples . Any way as long as your not doing to much Im sure it will all heal wonderfully.
Oh you asked about my family. My dad came to Australia as a displaced person after WW2. He was 28 .Left all his family behind in Ukrainian( at that particular time he had lost contact with most of them). My mum arrived about 12mths later with her patents,an older sister(married with a son) and three brothers. Mum was 19. They met and married in 1951. I grow up speaking Ukrainian( and English).
Take care.
NatalieHello Ladies...
Just checkin in as I got an email from Jessie. She actually lives in Toronto. I told her about Dr. Gladdy and she made contact and she too is going to see her. Wow, I am so happy for Jessie as she has some decisions to make for her next steps. I sure hope Dr. G can sort through it all with her and provide a good action plan.
I just wanted to pipe up on the chest xrays. I was actually in the hopsital in August (2 months before my biopsy) as I was at work and was experiencing some chest pains. Thought I was having a friggin heart attack. In the end it wasn't my heart, all my test were fine. BUT, I did have a chest xray and the tumor didn't register. I believe I read a CT or MRI is what is used rather than a chest xray. Google it again and see what comes up for diagnostic and screening.
Sure stinks not having this stuff covered. We are very lucky in Canada. People complain about our healthcare system but it's there when you need it.
Hope all is well with you ladies. AND Nat "good on ya" for making that appointment!!
JO
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Great that Jessie madeOntario48 said:Chest Xray
Hello Ladies...
Just checkin in as I got an email from Jessie. She actually lives in Toronto. I told her about Dr. Gladdy and she made contact and she too is going to see her. Wow, I am so happy for Jessie as she has some decisions to make for her next steps. I sure hope Dr. G can sort through it all with her and provide a good action plan.
I just wanted to pipe up on the chest xrays. I was actually in the hopsital in August (2 months before my biopsy) as I was at work and was experiencing some chest pains. Thought I was having a friggin heart attack. In the end it wasn't my heart, all my test were fine. BUT, I did have a chest xray and the tumor didn't register. I believe I read a CT or MRI is what is used rather than a chest xray. Google it again and see what comes up for diagnostic and screening.
Sure stinks not having this stuff covered. We are very lucky in Canada. People complain about our healthcare system but it's there when you need it.
Hope all is well with you ladies. AND Nat "good on ya" for making that appointment!!
JO
Great that Jessie made contact and that you were able to help get in contact with a good doc in Toronto.
In Denmark healthcare is free for everyone - we do however pay the higest taxes in all of the world for this. However i looked up what a MR scanning cost in a private hospital and it is like 500 us dollars for a scanning of the abdomin. I might go get one after my surgeon calls...
Nat are you going to regular checkups for your brain tumor? how did you find out? Have you had a biopsy? That must have caused a lot of scare being diagnosed with a brain tumor.
Take care
lone
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CheckupsLone111 said:Great that Jessie made
Great that Jessie made contact and that you were able to help get in contact with a good doc in Toronto.
In Denmark healthcare is free for everyone - we do however pay the higest taxes in all of the world for this. However i looked up what a MR scanning cost in a private hospital and it is like 500 us dollars for a scanning of the abdomin. I might go get one after my surgeon calls...
Nat are you going to regular checkups for your brain tumor? how did you find out? Have you had a biopsy? That must have caused a lot of scare being diagnosed with a brain tumor.
Take care
lone
Jo & Lone, nice to know Jessie is going to get some answers to her concerns. It's funny I touched base with a few other Aussies that have had DFSP over the last 6mths, but strangely I have had more contact with people from other parts of the world. Who would have thought that having a form of.cancer would lead me to 1.learning to use the internet on my phone( I have never bothered much with our home computer). 2. Learning more about DFSP than I.every imagined. 3. Made friends with such caring people. Now back to the heading "Check up" Yes I do have regular MRIs,but since the tumor hasn't changed in three yrs the neurosurgeon said I could leave it for 2yrs.( unless I notice any of the things he mentioned could happen of.it starts to grow). I was having a.CT scan for a totaly unrelated issue when the tumor was disscovered I had never had any symptoms to indicate it was there. I couldn't have a biopsy as it is located at the very top of my cerebellum and the location also makes it virtually inoperable. But it has been identified through scans as a meningioma. These type of brain tumors are not uncomen and only cause problems if the continue to grow. As we have no idea how long I've had it or when and why it stopped growing,all.I can do is avoid anything the might cause it to start growing. As I no longer water ski,snow ski, or go to amusement parks I reason that any sudden trauma to my head will be out of my control. So there you have it. Just as I was.coming up to the 2yrs all clear for that ordeal, when I found out about the DFSP. And now Im on another round-about of checkups. But that's OK Im here and reasonablly healthy. And when I count my blessings of which I have many. :-) life is pretty dam good. Hey Jo Coffey has chimed in again on the other thread. Bye ladies for now anyway. Nat.
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Can't find Coffeynatmcg said:Checkups
Jo & Lone, nice to know Jessie is going to get some answers to her concerns. It's funny I touched base with a few other Aussies that have had DFSP over the last 6mths, but strangely I have had more contact with people from other parts of the world. Who would have thought that having a form of.cancer would lead me to 1.learning to use the internet on my phone( I have never bothered much with our home computer). 2. Learning more about DFSP than I.every imagined. 3. Made friends with such caring people. Now back to the heading "Check up" Yes I do have regular MRIs,but since the tumor hasn't changed in three yrs the neurosurgeon said I could leave it for 2yrs.( unless I notice any of the things he mentioned could happen of.it starts to grow). I was having a.CT scan for a totaly unrelated issue when the tumor was disscovered I had never had any symptoms to indicate it was there. I couldn't have a biopsy as it is located at the very top of my cerebellum and the location also makes it virtually inoperable. But it has been identified through scans as a meningioma. These type of brain tumors are not uncomen and only cause problems if the continue to grow. As we have no idea how long I've had it or when and why it stopped growing,all.I can do is avoid anything the might cause it to start growing. As I no longer water ski,snow ski, or go to amusement parks I reason that any sudden trauma to my head will be out of my control. So there you have it. Just as I was.coming up to the 2yrs all clear for that ordeal, when I found out about the DFSP. And now Im on another round-about of checkups. But that's OK Im here and reasonablly healthy. And when I count my blessings of which I have many. :-) life is pretty dam good. Hey Jo Coffey has chimed in again on the other thread. Bye ladies for now anyway. Nat.
oHi Nat, thanks for letting me know but can't see anything for Coffey. My pages don't seem to refresh or something. Hope all is well there.
Jo
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Yyyyyyyyyeeeeeesssss I finally got the answer from the pathologyOntario48 said:Can't find Coffey
Hi Nat, thanks for letting me know but can't see anything for Coffey. My pages don't seem to refresh or something. Hope all is well there.
Jo
And it was a good answer. Actually they never found any dfsp in the lump the cut out which must be because my GP cut to edge of the tumor and got it all after all :-)
This means I have 1.5 mm clear margins.
Have a great Easter everyone
/Lone
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WONDERFUL CONGRATULATIONS.Lone111 said:Yyyyyyyyyeeeeeesssss I finally got the answer from the pathology
And it was a good answer. Actually they never found any dfsp in the lump the cut out which must be because my GP cut to edge of the tumor and got it all after all :-)
This means I have 1.5 mm clear margins.
Have a great Easter everyone
/Lone
Best news, sooo happy for you Lone,
Now you can relax and enjoy Easter with your family.
I have my 6mths checks up(a bit overdue) on the 3rd. I will probably discuss having a scan on my chest just so we have a reference should.I need it in the future.
Happy Easter Everyone :-)
Nat.0 -
Great News!Lone111 said:Yyyyyyyyyeeeeeesssss I finally got the answer from the pathology
And it was a good answer. Actually they never found any dfsp in the lump the cut out which must be because my GP cut to edge of the tumor and got it all after all :-)
This means I have 1.5 mm clear margins.
Have a great Easter everyone
/Lone
Hello Lone,
Very happy for you. Big relief!! Have a wonderful Easter.
Jo
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Worried Wife
When I met my husband in 2001 he had a round lump on the underside of his arm -about five inches from his shoulder- that bulged out. He said it's nothing, that he has had it forever. Forward to 2006 when my husband of three years finally got the courage to tell me that something was wrong, that he had a growth in his pelvic area, (in the joint of where the top of thigh met his groin). He showed it to me and it looked like a ball inside a sheath of skin dangling four to five inches from his groin--the ball slightly smaller than a golf ball. We were living in Canada (I'm Canadian, my husband was working in Canada temporarily) and had a great gp but she had just closed her practice so we went to a new Doctor across the border in Washington State. She looked at the growth, decided to snip it off close to his body and send the mass for a biopsy. It was easy, fast, closed with a couple of stitches. The biopsy came back as a type of fibrous tissue growth, non malignant, nothing to worry about we were told except that it would probably regrow.
Three weeks ago my husband told me that the area had started to return. Said it started about eight months ago but he couldn't take the time off to deal with it but now it was bothering him. This time it had a dangling bit, but the base was large and we could tell that there was a mass inside. We now live in Georgia, fairly new to the area, did not know who to go see so we started at the md's office where I had been going thinking that they could advise who to see. Couldn't get in to see Dr, saw a nurse practioner. She took a look and a picture, said it was more than she could deal with and got us in to the local dermatologist's office that afternoon - to the physician's assistant there. He looked, said it was no big deal he was going to remove the dangly bit and cauterize so that my husband would no longer be uncomfortable and that he could come in the following week and he would remove the rest so that it would not come back again. First biopsy from danging bit came back A-OK. I was not OK with the PA removing anything. I felt a surgeon or the very least the actual Doctor in the office but my husband felt that the guy sounded like he knew what he was doing so he went back the following week.
14 stitches and an appointment six days later to take out the stitches. The whole area is not good. We went back this past Wednesday afternoon to have his stitches removed but it soon became apparent that we weren't there to have his stitches removed. The biopsy of the main mass did not come back as expected, it showed the possibility of DFSP. He said that he was not able to remove it all, it has 'fingers' that he's not sure where they go, and that my husband needs to see a surgeon to have it removed. But we won't know for sure till the full pathology comes back and he knows a couple of surgeons in a small town that is the same distance from us as a major city with multiple health facilities. Needless to say we did not take him up on his offer of the 'good guy surgeons' in the small town. We asked him to refer us to a surgeon who worked in oncology out of a major hospital. The guy came back with a referral to a surgeon who specializes in bariatric surgeries with an appt at the end of April. Oh and when I called the following morning to find out when exactly all the biopsy pathology results would be in I was told that they were already back and it was DFSP.
Through making multiple calls and leaving messages for various Drs somehow I ended up being called at home by Dr Steven Attia at the Mayo Clinic. DFSP is what Dr Attia does. He organizes a conference for DFSP. While I was on the phone with this amazing man, he called a surgeon who specializes in sarcomas and between them they decided on a day that they could both see my husband. April 9.
My husband has not had a scan, an xray, an mri etc. He has had a biopsy result positive for DFSP. He has 14 stitches in his groin that are not healing and I'm scared to death. The wait to April 9th is very hard and I don't know what to do.
Tomorrow my plan is to get a copy of the picture and send it to Dr Attia as well as all three biopsy results. I thought that I'd also send a picture of what the stitches look like now.
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RHC the best is a good doctorRHC said:Worried Wife
When I met my husband in 2001 he had a round lump on the underside of his arm -about five inches from his shoulder- that bulged out. He said it's nothing, that he has had it forever. Forward to 2006 when my husband of three years finally got the courage to tell me that something was wrong, that he had a growth in his pelvic area, (in the joint of where the top of thigh met his groin). He showed it to me and it looked like a ball inside a sheath of skin dangling four to five inches from his groin--the ball slightly smaller than a golf ball. We were living in Canada (I'm Canadian, my husband was working in Canada temporarily) and had a great gp but she had just closed her practice so we went to a new Doctor across the border in Washington State. She looked at the growth, decided to snip it off close to his body and send the mass for a biopsy. It was easy, fast, closed with a couple of stitches. The biopsy came back as a type of fibrous tissue growth, non malignant, nothing to worry about we were told except that it would probably regrow.
Three weeks ago my husband told me that the area had started to return. Said it started about eight months ago but he couldn't take the time off to deal with it but now it was bothering him. This time it had a dangling bit, but the base was large and we could tell that there was a mass inside. We now live in Georgia, fairly new to the area, did not know who to go see so we started at the md's office where I had been going thinking that they could advise who to see. Couldn't get in to see Dr, saw a nurse practioner. She took a look and a picture, said it was more than she could deal with and got us in to the local dermatologist's office that afternoon - to the physician's assistant there. He looked, said it was no big deal he was going to remove the dangly bit and cauterize so that my husband would no longer be uncomfortable and that he could come in the following week and he would remove the rest so that it would not come back again. First biopsy from danging bit came back A-OK. I was not OK with the PA removing anything. I felt a surgeon or the very least the actual Doctor in the office but my husband felt that the guy sounded like he knew what he was doing so he went back the following week.
14 stitches and an appointment six days later to take out the stitches. The whole area is not good. We went back this past Wednesday afternoon to have his stitches removed but it soon became apparent that we weren't there to have his stitches removed. The biopsy of the main mass did not come back as expected, it showed the possibility of DFSP. He said that he was not able to remove it all, it has 'fingers' that he's not sure where they go, and that my husband needs to see a surgeon to have it removed. But we won't know for sure till the full pathology comes back and he knows a couple of surgeons in a small town that is the same distance from us as a major city with multiple health facilities. Needless to say we did not take him up on his offer of the 'good guy surgeons' in the small town. We asked him to refer us to a surgeon who worked in oncology out of a major hospital. The guy came back with a referral to a surgeon who specializes in bariatric surgeries with an appt at the end of April. Oh and when I called the following morning to find out when exactly all the biopsy pathology results would be in I was told that they were already back and it was DFSP.
Through making multiple calls and leaving messages for various Drs somehow I ended up being called at home by Dr Steven Attia at the Mayo Clinic. DFSP is what Dr Attia does. He organizes a conference for DFSP. While I was on the phone with this amazing man, he called a surgeon who specializes in sarcomas and between them they decided on a day that they could both see my husband. April 9.
My husband has not had a scan, an xray, an mri etc. He has had a biopsy result positive for DFSP. He has 14 stitches in his groin that are not healing and I'm scared to death. The wait to April 9th is very hard and I don't know what to do.
Tomorrow my plan is to get a copy of the picture and send it to Dr Attia as well as all three biopsy results. I thought that I'd also send a picture of what the stitches look like now.
It sound like you have best possible doctor and I'm sure he will make sure you're husband gets the mri/x-ray needed to see it the dfsp has spread. If you read the posts in here you will see that people have lived with this cancer undiagnosed for 10 or more years without it spreading much. I had my dfsp for 4,5 years without it spreading more than about 2 cm ( ~1 inch)
Make sure the lump on his arm is also checked. But even if it is the dfsp that has spread there are medicine such as Gleevec that can help kill the cancer. I will hope for the best.
I had 11 clamps removed from my groin/hip area wednesday before easter - 15 days after surgery. I think 6 days is not enough for healing, but i doubt that healing has anything to do with dfsp. Bad healing is usually more to do wiith smoking? Or lack of vitamin that you get from good green veggies. When i had a Caesarean the clamps stayed in for almost 3 weeks, that is of course a deeper cut through layers.
Best wishes
Lone
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Your in good handsLone111 said:RHC the best is a good doctor
It sound like you have best possible doctor and I'm sure he will make sure you're husband gets the mri/x-ray needed to see it the dfsp has spread. If you read the posts in here you will see that people have lived with this cancer undiagnosed for 10 or more years without it spreading much. I had my dfsp for 4,5 years without it spreading more than about 2 cm ( ~1 inch)
Make sure the lump on his arm is also checked. But even if it is the dfsp that has spread there are medicine such as Gleevec that can help kill the cancer. I will hope for the best.
I had 11 clamps removed from my groin/hip area wednesday before easter - 15 days after surgery. I think 6 days is not enough for healing, but i doubt that healing has anything to do with dfsp. Bad healing is usually more to do wiith smoking? Or lack of vitamin that you get from good green veggies. When i had a Caesarean the clamps stayed in for almost 3 weeks, that is of course a deeper cut through layers.
Best wishes
Lone
Hi worried wife, You have come to the right place for support and understanding. And you now have the best possible Drs looking after your husband. This rare cancer presents itself in so many different ways and it always resembles someother type of skin disorder, so it is no wonder it is misdiagnosed so often(actually I have not read one story where it has been diagnosed on the first occasion) . As I was reading you post I was thinking OMG this Man needs to get to a DFSP specialist or sarcoma specialist ASAP. Then I came to the ending and sighed a sigh of relief Feewww. Waiting is always the hardest part but nothing is going to change in the mean time and you are going to see the best people for this type of cancer. In regards to the wound not healing.....has the.wound been checked for infection? I was given a script for antibiotics and told to get them if my wound stated to get red around the edges or weepy. But with me the issue was I have become allergic to any kind of adhesive tape for wound dressing(even the hypoallergenic type) I never had this problem before so after my first excision when the area became red and itchy I assumed it was normal but then noticed that the redness and itching was radiating out to where I had been taped. This was also hindering the healing of the wound. So after my nxt surgery (Mohs to achieve clear margins) I made sure the wound only came in contact with sterile 100% cotton. Ok so this may not be of any concern to your husband but I just thought it was worth mentioning. As Lone mentioned there are lots of reasons why wounds heal differently. I havnt gone into the details of my DFSP ( if you want the details are accessible just click on my csn name or read through past posts there are two other DFSP threads here as well) but I was told for over 10yrs ago that I had a harmless little growth fatty tissue nothing to worry about ..yer sure!!!! Then last yr turned out to be DFSP. Lucky for me it's a slow growing cancer. Now Im all clear again..( for the time being anyway-)
Stay positive and good luck, pop in and let us know how hubby is doing and Thankyou for sharing I alway think that we are helping others if we make people aware of how this cancer can appear in so many different ways. Natalie0 -
Worried Wife Going Crazy
Thank you for responding to my post Lone and Nat. I am having a very difficult time my thoughts are going crazy.
My husband's mom died from pancreatic cancer, his dad has had both breast and colon cancer and his uncle (dad's brother) died from breast cancer--- the family owned a dry cleaning business for years and there is some question whether the breast cancer was environmental due to the now never used cleaning chemicals or because of genetics.
We have three boys, twins 10 and a 4 year old.
The thoughts/questions driving me nuts;
If he had one sarcoma on his arm for years, why did one start in his groin when they are usually one spot only?
Are they connected through his trunk somehow?
The one in his groin is next to his lympth node, there nothing to remove it from, it's not located in the meat of an arm or leg but in his joint, how are they going to get a 'clear margin' around it?
The dermatologist who attempted to remove it said it 'has fingers' and he doesn't know where or how far they go. In that area it's organs right?
If it is possible for surgery and a clear margin, is it day surgery? Radiation has been mentioned multiple times even without an mri, scan etc, what's that going to be like?
When a DFSP specialist says that it is going to be challenging, we r basically screwed right? That's what my head is telling me.
I have nothing to do but think and wait. I've got all the paperwork, faxed our lab results, registerd as a patient but we have to wait till the 9th. I'm not sleeping. I wonder how he can appear so healthy yet be in such danger.
Thank you for listening,
Helen
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Breath Helen now breath slowlyRHC said:Worried Wife Going Crazy
Thank you for responding to my post Lone and Nat. I am having a very difficult time my thoughts are going crazy.
My husband's mom died from pancreatic cancer, his dad has had both breast and colon cancer and his uncle (dad's brother) died from breast cancer--- the family owned a dry cleaning business for years and there is some question whether the breast cancer was environmental due to the now never used cleaning chemicals or because of genetics.
We have three boys, twins 10 and a 4 year old.
The thoughts/questions driving me nuts;
If he had one sarcoma on his arm for years, why did one start in his groin when they are usually one spot only?
Are they connected through his trunk somehow?
The one in his groin is next to his lympth node, there nothing to remove it from, it's not located in the meat of an arm or leg but in his joint, how are they going to get a 'clear margin' around it?
The dermatologist who attempted to remove it said it 'has fingers' and he doesn't know where or how far they go. In that area it's organs right?
If it is possible for surgery and a clear margin, is it day surgery? Radiation has been mentioned multiple times even without an mri, scan etc, what's that going to be like?
When a DFSP specialist says that it is going to be challenging, we r basically screwed right? That's what my head is telling me.
I have nothing to do but think and wait. I've got all the paperwork, faxed our lab results, registerd as a patient but we have to wait till the 9th. I'm not sleeping. I wonder how he can appear so healthy yet be in such danger.
Thank you for listening,
Helen
Hi, that's what I have learnt to do when things are crazy. This period of waiting is really the worst time in the process of ridding your husband of this cancer. I dearly wish I could answer all your questions. But your husband's DFSP has presented its in a way I have not read or head about. Has the lump on his arm been confirmed as DFSP? Or just the area in the groin? Gee I'm racking my brain here trying to see what I can help you with. Ok well Im just a DFSP survivor so Im not going to even try to explain stuff I don't understand. I'm regards to removing all the fingers(roots) to achieve clear margins I had Mohs surgery which means they cut a peice out after estimating have much area will need to be removed. This peice is frozen and pathology is done to determine if more skin, fat,muscle or bone need to be removed. in my case I had skin and fat tissue down to the muscle removed.
This is repeated until clear margins are achieved and is usually a day surgery. If they expect that a large amount will be removed then they may choose the other option which is wide excision. There are stories on another thread for DFSP of people who have had this on their head(including the face ) and the Drs have been able to do all sorts of wonderfully things to achieve clear margins and reconstruct the area. I'm sur once you talk to your team of drs net week it will all make more since. DFSP is not hereditary. It's just bad luck from what Iv read it can not be predicted. Children get it and there is no history DFSP in their families. So there is also no reason to think your children are at risk of getting it. Your not screwed!. Yes it may be a challenge,but they haven't said its not doable. You have done everything you can for now,and until your husband has talked to the specialists there isn't much else you can do . Unless you want.to ring them and see if tests can be organized before your appointment.
Try and keep busy, the time will pass quicker
Nat.0 -
A highly cureable cancer...RHC said:Worried Wife Going Crazy
Thank you for responding to my post Lone and Nat. I am having a very difficult time my thoughts are going crazy.
My husband's mom died from pancreatic cancer, his dad has had both breast and colon cancer and his uncle (dad's brother) died from breast cancer--- the family owned a dry cleaning business for years and there is some question whether the breast cancer was environmental due to the now never used cleaning chemicals or because of genetics.
We have three boys, twins 10 and a 4 year old.
The thoughts/questions driving me nuts;
If he had one sarcoma on his arm for years, why did one start in his groin when they are usually one spot only?
Are they connected through his trunk somehow?
The one in his groin is next to his lympth node, there nothing to remove it from, it's not located in the meat of an arm or leg but in his joint, how are they going to get a 'clear margin' around it?
The dermatologist who attempted to remove it said it 'has fingers' and he doesn't know where or how far they go. In that area it's organs right?
If it is possible for surgery and a clear margin, is it day surgery? Radiation has been mentioned multiple times even without an mri, scan etc, what's that going to be like?
When a DFSP specialist says that it is going to be challenging, we r basically screwed right? That's what my head is telling me.
I have nothing to do but think and wait. I've got all the paperwork, faxed our lab results, registerd as a patient but we have to wait till the 9th. I'm not sleeping. I wonder how he can appear so healthy yet be in such danger.
Thank you for listening,
Helen
Hello RHC,
I've have read lots of "cases" and test studies etc. and very very few have died from this cancer. Those who do have had complications with it after it has spread to the lungs (after a number of recurrences and bad management) which is extremely rare. I was very pleased to see you have a sarcoma specialist. I truely believe this is the way to go. Try not to jump ahead, it's hard but let the docs figure it out. The fact that he (like all of us) are healthy, no illness, side effects etc. says a lot. Most cancers that hide and grow produce acute side affects and typically are caught too late. This kind of cancer can take decades to grow and even the worst cases produce wonderful results once diagnosed.
I would guess from what you've wrote that hubby isn't a sit around and heal type of guy. Possibly the healing processes is delayed due to too much activity on his part and the location of the wound. I would expect it's challenging to not irritate that area without being absolutely immobile for some time...and you know how guys can be
Sounds like you are all over it, ask all the questions, keep a journal for the big day...April 9th will be here before you know it.
We are thinking of you, best wishes.
J
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Thank YouOntario48 said:A highly cureable cancer...
Hello RHC,
I've have read lots of "cases" and test studies etc. and very very few have died from this cancer. Those who do have had complications with it after it has spread to the lungs (after a number of recurrences and bad management) which is extremely rare. I was very pleased to see you have a sarcoma specialist. I truely believe this is the way to go. Try not to jump ahead, it's hard but let the docs figure it out. The fact that he (like all of us) are healthy, no illness, side effects etc. says a lot. Most cancers that hide and grow produce acute side affects and typically are caught too late. This kind of cancer can take decades to grow and even the worst cases produce wonderful results once diagnosed.
I would guess from what you've wrote that hubby isn't a sit around and heal type of guy. Possibly the healing processes is delayed due to too much activity on his part and the location of the wound. I would expect it's challenging to not irritate that area without being absolutely immobile for some time...and you know how guys can be
Sounds like you are all over it, ask all the questions, keep a journal for the big day...April 9th will be here before you know it.
We are thinking of you, best wishes.
J
Thank you for taking time to reply to my fearful rant. I flutter between being ok and crying - not in front of my husband. He's afraid too but we only talk about it at certain times. Today so far I'm good. I guess what keeps it in our face is the mess of the incision site where the dermatologist 'removed' it. As of last night 3 of the eight outside stitches are in place, it's gaping more everyday, there is redness spreading out and the idiot who did it is on vacation this week and regardless did not want to see my husband again anyway. Who do we see? I don't know if things will be ok to our April 9 appointment. There were fourteen stitches some on the inside and I worry about the ones I can't see. No bleeding though which is good. I guess I'll try to get him in to the nurse practioner today so that he can at least be looked at somewhere, he might need more antibiotics, and stitches.
From what I've read I understand that DFSP is highly treatable, and has a very low mortality rate but I also read qualifiers that say depending on the site, or location. I;m assuming that that refers to the lungs but I also can't tell you how -I dont want to say excited- eager our DFSP Dr is to have hubby as a patient because of the location, husband says that the Dr should be paying him for the opportunity!
It's wait and see, very hard to do. Kids are on spring break but we can't do anything so time's passing very slow.
Thank you again for sharing your experience and knowledge, and for grounding while things are spinning out of control,
Helen
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