After five beautiful years with my daughter, I was in operating room again, ready to bring my second borne into this bittersweet world.
He was borne at fifteen hundred hours, as the day was exhausting into soothing twilight... An anesthesist friend brought him to me, as I lay in OT table. I noticed his nose, similar to mine. I smiled. My pediatrician husband then took charge of the baby.
I was taken to postoperative room for the night. Two patients were already there, I was placed on the third bed. I was well acquainted with pain, from my previous caesarian section. As a doctor, I also knew I could comfortably rely on analgesics. However, other two ladies were winching, carefully fidgeting, so that any movement wouldn't throb their raw wounds.
Midnight passed. I was dozing off to sedative-induced drowsy sleep, when a wheeler rolled in. It carried a teenage newmom, after emergency operation. Her babygirl was put to her side. Some hospitals bring baby to mother's side immediately after operation, while others wait 24hours.
As the newborn started crying out of hunger, her mother didn't seem keen to feed her. At first, I thought it was probably because of pain and apprehension immediately atfer operation. Her mother in law was summoned for help. It was then, that I was astonished beyond words. Both women started cursing the newborn. They were so upset that it was a girlchild. They called her names, in harsh cruel offensive language. Mother-in-law angrily vanished out of the room into the darkness, blabbering all the while..... I sank in my bed in horrid disbelief. I found it brutal, close to barbarious. But it was kind of routine for caretaking nurses and obstetric staffs. They didn't react.
The baby was still howling, unaware of the harrowing cruel world she just came into. All she wanted... was her mom's suckle and granny's snuggle or her father rocking her to sleep.... :(
Nursing staff fetched the father in, hoping he could assist the new mom. This first time father was just a boy, perhaps in his late teens. He gently asked his wife to feed the child, but she started ranting again, vehemently. He seemed more level headed than both the ladies. He sat silently for few minutes. It seemed he wanted to help but had no idea what nursing or breastfeeding meant. Their first born was wailing all the time. But her mom was deafmuted to maternal emotions. After few requests, he gave up attempts of coaxing his wife and walked out of the room.
Meanwhile, baby seemed exhausted from crying. Her shrill screams became whimpers and then periodic sobs. Morning was less than hours away when she sobbed herself to sleep.
As the dawn pierced the gloomy dark night, bringing in pale yellow rays through the curtains, I woke up. To my surprise, my fellow mate was feeding her child. Even the granny had mellowed down a bit. She was spreading the light meal hospital allowed for the patient. It was as if the soft morning breeze had lightened their hearts. I understood they had finally amicably accepted the birth of a girl child. Then I heard the teenage mom talk to her child, a hint of tenderness in her voice. Love had sprouted amid the bitterness, anxiety and laments....
My heart crushed for them all. They were mere victims of a mindset, of social preference for a male child.
Sunday, October 15, 2017
Saturday, September 23, 2017
Why I didn't gain weight??
Everyone has been asking why I haven't gained weight after delivery or during pregnancy.
Its actually a long story, that I didn't wanna whine about in social media. Yes, our lives aren't exactly what we potray in facebook n instagram. We don't look as good as our pictures. I have dark circles, bags and perhaps much more. I haven't slept more than two hours in one stretch of a time in last two months, coz that's how frequently I need to feed my newborn.
Coming back to weight gain, my pregnancy and puerperium were more stormy than I ever imagined.
Pregnancy pukes were so horrible, I landed in ER and took IV drips. I had ketonuria, ie frequent vomiting made me pass glucose in urine. I had hyperemesis for first 4 months.
During last 3 months, I had severe iron deficiency n anemia. In my final month, I was bedridden coz of my preexisting illness, fibromyalgia. I couldnt eat, I couldnt sleep.
At 36 weekd, a random ultrasound showed that my uterus was just about to erupt or dehisce. Uterine wall thickness was less than 4 mm. I had to rush for emergency caesrian section. Operating gynecologist ma'am later informed that my uterus was plastic thin and baby's hair had already protruded out of the defect. I was rescued right before uterine rupture threatened both me and my baby's lives. Hubby told me later that day, that it was my second life.
But it was only the beginning of my countless sufferings....
My baby was taken to neonatal ICU for first 24 hours for TTN. My hubby informed me that my boy had heart murmur, a suspected VSD. I was petrified. Amidst so much pain, all I could think of, was my little boy's VSD. I cried, whined, sobbed and prayed. An ECHO revealed that the defect was small, which would most likely, close spontaneously. But only time would tell.
On the 3rd night, while still in the hospital, I got fever from breast engorgement. Severely painful milk expressions, day and night, for 4-5 days, and it dwindled a bit, only to be followed by wound infection, urinary tract infection and uterine wall infection. There was fluid collection(seroma) at wound site, which was drained via syringe.
At the end of second week, my wound hurt so bad that I couldnt empty bladder or bowel. It went on for a week before a senior gynecologist at Grande Hospital detected the source of infection. I took my third course of antibiotics. I was so weak, I couldnt eat or sleep well.
Just when the wound infection abated, and I thought all was well, I woke up in the middle of the night with fever, rigors and excruciating breast pain. Next day, I was told I had second bout of breast engorgement involving entire lower zone and risked forming an abscess. There I was, getting IV antibiotics again, fourth course. Running to hospital four times a day, as I refused admission coz I couldn't risk exposing my baby to hospital acquired infections. I was five weeks postpartum by then.
As that episode subsided, I had vestibulitis along with aphthae and dental impingement. I couldn't eat, again. My dose of antibiotics were escalated, as they feared my nasal infection had risks of passing into the connecting brain linings. With treatment, my swollen nose and eroded tongue was beginning to wane, and I had severe gastritis, forcing me to stop all antiobiotics.
Between all this, my wound pain had revived. And my gynecologist said I had scar adhesions, probably connecting to the uterus. He was apprehensive that I might need laparoscopic surgery for breaking adhesions if my pain won't subside. Maybe after 6months or so. But for me, any more surgery sounded like death sentence. I had suffered so much, any surgical intervention scared me.
Thankfully the wound pain vanished. And now, my baby is two months old, thriving well, with remarkable weight gain. And his murmur has disappeare. He has embraced my genes wholeheartedly, his light brown eyes, sharp nose, full lips and the dimples that light my world when he smiles.
During all the chaos, my baby's healthy weight gain was my only pride. And I learnt two things, pain is a constant, yet nothing lasts forever. I survived and I conquered.
Its actually a long story, that I didn't wanna whine about in social media. Yes, our lives aren't exactly what we potray in facebook n instagram. We don't look as good as our pictures. I have dark circles, bags and perhaps much more. I haven't slept more than two hours in one stretch of a time in last two months, coz that's how frequently I need to feed my newborn.
Coming back to weight gain, my pregnancy and puerperium were more stormy than I ever imagined.
Pregnancy pukes were so horrible, I landed in ER and took IV drips. I had ketonuria, ie frequent vomiting made me pass glucose in urine. I had hyperemesis for first 4 months.
During last 3 months, I had severe iron deficiency n anemia. In my final month, I was bedridden coz of my preexisting illness, fibromyalgia. I couldnt eat, I couldnt sleep.
At 36 weekd, a random ultrasound showed that my uterus was just about to erupt or dehisce. Uterine wall thickness was less than 4 mm. I had to rush for emergency caesrian section. Operating gynecologist ma'am later informed that my uterus was plastic thin and baby's hair had already protruded out of the defect. I was rescued right before uterine rupture threatened both me and my baby's lives. Hubby told me later that day, that it was my second life.
But it was only the beginning of my countless sufferings....
My baby was taken to neonatal ICU for first 24 hours for TTN. My hubby informed me that my boy had heart murmur, a suspected VSD. I was petrified. Amidst so much pain, all I could think of, was my little boy's VSD. I cried, whined, sobbed and prayed. An ECHO revealed that the defect was small, which would most likely, close spontaneously. But only time would tell.
On the 3rd night, while still in the hospital, I got fever from breast engorgement. Severely painful milk expressions, day and night, for 4-5 days, and it dwindled a bit, only to be followed by wound infection, urinary tract infection and uterine wall infection. There was fluid collection(seroma) at wound site, which was drained via syringe.
At the end of second week, my wound hurt so bad that I couldnt empty bladder or bowel. It went on for a week before a senior gynecologist at Grande Hospital detected the source of infection. I took my third course of antibiotics. I was so weak, I couldnt eat or sleep well.
Just when the wound infection abated, and I thought all was well, I woke up in the middle of the night with fever, rigors and excruciating breast pain. Next day, I was told I had second bout of breast engorgement involving entire lower zone and risked forming an abscess. There I was, getting IV antibiotics again, fourth course. Running to hospital four times a day, as I refused admission coz I couldn't risk exposing my baby to hospital acquired infections. I was five weeks postpartum by then.
As that episode subsided, I had vestibulitis along with aphthae and dental impingement. I couldn't eat, again. My dose of antibiotics were escalated, as they feared my nasal infection had risks of passing into the connecting brain linings. With treatment, my swollen nose and eroded tongue was beginning to wane, and I had severe gastritis, forcing me to stop all antiobiotics.
Between all this, my wound pain had revived. And my gynecologist said I had scar adhesions, probably connecting to the uterus. He was apprehensive that I might need laparoscopic surgery for breaking adhesions if my pain won't subside. Maybe after 6months or so. But for me, any more surgery sounded like death sentence. I had suffered so much, any surgical intervention scared me.
Thankfully the wound pain vanished. And now, my baby is two months old, thriving well, with remarkable weight gain. And his murmur has disappeare. He has embraced my genes wholeheartedly, his light brown eyes, sharp nose, full lips and the dimples that light my world when he smiles.
During all the chaos, my baby's healthy weight gain was my only pride. And I learnt two things, pain is a constant, yet nothing lasts forever. I survived and I conquered.
Friday, September 8, 2017
Happy Sixth
My dear daughter,
You are six now. You are this beautiful chirpy little thing that warms my heart and life.
Your shoes are getting bigger. And suddenly, I realise that one day you will out grow us and this house, to build your own shelter, or to find your own world. So I ask, why you can't be six forever?? Coz these are the best years of "you and me", coz you are innocent yet mischevious. Your pour your questions at us with utter amusement, and your little games add music to our souls.
Your father loves you, very deeply. As you will always fondly remember, he takes you places, shows you happiness and beauty. What you might not reckon, is that he subtly makes sure that sadness doesn't hover around you. He wants to protect you from the universe, from its chauvenism, judgements, patriarchy, etc. He acknowledges the charm of a girl child. At the same time, he understands the challenges of being a woman. and wishes so hard, that you don't encounter them. It makes him love you more everyday. That.... makes him the best father you could ever have. Happy Sixth Birthday.
You are six now. You are this beautiful chirpy little thing that warms my heart and life.
Your shoes are getting bigger. And suddenly, I realise that one day you will out grow us and this house, to build your own shelter, or to find your own world. So I ask, why you can't be six forever?? Coz these are the best years of "you and me", coz you are innocent yet mischevious. Your pour your questions at us with utter amusement, and your little games add music to our souls.
Your father loves you, very deeply. As you will always fondly remember, he takes you places, shows you happiness and beauty. What you might not reckon, is that he subtly makes sure that sadness doesn't hover around you. He wants to protect you from the universe, from its chauvenism, judgements, patriarchy, etc. He acknowledges the charm of a girl child. At the same time, he understands the challenges of being a woman. and wishes so hard, that you don't encounter them. It makes him love you more everyday. That.... makes him the best father you could ever have. Happy Sixth Birthday.
Saturday, May 6, 2017
So far.. in Nanjing
A petite brown-skinned woman in her early thirties, donning a blue long floral dress, has a backpack on her tiny shoulders, and an incubating pot-belly, protruding out of her rounded waist. She's at the airport, nervously fidgeting with her air-ticket, so uncertain of herself, for the first time in her life, daunted by fears of plausible upcoming challenges. At sixth month of pregnancy, she is traveling alone, to a place where English is an estranged language, where traffic signs, food menu and everything else is in Chinese. She can stutter few incoherent Chinese words, but her vocabulary is limited to countable ramblings. She looks at her five year old, one last time, shuddering at the thought of missing her desperately. Her daughter looks at her with piercing hopefulness, but in vain. With tearful sunken heart, she takes aching strides to the departure gate... "
This journey is a memoir I have to scribble about... too important a life event, too many memories to recount in years to come. I came to China for a training course of one month, all by myself, to a city I had never been to, without a single soul to call my acquaintance. It may not sound so unnerving, but my guts failed me because I was in vulnerable stage of life. I had lost my pace, recently overcame hyperemesis with ketonuria, and was regaining my health and stride back....
But the most striking part of my journey was the eager generosity people bestowed upon me. Be it random Chinese passerbys, handful Nepali students at the dorm or doctors at the hospital. I was greeted with exceptional kindness and love. Everyday I travel alone, to my faraway hospital, to shopping centers, electronic stores, groceries, and far off. I somehow find my way, without the google map, amid illegible Chinese signs, hoarding boards and bus routes. My full belly turns a lot of heads, and many helping hands too. Some instances are surreal and too-good-to-be-true. My beliefs of benevolence are reaffirmed very strongly in this presumed outlandish city...
... to be continued
Saturday, February 25, 2017
DAYCATION
A trend has set in. Any employee working under someone else
in Nepal, literally goes gaga over holidays during the weekend. Although it may sound bizzare to Westerners, for
whom two days long weekend, isn’t a luxury but a norm. More than 40 hours of
work week is overtime. But not in our country. So how do
we handle this exhilaration of a stretch of 48 hour long break? We go crazy, we
run to nearest staycation or daycation spot. And our facebook and instagram scroll
busier than usual, with photographs and captions.... of outings and contemplations of life etc.
In such similar strive, we drove to Namobuddha, an outing
closest to our abode. Beauty of this place cannot be confined to words. It’s
enrapturing placidity mirrors peace, stillness, faith and warmth. It has an
aroma of sophisticated mysticism and spirituality, as if an answer to all human
frailties, gluttony and malice. However, the last few strides to reach this
sanctuary is obnoxiously unpleasant. Our vehicle suffered bumps, curves, caves
and thuds along with sheets of mud. My four month old belly cramped all along
the unruly lane. We loathed the incompetence of our unstable government, which
gobbles hefty taxes from us, but is unable to suffice its obligations.
Just as we reach the destination, our disappointments of the
stumbling journey mists into breezy air. The spotless restfulness ripples at
Namobuddha. The yellow-capped hermitage rests at the hills of Kavre, various
wings of the monastery is terraced along its stairs. This place wasn’t a
stranger though.... We had hiked to this picturesque site, more than a decade ago,
in first year of med-school. We were teenagers, freshly paired up with each
other, and quite naïve about one another.... one of the fondest memories of maiden
years of love. Time has taken its swift flight, and here we are, a family of
three.
Our family trip was one of its kind this time, coz we had packed
home food with us. Sausages, cheese, bread, juice, papadum, vegetables, etc
were in the list. In a cozy nook of this peaceful hilltop, we spread our
lunch-pack enjoying the beaming sunshine. Aaliyah was especially elated, as it
was so refreshing. There were throngs of visitors from near and far off places,
from cities and villages alike. All of them were amusingly busy, taking pictures
of themselves, mostly selfies. Women and girls seemed more aware of their
dresses and makeup, than the serene scenery. An irony. Changing times. Men on
the contrary, were more self-reliant, absorbing the stunning backdrop
contently.
The site-seeing lasted a brief hour, and we were heading
back sooner than we had reached. Those sixty minutes were cleansing,
purgatory and delightful. We were weary but content. Gleeful. Happy. And just
like every tour, the journey back home seemed shorter. We were home before
twilight guzzled the Dhulikhel sky.
Thursday, December 1, 2016
Vitiligo: The scourge and the stigma- how the battle can be won
Humans are enthralled by the concept of beauty. And in our pursuit of vanity, mankind has many a times, rebuked any contrary to the norm. Be it leprosy, syphilis or tuberculosis, diseases have been loathed and ostracized ruthlessly since primeval times. How could vitiligo escape this coercive subjugation. Since its first documentation in Egyptian medical papyrus in 1550 BC, vilitiginous white spots have been noted by Indians, Japanese and Latins alike. The journey of demystifying vitiligo traverses almost four thousand years in time. And the path to unfurl its scientific genesis is still in progress.... Vitiligo stood apart from other diseases due to its deceitful appearance, despite naive harmlessness. An innocuous disorder raised such harsh abhoration in communities in the eighteenth and ninteenth century! Hence baptized "historical curse of depigmentation" Unlike our veteran vitiligans today, patients suffered despondent segregation from the society in the past. This stark stigma has aroused curiosity, resentment, distaste and sympathy across generations. Vitiligo patients are still divaricated from social throngs, as ugly ducklings. In our times, Michel Jackson catapulted the social standing of this disease to jolting acceptance. His unmatched contribution is etched in history. Vitiligans like Winnie Harlow, Lee Thomas further eased the battle by embracing their depigmented bodies, and shedding light on the disorder. Therefore, I believe that blemishes of vitiligo shall fade with time.
However, in developing countries like India and Nepal, the task of generating awareness about this disease is herculean. We lack vitiligo societies or foundations unlike in the West. It is still hurtful to disclose to a 10 year old that he/she has vitiligo, as it brings disgrace not just to the child, but the entire family. The prognosis maybe brighter in an adolescent, but the excruciating agony caused by the diagnosis, is hard to dampen, even with elaborate counseling. Hence, clarity about the disease and stupendous treatment efficacy will be the unwavering weapon against this discriminative illness.
The scientific task of delineating the etiopathogenesis has been arduous. Wide array of clinical causes have been postulated time after time, with newer theories emerging every now and then. As dermatologists, we are aware of the lists of various hypothesis. So lets take a brisk walk, down the lane of known etiopathogeneic factors. Autoimmunity, oxidative stress, cytorrhagia, traumatic, neural, genetic, biochemical factors are snippets of the dice we have yet to complete. Oxidative stress and autoimmunity are the titans that have had paramount significance. Others fall out in the fringes. Recently genetic linkage and associations are surfacing as strong determinants of both the onset and severity of the illness. Various susceptibility genes have been identified. Unfolded protein response(UPR), melanocortin and Raper mason enzyme related genes, genome with linkage and association studies are rising as susceptibility indicators. More concrete impact of gene analysis on disease predictability and prognosis, is yet to be disclosed.
Coming back to autoimmunity, tremendous association of vitiligo with other autoimmune conditions such as thyroid disorders is unputdownable. Studies show thyroid association in quarter of the childhood cases, and more than half of adult vitiligo cases. A study conducted in our center, have also reaffirmed the coexistence of thyroid disorders with vitiligo. Newer studies reveal autoantibodies and T cells predomination in diffuse and localized vitiligo. CD8T cells were positive in lesional skin in localized vitiligo. Depending on whether the cellular or the humoral response is predominant, extent of the disease maybe predictable in future.
My concern for autoimmune association, is regarding thyroid autoantibodies. To me, thyroid disorders and their treatment guidelines, are biased against cutaneous disorders. Thyroid associations in the West, specifically advocate against treating mild thyroid alterations despite cutaneous manifestations. Their cut off for thyroxine supplementation is TSH>10. We frequently witness patients with vitiligo, who have moderately increased TSH and positive Thyroid peroxidase (TPO) antibodies. Will autoimmune vitiligo improve as long as TPO remains escalated? Does mild TSH alteration shift the balance of skin homeostasis? Do we wait for endocrine storm to abate or we intervene? These questions need to be addressed in order to find a solution for autoimmune skin conditions.
In regards to management, counselling has a tremendous role. It is encouraged to make intelligible leaflets in patient’s language. For me, it is heart-crunching to see patients willing for painful surgeries for this asymptomatic condition. Hence, generating awareness in our community should be our prime priority.
Treatment modalities in vitiligo have metamorphosed over centuries, as we unravel this enigmatic condition. Treatment guidelines have been simplified, and rendered more precise in recent times. Dichotomy of segmental and nonsegmental vitiligo, treatment modalities according to body surface areas and stability of lesions are primary considerations for choosing treatment modalities.
Conventional treatment modalities such as steroids, are the veteran warhorse that still reign supreme in vitiligo. Oral steroids are the most potent tool to halt disease progression. Immunomodulators such as azathioprine, tacrolimus and phototherapy are prevailing steroid sparing alternatives. Phototherapy is an irrefutable asset. NB-UVB is superior to PUVA, with excellent color matching and minimal adverse effect profile. However, we have found rewards in Bath PUVA, turban PUVA and bathing suite PUVA in our vitiligo patients.
Newer molecule Tofacitinib has grabbed limelight of late. Tofacitinib inhibits the IFN-Y signalling via Jak pathway, hence halting progression and maintenance of vitiligo. Multiple clinical trials hint towards excellent potential role of Janus kinase inhibitors in near future.
Adjunctive or alternative therapies are topical gingko biloba, levamisole, latanoprost, vitamin D analogues, topical ruxolitinib and antioxidants.
Selenium in the form of selenomethionine or sodium selenite, has shown promise in cutting off the TPO levels. Selenium improves TPO profile, and also directly quenches the oxidative surge. Hence, it might emerge as a robust tool in autoimmune vitiligo. Some studies have shown the linkage between vitamin D deficiency and vitiligo. Vitamin D accentuates photo-induced melanogenesis and hinders cytokines linked to vitiligo via immune-modulating properties. Vitamin D deficiency related vitiligo might be more important in our skin types, as some reports have shown significant role of Vitamin D induced repigmentation with NB-UVB. Role of micronutrients such as selenium, zinc and copper should be further extrapolated.
Interventional strategies have gained momentum for some time now. Experts are fanatic about surgical grafting in patients with stable lesions. However, surgery maybe double edged sword, because of debacle of stability. Scoring these lesions, serial photographs and performing test grafts may aid in warranting stability. In test grafts, unequivocal repigmentation beyond 1mm from the border of the test graft is said to indicate stability. Individual lesional stability is cardinal before holding a scalpel. Evidence based practice will further uplift the surgical results in vitiligo patients. However, the despairing fact of failure of surgical grafts should be counselled even in the most promising patient.
Punch grafts were the harbinger of surgical interventions in vitiligo, and mini punch grafting still remains one of the most common surgeries. However, threats of cobblestone, lopsided repigmentation and anatomic restraints limits its utility.
Epidermal suction blister grafts, split skin grafts and tissue grafts are met by their rewards and hindrances. At present, non cultured epidermal cell suspension and cultured melanocyte suspensions are at the heart of vitiligo surgeries, as they address large recipient areas, provide excellent response and admirable color matching.
Hair transplantation, excision of small lesions have all been done with variable results. Nonsurgical interventions such as lasers and home-based phototherapy may prove to have snowball effect, as they gain momentum among patients with localized disease. Neon lasers, fractional lasers, microfocused bioskin phototherapy are glimmering in the horizon as promising innovations. In recent past, Mosenson et al. showed that vitiligo can be reversed through immune targeting with mutant Heat shock proteins(HSP70), given the evidence of association of Heat shock proteins (HSP) in depigmentation.
In conclusion, patient specific and lesion specific individualized approach in vitiligo management can defeat this colossal stigma. Unambiguous patient counselling at first patient visit should follow individual targeted therapy at achieving disease control and repigmentation. We stand at this glorious era in the history of vitiligo, where we have defined many uncharted spheres in etiogenesis and management. Future gleams in delight, as we discover newer prospects in battling this ancient disease.
However, in developing countries like India and Nepal, the task of generating awareness about this disease is herculean. We lack vitiligo societies or foundations unlike in the West. It is still hurtful to disclose to a 10 year old that he/she has vitiligo, as it brings disgrace not just to the child, but the entire family. The prognosis maybe brighter in an adolescent, but the excruciating agony caused by the diagnosis, is hard to dampen, even with elaborate counseling. Hence, clarity about the disease and stupendous treatment efficacy will be the unwavering weapon against this discriminative illness.
The scientific task of delineating the etiopathogenesis has been arduous. Wide array of clinical causes have been postulated time after time, with newer theories emerging every now and then. As dermatologists, we are aware of the lists of various hypothesis. So lets take a brisk walk, down the lane of known etiopathogeneic factors. Autoimmunity, oxidative stress, cytorrhagia, traumatic, neural, genetic, biochemical factors are snippets of the dice we have yet to complete. Oxidative stress and autoimmunity are the titans that have had paramount significance. Others fall out in the fringes. Recently genetic linkage and associations are surfacing as strong determinants of both the onset and severity of the illness. Various susceptibility genes have been identified. Unfolded protein response(UPR), melanocortin and Raper mason enzyme related genes, genome with linkage and association studies are rising as susceptibility indicators. More concrete impact of gene analysis on disease predictability and prognosis, is yet to be disclosed.
Coming back to autoimmunity, tremendous association of vitiligo with other autoimmune conditions such as thyroid disorders is unputdownable. Studies show thyroid association in quarter of the childhood cases, and more than half of adult vitiligo cases. A study conducted in our center, have also reaffirmed the coexistence of thyroid disorders with vitiligo. Newer studies reveal autoantibodies and T cells predomination in diffuse and localized vitiligo. CD8T cells were positive in lesional skin in localized vitiligo. Depending on whether the cellular or the humoral response is predominant, extent of the disease maybe predictable in future.
My concern for autoimmune association, is regarding thyroid autoantibodies. To me, thyroid disorders and their treatment guidelines, are biased against cutaneous disorders. Thyroid associations in the West, specifically advocate against treating mild thyroid alterations despite cutaneous manifestations. Their cut off for thyroxine supplementation is TSH>10. We frequently witness patients with vitiligo, who have moderately increased TSH and positive Thyroid peroxidase (TPO) antibodies. Will autoimmune vitiligo improve as long as TPO remains escalated? Does mild TSH alteration shift the balance of skin homeostasis? Do we wait for endocrine storm to abate or we intervene? These questions need to be addressed in order to find a solution for autoimmune skin conditions.
In regards to management, counselling has a tremendous role. It is encouraged to make intelligible leaflets in patient’s language. For me, it is heart-crunching to see patients willing for painful surgeries for this asymptomatic condition. Hence, generating awareness in our community should be our prime priority.
Treatment modalities in vitiligo have metamorphosed over centuries, as we unravel this enigmatic condition. Treatment guidelines have been simplified, and rendered more precise in recent times. Dichotomy of segmental and nonsegmental vitiligo, treatment modalities according to body surface areas and stability of lesions are primary considerations for choosing treatment modalities.
Conventional treatment modalities such as steroids, are the veteran warhorse that still reign supreme in vitiligo. Oral steroids are the most potent tool to halt disease progression. Immunomodulators such as azathioprine, tacrolimus and phototherapy are prevailing steroid sparing alternatives. Phototherapy is an irrefutable asset. NB-UVB is superior to PUVA, with excellent color matching and minimal adverse effect profile. However, we have found rewards in Bath PUVA, turban PUVA and bathing suite PUVA in our vitiligo patients.
Newer molecule Tofacitinib has grabbed limelight of late. Tofacitinib inhibits the IFN-Y signalling via Jak pathway, hence halting progression and maintenance of vitiligo. Multiple clinical trials hint towards excellent potential role of Janus kinase inhibitors in near future.
Adjunctive or alternative therapies are topical gingko biloba, levamisole, latanoprost, vitamin D analogues, topical ruxolitinib and antioxidants.
Selenium in the form of selenomethionine or sodium selenite, has shown promise in cutting off the TPO levels. Selenium improves TPO profile, and also directly quenches the oxidative surge. Hence, it might emerge as a robust tool in autoimmune vitiligo. Some studies have shown the linkage between vitamin D deficiency and vitiligo. Vitamin D accentuates photo-induced melanogenesis and hinders cytokines linked to vitiligo via immune-modulating properties. Vitamin D deficiency related vitiligo might be more important in our skin types, as some reports have shown significant role of Vitamin D induced repigmentation with NB-UVB. Role of micronutrients such as selenium, zinc and copper should be further extrapolated.
Interventional strategies have gained momentum for some time now. Experts are fanatic about surgical grafting in patients with stable lesions. However, surgery maybe double edged sword, because of debacle of stability. Scoring these lesions, serial photographs and performing test grafts may aid in warranting stability. In test grafts, unequivocal repigmentation beyond 1mm from the border of the test graft is said to indicate stability. Individual lesional stability is cardinal before holding a scalpel. Evidence based practice will further uplift the surgical results in vitiligo patients. However, the despairing fact of failure of surgical grafts should be counselled even in the most promising patient.
Punch grafts were the harbinger of surgical interventions in vitiligo, and mini punch grafting still remains one of the most common surgeries. However, threats of cobblestone, lopsided repigmentation and anatomic restraints limits its utility.
Epidermal suction blister grafts, split skin grafts and tissue grafts are met by their rewards and hindrances. At present, non cultured epidermal cell suspension and cultured melanocyte suspensions are at the heart of vitiligo surgeries, as they address large recipient areas, provide excellent response and admirable color matching.
Hair transplantation, excision of small lesions have all been done with variable results. Nonsurgical interventions such as lasers and home-based phototherapy may prove to have snowball effect, as they gain momentum among patients with localized disease. Neon lasers, fractional lasers, microfocused bioskin phototherapy are glimmering in the horizon as promising innovations. In recent past, Mosenson et al. showed that vitiligo can be reversed through immune targeting with mutant Heat shock proteins(HSP70), given the evidence of association of Heat shock proteins (HSP) in depigmentation.
In conclusion, patient specific and lesion specific individualized approach in vitiligo management can defeat this colossal stigma. Unambiguous patient counselling at first patient visit should follow individual targeted therapy at achieving disease control and repigmentation. We stand at this glorious era in the history of vitiligo, where we have defined many uncharted spheres in etiogenesis and management. Future gleams in delight, as we discover newer prospects in battling this ancient disease.
Monday, August 22, 2016
Journey with Fibromyalgia
I was just tender 22. One sunny summer noon, frens at med school planned an outing by the river-side of Dolalghat. We swam all day under the dazzling sun. And when I woke up next morning, i couldnt move. It was as if I was trapped in a casket. My hands and body crunched in pain. Oblivious to the source of pain, my friends tried giving me painkillers, massage and hotbags. None of that worked however. I was bedridden.
That was my first attack of fibromyalgia. ...
But it was only a harbinger of the upheaval.. that was about to turn my life upside down!
My hands and back felt foreign to me. I sat stiff, days after days, writhing, hurting, crying and devastated. Disabling pain pinged into my bones. I still sorely remember sitting by my hostel window, wearing jacket in summer heat, and trying to read my course books. I almost flunked my third year final exam. My friends were lost in their own stress of med-school. But i was at war, war i lost everyday. My dreams were thwarted, I sank in my wretchedness. I woke up every morning just to find the demons stronger and fiercer than the day before. I couldn't eat, dinner table sobs became a mundane routine. I was entangled in a vicious web of vexation. Thoughts of ending my sufferings constantly plagued me, and wished for euthanasia back then. My then boyfriend, and now spouse, was the only person who encouraged me to move on.
It took me more than a year to demystify the source of pain. I was temperature sensitive. I had allodynia and hyperalgesia. Temperature changes and wind triggered my attacks. But I didnt know how to avoid or abate it. Desperate for answers, I knocked all doors... specialists, traditional healers, fortune tellers and who not. Renouned orthopedician misdiagnosed me with arthritis and prescribed Methotrexate for a year, with no improvement. Rheumatologist at AIIMS Delhi, brushed off my condition as not arthritis, but wonder what...
Years passed, harrowing pain became a bitter constant. However, I didn't let it forestall my life goals. It wasnt one particular day or event, but when I looked back after 6-7 years of affliction, I realised I had won the battle. I wasn't cured, it still followed me like dark shadow. The disability still tainted my brightest days. During MBBS finals, MD finals or pregnancy, pain would shoot up, forcing me to immobility. But I worked. I worked when I was fine, I worked when it hurt. I worked when I was unable to hold a pen, I paddled through choppy waters. Now I am a proud Derm graduate. Despite days of bedlock right before MD finals, I am Kathmandu University's first distinction holder in Dermatology. Even today, my hands hurt during every hair transplant, while holding laser probes, in household chores and as I carry my daughter on my hips. But I do all of that, and the triumph is priceless.
I am sharing my journey because I know, there are so many others who live this chronicity, shunned and dejected. Life is a battle, one way or the other. Fibromyalgia is a havoc, it engulfs you if you succumb. You have to fight, you cant give up, just cant give up.
That was my first attack of fibromyalgia. ...
But it was only a harbinger of the upheaval.. that was about to turn my life upside down!
My hands and back felt foreign to me. I sat stiff, days after days, writhing, hurting, crying and devastated. Disabling pain pinged into my bones. I still sorely remember sitting by my hostel window, wearing jacket in summer heat, and trying to read my course books. I almost flunked my third year final exam. My friends were lost in their own stress of med-school. But i was at war, war i lost everyday. My dreams were thwarted, I sank in my wretchedness. I woke up every morning just to find the demons stronger and fiercer than the day before. I couldn't eat, dinner table sobs became a mundane routine. I was entangled in a vicious web of vexation. Thoughts of ending my sufferings constantly plagued me, and wished for euthanasia back then. My then boyfriend, and now spouse, was the only person who encouraged me to move on.
It took me more than a year to demystify the source of pain. I was temperature sensitive. I had allodynia and hyperalgesia. Temperature changes and wind triggered my attacks. But I didnt know how to avoid or abate it. Desperate for answers, I knocked all doors... specialists, traditional healers, fortune tellers and who not. Renouned orthopedician misdiagnosed me with arthritis and prescribed Methotrexate for a year, with no improvement. Rheumatologist at AIIMS Delhi, brushed off my condition as not arthritis, but wonder what...
Years passed, harrowing pain became a bitter constant. However, I didn't let it forestall my life goals. It wasnt one particular day or event, but when I looked back after 6-7 years of affliction, I realised I had won the battle. I wasn't cured, it still followed me like dark shadow. The disability still tainted my brightest days. During MBBS finals, MD finals or pregnancy, pain would shoot up, forcing me to immobility. But I worked. I worked when I was fine, I worked when it hurt. I worked when I was unable to hold a pen, I paddled through choppy waters. Now I am a proud Derm graduate. Despite days of bedlock right before MD finals, I am Kathmandu University's first distinction holder in Dermatology. Even today, my hands hurt during every hair transplant, while holding laser probes, in household chores and as I carry my daughter on my hips. But I do all of that, and the triumph is priceless.
I am sharing my journey because I know, there are so many others who live this chronicity, shunned and dejected. Life is a battle, one way or the other. Fibromyalgia is a havoc, it engulfs you if you succumb. You have to fight, you cant give up, just cant give up.
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