UI styling update

app/components/PackagingShipping/DNASamples.jsx

@@ -5,7 +5,7 @@ const DNASamples = () => {
   return (
     <div className="space-y-6">
       <div>
-        <h3 className="text-2xl font-semibold text-gray-700 mb-6">Shipping of DNA Samples</h3>
+        <h3 className="text-3xl font-bold text-teal-700 mb-4">Shipping of DNA Samples</h3>
       </div>
       
       <div className="flex flex-col lg:flex-row gap-6">

app/components/PackagingShipping/GeneralGuidelines.jsx

@@ -4,7 +4,7 @@ const GeneralGuidelines = () => {
   return (
     <div className="space-y-6">
       <div>
-        <h3 className="text-2xl font-semibold mb-6" style={{ color: '#555555' }}>General Guidelines</h3>
+        <h3 className="text-3xl font-bold text-teal-700 mb-4">General Guidelines</h3>
       </div>
       
       <div className="space-y-6">

app/components/PackagingShipping/PackagingGuideline.jsx

@@ -4,7 +4,7 @@ const PackagingGuideline = () => {
   return (
     <div className="space-y-6">
       <div>
-        <h3 className="text-2xl font-semibold mb-6" style={{ color: '#555555' }}>Packaging Guideline</h3>
+        <h3 className="text-3xl font-bold text-teal-700 mb-4">Packaging Guideline</h3>
       </div>
       
       <div className="space-y-6">

app/components/PackagingShipping/RNASamples.jsx

@@ -4,40 +4,50 @@ const RNASamples = () => {
   return (
     <div className="space-y-6">
       <div>
-        <h3 className="text-2xl font-semibold mb-6" style={{ color: '#555555' }}>Shipping of RNA Samples</h3>
+        <h3 className="text-3xl font-bold text-teal-700 mb-4">Shipping of RNA Samples</h3>
       </div>
       
       <div className="space-y-6">
-        <p className="leading-relaxed" style={{ color: '#555555' }}>
+        <ul className="list-disc list-inside space-y-4 leading-relaxed pl-4">
+          <li className="text-justify" style={{color: '#faae31'}}>
+            <span style={{color: '#555555'}}>
               Bioanalyzer QC report is advised to be shared from the client's end, in the
               absence of which an agarose Gel Electrophoresis and Nanodrop quantification
               to confirm the integrity of RNA must be shared. Samples with A260/280 ratio
               values of ~1.8 are considered "pure" for DNA and will be accepted for
               processing further.
-        </p>
+            </span>
+          </li>
           
-        <p className="leading-relaxed" style={{ color: '#555555' }}>
+          <li className="text-justify" style={{color: '#faae31'}}>
+            <span style={{color: '#555555'}}>
               We require Bioanalyzer traces (or similar) for all customer-submitted
               sequencing libraries and total RNA samples. If traces are not provided, we
               will perform Bioanalyzer QC for an additional fee. If you can supply traces,
               please include them into the shipment in hard copy. Also, ensure that your
               samples meet the specified sample or library requirements [LINK].
-        </p>
+            </span>
+          </li>
           
-        <p className="leading-relaxed" style={{ color: '#555555' }}>
+          <li className="text-justify" style={{color: '#faae31'}}>
+            <span style={{color: '#555555'}}>
               For large-scale projects, RNA samples can be submitted in strip tubes with
               individually attached RNase-free caps. Pack the strips into racks (e.g.,
               empty pipet tip boxes) and ensure they are secured to prevent movement
               during transport.
-        </p>
+            </span>
+          </li>
           
-        <p className="leading-relaxed" style={{ color: '#555555' }}>
+          <li className="text-justify" style={{color: '#faae31'}}>
+            <span style={{color: '#555555'}}>
               RNA, cells, bacteria, and frozen tissue samples should be stored in liquid
               nitrogen for rapid freezing and then transported with dry ice. For longer
               shipments, RNA samples can also be successfully shipped dry at room
               temperature after LiCl/ethanol precipitation and ethanol washes; make sure
               to mark the pellet's position on the tubes.
-        </p>
+            </span>
+          </li>
+        </ul>
       </div>
     </div>
   );

app/components/PackagingShipping/ShippingSchedule.jsx

@@ -4,7 +4,7 @@ const ShippingSchedule = () => {
   return (
     <div className="space-y-6">
       <div>
-        <h3 className="text-2xl font-semibold mb-6" style={{ color: '#555555' }}>Shipping Schedule and Address</h3>
+        <h3 className="text-3xl font-bold text-teal-700 mb-4">Shipping Schedule and Address</h3>
       </div>
       
       <div className="space-y-6">

app/components/PackagingShipping/ShippingTemperatureTable.jsx

@@ -129,7 +129,7 @@ const ShippingTemperatureTable = () => {
   return (
     <div className="space-y-6">
       <div>
-        <h3 className="text-2xl font-semibold text-gray-700 mb-6">Shipping Temperature and Condition</h3>
+        <h3 className="text-3xl font-bold text-teal-700 mb-4">Shipping Temperature and Condition</h3>
       </div>
       
       <div className="space-y-6">

app/components/SampleGuideline/ContentSection.jsx

@@ -18,7 +18,7 @@ const ContentSection = () => {
 
   return (
     <section className="pt-4 pb-8">
-      <div className="container mx-auto max-w-none px-4">
+      <div className="container max-w-none px-4">
         <div className="grid xl:grid-cols-[280px_1fr] gap-8">
           {/* LEFT SIDEBAR */}
           <div className="xl:sticky xl:top-8">

app/components/SampleGuideline/GeneralGuidelines.jsx

@@ -4,46 +4,58 @@ const GeneralGuidelines = () => {
   return (
     <div className="space-y-6">
       <div className="mb-6">
-        <h3 className="text-2xl font-semibold text-gray-600 mb-4">General Guidelines</h3>
+        <h3 className="text-3xl font-bold text-teal-700 mb-4">General Guidelines</h3>
       </div>
       
       <div className="prose max-w-none">
-        <ul className="space-y-4 text-gray-700 leading-relaxed pl-5">
-          <li className="list-disc">
+        <ul className="space-y-4 text-gray-700 leading-relaxed pl-5" style={{listStyleType: 'disc'}}>
+          <li className="list-disc" style={{color: '#faae31'}}>
+            <span style={{color: '#374151'}}>
               Please complete the Sample Initiation Form (SIF), ensuring that the
               sample names on the form match the labels on the sample tubes. We also
               request that you send an electronic copy of the form and any required QC
               data via email.
+            </span>
           </li>
-          <li className="list-disc">
+          <li className="list-disc" style={{color: '#faae31'}}>
+            <span style={{color: '#374151'}}>
               Each tube should be labeled on the lid with a maximum of 4-6
               alphanumeric characters (e.g., 4B0001). Use a black permanent marker to
               write sample names on the top and side of each tube. Avoid writing
               directly on the tube wall or cover with an oil pen.
+            </span>
           </li>
-          <li className="list-disc">
+          <li className="list-disc" style={{color: '#faae31'}}>
+            <span style={{color: '#374151'}}>
               DNA can be submitted in DNase-free water, Elution Buffer, or 10mM Tris
               pH 8.0. DNA samples should have an OD260/280 ratio as close to 1.8~2.0
               as possible. All DNA should be RNase-treated and free from degradation
               or contamination. Ship with ice packs. The total amount of DNA required
               depends on the specific application.
+            </span>
           </li>
-          <li className="list-disc">
+          <li className="list-disc" style={{color: '#faae31'}}>
+            <span style={{color: '#374151'}}>
               RNA can be submitted in RNase-free water, RNA Stabilization Reagent, or
               10mM Tris pH 8.0. All total RNA samples should be DNA-free, with an OD
               A260/A280 ratio ≥ 1.8, A260/230 ratio ≥ 1.8, and a RIN ≥ 6. Ship with
               dry ice. The total amount of RNA required depends on the specific
               application. For Long Read Sequencing, RNA samples should have a RIN ≥
               8.
+            </span>
           </li>
-          <li className="list-disc">
+          <li className="list-disc" style={{color: '#faae31'}}>
+            <span style={{color: '#374151'}}>
               The listed concentrations should be determined by fluorometry (e.g.,
               PicoGreen/Qubit/RiboGreen). If using spectrophotometry (e.g., Nanodrop),
               increase concentrations by approximately twofold.
+            </span>
           </li>
-          <li className="list-disc">
+          <li className="list-disc" style={{color: '#faae31'}}>
+            <span style={{color: '#374151'}}>
               The quality inspection method for the sizes and concentrations of the
               Ready To Run Library is Qubit and Agilent Bioanalyzer.
+            </span>
           </li>
         </ul>
       </div>

app/components/SampleGuideline/IntroSection.jsx

@@ -2,11 +2,11 @@ import React from 'react';
 
 const IntroSection = () => {
   return (
-    <section className="bg-white mx-4 md:mx-8  mt-4 mb-4 py-4">
-      <div className="container mx-auto max-w-none px-4">
-        <div className="text-gray-600 max-w-none leading-relaxed text-center">
-          <div className="text-base text-justify">
-            <p className="m-0">
+    <section className="py-0">
+      <div className="container-fluid">
+        <div className="bg-gradient-to-br from-teal-600 to-teal-700 text-white p-8 lg:p-8  flex items-center">
+          <div className="w-full">
+            <p className="leading-relaxed text-base text-justify m-0">
               We humbly offer a wide range of services, including genomics, transcriptomics,
               metagenomics, epigenomics, single-cell sequencing, genotyping, microarray,
               bioinformatics, and more. To help us deliver the best results for you, we request you to

app/components/SampleGuideline/SearchSampleRequirements.jsx

@@ -67,7 +67,7 @@ const SearchSampleRequirements = () => {
   return (
     <div className="space-y-6">
       <div className="mb-6">
-        <h3 className="text-2xl font-semibold text-gray-600">Search Sample Requirements</h3>
+        <h3 className="text-3xl font-bold text-teal-700 mb-4">Search Sample Requirements</h3>
       </div>
       
       <SearchFilters

app/components/SampleInitiation/ProcessSection.jsx

@@ -5,11 +5,11 @@ import SubmissionOptions from './SubmissionOptions';
 const ProcessSection = () => {
   return (
     <section className="bg-white">
-      <div className="container mx-auto max-w-none px-4">
+      <div className="container max-w-none">
         <div className="bg-white p-4 md:p-6">
           {/* Main Title */}
           <div className="text-left mb-4">
-            <h2 className="text-2xl md:text-4xl text-gray-600 font-normal">
+            <h2 className="text-3xl font-bold text-teal-700 mb-4">
               Welcome to Our Online Submission Portal!
             </h2>
           </div>

app/components/SampleInitiation/ProcessSteps.jsx

@@ -46,8 +46,10 @@ const ProcessSteps = () => {
             </h3>
             <ul className="list-disc list-inside space-y-2 text-gray-700 leading-relaxed pl-4">
               {step.items.map((item, index) => (
-                <li key={index} className="text-justify">
+                <li key={index} className="text-justify" style={{color: '#faae31'}}>
+                  <span style={{color: '#374151'}}>
                     {item}
+                  </span>
                 </li>
               ))}
             </ul>

app/components/SampleInitiation/SampleInitiationPage.jsx

@@ -1,14 +1,14 @@
 import React from 'react';
 import PageTitle from './PageTitle';
 import ProcessSection from './ProcessSection';
-import ContactNote from './ContactNote';
+// import ContactNote from './ContactNote';
 
 const SampleInitiationPage = () => {
   return (
     <div className="page-content">
       <PageTitle />
       <ProcessSection />
-      <ContactNote />
+      {/* <ContactNote /> */}
     </div>
   );
 };

app/dna-sequencing/components/AboutDNA.jsx

@@ -4,24 +4,21 @@ import React from 'react';
 const AboutDNA = () => {
   return (
     <section className="pt-6 bg-white">
-      <div className="container mx-auto px-6">
-        <h2 className="text-4xl font-bold text-gray-700 text-left pb-2">
+      <div className="container max-w-none px-6">
+        <h2 className="text-4xl font-bold text-teal-700 mb-4">
           About DNA Sequencing
         </h2>
         <h2 className="text-lg font-semibold text-gray-600 mb-4">
           Exploring Life's Blueprint with Every Sequence
         </h2>
         
-        <div className="mb-6 text-justify">
+        <div className="mb-4 text-justify">
           <p className="text-gray-600 leading-relaxed text-base mb-4">
             DNA sequencing is a method used to determine the precise order of nucleotides 
             (adenine, thymine, cytosine, and guanine) in a DNA molecule. This information is 
             critical for understanding genetic information, mutations, and their roles in disease, 
             evolution, and various biological processes.
           </p>
-          <p className="text-gray-600 leading-relaxed text-base">
-            Different DNA sequencing approaches using Next Generation sequencing are listed below:
-          </p>
         </div>
       </div>
     </section>

app/dna-sequencing/components/DNATable.jsx

@@ -115,17 +115,17 @@ const DNATable = () => {
   ];
 
   return (
-    <section className="pt-6 bg-white">
-      <div className="container mx-auto px-6">
-        <h3 className="text-2xl font-semibold text-gray-700 mb-6">DNA Sequencing Approaches</h3>
+    <section className="pt-4 bg-white">
+      <div className="container max-w-none px-6">
+        <h3 className="text-lg font-semibold text-gray-600 mb-4">DNA Sequencing Approaches</h3>
         <div className="mb-6 text-justify">
           <p className="text-gray-600 leading-relaxed text-base">
             Different DNA sequencing approaches and their applications are summarized below:
           </p>
         </div>
 
-        <div className="overflow-x-auto mb-8">
-          <table className="w-full border-collapse border border-gray-300 text-sm bg-white shadow-sm">
+        <div className="overflow-x-auto mb-8 justify-center">
+          <table className="w-full border-collapse border border-gray-300 text-sm bg-white shadow-sm ">
             <thead>
               <tr className="bg-teal-50">
                 <th className="border border-gray-300 px-4 py-3 text-left font-semibold text-teal-700">
@@ -146,7 +146,7 @@ const DNATable = () => {
               {sequencingData.map((row, index) => (
                 <tr key={index} className={`${index % 2 === 1 ? 'bg-gray-50' : 'bg-white'} hover:bg-teal-25 transition-colors`}>
                   <td className="border border-gray-300 px-4 py-3 align-top">
-                    <a href={row.approach.link} className="text-teal-600 hover:underline font-medium text-base">
+                    <a href={row.approach.link} className="text-gray-600 hover:underline font-medium text-base">
                       {row.approach.name}
                     </a>
                   </td>

app/health/Components/ClinicalAreas.jsx

@@ -6,12 +6,12 @@ export default function ClinicalAreas() {
   return (
     <div className="mx-auto px-10 py-4">
       {/* Heading */}
-      <h2 className="text-4xl font-bold text-gray-700 text-left pb-2 mb-4">
+      <h2 className="text-3xl font-bold text-teal-700 mb-4">
         Precise Solutions for Clinical Areas
       </h2>
 
       {/* Subtext */}
-      <p className="text-gray-600 leading-relaxed text-base mb-8 max-w-3xl text-justify">
+      <p className="text-gray-600 leading-relaxed text-base mb-4 text-justify">
         Empowering you with precise, tailored approaches to diagnostics and care — 
         addressing the unique needs of each clinical area to improve patient outcomes.
       </p>

app/health/Components/HealthIntro.jsx

@@ -4,46 +4,40 @@ import Link from "next/link";
 
 export default function AboutHealth() {
   return (
-    <div className="mx-auto px-10 pt-12">
-      {/* Title */}
-      <h1 className="text-4xl font-bold text-gray-700 text-left pb-2 mb-4">About Health</h1>
-
-      {/* Intro Section */}
-      <div className="grid grid-cols-1 md:grid-cols-2 gap-8 items-center mb-12">
-        {/* Left Content */}
-        <div>
-          <p className="text-gray-600 leading-relaxed text-base mb-4 text-justify">
+    <section className="py-0">
+      <div className="container-fluid">
+        <div className="bg-gradient-to-br from-teal-600 to-teal-700 text-white p-8 lg:p-8 flex items-center">
+          <div className="w-full">
+            <ul className="list-disc list-inside space-y-4 leading-relaxed pl-4">
+              <li className="text-justify" style={{color: '#faae31'}}>
+                <span style={{color: '#ffffff'}}>
                   At Operify Health, we believe every patient deserves answers that are not only
                   accurate — but actionable. By harnessing the power of Next Generation Sequencing
                   (NGS), we transform patient samples into rich genomic insights that enable
                   clinicians and oncologists to make informed, personalized decisions. From rare
                   genetic disorders to complex oncological cases, our solutions help uncover what
                   traditional diagnostics often miss.
-          </p>
-          <p className="text-gray-600 leading-relaxed text-base mb-4 text-justify">
+                </span>
+              </li>
+              <li className="text-justify" style={{color: '#faae31'}}>
+                <span style={{color: '#ffffff'}}>
                   Our strength lies in our multidisciplinary team of researchers, bioinformaticians,
                   and data scientists who use custom-built algorithms and cutting-edge analytics to
                   interpret genetic data with unmatched depth. Backed by curated scientific evidence
                   and real-world clinical findings, we deliver recommendations that are current,
                   relevant, and patient-focused.
-          </p>
-          <p className="text-gray-600 leading-relaxed text-base text-justify">
+                </span>
+              </li>
+              <li className="text-justify" style={{color: '#faae31'}}>
+                <span style={{color: '#ffffff'}}>
                   With every genome we decode, we move closer to truly personalized medicine —
                   bridging data and care, science and life.
-          </p>
-        </div>
-
-        {/* Right Image */}
-        <div className="flex justify-center">
-          <Image
-            src="images/health/dna-placeholder.jpg" // Replace with your actual image path in /public
-            alt="DNA Strand"
-            width={500}
-            height={500}
-            className="rounded-lg object-cover"
-          />
+                </span>
+              </li>
+            </ul>
           </div>
         </div>
       </div>
+    </section>
   );
 }

app/health/Components/HealthTitle.jsx

@@ -3,7 +3,7 @@ import React from 'react';
 const HealthTitle = () => {
   return (
     <section 
-      className="relative bg-cover bg-center py-6 h-24" 
+      className="relative bg-cover bg-center py-6 h-[7rem]" 
       style={{ backgroundImage: "url('/images/bredcrumb.jpg')" }}
     >
       {/* Breadcrumb */}

app/health/components/ClinicalAreas.jsx

@@ -6,12 +6,12 @@ export default function ClinicalAreas() {
   return (
     <div className="mx-auto px-10 py-4">
       {/* Heading */}
-      <h2 className="text-4xl font-bold text-gray-700 text-left pb-2 mb-4">
+      <h2 className="text-3xl font-bold text-teal-700 mb-4">
         Precise Solutions for Clinical Areas
       </h2>
 
       {/* Subtext */}
-      <p className="text-gray-600 leading-relaxed text-base mb-8 max-w-3xl text-justify">
+      <p className="text-gray-600 leading-relaxed text-base mb-4 text-justify">
         Empowering you with precise, tailored approaches to diagnostics and care — 
         addressing the unique needs of each clinical area to improve patient outcomes.
       </p>

app/health/components/HealthIntro.jsx

@@ -4,46 +4,40 @@ import Link from "next/link";
 
 export default function AboutHealth() {
   return (
-    <div className="mx-auto px-10 pt-12">
-      {/* Title */}
-      <h1 className="text-4xl font-bold text-gray-700 text-left pb-2 mb-4">About Health</h1>
-
-      {/* Intro Section */}
-      <div className="grid grid-cols-1 md:grid-cols-2 gap-8 items-center mb-12">
-        {/* Left Content */}
-        <div>
-          <p className="text-gray-600 leading-relaxed text-base mb-4 text-justify">
+    <section className="py-0">
+      <div className="container-fluid">
+        <div className="bg-gradient-to-br from-teal-600 to-teal-700 text-white p-8 lg:p-8 flex items-center">
+          <div className="w-full">
+            <ul className="list-disc list-inside space-y-4 leading-relaxed pl-4">
+              <li className="text-justify" style={{color: '#faae31'}}>
+                <span style={{color: '#ffffff'}}>
                   At Operify Health, we believe every patient deserves answers that are not only
                   accurate — but actionable. By harnessing the power of Next Generation Sequencing
                   (NGS), we transform patient samples into rich genomic insights that enable
                   clinicians and oncologists to make informed, personalized decisions. From rare
                   genetic disorders to complex oncological cases, our solutions help uncover what
                   traditional diagnostics often miss.
-          </p>
-          <p className="text-gray-600 leading-relaxed text-base mb-4 text-justify">
+                </span>
+              </li>
+              <li className="text-justify" style={{color: '#faae31'}}>
+                <span style={{color: '#ffffff'}}>
                   Our strength lies in our multidisciplinary team of researchers, bioinformaticians,
                   and data scientists who use custom-built algorithms and cutting-edge analytics to
                   interpret genetic data with unmatched depth. Backed by curated scientific evidence
                   and real-world clinical findings, we deliver recommendations that are current,
                   relevant, and patient-focused.
-          </p>
-          <p className="text-gray-600 leading-relaxed text-base text-justify">
+                </span>
+              </li>
+              <li className="text-justify" style={{color: '#faae31'}}>
+                <span style={{color: '#ffffff'}}>
                   With every genome we decode, we move closer to truly personalized medicine —
                   bridging data and care, science and life.
-          </p>
-        </div>
-
-        {/* Right Image */}
-        <div className="flex justify-center">
-          <Image
-            src="images/health/dna-placeholder.jpg" // Replace with your actual image path in /public
-            alt="DNA Strand"
-            width={500}
-            height={500}
-            className="rounded-lg object-cover"
-          />
+                </span>
+              </li>
+            </ul>
           </div>
         </div>
       </div>
+    </section>
   );
 }

app/health/components/HealthTitle.jsx

@@ -3,7 +3,7 @@ import React from 'react';
 const HealthTitle = () => {
   return (
     <section 
-      className="relative bg-cover bg-center py-6 h-24" 
+      className="relative bg-cover bg-center py-6 h-[7rem]" 
       style={{ backgroundImage: "url('/images/bredcrumb.jpg')" }}
     >
       {/* Breadcrumb */}

app/health/oncology/Components/HereditaryCancerPanel.jsx

@@ -9,29 +9,32 @@ export default function HereditaryCancerPanel() {
     { title: "Genetic Counseling Support", desc: "Optional access to pre- and post-test counseling for patient education and informed decision-making." }
   ];
 
+  const points = [
+    "About 5-10% of all cancers are linked to inherited genetic mutations, often going undetected until late stages or after multiple family members are affected.",
+    "The Operify Hereditary Cancer Panel screens key high- and moderate-risk genes associated with hereditary cancer syndromes like HBOC, Lynch Syndrome (LS), Li Fraumeni Syndrome (LFS), Familial Adenomatous Polyposis (FAP), Cowden Syndrome (CS), Peutz-Jeghers Syndrome (PJS), Neurofibromatosis (NF) etc.",
+    "Early identification of germline mutations enables proactive clinical decisions, including risk-reducing strategies, targeted surveillance, and family cascade testing.",
+    "Studies show that genetic testing in hereditary cancer cases improves outcomes and informs care for both patients and at-risk relatives."
+  ];
+
   return (
-    <section className="mx-auto px-10 pt-12">
-      <h2 className="text-3xl font-bold text-gray-700 text-left pb-2 mb-4">Operify Hereditary Cancer Panel</h2>
+    <section className="mx-auto px-8 pt-8">
+      <h2 className="text-3xl font-bold text-teal-700 pb-2 mb-4">Operify Hereditary Cancer Panel</h2>
       
       <div className="mb-8">
-        <p className="text-gray-600 leading-relaxed text-base mb-4 text-justify">
-          <strong>About 5-10% of all cancers are linked to inherited genetic mutations</strong>, often going 
-          undetected until late stages or after multiple family members are affected.
-        </p>
-        <p className="text-gray-600 leading-relaxed text-base mb-4 text-justify">
-          The Operify Hereditary Cancer Panel screens key high- and moderate-risk genes associated 
-          with hereditary cancer syndromes like HBOC, Lynch Syndrome (LS), Li Fraumeni Syndrome (LFS), 
-          Familial Adenomatous Polyposis (FAP), Cowden Syndrome (CS), Peutz-Jeghers Syndrome (PJS), 
-          Neurofibromatosis (NF) etc.
-        </p>
-        <p className="text-gray-600 leading-relaxed text-base mb-4 text-justify">
-          Early identification of germline mutations enables proactive clinical decisions, including 
-          risk-reducing strategies, targeted surveillance, and family cascade testing.
-        </p>
+        <ul className="space-y-4">
+          {points.map((point, idx) => (
+            <li key={idx} className="flex items-start">
+              <span 
+                className="w-2 h-2 rounded-full mt-2 mr-3 flex-shrink-0"
+                style={{backgroundColor: '#faae31'}}
+              ></span>
               <p className="text-gray-600 leading-relaxed text-base text-justify">
-          Studies show that genetic testing in hereditary cancer cases improves outcomes and informs 
-          care for both patients and at-risk relatives.
+                <strong>{idx === 0 ? "About 5-10% of all cancers are linked to inherited genetic mutations" : ""}</strong>
+                {idx === 0 ? ", often going undetected until late stages or after multiple family members are affected." : point}
               </p>
+            </li>
+          ))}
+        </ul>
       </div>
 
       <h3 className="text-2xl font-semibold text-gray-700 mb-4">Key Features</h3>
@@ -45,7 +48,7 @@ export default function HereditaryCancerPanel() {
           </thead>
           <tbody>
             {features.map((feature, idx) => (
-              <tr key={idx} className="hover:bg-gray-50">
+              <tr key={idx} className="hover:bg-teal-50">
                 <td className="border border-gray-300 px-6 py-3 text-gray-700 font-medium">{feature.title}</td>
                 <td className="border border-gray-300 px-6 py-3 text-gray-600">{feature.desc}</td>
               </tr>

app/health/oncology/Components/OncologyIntro.jsx

@@ -1,31 +1,52 @@
 export default function OncologyIntro() {
   return (
-    <section className="mx-auto px-10 pt-12">
-      <h1 className="text-4xl font-bold text-gray-700 text-left pb-2 mb-4">Oncology</h1>
-      <h2 className="text-2xl font-semibold text-gray-700 mb-4">Turning Complexity into Clarity</h2>
-      <p className="text-gray-600 leading-relaxed text-base mb-4 text-justify">
+    <section className="py-0">
+      <div className="container-fluid">
+        <div className="bg-gradient-to-br from-teal-600 to-teal-700 text-white p-8 lg:p-8 flex items-center">
+          <div className="w-full">
+            <h2 className="text-3xl font-bold text-white mb-6 leading-tight">
+              Turning Complexity into Clarity
+            </h2>
+            <ul className="space-y-4">
+              <li className="flex items-start gap-3">
+                <div className="w-2 h-2 rounded-full mt-2 flex-shrink-0" style={{backgroundColor: '#faae31'}}></div>
+                <span className="leading-relaxed text-justify">
                   Cancer is not a single disease—it's a highly complex and dynamic group of disorders, 
                   often driven by a multitude of genomic alterations. Despite advancements in treatment, 
                   many patients still face uncertainty due to incomplete or delayed molecular diagnoses.
-      </p>
-      <p className="text-gray-600 leading-relaxed text-base mb-4 text-justify">
+                </span>
+              </li>
+              <li className="flex items-start gap-3">
+                <div className="w-2 h-2 rounded-full mt-2 flex-shrink-0" style={{backgroundColor: '#faae31'}}></div>
+                <span className="leading-relaxed text-justify">
                   At Operify Health, we recognize that behind every tumor is a unique genetic story waiting 
                   to be told. Our precision oncology solutions utilize high-throughput Next Generation 
                   Sequencing (NGS) to analyze both somatic and germline mutations—providing clinicians 
                   with actionable insights that inform targeted therapies, immunotherapy decisions, and 
                   hereditary cancer risk assessments.
-      </p>
-      <p className="text-gray-600 leading-relaxed text-base mb-4 text-justify">
+                </span>
+              </li>
+              <li className="flex items-start gap-3">
+                <div className="w-2 h-2 rounded-full mt-2 flex-shrink-0" style={{backgroundColor: '#faae31'}}></div>
+                <span className="leading-relaxed text-justify">
                   This genomic-driven approach is especially critical in advanced and treatment-resistant 
                   cancers, where conventional methods often fall short. Studies have shown that integrating 
                   broad-panel NGS into cancer care can impact clinical decision-making in up to 30% of cases, 
                   leading to more personalized and effective treatment strategies.
-      </p>
-      <p className="text-gray-600 leading-relaxed text-base text-justify">
+                </span>
+              </li>
+              <li className="flex items-start gap-3">
+                <div className="w-2 h-2 rounded-full mt-2 flex-shrink-0" style={{backgroundColor: '#faae31'}}></div>
+                <span className="leading-relaxed text-justify">
                   By combining cutting-edge sequencing, advanced bioinformatics, and curated clinical evidence, 
                   Operify Health empowers oncologists to move from uncertainty to precision—ensuring every cancer 
                   patient's care is as individualized as their diagnosis.
-      </p>
+                </span>
+              </li>
+            </ul>
+          </div>
+        </div>
+      </div>
     </section>
   );
 }

app/health/oncology/components/HereditaryCancerPanel.jsx

@@ -9,29 +9,32 @@ export default function HereditaryCancerPanel() {
     { title: "Genetic Counseling Support", desc: "Optional access to pre- and post-test counseling for patient education and informed decision-making." }
   ];
 
+  const points = [
+    "About 5-10% of all cancers are linked to inherited genetic mutations, often going undetected until late stages or after multiple family members are affected.",
+    "The Operify Hereditary Cancer Panel screens key high- and moderate-risk genes associated with hereditary cancer syndromes like HBOC, Lynch Syndrome (LS), Li Fraumeni Syndrome (LFS), Familial Adenomatous Polyposis (FAP), Cowden Syndrome (CS), Peutz-Jeghers Syndrome (PJS), Neurofibromatosis (NF) etc.",
+    "Early identification of germline mutations enables proactive clinical decisions, including risk-reducing strategies, targeted surveillance, and family cascade testing.",
+    "Studies show that genetic testing in hereditary cancer cases improves outcomes and informs care for both patients and at-risk relatives."
+  ];
+
   return (
-    <section className="mx-auto px-10 pt-12">
-      <h2 className="text-3xl font-bold text-gray-700 text-left pb-2 mb-4">Operify Hereditary Cancer Panel</h2>
+    <section className="mx-auto px-8 pt-8">
+      <h2 className="text-3xl font-bold text-teal-700 pb-2 mb-4">Operify Hereditary Cancer Panel</h2>
       
       <div className="mb-8">
-        <p className="text-gray-600 leading-relaxed text-base mb-4 text-justify">
-          <strong>About 5-10% of all cancers are linked to inherited genetic mutations</strong>, often going 
-          undetected until late stages or after multiple family members are affected.
-        </p>
-        <p className="text-gray-600 leading-relaxed text-base mb-4 text-justify">
-          The Operify Hereditary Cancer Panel screens key high- and moderate-risk genes associated 
-          with hereditary cancer syndromes like HBOC, Lynch Syndrome (LS), Li Fraumeni Syndrome (LFS), 
-          Familial Adenomatous Polyposis (FAP), Cowden Syndrome (CS), Peutz-Jeghers Syndrome (PJS), 
-          Neurofibromatosis (NF) etc.
-        </p>
-        <p className="text-gray-600 leading-relaxed text-base mb-4 text-justify">
-          Early identification of germline mutations enables proactive clinical decisions, including 
-          risk-reducing strategies, targeted surveillance, and family cascade testing.
-        </p>
+        <ul className="space-y-4">
+          {points.map((point, idx) => (
+            <li key={idx} className="flex items-start">
+              <span 
+                className="w-2 h-2 rounded-full mt-2 mr-3 flex-shrink-0"
+                style={{backgroundColor: '#faae31'}}
+              ></span>
               <p className="text-gray-600 leading-relaxed text-base text-justify">
-          Studies show that genetic testing in hereditary cancer cases improves outcomes and informs 
-          care for both patients and at-risk relatives.
+                <strong>{idx === 0 ? "About 5-10% of all cancers are linked to inherited genetic mutations" : ""}</strong>
+                {idx === 0 ? ", often going undetected until late stages or after multiple family members are affected." : point}
               </p>
+            </li>
+          ))}
+        </ul>
       </div>
 
       <h3 className="text-2xl font-semibold text-gray-700 mb-4">Key Features</h3>
@@ -45,7 +48,7 @@ export default function HereditaryCancerPanel() {
           </thead>
           <tbody>
             {features.map((feature, idx) => (
-              <tr key={idx} className="hover:bg-gray-50">
+              <tr key={idx} className="hover:bg-teal-50">
                 <td className="border border-gray-300 px-6 py-3 text-gray-700 font-medium">{feature.title}</td>
                 <td className="border border-gray-300 px-6 py-3 text-gray-600">{feature.desc}</td>
               </tr>

app/health/oncology/components/OncologyIntro.jsx

@@ -1,31 +1,52 @@
 export default function OncologyIntro() {
   return (
-    <section className="mx-auto px-10 pt-12">
-      <h1 className="text-4xl font-bold text-gray-700 text-left pb-2 mb-4">Oncology</h1>
-      <h2 className="text-2xl font-semibold text-gray-700 mb-4">Turning Complexity into Clarity</h2>
-      <p className="text-gray-600 leading-relaxed text-base mb-4 text-justify">
+    <section className="py-0">
+      <div className="container-fluid">
+        <div className="bg-gradient-to-br from-teal-600 to-teal-700 text-white p-8 lg:p-8 flex items-center">
+          <div className="w-full">
+            <h2 className="text-3xl font-bold text-white mb-6 leading-tight">
+              Turning Complexity into Clarity
+            </h2>
+            <ul className="space-y-4">
+              <li className="flex items-start gap-3">
+                <div className="w-2 h-2 rounded-full mt-2 flex-shrink-0" style={{backgroundColor: '#faae31'}}></div>
+                <span className="leading-relaxed text-justify">
                   Cancer is not a single disease—it's a highly complex and dynamic group of disorders, 
                   often driven by a multitude of genomic alterations. Despite advancements in treatment, 
                   many patients still face uncertainty due to incomplete or delayed molecular diagnoses.
-      </p>
-      <p className="text-gray-600 leading-relaxed text-base mb-4 text-justify">
+                </span>
+              </li>
+              <li className="flex items-start gap-3">
+                <div className="w-2 h-2 rounded-full mt-2 flex-shrink-0" style={{backgroundColor: '#faae31'}}></div>
+                <span className="leading-relaxed text-justify">
                   At Operify Health, we recognize that behind every tumor is a unique genetic story waiting 
                   to be told. Our precision oncology solutions utilize high-throughput Next Generation 
                   Sequencing (NGS) to analyze both somatic and germline mutations—providing clinicians 
                   with actionable insights that inform targeted therapies, immunotherapy decisions, and 
                   hereditary cancer risk assessments.
-      </p>
-      <p className="text-gray-600 leading-relaxed text-base mb-4 text-justify">
+                </span>
+              </li>
+              <li className="flex items-start gap-3">
+                <div className="w-2 h-2 rounded-full mt-2 flex-shrink-0" style={{backgroundColor: '#faae31'}}></div>
+                <span className="leading-relaxed text-justify">
                   This genomic-driven approach is especially critical in advanced and treatment-resistant 
                   cancers, where conventional methods often fall short. Studies have shown that integrating 
                   broad-panel NGS into cancer care can impact clinical decision-making in up to 30% of cases, 
                   leading to more personalized and effective treatment strategies.
-      </p>
-      <p className="text-gray-600 leading-relaxed text-base text-justify">
+                </span>
+              </li>
+              <li className="flex items-start gap-3">
+                <div className="w-2 h-2 rounded-full mt-2 flex-shrink-0" style={{backgroundColor: '#faae31'}}></div>
+                <span className="leading-relaxed text-justify">
                   By combining cutting-edge sequencing, advanced bioinformatics, and curated clinical evidence, 
                   Operify Health empowers oncologists to move from uncertainty to precision—ensuring every cancer 
                   patient's care is as individualized as their diagnosis.
-      </p>
+                </span>
+              </li>
+            </ul>
+          </div>
+        </div>
+      </div>
     </section>
   );
 }

app/health/rare-disorders/components/ClinicalAreasGrid.jsx

@@ -21,8 +21,8 @@ export default function ClinicalAreasGrid() {
   ];
 
   return (
-    <section className="mx-auto px-10 pt-12">
-      <h2 className="text-3xl font-bold text-gray-700 text-left pb-2 mb-4">Clinical Areas</h2>
+    <section className="mx-auto px-8 pt-8">
+      <h2 className="text-3xl font-bold text-teal-700 pb-2 mb-4">Clinical Areas</h2>
       <div className="grid sm:grid-cols-2 md:grid-cols-3 lg:grid-cols-4 gap-4">
         {areas.map((area, idx) => (
           <div

app/health/rare-disorders/components/OperifyExome.jsx

@@ -9,30 +9,34 @@ export default function OperifyExome() {
     { title: "Dynamic Reanalysis", desc: "Reanalysis as scientific knowledge evolves." }
   ];
 
+  const points = [
+    "Whole Exome Sequencing (WES) targets the protein-coding regions of the genome, where most disease-causing mutations are found.",
+    "With over 7,000 rare diseases identified—80% of which have a genetic basis—WES offers a powerful approach to uncover their causes.",
+    "Traditional diagnostic methods can be slow, costly, and inconclusive; WES streamlines the process by delivering broad genetic insights in a single test.",
+    "Operify Exome enhances WES by combining comprehensive coverage with advanced interpretation, improving diagnostic yield and patient outcomes."
+  ];
+
   return (
-    <section className="mx-auto px-10 pt-12">
-      <h2 className="text-3xl font-bold text-gray-700 text-left pb-2 mb-4">Operify Exome</h2>
+    <section className="mx-auto px-8 pt-8">
+      <h2 className="text-3xl font-bold text-teal-700 pb-2 mb-4">Operify Exome</h2>
       
       <div className="mb-8">
-        <p className="text-gray-600 leading-relaxed text-base mb-4 text-justify">
-          Whole Exome Sequencing (WES) targets the protein-coding regions of the genome, where most
-          disease-causing mutations are found.
-        </p>
-        <p className="text-gray-600 leading-relaxed text-base mb-4 text-justify">
-          With over 7,000 rare diseases identified—80% of which have a genetic basis—WES offers a 
-          powerful approach to uncover their causes.
-        </p>
-        <p className="text-gray-600 leading-relaxed text-base mb-4 text-justify">
-          Traditional diagnostic methods can be slow, costly, and inconclusive; WES streamlines the 
-          process by delivering broad genetic insights in a single test.
-        </p>
+        <ul className="space-y-4">
+          {points.map((point, idx) => (
+            <li key={idx} className="flex items-start">
+              <span 
+                className="w-2 h-2 rounded-full mt-2 mr-3 flex-shrink-0"
+                style={{backgroundColor: '#faae31'}}
+              ></span>
               <p className="text-gray-600 leading-relaxed text-base text-justify">
-          Operify Exome enhances WES by combining comprehensive coverage with advanced interpretation, 
-          improving diagnostic yield and patient outcomes.
+                {point}
               </p>
+            </li>
+          ))}
+        </ul>
       </div>
 
-      <h3 className="text-2xl font-semibold text-gray-700 mb-4">Key Features</h3>
+      <h3 className="text-2xl font-semibold text-teal-700 mb-4">Key Features</h3>
       <div className="overflow-x-auto">
         <table className="w-full border-collapse border border-gray-300 rounded-lg">
           <thead>

app/health/rare-disorders/components/OperifyExomeMito.jsx

@@ -14,52 +14,48 @@ export default function OperifyExomeMito() {
     { genome: "Mitochondrial genome", coverage: "37 genes" }
   ];
 
+  const points = [
+    "The Operify ExomeMito Panel offers a unified solution by integrating whole exome sequencing with complete mitochondrial genome analysis—addressing both nuclear and mitochondrial causes of disease.",
+    "This combined approach is especially valuable in diagnosing complex, multisystemic, and rare disorders, where variants may exist across both genomes.",
+    "Mitochondrial disorders, though individually rare, are clinically significant, affecting approximately 1 in 5,000 individuals and often missed in standard testing.",
+    "Studies show that adding mitochondrial sequencing to exome testing increases diagnostic yield by up to 20%, offering greater clarity and clinical confidence. (PMID: 30369941)",
+    "While screening for rare genetic disorders, it's essential not to overlook the rarest among them-mitochondrial disorders, which occur in approximately 1 in 5,000 individuals. Although individually rare, their cumulative impact is significant in the context of rare disease diagnostics. Multiple studies have demonstrated a substantial increase in diagnostic yield—up to 20%—when mitochondrial genome sequencing is performed alongside whole exome sequencing. Reference: PMID: 30369941"
+  ];
+
   return (
-    <section className="mx-auto px-10 pt-12">
-      <h2 className="text-3xl font-bold text-gray-700 text-left pb-2 mb-4">Operify ExomeMito</h2>
+    <section className="mx-auto px-8">
+      <h2 className="text-3xl font-bold text-teal-700 pb-2 mb-4">Operify ExomeMito</h2>
       <h3 className="text-xl font-semibold text-gray-700 mb-4">Boost diagnostic yield with Exome + Mito Sequencing</h3>
       
-      <div className="mb-8">
-        <p className="text-gray-600 leading-relaxed text-base mb-4 text-justify">
-          The Operify ExomeMito Panel offers a unified solution by integrating whole exome sequencing 
-          with complete mitochondrial genome analysis—addressing both nuclear and mitochondrial causes 
-          of disease.
-        </p>
-        <p className="text-gray-600 leading-relaxed text-base mb-4 text-justify">
-          This combined approach is especially valuable in diagnosing complex, multisystemic, and rare 
-          disorders, where variants may exist across both genomes.
-        </p>
-        <p className="text-gray-600 leading-relaxed text-base mb-4 text-justify">
-          Mitochondrial disorders, though individually rare, are clinically significant, affecting 
-          approximately 1 in 5,000 individuals and often missed in standard testing.
-        </p>
-        <p className="text-gray-600 leading-relaxed text-base mb-4 text-justify">
-          Studies show that adding mitochondrial sequencing to exome testing increases diagnostic 
-          yield by up to 20%, offering greater clarity and clinical confidence. <em>(PMID: 30369941)</em>
-        </p>
+      <div className="mb-6">
+        <ul className="space-y-4">
+          {points.map((point, idx) => (
+            <li key={idx} className="flex items-start">
+              <span 
+                className="w-2 h-2 rounded-full mt-2 mr-3 flex-shrink-0"
+                style={{backgroundColor: '#faae31'}}
+              ></span>
               <p className="text-gray-600 leading-relaxed text-base text-justify">
-          While screening for rare genetic disorders, it's essential not to overlook the rarest among 
-          them-mitochondrial disorders, which occur in approximately 1 in 5,000 individuals. Although 
-          individually rare, their cumulative impact is significant in the context of rare disease 
-          diagnostics. Multiple studies have demonstrated a substantial increase in diagnostic yield—up 
-          to 20%—when mitochondrial genome sequencing is performed alongside whole exome sequencing. 
-          <em>Reference: PMID: 30369941</em>
+                {point}
               </p>
+            </li>
+          ))}
+        </ul>
       </div>
 
       <div className="mb-8">
-        <h3 className="text-2xl font-semibold text-gray-700 mb-4">Genome Coverage</h3>
+        <h3 className="text-2xl font-semibold text-teal-700 mb-4">Genome Coverage</h3>
         <div className="overflow-x-auto">
           <table className="w-full border-collapse border border-gray-300 rounded-lg">
             <thead>
-              <tr className="bg-gray-50">
-                <th className="border border-gray-300 px-6 py-3 text-left text-gray-700 font-semibold">Genome</th>
-                <th className="border border-gray-300 px-6 py-3 text-left text-gray-700 font-semibold">Coverage</th>
+              <tr className="bg-teal-50">
+                <th className="border border-gray-300 px-3 py-2 text-left font-semibold text-teal-700">Genome</th>
+                <th className="border border-gray-300 px-3 py-2 text-left font-semibold text-teal-700">Coverage</th>
               </tr>
             </thead>
             <tbody>
               {genomeCoverage.map((item, idx) => (
-                <tr key={idx} className="hover:bg-gray-50">
+                <tr key={idx} className="hover:bg-teal-50">
                   <td className="border border-gray-300 px-6 py-3 text-gray-700 font-medium">{item.genome}</td>
                   <td className="border border-gray-300 px-6 py-3 text-gray-600">{item.coverage}</td>
                 </tr>
@@ -69,18 +65,18 @@ export default function OperifyExomeMito() {
         </div>
       </div>
 
-      <h3 className="text-2xl font-semibold text-gray-700 mb-4">Key Features</h3>
+      <h3 className="text-2xl font-semibold text-teal-700 mb-4">Key Features</h3>
       <div className="overflow-x-auto">
         <table className="w-full border-collapse border border-gray-300 rounded-lg">
           <thead>
-            <tr className="bg-gray-50">
-              <th className="border border-gray-300 px-6 py-3 text-left text-gray-700 font-semibold">Feature</th>
-              <th className="border border-gray-300 px-6 py-3 text-left text-gray-700 font-semibold">Description</th>
+            <tr className="bg-teal-50">
+              <th className="border border-gray-300 px-3 py-2 text-left font-semibold text-teal-700">Feature</th>
+              <th className="border border-gray-300 px-3 py-2 text-left font-semibold text-teal-700">Description</th>
             </tr>
           </thead>
           <tbody>
             {features.map((feature, idx) => (
-              <tr key={idx} className="hover:bg-gray-50">
+              <tr key={idx} className="hover:bg-teal-50">
                 <td className="border border-gray-300 px-6 py-3 text-gray-700 font-medium">{feature.title}</td>
                 <td className="border border-gray-300 px-6 py-3 text-gray-600">{feature.desc}</td>
               </tr>

app/health/rare-disorders/components/RareIntro.jsx

@@ -1,18 +1,33 @@
 export default function RareIntro() {
   return (
-    <section className="mx-auto px-10 pt-12">
-      <h1 className="text-4xl font-bold text-gray-700 text-left pb-2 mb-4">Rare Disorders</h1>
-      <h2 className="text-2xl font-semibold text-gray-700 mb-4">Transforming Delays into Diagnoses</h2>
-      <p className="text-gray-600 leading-relaxed text-base mb-4 text-justify">
+    <section className="py-0">
+      <div className="container-fluid">
+        <div className="bg-gradient-to-br from-teal-600 to-teal-700 text-white p-8 lg:p-8 flex items-center">
+          <div className="w-full">
+            <h2 className="text-3xl font-bold text-white mb-6 leading-tight">
+              Transforming Delays into Diagnoses
+            </h2>
+            <ul className="space-y-4">
+              <li className="flex items-start gap-3">
+                <div className="w-2 h-2 rounded-full mt-2 flex-shrink-0" style={{backgroundColor: '#faae31'}}></div>
+                <span className="leading-relaxed text-justify">
                   There are over 7,000 identified rare diseases, many of which begin in childhood—and
                   nearly 80% have a genetic cause. Yet, the average time to diagnose a rare disorder is
                   still 4.8 years, with some cases taking up to 20 years.
-      </p>
-      <p className="text-gray-600 leading-relaxed text-base text-justify">
+                </span>
+              </li>
+              <li className="flex items-start gap-3">
+                <div className="w-2 h-2 rounded-full mt-2 flex-shrink-0" style={{backgroundColor: '#faae31'}}></div>
+                <span className="leading-relaxed text-justify">
                   At Operify Health, we leverage advanced Next Generation Sequencing (NGS) and proprietary
                   bioinformatics to deliver rapid, reliable insights—helping reduce the diagnostic journey
                   from years to days.
-      </p>
+                </span>
+              </li>
+            </ul>
+          </div>
+        </div>
+      </div>
     </section>
   );
 }

app/health/rare-disorders/components/SampleRequirements.jsx

@@ -1,36 +1,49 @@
+import Image from "next/image";
+
 export default function SampleRequirements({ title, items }) {
+  const requirements = [
+    {
+      icon: "/images/icons/clock.png", // Replace with your actual icon path
+      title: "Turnaround Time",
+      description: "21 Days"
+    },
+    {
+      icon: "/images/icons/sample.png", // Replace with your actual icon path
+      title: "Sample Requirement", 
+      description: "Blood/Saliva/Cheek Swab/Genomic DNA/Dry Blood Spot"
+    }
+  ];
+
   return (
-    <section className="mx-auto px-10 pt-8 pb-12">
-      <div className="bg-gray-50 rounded-lg p-6">
-        <h3 className="text-2xl font-semibold text-gray-700 mb-6">{title} Sample Requirements</h3>
+    <section className="mx-auto px-8 pt-8 pb-12">
+      <h3 className="text-3xl font-bold text-teal-700 mb-6">{title} Sample Requirements</h3>
       
-        <div className="grid md:grid-cols-2 gap-6">
-          {/* Turnaround Time */}
+      <div className="grid grid-cols-1 sm:grid-cols-2 gap-6 max-w-5xl mx-auto">
+        {requirements.map((req, idx) => (
+          <div 
+            key={idx}
+            className="rounded-lg p-6 hover:shadow-sm transition-shadow cursor-pointer" 
+            style={{backgroundColor: '#f2fcfc'}}
+          >
             <div className="flex items-start gap-4">
-            <div className="flex-shrink-0 w-10 h-10 bg-teal-100 rounded-full flex items-center justify-center">
-              <svg className="w-5 h-5 text-teal-600" fill="none" stroke="currentColor" viewBox="0 0 24 24">
-                <path strokeLinecap="round" strokeLinejoin="round" strokeWidth={2} d="M12 8v4l3 3m6-3a9 9 0 11-18 0 9 9 0 0118 0z" />
-              </svg>
+              <div className="flex-shrink-0 mt-1">
+                <Image
+                  src={req.icon}
+                  alt={req.title}
+                  width={40}
+                  height={40}
+                  className="object-contain"
+                />
               </div>
-            <div>
-              <h4 className="text-lg font-semibold text-teal-600 mb-1">Turnaround Time</h4>
-              <p className="text-gray-600 leading-relaxed text-base">21 Days</p>
-            </div>
-          </div>
-
-          {/* Sample Requirement */}
-          <div className="flex items-start gap-4">
-            <div className="flex-shrink-0 w-10 h-10 bg-teal-100 rounded-full flex items-center justify-center">
-              <svg className="w-5 h-5 text-teal-600" fill="none" stroke="currentColor" viewBox="0 0 24 24">
-                <path strokeLinecap="round" strokeLinejoin="round" strokeWidth={2} d="M19.428 15.428a2 2 0 00-1.022-.547l-2.387-.477a6 6 0 00-3.86.517l-.318.158a6 6 0 01-3.86.517L6.05 15.21a2 2 0 00-1.806.547M8 4h8l-1 1v5.172a2 2 0 00.586 1.414l5 5c1.26 1.26.367 3.414-1.415 3.414H4.828c-1.782 0-2.674-2.154-1.414-3.414l5-5A2 2 0 009 10.172V5L8 4z" />
-              </svg>
-            </div>
-            <div>
-              <h4 className="text-lg font-semibold text-teal-600 mb-2">Sample Requirement</h4>
-              <p className="text-gray-600 leading-relaxed text-base">Blood/Saliva/Cheek Swab/Genomic DNA/Dry Blood Spot</p>
+              <div className="flex-1">
+                <h4 className="text-lg font-semibold text-gray-900 mb-2">{req.title}</h4>
+                <p className="text-gray-500 text-sm leading-relaxed">
+                  {req.description}
+                </p>
               </div>
             </div>
           </div>
+        ))}
       </div>
     </section>
   );

app/health/rare-disorders/components/SolutionsOffer.jsx

@@ -11,19 +11,30 @@ export default function SolutionsOffer() {
   ];
 
   return (
-    <section className="mx-auto px-10 pt-12">
-      <h2 className="text-2xl font-semibold text-gray-700 text-left pb-2 mb-4">Our Rare Disease Solutions Offer</h2>
-      <div className="grid sm:grid-cols-2 gap-6">
+    <div className="mx-auto px-8 py-6">
+      <h2 className="text-3xl font-bold text-teal-700 mb-4">Our Rare Disease Solutions Offer</h2>
+      
+      <p className="text-gray-600 leading-relaxed text-base mb-4 text-justify">
+        Comprehensive genomic sequencing solutions designed to unlock genetic insights 
+        and accelerate diagnosis for rare disease patients and their families.
+      </p>
+
+      <div className="grid grid-cols-1 sm:grid-cols-2 gap-6">
         {solutions.map((sol, idx) => (
           <div
             key={idx}
-            className="border rounded-lg p-6 hover:shadow-lg transition-shadow cursor-pointer"
+            className="rounded-lg p-6 hover:shadow-sm transition-shadow cursor-pointer"
+            style={{backgroundColor: '#f2fcfc'}}
           >
-            <h3 className="text-xl font-semibold text-gray-700 mb-2">{sol.name}</h3>
-            <p className="text-gray-600 leading-relaxed text-base">{sol.desc}</p>
+            <div className="flex items-start">
+              <div className="flex-1">
+                <h3 className="text-lg font-semibold text-gray-900 mb-2">{sol.name}</h3>
+                <p className="text-gray-500 text-sm leading-relaxed">{sol.desc}</p>
+              </div>
+            </div>
           </div>
         ))}
       </div>
-    </section>
+    </div>
   );
 }

app/health/rare-disorders/components/WESInfo.jsx

@@ -1,22 +1,28 @@
 export default function WESInfo() {
+  const points = [
+    "Whole Exome Sequencing (WES) is recommended for individuals with unexplained genetic disorders, complex or atypical clinical presentations, or when prior genetic tests have been inconclusive.",
+    "It is especially valuable in diagnosing rare inherited diseases, uncovering the cause of developmental delays, intellectual disabilities, or early-onset neurological conditions, and providing insights for personalized treatment planning.",
+    "WES can help identify genetic causes in a wide range of rare disorders."
+  ];
+
   return (
-    <section className="mx-auto px-10 pt-12">
-      <h2 className="text-2xl font-semibold text-gray-700 text-left pb-2 mb-4">
+    <section className="mx-auto px-8 pt-4">
+      <h2 className="text-3xl font-bold text-teal-700 pb-2 mb-4">
         Who Should Consider Whole Exome Sequencing (WES)?
       </h2>
-      <p className="text-gray-600 leading-relaxed text-base mb-4 text-justify">
-        Whole Exome Sequencing (WES) is recommended for individuals with unexplained genetic
-        disorders, complex or atypical clinical presentations, or when prior genetic tests
-        have been inconclusive.
-      </p>
-      <p className="text-gray-600 leading-relaxed text-base mb-4 text-justify">
-        It is especially valuable in diagnosing rare inherited diseases, uncovering the cause
-        of developmental delays, intellectual disabilities, or early-onset neurological
-        conditions, and providing insights for personalized treatment planning.
-      </p>
+      <ul className="space-y-4">
+        {points.map((point, idx) => (
+          <li key={idx} className="flex items-start">
+            <span 
+              className="w-2 h-2 rounded-full mt-2 mr-3 flex-shrink-0"
+              style={{backgroundColor: '#faae31'}}
+            ></span>
             <p className="text-gray-600 leading-relaxed text-base text-justify">
-        WES can help identify genetic causes in a wide range of rare disorders.
+              {point}
             </p>
+          </li>
+        ))}
+      </ul>
     </section>
   );
 }

app/rna-sequencing/components/AboutRNA.jsx

@@ -4,8 +4,8 @@ import React from 'react';
 const AboutRNA = () => {
   return (
     <section className="pt-6 bg-white">
-      <div className="container mx-auto px-6">
-        <h2 className="text-4xl font-bold text-gray-700 text-left pb-2">
+      <div className="container max-w-none px-6">
+        <h2 className="text-4xl font-bold text-teal-700 mb-4">
           About RNA Sequencing
         </h2>
         <h2 className="text-lg font-semibold text-gray-600 mb-4">
@@ -16,9 +16,6 @@ const AboutRNA = () => {
           <p className="text-gray-600 leading-relaxed text-base mb-4">
             RNA sequencing (RNA-Seq) is a method used to determine the sequence and quantity of RNA present in a sample, providing insight into gene expression, alternative splicing, and non-coding RNA functions. It is essential for understanding various biological processes, including disease mechanisms, gene regulation, and cellular responses.
           </p>
-          <p className="text-gray-600 leading-relaxed text-base">
-            Different RNA sequencing approaches using Next-Generation Sequencing (NGS) are listed below:
-          </p>
         </div>
       </div>
     </section>

app/rna-sequencing/components/RNATable.jsx

@@ -106,7 +106,7 @@ const RNATable = () => {
 
   return (
     <section className="pt-6 bg-white">
-      <div className="container mx-auto px-6">
+      <div className="container max-w-none px-6">
         <h3 className="text-2xl font-semibold text-gray-700 mb-6">RNA Sequencing Approaches</h3>
         <div className="overflow-x-auto mb-8">
           <table className="w-full border-collapse border border-gray-300 text-sm bg-white shadow-sm">
@@ -130,7 +130,7 @@ const RNATable = () => {
               {sequencingData.map((row, index) => (
                 <tr key={index} className={`${index % 2 === 1 ? 'bg-gray-50' : 'bg-white'} hover:bg-teal-25 transition-colors`}>
                   <td className="border border-gray-300 px-4 py-3 align-top">
-                    <a href={row.approach.link} className="text-teal-600 hover:underline font-medium text-base">
+                    <a href={row.approach.link} className="text-gray-600 hover:underline font-medium text-base">
                       {row.approach.name}
                     </a>
                   </td>