Mohs Surgery Pictures, Preparation and Recovery
If you’re about to have a Mohs procedure, let me help you get prepared. I’m sharing my Mohs surgery pictures so you’ll have a better idea of how it will go. I cried. And you might, too. And that’s perfectly ok.
When I had to have a basal cell carcinoma removed in 2013, I was stunned.
Growing up in Southern California, I spent a lot of time in the sun. But I never expected that I would have to worry about skin cancer.
“So…I had skin cancer. I had surgery. I’m totally fine. I just wanted you to know because we are having dinner in a few days and I didn’t want you to freak out when you see a huge wound on my neck.” That is how my phone conversation went with a really good friend after my Mohs surgery.
Because although the doctor told me what would happen, you truly don’t understand what the recovery will look like. But I want to help you plan ahead.
IF YOUR SKIN GETS IRRITATED BY REGULAR MEDICAL TAPE…
I just used these bandaids for the first time and they are AMAZING! I recently had stitches for 2 weeks and these were the only bandaids that weren’t awful on my skin! The stitches were above my knee near my inner thigh where the skin is thinner and sensitive. These bandaids were a dream! They were way better than sensitive skin bandaids.
You can also try this dressing tape if regular bandaids irritate your skin but this tape also irritated my leg when I tried it. It is better for tougher skin.
Basal Cell Carcinoma on my Neck
This post is about my experience with basal cell carcinoma skin cancer and how I had it removed with Mohs surgery.
And it’s also about how I became depressed. I want to share my story in case you know anyone who has one of the “better” skin cancers, like basal cell, or you have it yourself.
It is ok to be scared. Even though a lot of people will not give it a second thought, it is ok to feel uneasy about it.
WARNING: I share photos with my stitches. If you are squeamish, you may want to skip it. I mean, it’s not all that grotesque but I want to give a fair warning.
Discovering the Basal Cell
My dad had been dealing with his own skin cancer issues for the last few years. I take after his light complexion so I thought it couldn’t hurt to get a doctor’s opinion.
I had a little red mark, that had been on my neck for about two months (effing eczema, I thought). I was referred to a dermatologist and I’m so grateful I was. My primary care doctor wasn’t worried about the red mark, but it turned out to be basal cell cancer.
If you think something is wrong but your doctor isn’t listening, for sure get a second opinion!
Dealing with Skin Cancer
Most often you will have a biopsy done of the trouble spot. Typically they quickly numb up the area surrounding what they want to biopsy and they will slice off the whole mole or spot or a portion of it.
They send it off to the lab and in about a week, you’ll get a phone call following up. Often they will also send a letter in the mail letting you know about the mole and what the findings were.
Most of mine are irregular but not cancerous. I’ve had Mohs done once because of basal cell. But I’ve had excision biopsies 4 times (I’ll explain that in a moment).
On this particular visit, my dermatologist said “If I call you, don’t freak out. It doesn’t necessarily mean something is wrong.” But then when the call came, he said, “You know if I’m calling, something isn’t right…” Geez.
That was my neck. And it was basal cell.
It was decided that Mohs was the best way to deal with the basal cell and the appointment was scheduled.
He explained that because of where it was (in a very visible spot on my neck), he would refer me to another dermatologist who specializes in plastic surgery who would do a procedure to remove all the skin cancer cells.
I didn’t know until right before the surgery that it would be Mohs Surgery, the same that my dad had a few months before.
So leading up to it, I just thought it would be pretty similar to the mole removals I had done so far, which required a small bandage for about a week.
To be fair, I do remember my dermatologist telling me that I may end up with a few stitches but I’ve never had stitches, aside from child-birth (hey if I’m sharing, I’m sharing everything) so even a few stitches seemed insignificant.
I didn’t really know how to feel about the news. I was kind of scared but most people I talked to were not that worried. I went out to dinner the night that I found out about my basal cell diagnosis.
One close friend said, “yeah I had that, they just take it off, right?” And we moved on.
Several of the moms from my son’s elementary school have had basal cell carcinomas and they seemed totally low key about the whole situation. And knowing that my dad had the surgery, that it was “no big deal” and was pretty common left me feeling, well, it left me not feeling.
I never really thought about it. So I didn’t make any special phone calls to friends with news of my skin cancer. I didn’t need any extra support.
What is Mohs Surgery?
Here is my, probably very wrong, description of what Mohs Surgery is. First they remove the area that they believe to contain the cancer cells.
There is a pathologist right on site who evaluates the cells and determines if they need to go back and take more tissue. They do this as many times as they need to in order to remove all cancer cells and get a clear margin around the area.
So the Tuesday before Thanksgiving, my husband took the day off of work and went with me to the most gorgeous dermatologists office ever in Newport Beach, CA.
I have not seen any bills from this procedure yet and I will probably have to sell everything I own to pay it but at that moment, I needed all the amenities they provided (update: the bills were reasonable and I don’t believe I paid anything over what insurance would normally cover! A DREAM COME TRUE!).
The most amazing front desk gal had called a few days before and explained that I should plan on being there the whole day. Up to this point, I really thought I would be in and out.
I asked my mom, who would watch the kids during the procedure, if she would just keep them overnight since I had no idea when I would get home.
The office smelled like a spa. The music was relaxing and everyone was beyond friendly. But I was starting to get pretty darn nervous.
My father’s Mohs Surgery experience was much different from mine. I was given my own private room with space for my husband to work and a TV to watch. The entire procedure would be done in this room and the doctor would come to me.
I was free to get comfy and enjoy the time there as much as possible. And I totally did at first!
My dad’s surgery, on the other hand, was done similar to how a lab is set up. The patient is called back in to a room, cuts are made, and then they are sent back out to the waiting room with everyone else.
That part alone would have probably done me in. But I do hear that is how most people experience it. I think I was super lucky to have found such an amazing doctor.
Basal Cell Carcinoma Before and After Pictures
To start, they marked and measured me. The red area in the circle is the basal cell carcinoma. Not that big of an area, or so I thought. Remember the front office gal I mentioned?
Well, she was like the best hostess ever. She brought me coffee. And teased me with treats she would be bringing around later. It was nice to spend some time with my husband. It was all very relaxed and enjoyable.
My husband and I, still in good spirits, took joke pictures to send to his mom. He doesn’t do well in medical situations so we thought this photo, of him pretending to have passed out, seemed appropriate.
The dermatologist did round one. They laid me back, numbed me up and made an incision. It took just a few minutes. It wasn’t awesome, but it was manageable. They removed some cells and took them to their onsite lab to evaluate.
Just a little bit of cotton and tape were put over the incision while we waited to see what would happen next. We were told results would take about an hour so we just had to relax and wait.
Sweet, sweet lady. First my husband and I were brought warm cinnamon swirl bread from the front office gal. Then an hour later she came by with these abelskivers from Trader Joes! I loved this place! They really did their best to make you comfortable.
The doctor came in and said they needed to take more cells. For the second round they needed to do some cauterizing. I’m not going to explain it. It’s necissary but gross. But it made everything a little more real. Like, hold up, this isn’t just a little cut anymore.
They ended up going in to take more cells a third time before I was finally told they got all the area they needed. As it was now lunchtime, we were brought delicious sandwiches! I made a joke about when the masseuse would show up and was very seriously told 4:30pm!
But I wouldn’t be there that long. At this point, I just needed to be stitched up. So while the original red mark appeared to be very small, the cancer was actually much larger below the surface.
I was pretty ready to go home at this point. I had been sitting all day in the same chair.
The nurse laid me back and began prepping me for stitches. I got REAL nervous. The doctor explained that I would be getting two rows of stitches, one inside that would dissolve on its own, and one outside that I would have to get removed a week later.
When the doctor started stitching, I totally lost it. I started crying and they were so confused.
I was not in any pain but I think the magnitude of the procedure finally hit me and I was choosing to deal with all the emotion that I had repressed during the stitches.
I just couldn’t stop. I was a hot and sweaty mess. And then I saw how many stitches I had. Wait, what? From that small red mark?
I was given care instructions – keep that first dressing on for 48 hours without getting it wet, then change the dressing twice a day for a week. Wait, what? I couldn’t take a shower for 2 days? That would mean I’d be a few days unshowered for Thanksgiving…
That wasn’t in the plan! I had to come back in a week for stitches to be removed? I couldn’t exercise for a month? Well, that one I was totally on board with but everything else, a total shock.
Recovery
They didn’t give me any pain medicine and said I should only need a Tylenol. That first dressing was so big that I had trouble turning my head. The tape pulled like crazy and I was really uncomfortable. We got out of the doctor’s office around 2:30pm.
And headed straight to Toys R Us. Wait, what? Yup. Since I had no idea how invasive the procedure was, my plan was to head straight to the toy store to pick up a Christmas gift for my son that was starting to sell out.
My husband drove me. I think at that point he would have done anything to make sure I didn’t start crying again. In hindsight, I don’t think going to Toys R Us was the best decision I’ve ever made.
I got the toy and some other shopping done, but I was uncomfortable, exhausted, cranky and needed to be cozy in bed.
Because of the stitches from Mohs surgery, I couldn’t pick up my boys or lift anything heavy. I had not prepared for that. I hadn’t stocked up on food at the grocery store in preparation.
I hadn’t planned ahead for anything because in my head it wasn’t going to be a big deal (which is also how all the doctors treated it). This was the picture we sent the boys that first night. I didn’t want them to freak out or worry so I put on a happy face.
But I really felt more like this. I couldn’t sleep on my side because the tape pulled so much. It was hard to get out of bed without my neck muscles pulling.
I rolled into Thanksgiving dinner with no makeup on and 2 day old dirty hair (which I don’t do – it is NOT cute on me). I put clothes on but I would have much rather stayed in my pajamas.
That night I could take the dressing off for the first time and finally got my shower. I broke down again when I saw the stitches. I just wasn’t prepared. For any of this. The next day I was in a good deal of pain (mostly achey) and managed it with over the counter meds.
WARNING: AFTER PICTURE OF MOHS SURGERY STITCHES COMING UP!
Each day got a little easier. But I had to wear this gigantic dressing. I got a lot of looks. The tape was still pulling on my skin. It was hard to tell if the stitches hurt or if it was the tape.
So I was extra cautious and held my head in odd positions to baby my neck. I ended up super stiff and with headaches. So lame. And I became depressed. Self diagnosed, but still counts I think.
I didn’t want to go anywhere, I didn’t want to see anyone. All a sudden it had become a pretty big deal but most people didn’t even know about it. How do you ask for help or support when no one knows you need it?
It really wasn’t a big deal. The cancer can grow but not really spread anywhere. It is highly curable. So I was conflicted. I chose to spend a lot of time in bed. I left only when I had to.
The tape made my skin SO angry. I hated wearing the dressing more than anything else. Now, years later, my new dermatologist says most people react to the tape and are usually fine with the stitches.
If you are sensitive, be sure to let your doctor know in case there are other options they can use.
IF YOUR SKIN GETS IRRITATED BY REGULAR MEDICAL TAPE…
I just used these bandaids for the first time and they are AMAZING! I recently had stitches for 2 weeks and these were the only bandaids that weren’t awful on my skin! The stitches were above my knee near my inner thigh where the skin is thinner and sensitive. These bandaids were a dream! They were way better than sensitive skin bandaids.
You can also try this dressing tape if regular bandaids irritate your skin but this tape also irritated my leg when I tried it. It is better for tougher skin.
The day that I got the stitches out I was a wreck. I think I started crying before they even did anything. It wasn’t really that bad but it didn’t matter. I’m sure the office staff still talks about me and my crazy emotions.
Mohs Surgery Scar Pictures
At my check up, the doctor liked how the scar was looking so he put something called a steri strip on it. They glued it to my skin and it would fall off on its own in 1-3 weeks. When it fell off, I was to go back to the dressings again.
I did everything I could to make sure that steri strip stayed on so I didn’t have to put that awful tape back on.
It stayed on until my follow-up appointment about 3 weeks later. They removed it and were very pleased with the progress. They told me I didn’t need to use dressings anymore which was a dream come true. I was okayed to exercise. Eff that.
I am so grateful for my family for taking such good care of me. My husband was a trooper and was so strong. He comforted me, he let me sulk, he handled the boys. I really couldn’t have done it without him.
A very dear friend, Kayla, was a rock for me. She let me cry, she always knew what to say and she would just send me texts letting me know she was there for me.
But I also thank those people who would have been there for me had they known. I know there are many more people who would have dropped everything to help me if I had given them the chance.
My head was just so jumbled. I was in a pretty dark place for those couple of weeks.
This is how the basal cell carcinoma scar looked on Christmas (about a month after the Mohs surgery). I had minor (really minor) pain for a month or so. And because of the placement on my neck, sweaters would rub right there.
You can see how my basal cell carcinoma scar looked a year after this surgery in this post.
Thoughts on my Mohs Surgery Journey
Everything we go through is an experience. I think we go through life trying to be so stoic and act as if we are unflappable. But we are all vulnerable. It is okay to be scared of things that others might be fine with.
It is okay to call your friends up out of the blue and tell them you need them. And it is okay to spend lots of time at home in your pajamas watching Bravo if that is what you need to do.
The scar was kind of red and little puffy on one side for a little while. I had a follow up appointment in February and then was released and went on about my life.
I see my regular dermatologist every few months. We evaluate moles and other marks and talk through what we need to do about them.
I finally feel like I know what questions to ask about how we will handle these and other moles going forward. I always learn things I didn’t know about skin cancer before and I feel really good in his care. I feel like we have a plan and I have to rely on that.
I can’t say that I’m not worried about finding more or other types of skin cancer. But I am a little more versed in it now. It took awhile to not feel depressed. I told myself I could cry about stitches if I wanted to. And I could take as long to recover from these procedures as I wanted.
Since this Mohs surgery, I had to have multiple places removed and biopsies. Some have looked like regular moles. One was a purple mole that looked like my kid drew it on me with a marker.
For that one, they wanted to take a larger area to biopsy which would require stitches.
I convinced my doctor, instead, to do a punch biopsy. That biopsy came back with them wanting to take more action so I had to do an excisional biospy, that was pretty similar to Mohs surgery.
Which meant more stitches. That I cried through. I had even gone to my doctor for Xanax but my anxiety proved to be too strong. In all of this, I found out I’m pretty much a sissy when it comes to medical procedures. And I’m ok with that. I will just take each biopsy as it comes.
Related Post: Basal Cell Carcinoma Update and Excisional Biopsies
Have you ever had to have basal cell skin cancer removed with Mohs surgery? Skin cancer sucks. For real.
After the basal cell, I began the journey of having moles biopsied pretty regularly. Over my first few visits, the dermatologist evaluated my moles and skin (head to toe check!) and we’ve set about prioritizing what we need to focus on first.
For the first few years after the basal cell I was seen by my dermatologist every six months. But over the years it has slowed to about every 6 months. Find a dermatologist you like and talk to them about what your journey should look like.
If you are about to get the procedure, I wish you luck! However you are feeling is right. Sending best wishes!
I thought my experience was pretty crazy so I wanted to make sure to share it in case it would help someone else. And what I’m finding is that many of you have similar experiences.
If you’re looking for Moh’s Surgery pictures, hopefully, these will help you plan for your own procedure and know what to expect.
Hi, I just had Mohs surgery to remove SCC on my left cheek. Left with an inch-long scar. It’s still within its first week, and I have been very emotional and upset over the whole thing. This giant bandaid covering half my face is making me feel embarrassed to walk about, and I don’t want to start explaining to everyone.
I was really not prepared for this size scar or the mountain of emotions that followed the surgery. It’s nice to know it’s not only me, and there is a faded scar at the end of the tunnel…
And by the way, I cried in the doctors’ office before, during and after the surgery, so you’re in good company there!
Thanks so much for commenting. By my third procedure I knew that my emotions could be helped with a yummy waffle sandwich from a local restaurant. :) Wishing you fast healing!!
Thanks for posting this. I have my surgery scheduled for tomorrow. I’ve know about it for over a month, but was able to distract myself with kids, husband, work, life… I’m getting really nervous now. I might cry too. I’ll embarrass myself, I’m sure. Geez, it’s on my face too, right near my eye. I don’t want to go! Waa! But, thanks for posting your story. I know it’s been awhile for you, and soon enough It will have been awhile for me too. Looking forward to that. :)
Like the other posters I appreciate hearing about your experience. I just had a BCC removed from my chin yesterday. It took two rounds they had to go pretty deep. The worst part was the reconstruction afterwards. To try to cover the hole left they had to cut pretty far across and even down my chin. I lost count how many stitches I got. If I had to hazard a guess it was 2 dozen under and at least 35 on top! I woke up in the middle of the night in pain and swollen. Seeing your experience makes me feel better. Almost everywhere I looked the remarks were oh it was nothing, no pain. I was thinking what is wrong with me. Your candor makes feel less alone. Thank you!
I’m so sorry, Carla! I’m glad my experience could help in some way. I think we are all built to tolerate pain differently and I don’t like it one bit! I also don’t think you need to be brave every second of the day. It’s ok to take some time and be sad, mad, whatever you need to be! I hope that is the last time you have to do the surgery, but if it isn’t, you can prepare a little more for the next time and plan your recovery the way you need it or want it to be. For me, that means watching a lot of reality shows in my pajamas. :)
I am scheduled to have mohs on my upper ear right next to my scalp. I had a large growth that was cut off by the dermatologist for biopsy and it came back basal. Also they cut a piece out of the side of my neck which is also basal. I have an appointment on 30 Nov to have mohs on my ear. They are then sending me to a plastic surgeon to close my ear and do my neck. Has anyone else had to use two different doctors? Why can’t they do mohs on my neck? Any info would be greatly appreciated. I’m freaking out.
I think using two doctors is quite common. I was lucky that I didn’t have to do that. But I know other people who have. I’m not sure why they can’t do Mohs on your neck. I suggest asking your doctor more questions so you understand it better. For me, when they wanted to remove a purple mole, it didn’t come back cancerous so they didn’t do Mohs, but rather sent out what they did remove to make sure the margins were clean. They weren’t so I had to go back a second time for them to take more. It could have been done all at once with Mohs but maybe their hands are tied as to what they can do Mohs for. I wish you the best of luck with your procedures!
Sharon, I am so happy you posted your story. My skin cancer is approx 2 inches below where yours was right where my necklaces hang a little to the right so I am really freaked out about having a scar there. My skin cancer is similar to Basal cell carcinoma but pathologists are calling it “Basaloid” carcinoma. The best way it was described to me was it was like basal cell carcinoma but more aggressive. They tested it for breast cancer and did a diagnostic mammogram and that was all ok. The first oncologist I saw said she would treat this just like melanoma. She would cut all the way down to the muscle and 5 inches across. I completely fell apart. Cried for 2 days non stop! I consulted a mohs dermatologist who told me he wouldn’t even touch what I had because he’d never seen this skin cancer before. I finally found Dr. Glen Bowen at the Huntsman Cancer Institute here in Utah who has seen this form of skin cancer before and said he could do mohs surgery saving as much skin tissue as possible. I’m still terrified, but your story and healed pictures have eased my mind so much! Can I ask you if you ever had any laser treatment or cortisone injections to improve your scar after? I can’t even see your scar now. Beautiful job! Also how long was your incision and how many stitches? I’ve heard so many times the chest wall is a bad place for scaring. Trying to remain optimistic! This will be my 6th skin cancer removed, 2 on my stomach, 3 on my back and now this one on my chest. I don’t care as much about the other scars because they aren’t in places that show most of the time. But this one really scares me. Holly Jo
Thank you for giving me permission to sob like a blubbering baby! So many different people have been so nanchalant about their Mohs experience, I thought there must be something wrong with me for wanting to cry.
Your blog has made me feel so much better about hating this whole experience and finding it excruciatingly uncomfortable. Just had a huge chunk of my nose removed on Tuesday.
Oh, forgot to include a link to my blog entry spit Mohs I went to a MUCH less plush doctors office than yours! I’m super jealous of how they pampered you!!!!
Just so you know, I too had MOHS done on my left cheek of my face. I found a healing technique that was not recommended nor suggested by anyone. Nine weeks after surgery, My 2 inch incision was red and had bumps on it most likely scar tissue under the first layer of skin. I decided to use Neospurin which healed my face in less than 5 days, where the redness left and the bumps were reduced. I am still healing, but at least now I am seeing results. Too bad no one told me about using it. I just tried out of frustration.
I was told not to use it. I don’t think it had a negative side effect they just didn’t think it really helped. But glad to hear it helped you!!! Believe me, I stood in the band aid aisle and looked at all of those creams. :)
Hi Suzy! I think that is why I was so weirded out by the whole thing! I was sobbing but no one understood why! But when you think about it, it’s a pretty big deal! But I’ve had my chance to process and figure out a better way to cope with having to be poked and prodded by a dermatologist for the rest of my life. I don’t cry as much but I am eating an enormous amount of NERDS candies. ;)
I’m 74 and this past Tuesday had a large chunk removed on the the left side of my nose and was sobbing on Friday when it was time to take bandage off and saw the hole. I’m still very upset. Reading about your reaction and feelings helped me. Its not life or death but to know you have cancer is very upsetting to me.
Yes! I’m glad you are doing ok and I’m glad that you got your cry out! Everyone needs to process it how they see best. Wishing you the best, my friend!
So glad I read this. I had the mohs on the left side of my nose Tuesday. 6 hours later I had 30 stitches going down my nose and cheek. They had to go so deep the doctor had to take skin from my cheek for
Reconstructive surgery. I thought I was crazy with all my crying but it’s nice to know it must be normal. It’s scary to to think what’s next? I’m only 42. I have a huge bandage and I’m already dreading work Monday. I’m not a vain person. Well I didn’t think I was at least. I’m trying to be positive. I’m thankful it was basil cell and not melonoma. Thanks for your post. It made me feel better to know I’m not alone. Hope your thanksgiving was better this year!!
Glad to hear you are ok Kim! I was so surprised at how well my scars have healed! I know having it on your face is super scary. My friend, who has had Mohs on her nose, had a cosmetic procedure with a laser done a few years ago to feel better about her scars. I don’t think it is vanity at all. I wish you a quick recovery and don’t feel bad about the crying. It just happens!
Thank you so much for sharing this, Sharon! I recently went to my dermatologist for a “mole” I had on my face and it turns out it is Basal Cell Carcinoma. I’m such a big baby when it comes to hearing about negative things and of course I cried. I kept researching and researching until I came across your page. Your story made me cry so much, but it also helped me prepare for what I am about to face. I received the call today with the results for the biopsy and now just have to wait for my dermatologist to call back and schedule for surgery. My main concern when I first heard that word, “surgery” was how the heck will I pay for this?! As I continued to read on it and YouTube it, that’s when I was more alarmed and then reading and seeing you pictures…I can only hope that I won’t go through this alone! I haven’t yet mentioned it to my husband or my kids, I actually haven’t mentioned it to anyone yet… I just wonder how they’ll take it. It may not be a big deal, hopefully not, but I can’t help but worry. It’s unfortunate that you weren’t prepared for all you went through, but I am glad everything came out well and I thank you so much for this!
Strong. Brave. Beautiful. That’s what you are my friend.
Thanks my friend!!
you are super brave for writing this — i love honest, real life blog posts like this. i’m glad you’re okay!! keep getting checked :)
Cancer sucks. That’s all there is to it. My father in law passed away a little over a year ago from Melanoma. Since then my BIL had melanoma removed from his foot, and a couple of weeks ago my husband had three cancerous moles removed. We are on the get moles checked every six months plan. It’s so vital to be your own advocate and get checked like you did. Things could have been different if my father in law was more proactive with his own health. I’m sorry you have had to go through this, it’s lame. Thank goodness for modern medicine. I say when it doubt – get it checked out!
I’m sorry to hear about your father-in-law. :( I’m with you, better to get checked! My poor dermatologist. Every time I go in I’m like okay, look at this…now what about under my hair…or I heard this descriptive term and I think this mole matches that, can you check? And then I think ok, we are managing it now, but what about in 20 years, what is going to come up then? I just have to live each day at a time and not guess but he said my cancer would have been from sun when I was in elementary school. I feel like my tan years came in high school so…
Hi Sharon,
Wow you are such an inspiration, I think it is really brave to open up with a post like this and I really admire that. I am so glad that you are ok and as freckly red head I appreciated all the good info, I’ve been warned my whole life about this kind of thing. I usually laugh because I imagine a dermatologist trying to find an irregular shaped dark spot on my skin and liken it to a session of Where’s Waldo among all my freckles. Cheers to you!
Your comment made me laugh! :) Thank you.
This post totally made me laugh and cry at the same time. And I’m glad you cleared up the whole “ripple” thing hahaha. So happy everything is ok now! I heart you Sharon :)
Awww, I heart you Tammy. :)
I write this with tears filled in my eyes. You’re so brave to share this! I can relate to the flood of emotions you had while getting your stitches.. I will always keep you in my prayers and I’m so glad you had this done in such a wonderful office! Sending you a big hug.
hey girl – thanks for being so open about this all. Glad to see it is working out for you & I will send prayers your way that it continues to be ok with the remaining ones you are having checked. I am going through something as well & meeting with my dr. to get my pathology results THIS Monday. Mine is different as 2 weeks ago Friday I had a total hysterectomy because I had to. Now I wait to see if I have cancer – uterine cancer. {sigh} It DOES suck sharing your feelings and whether or not to share on our blogs or not. You wonder if people will think you’re weird or say ‘did they reallly just share that?”. But I look at it this way – if our stories help just ONE person, then it’s worth it right? I can totally relate about being a mess & crying – I haven’t stopped – everyday is a new day, but it is a struggle dealing with ALL the emotions. Dealing with all the ‘what-ifs’ – it is maddening. I keep thinking the paddy wagon will pull up to my home any minute because I also think I’m going crazy! lol Anyway – I will keep following & hope for the BEST for you. Feel free to contact me if you would like to chat. =) laura
Laura, I will pray for you as well. Thank you for sharing your story. The emotions are crazy! Keep your chin up and find a good support system. Friends and family really help!
Thank you so much for sharing your story.. I am SO glad to hear that you are mending and getting care.
Thanks, friend! Feeling like my old self again! :)
This is what I just wrote to family and friends: I want to share a my experience, so it won’t happen to you!
I wanted to let you know that for the first time, when my sister mentioned she goes to the dermolotigist annually, I made an appointment for the dermotologist last Friday (I really didn’t expect a problem, as I use SPF 25 and make up with SPF, haven’t been to the beach in 25 years and don’t usually go out in the sun except to garden or cut grass. Well, to my shock, by Tuesday morning, I was sitting in a MOHS office facing disfiguring, uncomfortable surgery! (I was really praying, not scared.)
I was diagnosed with BCC on the left side of my nose. After giving an initial sample on Friday, on Tuesday morning, I had two more scrapings of the area. The BCC was so deep on the side of my nose, I needed a skin graft, which was taken from my neck behind my ear.(I asked the doctor to take some from an area he could do a facelift.) I now have bandages on my nose (hope I don’t get a cold) and neck, can’t lift anything heavy, can’t do strenuous work, and face months of healing; the doctor ( a military-trained surgeon) said it usually comes back somewhere else on the body (so he will always have a job).
Fortunately, BCC is not the bad kind of cancer: I can still donate blood, stay on the donor registery and donate my organs at the end of life, but BCC can be hereditary. The medical forms I completed asked questions about family history (I knew of none; not with mom or dad), but if you’re over 60, it may appear.
So if your insurance covers a visit to the dermotologist, consider going. You can look up more information on the web, but please pass this information on to siblings whom I may have missed.
Love, Cousin/sister/Aunt/Godmother Betty